ML20069B843
| ML20069B843 | |
| Person / Time | |
|---|---|
| Issue date: | 05/31/1994 |
| From: | Borges T, Carter D, Lu P, Stafford R Office of Nuclear Reactor Regulation, OAK RIDGE NATIONAL LABORATORY |
| To: | NRC OFFICE OF NUCLEAR REGULATORY RESEARCH (RES) |
| References | |
| CON-FIN-L-2416 NUREG-CR-6204, ORNL-TM-12690, NUDOCS 9405310172 | |
| Download: ML20069B843 (111) | |
Text
NUREG/CR-6204 ORNL/TM-12690 Questions anc Answers Basec.
on Revisec.10 CFR Part 20 1
Prepared by
'l: Horges, R. S. Stafford P. Y. Lu/ORNL D. Carter /NRC Oak Ridge National Laboratory Prepared for U.S. Nuclear Regulatory Commission l
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i AVAILABluTY NOTICE I
Availab&ty of Reference Matends Cated in NRC Publications f
Most documents cited in NRC publications will be available from one of the following sources:
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The NRC Public Docurnent Room. 2120 L Street, NW,, Lower Level, Washington, DC 20555-0001 2.
The Superintendent of Documents. U.S. Government Printing Office, Mall'Stop SSOP, Washington, DC j
20402-9328 3.
The National Technical information Service, Springfield, VA 22161 Although the listing that follows represents the majority of documents cited in NRC publications, it is not in-tended to be exhaustive.
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Referenced documents available for inspection and copying for a fee from the NRC Public Document Room
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Include NRC correspondence and internal NRC memoranda: NRC bulletins, circulars, information notices, in-spection and investigation notices; licensee event reports; vendor reports and correspondence; Commission
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papers; and applicant and licensee documents and correspondence.
The following documents in the NUREG ser6es are available for purchase from the GPO Sales Program: formal NRC staff and contractor reports. NRC-sponsored conf erence proceedings, international agreement reports, grant publications, and NRC booklets e id brochures. Also available are regulatory guides NRC regulations in the Code of Federal Regulations, an Nuclear Regulatory Commission Issuances.
Documents ava!!able from the National Technicat inf orma' ion Service include NUREG-series reports and tech-nical reports prepared by other Federal agencies and reports prepaced by the Atomic Energy Commission, forerunner agency to the Nuclear Regulatory Commission.
Documents available from public and special technicallibrarios include all open literature items, such as books, journal articles, and transactions. Federal Register notices Federal and State legislation, and congressional reports can usually be obtained from these libraries.
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Documents such as theses, dissertations, foreign reports and translations, and non-NRC conference pro-l ceedings are available for purchase from the organization sponsoring the publication cited.
t Singie copies of NAC draf t reports are available f ree, to the extent of supply. upon written request to the Office of Administration, Distribution and Mall Services Section, U.S. Nuclear Regulatory Commission Washington.
DC 20555-0001.
l Copies of industry codes and standards used in a substantive manner in the NRC regulatory process are main-l tained at the NRC Library,7920 Norfolk Avenue, Bethesda. Maryland, for use by the public. Codes and stan-dards are usually copynghted and may be purchased from the originating organization or, if they are American i
National Standards, from the American National Standards institute,1430 Broadway, New York, NY 10018.
DISCLAIMER NOTICE This report was prepared as an account of work spaed by an agency of the United States Government.
Neither the United States Government nor any agency thereof, or any of their employees, makes any warranty, expressed or implied, or assumes any legal liability of responsibility for any third party's use, or the results of such use, of any information, apparatus, product or process disclosed in tnis report, or represents that its use by such third party would not infringe privately owned rights.
NUREG/CR--6204 ORNUTM-12690 Questions and Answers Based on Revised 10 CFR Part 20 l
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Manuscript Completed: April 1994 Date Published: May 1994 Prepared by T. Borges, R. S. Stafford, P. Y. Lu, Oak Ridge National Laboratory D. Carter, U.S. Nuclear Regulatory Commission Oak Ridge National Laboratory Operated by Martin Marietta Energy Systems, Inc.
Oak Ridge National Laboratory Oak Ridge, TN 37831-6050 Prepared for Division of Regulatory Applications Office of Nuclear Regulatory Research U.S. Nuclear Regulatory Commission Washington, DC 20555-0001 NRC FIN L2416 Under Contract No. DE-AC05-840R21400
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ABSTRACT NUREO/CR4204 is a collection of questions and answers that were originally issued in seven sets ami which pertain to
-l revised 10 CFR Part 20. W questions came from both outside and wittun the NRC. W answers were compiled and provided by NRC staff withm the offices of Nuclear Reactor Regulation, Nuclear Material Safety and Safeguants, Nuclear.
Regulatory Research, the Office of State Programs, and the five regional offices. Although all of the questions and answers have been reviewed by attorneys in the NRC Office of the General Counsel, they do not constitute official legal interpretations relevant to revised 10 CFR Part 20. h questions and answere do, however, reflect NRC staff decisions and technical opunons on aspects of the revised 10 CFR Part 20 regulatory requirements. This NUREO is being made available to encourage communication among the public, industry,'ami NRC staff cawernmg the major revisions of the NRC's starvlards for protection against taliation.
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TABLE OF CONTENTS Abstract....................................................iii Forewo rd................................................... vii
- 1. Introduction
................................................ I
- 2. Questions and Answers 3
2.1 Subpart A - General Provisions....................................3 j
10 CFR 20.1001 - Purpose....................................... 3 10 CFR 20.1002 - Scope.......................................
3 10 CFR 20.1003 - Definitions
....................................3 i
10 CFR 20.1004 - Units of Radiation Dose............................... 11 10 CFR 20.1008 - Implementation................................... 11 2.2 Subpart B - Radiation Protection Programs...............................12 10 CFR 20.1101 - Radiation Protection Programs............................ 12 2.3 Subpart C - Occupational Dose Limits.................................14 10 CFR 20.1201 -Occupational Dose Limits for Adults.......................... 14 10 CFR 20.1202 - Compliance with the Requirements for Summation of External and Internal Doses...... 19 10 CFR 20.1203 - Determination of External Dose from Airborne Radioactive Material........... 20 l
10 CFR 20.1204 - Determination of Internal Exposure.......................... 20 10 CFR 20.1206 - Planned Special Exposures.............................. 22 10 CFR 20.1208 - Dose to an Emb:yo/ Fetus............................... 24 2.4 Subpart D - Radiation Dose Limits for Individual Members of the Public.................. 26 10 CFR 20.1301 - Dose Limits for Individual Members of the Public.................... 26 10 CFR 2.0.1302 - Compliance with Dose Limits for Individual Members of the Public............ 29 2.5 Subpart F - Surveys and Monitoring.................................. 32 10 CFR 20.1501 - Surveys and Monitoring-General........................... 32 10 CFR 20.1502 - Conditions Requiring Individual Monitoring of Internal and External Occupational Dose.....................................
.... 32 2.6 Subpart G - Control of Exposure from External Sources in Restricted Areas................. 38 10 CFR 20.1601 - Control of Access to High Radiation Areas....................... 38 10 CFR 20.1602 -Control of Access to Very High Radiation Areas.................... 40 10 CFR 20.1603 - Control of Access to Very High Radiation Areas-Irradiators............... 41 2.7 Subpart H - Respiratory Protection and Controls to Restrict Internal Exposure in Restricted Arean.....................................42 10 CFR 20.1701 - Use of Process or Other Engineering Controls.....................42 10 CFR 20.1702 - Use of Other Controls................................ 42 10 CFR 20.1703 - Use of hxlividual Respiratory Protection Equipment................... 44 2.8 Subpart I - Storage and Control of Licensed Material........................... 46 10 CFR 20.1801 - Security of Stored Material.............................. 46 2.9 Subpart J - Precautionary Procedures.................................. 47 10 CFR 20.1902 - Posting Requirements................................ 47 10 CFR 20.1903 - Exceptious to Posting Requirements.......................... 49 10 CFR 20.1904 - Labeling Containers.....................
...........50 10 CFR 20.1906 - Procedures for Receiving and Opening Packages.................... 50 2.10 Subpart K - Waste Disposal...................................... 52 10 CFR 20.2001 - Waste Disposal - General............................... 52 10 CFR 20.2003 - Disposal by Release into Sanitary Sewerage......................53 v
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Table of Contents 2.11 Subpart L - Records.........................................54 10 CFR 20.2101 - Records, General Provisions............................. 54 1
10 CFR 20.2104 - Deternunation of Prior Occupational Dose....................... 54 10 CFR 20.2105 Records of Planned Special Exposures
........................57 5
10 CFR 20.2106 - Records of Individual Monitoring Results........................57 10 CFR 20.2107 - Records of Dose to Individual Members of the Public.................. 59 10 CFR 20.2110 - Form of Records.................................. 60 -
2.12 Subpart M - Reports......................................... 60 10 CFR 20.2202 - Notification of lacidents............................... 60 l
10 CFR 20.2203 - Reports of Exposures, Radiation levels, Etc....................... 60 10 CFR 20.2206 - Reports of Individual Monitoring........................... 60 2.13 10 CFR 20 Appendices......................................... C2 10 CFR Part 20 Appendix A...................................... 62 10 CFR Part 20 Appendix B.....................................63 l
2.14 10 CFR 19 - Notices, Instructions, and Reports to Workers: Inspection and Investigations.......... 65 -
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10 CFR 19.12 - Instructions to Workers................................. 65 10 CFR 19.13 - Notification and Reports to Individuals.......................... 66 l
2.15 10 CFR 50 - Domestic Licensing of Production and Utilization Facilities.................. 68 10 CFR Part 50........................................... 68 1
2.16 Regulatory Guides.......................................... 69 Regulatory Guides - General....................................... 69 Regulatory Guide 1.109.,...................................... 69 Regulatory Guide 8.25........................................ 69 Regulatory Guide 8.36........................................ 69 Regulatory Guide 8.7, Rev. 1..................................... 70 2.17 Technical Specifications........................................ 70 I
Reactor Technical Specifications.................................... 70 Power Reactor Technical Specifications and Materials Licenses...................... 71.
2.18 Other Questions............................................ 72 Appendix A - Numerical List of Questions and Answers.............................75 Appendix B Regulatory References Cited in Text................................ 89 Appendix C - Questions and Answers by Regulatory Reference.......................... 93 1
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NUREO/CR-6204 vi I
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FOREWORD This report contains questions and answers concerning the major revision of 10 CFR Part 20 (10 CFR Part 20 Sections 20.1001 y 20.2402) and its implementation. The questions and answers in this report have been available to the public previously as seven separate consecutive sets of questions and answers in the NRC Public Document Room; however, this report makes all of the questions and answers from the seven separate documents available in a single, more convenient, form.' (The NRC staff expects to prepare, and make publicly available, additional questions and answers on this subject as questions arise during the implemeni tation of the revised 10 CFR Part 20.)
These questions and answers were compiled by the NRC headquarters radiation protection staff pnmarily for use in training NRC regional inspection staffmembers. As each set of question and answers was completed, it was made publicly available for -
information ofinterested individuals and orgamzations and to encourage communications between the public and the NRC staff concermng this major revision of the NRC's standards for pmtection against radiation.
The questions were provided by individuals and organizations outside the NRC 'and by NRC staffmembers. Answers to these.
questions have been prepared and reviewed by NRC staff members in the NRC Offices of Nuclear Reactor Regulation (NRR), -
Nuclear Material Safety and Safeguards (NMSS), Nuclear Regulatory Research (RES), Office of State Pmgrams (OSP), and the
. five NRC Regional Offices. The questions and answers also have been reviewed by attorneys in the NRC Office of the General Counsel.
The questions and answesi in this report are NRC staff positions on NRC regulatory requirements and guidance for radiation protection (health physics). Therefore, these questions and answers are " health physics positions". as this term is defined in NRC report number NUREG/CR 5569 Rev.1 Health Physics Positions Database, February 1994. Because all of the questions in this report concern the new revision of 10 CFR Part 20 and related requirements, they have been compiled as a separate data base rather than combining them with other health physics positions in a single data base. Consideration will be given in the future to consolidating the two da's bases. Users of these data bases are invited to comment on the desirability of this potential consolidation.
On February 3,1994, the NRC published a notice of proposed rulemaking (59 FR 5132) that would amend 10 CFR Parts 19 and
- 20. This proposed rule would: (1) delete the definition of" controlled area" to make it clear that any area to which access is restricted for the purpose of radiological protection is a " restricted area" as dermed in the regulation, (2) revise tle dermition of
" occupational dose" to delete reference to the " restricted area," (3) revise the definition of" unrestricted area" to be consistent with the deletion of the controlled area, (4) revise the provision entitled " Instructions to Workers," so that radiation protection training will be provided to all persons with the potential to be occupationally exposed and (5) restore a provision to Part 20 that whenever licensees are required to report exposures ofindividual members of tlw public to the NRC, then those individuals are to receive copies of the report These proposed =_m-Imants, ifissued in final form, would result in changes to the following (and possibly other) questions and answers:
Section Question Numbers Section Question Numbers 10 CFR 19.12
- 95,#411,#422 10 CFR 20.I301
- 106,#203,#206,#384 10 CFR 20.1003
- 25,#26,#66,#67,#80,#94, 10 CFR 20.1302
- 28,#29,#104,#417
- 119,#148,#412,#413 10 CFR 20.1502
- 82,#126,#213,#429,#444 10 CFR 20.1201
- 31,#33,#34,#77 10 CFR 20.1801
- 129,#419,#450 10 CFR 20.1206
- 136 10 CFR 20.1902
- 27,#53 10 CFR 20.1208
- 442 10 CFR 20.2107
- 391 vii NUREG/CR-6204
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- l Foreword
~1 The answers to questions in this report do not constitute official legal interpretations, which can only be provided by the General Counsel, and they do not reflect official NRC policy as approved by the Commission. The answers do reflect NitC staff decisions and technical opinions on specific aspects of regulatory requirements.
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LeMoine J. Cunningham,'C f,
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Radiation Protection Branch.
Division of Radiation Safety and Safeguards -
Office of Nuclear Reactor Regulation l
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- 1. INTRODUCTION This report contains questions asked by individuais outside numerical listing of the questions and answers, the question the NRC concerning the implementation, relevance, and and answer set in which it was issued, and the most relevant applicability of the revised 10 CFR Pan 20. Other ques-section under which it appeared are given. Appendix B of tions and answers in this report were developed by the NRC this report contains a listing of the of the regulatory refer-to further explain the revised regulations. b answers to ences cited in this report. 'Ibese include 10 CFR Part 19, the questions have been provided by NRC staff members revised 10 CFR Part 20,10 CFR Part 34,10 CFR Part 50, within the offices of Nuclear Reactor Regulation, Nuclear NUREO documents, Regulatory Guides, and others. In Material Safety and Safeguards, Nuclear Regulatory Re-Appendix C of the report, all questions and answers that search, Office of State Programs, and the five regional pertain to a particular regulatory reference are listed.
offices.
Each question and answer appears under the section of the This report is the unedited contents of the original seven revised 10 CFR Part 20 to which it is most closely related.
question and answers sets. These were placed in the NRC The sections of revised 10 CFR Part 20 are in urn arrang-a Public Document Room identified by their dates of issuance ed in order of their appearance in the revised coCe of federal and NRC accession numbers as shown below. The acces-regulations. Following the 10 CFR Part 20 sections are sion numbers are used by NRC staff to retrieve the original questions and answers relating to 10 CFR Part 19,10 CFR documents from the NUDOCS system and by members of Part 50, regulatory guides, technical specifications, arx!
the public to obtain copies from the NRC Public Document other topics. Unless otherwise indicated, references to the Room.
Federal Register refer to a page number in the May 21, 1991 edition. This edition contained the major revisign of Set Date Inued PDR Number 10 CFR Part 20 as a final rule on pages 23360-23474., b questions and answers in this compilation include cor-First 12/06/91 PDR-9112190258 rections that were issued with question and answer sets 2-7, Second 04/17/92 PDR-9205010117 inclusive, and other corrections of typogralaical errors.
Third 07/23/92 PDR-9207300261 Fourth 09/14/92 PDR-9209230012 With issuance by the U. S. Department of Energy (DO E) of Fifth 06/08/93 PDR-9306110303 the U.S. DOE Radiological Control Manual (DOE /EH-Sixth 09/28/93 PDR 9310070005 0256T) in June 1992, the committed effective dose equive Seven 10/29/93 PDR-9311050284 lent (rather than the " annual effective dose equivalent") is used by DOE to assign internal dose received by personnel The NRC public document room can be contacted for copies at DOE facilities. This information updates the information of the individual question and answer sets at the following previously provided in the answer to Questiom 76 and 83 address and phone number:
(under 10 CFR 20.1204) and to Question 113 (under 10 CFR 20.2104).
Write: U.S. Nuclear Regulatory Commission Public Document Room 10 CFR 20.1603, " Control of Access to Very High 2120 L Street, N.W.
Radiation Areas -Irradiators," which is the subject of Room LL4 question 130, was deleted from Part 20 effective 7/1/93.
Washington, DC 20013-7082 Telephone: (202) 634-3273 FAX: (202) 634-3343 Each question included in this report was assigned a unique number for identification purposes, but not necessarily in raunerical order. It must be noted, however, that the numbers were not all inclusive. Many of the question numbers, particularly those in the range 151 - 370, were not used, whereas others were deleted prior to the release of the question and answer sets. In Apperulix A of this report, a 1
NUREO/CR-6204
- 2. QUESTIONS AND ANSWERS 2.1 SUBPART A - GENERAI, c*ml of raium tint nmy 14 incidwal to NRC-licensed operations is evaluated by NRC as required by NEPA.
PROVISIONS Reiemm of,adium f,om.,;te, otse, than from NRC-bcensed material (ores or tailings), may be required to meet 10 CFR 20.1001 - Purpose State release H=h=. Also, an NRC heensee may be requir- -
ed to get a State license for the radium in naturally occur-ring radioactive material (NORM) if the State requires a lic-Questlom 407: (a) Does Part 20 apply to emergency ense for the use and possession of this material. (Referen-ces: 10 CFR 20.1001,10 CFR 20.1002,10 CFR 20.1003) t rasponse psrsonnel such as city fire fighters? (b)If Part 20 does apply, wouki the radiation dose received by the work-ers be considered to be an occupational dose or a public dose?
10 CFR 20.1003 - Definitions Answer: (a) No. As stated in 10 CFR 20.1001, "Pur-pose," Part 20 applies to activities conducted under licenses Question 1: If a licensee decides to implement Part 20 in issued by the NRC. Emergency response activities such as mid-year, how does the. licensee trent the annual dose lim-fire fighting by employees of a city fire department are not its? Prorated?, Add contnhutions from beginning of year -
. conducted under a license issued by the NRC (even when before the revised Part 20 was adopted?
the fire being fought is in a facility of an NRC heensee).
Furthermore, as stated in 10 CFR 21.1001, nothms in Part Answer: b licensee must derme the " year" consistent 20 shall be construed as limiting actions to protect health with the definition in 10 CFR 20.1003. If a licensee intends and safety. 'Ihus, Part 20 does not apply to emergency to implement tim revised Part 20 at any time other than the response activities and workers such as fire fighting by beginning of the year, the licensee snust subtract the dose '
employees of a city fire department.'
received for the current year prior to the revised Part 20 dose being adopted from the revised Part 20 dose limit. : The For NRC licensees, it is the Commission's intent that the difference need not be prorated. For example, assume a regulations be observed to the extent practicable dunns licensee adopts tim avised Part 20 on July 1,1992, and emergencies, but that conformance with the regulations defines its dose year as January 1 - December 31. If the should not hinder any actions that are necessary to protect worker'ind received 1.5 rems between January 1 and June J
public health and safety such as lifesaving or mandmininf 30,1992, he or she woukt have (5 - 1.5) = 3.5 roms avail-1 coJmement of radioactive materials (36 FR 23365). Also, able for the rananvtar of the year. If the worker alrondy for nuclear power reactor heensees, a different part of the
' has more than 5 rem (e.g., two 3-rem quarters), the licensee regulations,10 CFR Part 50, includes a requirement, in 10 must shiA tie worker to tasks in which the worker will CFR 50.47(b)(11), that the offsite emergency response plans
- receive no occupational radiation exposure. (
Reference:
10 must include means for controlling radiological exposure of CFR 20.1003) emergency workers in an emergency. (
Reference:
Question 4: How is the dose from redon considered? What -
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about technologically enhanced redon at a licensed facility?..
10 CFR 20.1002 - Scope
[ Note: Technologically enhanced natural radiation sources '
have been defined as "truly natural sources of radiation...
which woukt not occur without (or wouki be increased by)
Question 5: Who is responsible for regulating radium 4 the some technological activity not exprwaly designed to State or NRC7 produce radiation."
Reference:
T.F. Gesell and H.M.
Prichard, ilaalth Phyama 28, 361-366,' April 1975.]
Answer: b NRC regulates radium when it is in NRC-Licensed uramum or thornun ores (source naterial, as de.
Answer: How the dose from redon is treated depends f
fined in Part 20) or in tailings or wastes from processing upon the source of the redon. If the source is NRC-licensed 1
these cres (byproduct material, as defined in Part 20). The material such as mill tailings or ores, then the dose from'-
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Questions and Answers redon and its particulate daughters should be included in defmition of " occupational dose") a dose received "in the :
I estimates of doses to workers or to mamhers of the general course of employment in which the individual's assigned public (except for 40 CFR Part 190 evaluations which duties involve exposure to radiation and to radioactive exclude redon). If the source of the redon is from radium material from licensed and unlicensed sources of radiation, -
J that is not hcensed or controlled by any agency, then the whether in the possession of the licensee or other person' "
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. dose from radon and its daughters is considered background e in other words, outside " restricted areas"fwhether the dose
-l radiation and may be excluded from occupational or public to an individual is an " occupational dose" or a "public done" dose estimates, whether there is any technological enhance.
(and whether the occopational dose limits or the public close ment of the concentrations or not. Many states are working limits apply to the individual) depends on what the toward licensing certam matenals contammg radium and individual is doing arul ant on 'what aren (controlled or these _ sources will need to be known to bcensees even if they.
unrestricted area) the individual is in when the dose is
'l cro not the persons licensed by the States. (See definitions received.
of " background radiation," " source matenal," and "bypro-duct material" in 10 CFR 20.1003). (
References:
10 CFR Different understandings of the meanmg of the second part 20.1001,10 CFR 20.1002,10 CFR 20.1003) -
of the defmition of " occupational dose" (which begins "...
or in the course of employment...") has been a source of much of the confusion with respect to applicable dose limits.
l Q=ada= 25: Does the definition of a " member of the '
Generally, this part of the defmition does not mean that any.
public" mean "all" individuals? If so why is the exception
' dose received by an individual while working, regardless of -
statement added to the definition?
the type of work, is an " occupational dose." Doses receiv.
I ed by an individual while working outside a~ restricted area.
Answer: No. A particular individual can be a " member of (in a controlled or unrestricted area) usually woukt be cate-the public" at some times and not at others. For example, gorized as public dose when the dose received is within the -
an individual who works at a nuclear power plant and re-public dose limit (and is not likely to exceed that limit) and !
~ccives an " occupational dose" is not a member of the public the work being done is not closely connected (i.e., is only
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- while at work, but is a " member of the public" durms offa casually connected) to the licensed activity.
hours at home. (
Reference:
I b-niminn Question 26(a): bre has been some confusion about the revised Part 20 r-;i with respect to controlled The regulations (revised Part 20) allow licensees a certain creas and when individuals are receiving a public or an oc.
amount of discretion in developing a radiation protection cupational dose. Before asking questions involving specific program that is suitable and practical to implement at the exposure scenarios (in parts b, c, and d of this question),
licensee's location and for the licensee's particular set of -
does the NRC staff have any general guidance on these working conditions. For example, licensees are permitted by topics?
the regulations to select the boundaries for restricted areas and controlled areas. (Because licensees are not required by Answer: Anyone attempting to answer questions about 10 CFR Part 20 to have controlled areas they may choose -
which dose limits apply in a particular situation shoukt be -
whether or not to have controlled areas.) When an individ-familiar with the requirements of 10 CFR 20.1201,10 CFR ual is to work in a controlled area or an unrestricted area, 20.1207,10 CFR 20.1208, and 10 CFR 20.1301, and with -
the licensee shouki evaluate the individual's assigned duties
- i the dormitions of the following terms in 10 CFR 20.1003:
and determine whether a does woukt be categorized as a i
occupational dose, public dose, member of the public, re-public dose or an occupational dose in accordance with the i
stricted area, controlled area, and unrestricted area.
definitions of these terms in 10 CFR 20.1003.
1 h - dan.i % va una na==
h following criteria that include both regulatory require-i ments and basic radiation protection philosophy will be used By definition, and with the exceptions given in the def-in the NRC inspection program.
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initions of " occupational dose", any dose received by any individual in a " restricted aren" is an " occupational dose."
hatN Area No one in a resencted area is a "snamher of the public."
Outside " restricted areas" (i.e., in " controlled areas" or in When an area satisfies both the dermition of a restricted
" unrestricted areas"), whether the dose to an individual is an area in Part 20 and the defmition of a protected area in
' occupational dose" or a "public dose" depends on whether Part 73,-it is considered to be a restricted area for the dose received by the individual is (as specified in the purposes of compliance with 10 CFR Part 20.'
NURBO/CR-6204 4
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Questions and Answers Doses are to be categorized as public doses (i.e., public Boundaries of restricted areas may be selected by licen-dose limits apply) whenever reasonable and practical sees but being selected, they shoukt be documented (good practice) (except for occupational doses).
(recorded) (good practice).
In deternunmg whether an individual in a controlled Access to restricted areas must be controlled, e.g., by area is to be categorized as an individual who receives barriers, signs, or guards ($20.1003). Note: Areas an occupational dose or as a member of the general that can have personnel access controlled but that are public, the more difficult decisions concern individuals not being controlled (e.g., because the radiation source who may be occasionally exposed or whose assigned has been removed) are not restricted aream, duties are not closely connected to the licensed activity.
Such individuals include messengers, delivery men and Posting of a restricted area as a restricted area is not women, custodial workers, secretaries, clerical work-required although other posting may be required within ers, hospital volunteers, etc. Usually, such indivkhtals the area (620.1902).
are considered to be members of the public and the doses they receive are well within the limits for mem-Doses received by allindividuals in restricted areas are bers of the public. However, if the assigned duties of occupational doses (520.1003),
these individuals are closely and frequently connected to the licensed activity, and their doses may approach Individuals working in or frequenting a restricted area or exceed the limits for members of the public, the must be provided training, as appropriate (619.12),
doses such individuals receive are better treated as occupational doses.
Individuals entering a restricted area must be informed Only when doses are to be categorized as occupational that they are subject to occupational dose limits.
doses (i.e., occupational dose limits apply) do the fo!-
Effort must be made to maintain all doses ALARA lowing conditions apply:
($20.1101).
- A decision must be mad 3 as to whether monitor-A decision must be made as to whether monitoring is ing is required (620.1502).
required ($20.1502).
- The licensee should have the ability to exercise enntrnlled Area positive control over the individual's activities in a
the controlled area.
Controlled areas are not required (620.1003).
- The licensee should provide appropriate instruc-As indicated in the preceding section, an area that tions.
satisfies both the definition of a restricted area and the definition of a controlled area is considered to be a
- The licensee shouki inform the individual that restricted area for purposes of compliance with 10 CFR he/she is subject to occupational dose limits rather Part 20.
than public dose limits (619.12-this is an implied requirement).
Boundaries of controlled areas may be selected by licensees but shouki be documented (reconfed) (good indiviAn=1 Member = nf tha puhtin practice).
Individuals in controlled areas and unrestricted areas Posting of a controlled area as a controlled area is not are members of the public unless they are receiving an required (120.1902),
occupational dose (620.1003 & 620.1301).
Licensees shoukt apply lower dose limits (public dose Doses received in controlled areas may be occupational doses or public doses. Generally doses will be public limits) to non-workers whenever possible and doses except when the licensee determmes that an reasonable (good practice).
individual receives exposure to radiation "in the course An individual is not a member of the public when they of employment...." [$20.1003, $$20.1301(b)].
enter a restricted area (520.1003).
Questions and Answers
-I Effort naast be made to achieve doses that are ALARA procedures will not be rescheduled. "Ihe ducts are not used I
o (620.1101),
to ventilate the hot lab.
l
' 2. Individual B is an emergency room nurse employed by i
Question 26 (b): Do occupational dose limits or public the hospital. On frequent occasions she accompames dose limits apply to the doses received by the individnals patients to the nuclear medicine department for emergency described in the following scenanos for nuclear power lung scans.
l plants?
j i
- 3. Individual C is not employed by the hospital but visits j
- 1. Assume an indivaal employed by a heensee working at the hospital on a weeklf basis for the purpose of performing
{
a two-unit site (one nuclear plant and one fossil plant) is preventive mamtenance on the gamma cameras. He fro-permanently employed at the fossil plant, which is inside the quently observes the nuclear medicine technologist during.
nuclear plant's controlled area. b individual does not -
patient studies to verify equipment operation.
enter any restricted areas. What dose limits apply to that individual while' working at the fossil plant?
- 4. Individual D is employed by the hospital as a caretaker.
During the sununer he routinely cuts the grass outside the
- 2. What dose limits apply to a pregnant taxi driver while hospital. Note: b hot lab has at least one outside wall.
she is picking up and discharging passengers withm the controlled area (outside the restricted area) of a nuclear Answer: Occupational dose limits apply to individuals B.
l power plant?
(emergency room nurse)'and C (who maintams gamma
'l cameras), h assigned duties ofindividuals B and C are J
3L What dose limits apply (a) to construction workers who closely and frequently connected to the hcensed activities, cre building a second nuclear power plant within the con.
Linuts for members of the public apply to Individuals A _
trolled area (outside the restricted area) of the first nuclear (who repairs a ventilation duct) and D (caretaker who cuts power plant at that site and (b) to secretanes in the adminis-grass), h assigned duties ofIndividuale A and D are only l
trative buikling within the controlled area (outside the re-remotely (and, in the case ofIndividual A, infrequently),
stricted aren)?
connected to the licensed activity and it is reasonable and practical to apply the public dose limits.
Answer: For scenarios #1,2, and 3, the dose limits for members of the public apply. However, if turbine shine Question 26 (d):. Do occupational doses limits or public from the nuclear plant is such that the individuals in scen-dose limits apply to the doses received by the individuals -
{
orios #1 (fossil plant workers) and #3 (constmetion workers described in the following scenarios for a radiography com-and secretaries) are likely to exceed the dose limits for pany?
members of the public, the licensee should consider the individual doses to be occupational doses and meet the A large radiography company performs radiography both in requirements for individuals who receive occupational the fieki amt in a hot cell within its plant. b hot cell is doses.
located in the delivery bay. The company shares its physi-cal plant with an affiliated company. UPS deliveries for l
Question 26(c): Do occupational dose limits or gniblic dose both compames come to the same bay area. h radio-limits apply to the doses received by the individuals des-graphy company has dermed its restricted area to be the hot cribed in the following scenarios for a hospital?
cell and its controlled area to be the delivery bay.
A hospital has dermed a controlled area as all areas within
- 1. Individual E is a secretary employed by the radiography.
the main buikling. These areas can only be accessed by company. Her desk, where she performs all admimstrative doors which open to the outside environment. In addition, assignments, is located in the delivery bay, adjacent to the they have designated the hot lab as a restricted area. b hot cell.
hot lab can only be accessed through the nuclear medicine department.
- 2. Individual F is a data entry clerk at the affiliated com-pany. He is employed by a temporary agency on a 12-
- 1. Individual A is a maintenance worker. He is employed month assignment. He is responsible for picking up all UPS by the hospital and has been assigned to repair ventilation shipments (within the controlled area),
ducts in the nuclear medicine (NM) department. b job
. must be performed during normal work hours; patient
- 3. Individual G is a co-worker of Individual E. He fre-l-
quently enters Individual E's office to use the telephone to l
l L
NUREO/CR-6204 6
l
Questions and Answers make personal calls during the course of a normal work Question 66: his question concerns restricted area
- day, limitations. At some sites for nuclear power plants the restricted area has been defmed as the site boundary, in Answer: Individual E (secretary): Assuming that the sec-some areas routine public access was available with the retary's location near a hot cell is essential, the occupational urxlerstanding that, shoukt the need arise, public use of dose limits apply, these areas coukt be prohibited. Examples of this type of access include fishing, visitor centers, and farming. This Indivkhial F (clerk): Limits for the general public apply.
type of use now appears to fall within the intent of the def-bre is only a casual connection between the individual's inition of controlled area and therefore, a new restricted assigned duties and the licensed activity that results in the area boundary located somewhat nearer the plant must be individual's exposure, dermed, in places where such uses exist.
Individual O (co-worker): his indivklual is subject to the b next physical boundary is a single fenced area, roughly dose limits for a member of the general public. He has not corresponding to the security definition of owner controlled entered a restricted area and his assigned duties do not area. Station parking is routinely within this area and ac-involve exposure to radiation and to radioactive material cess is provided through openings in the single fence which from licensed and unlicensed sources of radiation.
are not continuously guarded. These openings are posted,
(
Reference:
"No Trespassing " b direct questions involved are, f
Can this area (single fenced area) qualify as the restrict-a.
Question 40: Assume a licensee has dermed its compliance ed area boundary?
year as January 1,1993 to December 31,1993. What is the mechanism to change its defmition of year? For example, b.
If so, are postings sufficient or woukt guards be the licensee wants to monitor from January 31,1994 to required?
January 30,1995, how shoukt it account for the lost days January 1 - 30, 19947 Is it acceptable to prorate the doses?
c.
If posting is sufficient, what is the acceptable wording?
Answer: No. b question refers to the definition of Answer:
)
" year" in 10 CFR 20.1003. h licensee is not allowed to a.
Yes, access to this area coukt be limited so as to meet j
make the one-step change as postulated in the example in the question because that change involves omitting certain the dermition of a restricted area. However, it shouki be days. Omitting days, even with dose proration, is not recognized that the dose received by an individual in a re-allowed. However, the license coukt accomplish the desired stricted area is an occupational dose that is subject to the change in two steps, one step in each of two consecutive occupational dose limits in Subpart C of tim revised Part 20 years, that wouki give a " year" beginning 1/31 of one calen-(or to the occupational dose limits of 10 CFR 20.101 in the dar year and ending 1/30 of the following year. b first oki Part 20) and the requirements in 10 CFR 19.12 on step, using the example, wouki be a change, at the begin-instructions to workers. (See defmitions of " restricted area" ning of 1993, to a " year" of 1/1/93 to 1/30/94 (13 months).
and " occupational dose.")
The second step wouki be a change, at the beginning of 1994, to a " year" of 1/31/94 to 1/30/95. This two-step b.
Although neither posting nor guards are required speci.
change meets the requirement of " years" that begin in fically, access to a restricted area must, by definition, be January with no day omitted or duplicated in consecutive controlled. In the situation desenhed in the question, access years. (
Reference:
10 CFR 20.1003) control couki be accomplished by posting or use of guards Since posting is not specifically required (see b. above),
Question 57: b definition of a very high radiation area c.
(10 CFR 20.1003) and the requirement for control of access the wording is leR to the discretion of the licensee.
to very high radiation areas specify an absorbed dose of 500 rads in an hour. Is this a deep dose, a shallow dose, or an NOTFh This answer also applies to research and test reac-eye dose?
tors, fuel fabrication plants, and major radioactive materials processors insofar as the conditions desented in the ques.
Answer: The 500-rad dose is intended to be a deep dose, tion for nuclear power plants apply to these other facilities.
evaluated at a tissue depth of I cm (1000 mg/cm').
(
References:
10 CFR 20.1003,10 CFR 20.1201,10 CFR
(
References:
10 CFR 20.1003,10 CFR 20.1602) 20.1206,10 CFR 20.1207,10 CFR 20.1208,10 CFR 19.12) 7 NUREO/CR-6204
Questions and Answers ed due to radiological exposure considerations. This Question 67: This question concerns water approaches to concep is consistent with the revised mle.
nuclear sites. Several sites for nuclear power plants include portions of navigable lakes or rivers within their licensed Will the defmitions of " member (s) of the public" in Generic exclusion areas. Obviously, the utility does not own these Letter 89-01, Supplement 1 (NUREGs 1301 and 1302) be areas. Would such boundaries as dermed in our licenses changed to be consistent with the defimition of " member of qualify as restricted areas, controlled areas, or unrestricted the public" in the revised Part 20?
areas?
Answer: Yes. The NUREGs themselves will not be Answer: b licensee cannot limit access to navigable changed; however, in a forthcoming Generic Letter on lakes or rivers that the licensee does not own; therefore, model Technical Specifications that incorporate provisions these bodies of water cannot be part of a restricted area or of revised Part 20, the definition of " member (s) of the controlled area arxl must be considered to be unrestricted public* will be changed to be consistent with revised Part creas. However, for the dose calculations for airborne ef-
- 20. See Question 26 and answer in the fourth set of fluents that are required by reactor technical specifications questions and answers for clarification of the definition of and that are related to 10 CFR 50 Appendix I, doses are not
" occupational dose." (
References:
10 CFR 20.1003, required to be calculated over such bodies of water.
(
Reference:
Question 93: In the definition of individual monitoring Question 74: Dose rates are used to establish posting devices, is there any reason electmnic monitoring devices requirements for radiation areas, high radiation areas, and are not mentioned?
very high radiation areas. 10 CFR 20.1601(a)(1), " Control of Access to High Radiation Areas." refers to a " deep-dose Answer: No b particular devices inchided in this equivalent" in describing when a control device shouki be dermition are a few examples, not a comprehensive listing, provided to reduce radiation doses below 0.1 rem in one of such devices. (
Reference:
hour, thus implying that the " dose equivalent" in the defmi-tion of a "high radiation area" is the " deep dose equivalent"
[at a tissue depth of I cm (1000 mg/cm2)). Are the " dose Question 94: Why was the " controlled area" defined?
equivalent" in the defmitions of " radiation area" arul "high radiation area" and the " dose" in the definition of "very Answer: h " controlled area," which is not defined or high radiation area" all considered to be at a tissue depth of used in the old Part 20, was defmed and used in the revised 1 cm (1000 mg/cm2)?
Part 20 to provide regulatory recognition of the existence of such areas and to clarify their regulatory status within the Answer: Yes, in addition see Question 57. (
References:
context of 10 CFR Part 20. In a related change, in revised
)
10 CFR 20.1003,10 CFR 20.1601)
Part 20, occupational dose limits no longer apply only in restricted areas, and lower (public) dose limits no longer apply to raervnna outside a restricted area. Es, under the Question 80: The revised Part 20 ($20.1003) provides old Part 20, an individual who receives an occupational dose defmitions of " member of the public," "public dose," and in a controlled area is subject to the same (low) dose limit as
" occupational dose." These definitions are not consistent a member of the public in that same area. Under the revis.
with the definition of " member (s) of the public" dermed (for ed Past 20, an individual who receives an occupational dose nuclear power plants) in Generic Letter 89-01, Supplement in a controlled area is subject to the occupational dose 1 (NUREGs 1301 and 1302).
limits, but a member of the public in the same controlled area is subject to the (lower) dose limits for members of the Consider that typically, one woukt expect any individual public. (
Reference:
entering the " restricted area" wouki be considered to be occupationally exposed and not classified as a " member of the public." All individuals, including utility employees, Question 96: (a) h roentgen (R) is not defined or used in their contractors, and delivery people outside the " restricted revised Part 20; however, many survey instruments and area," in the " controlled area," woukt be considered as computer records show dose rates in terms of "mR/h" or
" members of the public." h only exception is where a "R/h." Will these survey instrument face pieces and com-utility employee or its contractor doing work in a portion of puter forms have to be changed when revised Part 20 is im-the " controlled area" where public access has been restrict-plemented? (b) Most radiation instrumentation is currently NUREG/CR4204 8
Questions and Answers calibrated in units of roentgens rather thaa rads. A roentgen means an individual in a controlled or unrestricted area (not of x-or gamma-radiation in the energy range of 0.1 - 3 an individual in a restricted area). Therefore, the occupa-MeV produces 0.% rad in tissue. Will these instruments tional dose limits (and not the dose limits for individual need to be recalibrated to account for this difference.
members of the public) apply to the dose received by any individual in a restricted area. See related Question 26.
Answer: (a) No. The survey instruments will not need to
(
Reference:
be changed. See Question 428 for acklitional information conceming the use of the unit " roentgen
- arxl its subunits.
Question 149: 10 CFR 20.1003 dermes the shallow-dose (b) No. It may be assumed that one roentgen equals one equivalent as the dose equivalent at a tissue deph of 0.007 rem or a more accurate conversion factor may be used.
cm. (a) Does this mean that the dose to the skin of the
(
References:
10 CFR 20.1003,10 CFR 20.2101),
whole body is the sum of the non-penetrating dose equivalent (beta and low energy photons) and the deep dose equivalent? (b) is it proper to calculate the extremity dose Question 119: Is it permissible under 10 CFR Part 20 for a by summmg the dose equivalent nwasured on an extremity bcensee to have a controlled area that is controlled for dosimeter (which may only be worn for part of the prposes of radiation protection but that is not a restricted monitoring period) with the deep dose equivalent?
area?
Answer: General response: 10 CFR 20.1502 requires Answer: No. By definition, in Part 20, a " restricted area monitoring of external dose for individuals who are likely to means an area, access to widch is limited by the licensee for receive, in a year, a dose in excess of 10% of the applicable the purpose of protecting individuals against undue risks limits. Requirements to measure / assess the dose equivalent from exposure to radiation and radioactive materials." As at dephs of 0.007,0.3, and I cm exist under old Part 20 as stated in the answer to Question 26(a) under the heading well as revised Part 20. In oki Part 20, these requirements
" Controlled Area" ".. an area that satisfies both the are included in the instmetions for item 5 of NRC Form 5.
definition of a restricted area and the definition of a la the revised Part 20, these requirements are in Part 20
)
controlled area is considered to be a restricted area for itself, together with new dose limits and special names in purposes of compliance with Part 20." (
Reference:
10 CFR the definitions for the dose equivalents at these three dephs.
i 20.1003)
The only explicit requirements concerning the precision and accuracy of personnel dosimetry are the NVLAP accreditation requirements, which are the same in old Part Question 144: When will licer' sees be permitted to use 20 [10 CFR 20.202(c)] arxl revised Part 20 [10 CFR weighting factors other than one to determine and record 20.1501(c)]. Methods that have been acceptable for extemal whole body dose (effective dose equivalent from measuring / assessing dose equivalent at these three depths in external sources) as the occupational dose of record?
the past shouki continue to be acceptable in the future.
Answer: After the NRC has received and approved an Answers to the specific questions are as follows:
application for the use of weighting factors (W) other than one for obtaining the effective dose equivalent. See the (a) No. The " dose to the skin of the whole body" is the discussion of the comment on the use of effective dose equi-shallow dose equivalent. The shallow-dose equivalent is the 2
valent for external exposure in the Statement of Considera-dose equivalent at a depth of 0.007 cm (7 mg/cm ) from all tions (56 FR 23368, third column arxl 23369, first column).
types of radiation, whether " penetrating" (such as gamma The response to the comment concludes with the statement rays and neutrons) or "non-penetrating" (such as weak beta that "The use of other weighting factors for external radiation and lower energy x-rays).
exposure may be approved on a case-by-case basis upon request to the NRC." (
Reference:
(b) No, not in general. The question does not make it clear whether or not the dose summmg is for dose during the same time period. It is never proper to calculate an ex-Question 148: What is the dose limit for a member of the tremity dose (shallow-dose equivalent) for a particular time pblic in a restricted area?
period by adding a deep dose equivalent to the shallow-dose equivalent. If the question refers to a monitoring period Answer: By definition (10 CFR 20.1003), the dose re-during which an extremity dosimeter (measuring shallow-ceived by an individual in a restricted area is an occupa-dose equivalent) was used only part of the time, but during tional dose. Also, by definition, " member of the public" which a whole-body dosimeter was used all of the time, the 9
Questions ard Answers answer deperds on the circumstances of the individual's struction workers, or secretaries (but not the pregnant taxi exposure. It wouki be acceptable to assume, for the times driver) "... are likely to exceed the dose limits for mem-during which the extremity dosimeter is not used, that the bers of the public, the licensee should consider the indivi-extremity dose (shallow dose equivalent) is equel to the dual doses to be occupational doses and meet the requim-shallow. dose equivalent measured by the whole-body dosi-ments for individuals who receive occupational doses." ne meter. If only the deep-dose equivalent is measured by the basis for this answer is the NRC staff's understanding of the whole-body dosimeter, it would be acceptable to assume, intent of the defmition of " occupational dose", specifically, for times during which the extremity dosimeter is not used, that portion which states that " occupational dose means the that the extremity dose is equal to the deep-dose equivalent dose received by an individual... in the course of employ-(measured by the whole-body dosimeter) if it can be shown ment in which the individual's assigned duties involve that types ard levels of radiation to which the extremity was exposure to radiation...." This understanding of the exposed wouki not have resulted in a significantly higher dermition is also expressed in more general terms in the shallow dose equivalent to the extremity than the deep dose answer to Question 26(a). (
Reference:
10 CFR 20.1003) equivalent to the whole body. (
Reference:
Question 413: This question refers to the answers to Questions 66 and 31 under $20.1003 and $20.1201, respec-Question 150: 10 CFR 20.1003 defmes tissue monitoring tively, and to Question 26(d) under $20.1003. Simply depths of 0.007,0.3, and 1 cm for shallow, eye, and deep.
designating an area as a restricted area so you can control dose, respectively; (a) Is it important to measure at (or everyone at occupational dose limits is a perversion of every extrapolate the measurements to) these exact depths? (b) radiation protection principle published. Of course, this is couki the eye and deep-dose both be determmed at 0.3 cm?
just my opinion. I hope NRC will revise its interpretation of this defmition.
Answer: See the " general response" in the answer to Question 149.
For example, a secretary in a nuclear medicine clinic with-out any direct person-to-person contact with patients shouki (2) As under the ok! Part 20, it is important to measure (or not be subject to occupational limits just because she is in a to extrapolate measurements to, or otherwise assess the dose restricted area. Many other examples coukt be cited, and equivalent) at a reasonable approximation of these depths.
some that are more in the gray area shouki be examined carefully. Clearly, there is a significant population of (b) No. The deep < lose equivalent is, by defmition, the exposed persons that are not being hekt to the proper dose equivalent at a depth of I cm, not 0.3 cm. However, standard. The following statement refers to the answer to the dose at 0.3 cm (eye dose) woukt usually be a Question 26(d) concerning " individual E." la spite of the conservative approximation (overestimate) of the dose at I definition of occupational dose, mere geography is not cm (deep < lose). (
References:
10 CFR 20.1003) justification for classifying a person as a radiation worker.
Answer: The questioner appears to object to the dermition Question 412: This question refers to the answer to of " occupational dose" that states that " occupational dose Question 26(b) urder $20.1003. What is the basis for using means the dose received by an individual in a restricted area a dose threshoki to decide whether a person is categorized or...." The NRC cannot change this defmition by as a member of the public or as occupationally exposed?
revising its " interpretation of this definition." The definition The definitions do not specify a dose thresboki.
can only be changed by rulemaking.
Answer: Question 26(b) asked whether occupational or While there may have been a lack of clarity in the referenc-public dose limits apply to individuals, described in three ed answers, our intention is that licensees shouki not engage different scenarios, who are exposed within controlled areas in a practice of " simply designating an area as a restricted J
(outside any restricted areas) at a nuclear power plant.
area so you can control everyone at occupational dose i
These scenarios described (1) a fossil plant worker, (2) a limits." Question 66 asks if a simple fenced area can quali-pregnant taxi driver, and (3) construction workers building a fy as a restricted area and the answer is yes, provided it is second nuclear power plant argl secretaries in the adminis-the licensee's purpose to limit access for the purpose of trative buikling. He answer to Question 26(a) states that controlling radiation exposures. Question 31 asks if stu-the public dose limits apply to the individuals in all three dents and volunteers (such as nuclear medicine students and scenarios, but the answer also states that if turbine shine
" candy stripers" who transport nuclear medicine patients or from the nuclear plant is such that fossil plant workers, con-perform volunteer work in a nuclear medicine department)
NUREO/CR-6204 10
Questions and Answers ere subject to occupational dose limits. The answer to this used in experiments at some research reactor facilities.
question is that these individuals are subject to the occupa.
What values of the quality factor, Q, and the fluence per tional dose limits because, and provided that (as the question unit dose equivalent shoukt be used for " cold" neutrons?
implies), the type of work they are assigned involves ex-j posure to rr.diation; it does not matter where (in which area)
Answer: The values for " thermal neutrons" should be used
]
they are working Question 26(d) asks if the occupational until the use of other values is approved by the NRC.
i doio limits or public dose limits apply to " Individual E," a
(
Reference:
10 CFR 20.1004 Table 1004(b).2) secretary for a radiography company, who works in a
" controlled area" next to a " restricted area" containing a hot cell. The answer is that the occupational dose limits apply),
10 CFR 20.1008 - hnpleinentation again because the type of work assigned presumably in-volves exposure to radiation since it must be perfomied near the hot cell. (
References:
10 CFR 20.1003,10 CFR Question 30: If a license condition ties the licensee to a 20.1201).
section in the old Part 20 and there is no corresponding section in the revised Part 20, does the requirement in the old Part 20 stay in effect after implementation of the revised Question 434: llow are occupational dose limits applied in Part 20.
regard to the revised Part 20 definition of " year"? The purpose of this question is to obtain additional clarification Answer: Yes. See 10 CFR 20.1008(e). The license of the intent and application of the " year" as it is defined in condition that ties the licensee to a section in the old Part 20 the revised Part 20 and discussed previously in Question 40.
remains in force until there is a technical specification Apparently, licensees may establish a year that is other than change, license amendment, or a license renewal that January 1 through December 31 (e.g., Question 40 address-modifies or removes this condition." (
Reference:
10 CFR es a year that is from January 31 of one year through 20.1008(e))
January 30 of the following year). In responding to the question, consider the following example. A worker receives dose sequcntially at facilities of two different Question 58: Before implementing all of the provisions of licensees, the first licensee using a year of January 1 -
the revised Part 20, would a licensee be in violation of 10 December 31 n1 the second licensee using a year of CFR 20.1008(a)if the licensee voluntarily adopted the pro-January 31 - January 30. The worker receives 4 rems total visions of 10 CFR 20.1208 for protection of the embryo /
effective dose equivalent (TEDE) at the facility of the first fetus?
licensee during the period January 1 January 30, and then transfers to the second licensee's facility, arriving for work Answer: No, licensees can voluntarily provide protection on February 1. For work performed at the second licen-for the embryo / fetus in accordance with the provisions of 10 see's facility, is the individual's remaining available TEDE CFR 20.1208 before implementing all of the provisions of I rem or 5 rems?
revised Part 20. Ilowever, licensees wouki have to be clear that they are not " adopting Part 20" because that wouki Answer: Five rems. For a particular licensee, the relevant require it to be adopted in full. (
References:
10 CFR time period for determmmg compliance with an annual dose 20.1008(a),10 CFR 20.1208) limit is the year beginning and ending on the dates specified by that licensee, providing that the time period chosen by the licensee is consistent with the definition of " year" in 10 Question 65: The following question concerns OMB CFR 20.1003. In the example provided, the worker started approval of the information collection requirements of the work at the facility of the second licensee at the beginning revised Part 20. Section 20.1008 indicates that licensees of that licensee's " year" and, therefore, the worker had no shall implement the provisions of all sections of revised Part prior occupational dose during that licensee's " year."
20 on or before January 1,1993 and that if a licensee
(
Reference:
chooses to implement revised Part 20 before then, the licensee shall implement all provisions of revised Part 20 not othmvise exempted by subsection 20.1008(d). How-10 CFR 20.1004 - Units of Radiation Dose ever, section 20.1009 says that the information collection requirements of the revised Part 20 will not becorne effec-tive urJil OMB approves them. Does this mean that before Question 73: Table 1004(b).2 does not include entries for OMB approval is obtamed, a licensee can implement all of "cok!" neutrons, (e.g.,7 x 10* MeV neutrons) which are 11 NUREO/CR-6204
l Questions and Answers the provisions of the revised Part 20 ascent the infonnation of inspections with respect to ALARA and, therefore, no collection requirements?
significant change in the inspection program and proce-dures. NRC headquarters does plan to review all draR '
Answen OMB approval of the infonnation collection notices of violation of 10 CFR 20.1101(b) in order to requirements of revised Part 20 was obtamed on January 24, mosutor proposed enforcement actions in this area to ensure 1992, with the exception of NRC Forms 4 and 5. OMB that a reasonably consistent approach is established. Con-cpproval for these forms is expected in the future.
sistent with current and past policy, the NRC Regional -
(
References:
10 CFR 20.1008,10 CFR 20.1009)
Offices will continue to allocate increased inspection re-sources (e.g., ALARA team inspections) to inspections of poor ALARA performers. (
References:
10 CFR 2.2 - SUBPART B - RADIATION 20.110i(bn PROTECTION PROGRAMS Question 99: b following questions concern the relation-
' ship of emergency plans for nuclear power plants to 10 CFR 10 CFR 20.1101 - Radhtlon Protection 20.1001 (" Purpose") and 10 CFR 20.1101 )" Radiation Progrants Protection Programs").. (a) To what extent do radiation protection programs need to be established such that during emergency conditions, the revised Part 20 can be complied Question 7: Relative to 10 CFR 20.1101, radiation protec-with? (b) For example, in order to comply with the new EPA "Mamial of Protective Actions For Nuclear Incidents" tion programs, what wouki a typical radiography licensee have to do beyond what that licensee is doing now?
October 15,1991, do germanium counting systems need to be established to analyze air samples for iodines and par-Answen Ensure that the pmgram was documented amt ticulates, and computer programs to calculate CEDE, so that review the program's content and hnplementation periodi-CEDE can be added to external dose to get TEDE7 (c) Do cally (at least annually). (See Regulatory Guide 10.6 for emergency smvey/ plume chase teams need to wear breath-additional information). If the licensee does not have a -
ing zone air samplers?
radiation protection program, then such a program must be developed. (
Reference:
Answen (a) In general, the revised Part 20 contains no new requirements that would make ' hanges necessary in c
existing radiation protection programs as they relate to Question 11: Shoukt the Radiation Protection Program be a emergency conditions. 10 CFR 20.1001 includes the sen-stand-alone document or can it be the sum of many docu.
tence, "However nothmg in this past shall be construed as monts or manuals (e.g., a requirement for HP audits includ.
limiting actions that may be necessary to protect public ed as part of a QA audit program document)?
heahh and safety," and the intent of this sentence is discus-sed in the statement of considerations (56 FR 23365, first Answen Section20.1101 requires a documented radiation column). NRC requirements concerning emergencies at protection program. This documentation does not have to NRC-licensed facilities (i.e., nuclear power' plants and fuel-be a stand-alone document but it must be reviewed annually, cycle licensees) are contained in 10 CFR Parts 30,40,50,
(
Reference:
10 CFR 20.1101) and 70, and no conforming changes to these requirements were needed as a result of the revised Part 20. (b)'and (c)
See answer to (a). With regard to the offsite emergency
)
Question 62: With 10 CFR 20.1101(b) makmg ALARA a workers such as fire fighters, law enforcement officers, civil i
requirement ("shall" instead of a "shouk!"), does the NRC defense workers and environmental fiekt team members, the staff' plan or anticipate any significant change in inspection EPA manual provides guidance given in Table 2-2 titled program focus or in enforcement activity with respect to "Ouidance on Dose Limits for Workers Performing Emer.
ALARA for occupational exposure at nuclear power plants?
gency Services." In addition to the refinements in the dose limits, the revised EPA Manual uses the CEDE and the Answen No. In general, the recent performance of the TEDE concept bre are no changes necessary with nuclear power reactor industry has been good with respect respect to the momtoring of the external exposure levels of to efforts to achieve occupational doses that are ALARA.
these workers in the early phase of an accident except as Collective doses (person-rem) for both PWRs and BWRs noted in the referenced table, b question is, therefore,
.l have been declining since the early 1980s. b NRC staff how to account for the inhalation dose of offsite emergency is not planmng any significant change in the depth or scope workers to prevent them from exceeding their limits. Due NUREG/CR-6204 12
Questions and Answers to the urgency of offsite response in the early phase of an Offsite (corporate or contract) audits and evaluations accident, it will not be practical to set up air samplers at shouki be performed to determine whether the radiation numerous locations and analyze those samples in a timely protection program complies with the regulations and manner. Air samples and radiation measurements taken by other requirements and whether plant. wide objectives the fiek! monitoring teams will be valuable to determine the are being met as well as to identify needed program dose to emergency workers after the fact, but will be of improvements. (
Reference:
10 CFR 20.1101) little value during the actual performance of emergency tasks, since some form of real time exposure rate inlication is needed. To create this real time indication, a correction Question 133: 10 CFR 20.1101(b) requires licensees to factor can be developed that when multiplied by the emer-use, to the extent " practicable," procedurea and engineering gency worker's dosimeter reading can provide a conserva-controls based upon sound radiation protection principles to tive estimate of the inhalation dose. The NRC and FEMA achieve dosee that are ALARA. The ALARA concept cre currently investigating this issue. After appropriate emphasizes dose-reduction techniques that are reasonable review the NRC and FEMA will provide guidance for considering costs.
offsite agencies to use. (
References:
10 CFR 20.1001,10 CFR 20.1101,10 CFR 50.47) liowever, " practicable" may imply something that has been proposed and seems feasible but has not been actually tested in use. " Practical" is more consistent with the ALARA con-Question 118: 10 CFR 20.1101(c) requires that each cept because " practical" implies " sensible", " involving good licensee " periodically (at least annually) review the radiation judgement" and " proven success in meeting the demands program content and implementation." A nuclear power made by actual living or use." In making decisions about plant has many reviews and atulits (including quality assur-ALARA procedures and engineering controls, will licensees ance audits) of various aspects of their radiation protection be permitted to interpret " practicable" as " practical"?
programs during a year and reviews are on a schedule that covers all phases of the program on a 2-3-year review cycle.
Answer: In the context of this regulation, the word "prac-la this acceptable to the NRC7 ticable does not have the connotations attributed to it in the question. 10 CFR 20.1003 states that "ALARA... means Answer: Yes, provided that the combination of these making every r=-hla effort to maintain exposures to reviews and audits covers program content and implemen-radiation as far below the dose limits in this part as is tation. Reviews and audits at nuclear power plants should prarteral... * (emphasis added). The discussion of 10 incorporate the following features to assess procedural CFR 20.1101(b) in the preamble to revised Part 20 (56 FR compliance, technical performance, implementation, and 23367) includes the following statement: " Compliance with effectiveness of the facility radiation protection program, this requirement [10 CFR 20.1101(b)] will be judged on whether the licensee has incorporated measures to track Radiation protection supervisoiy reviews and, if necessary, to reduce exposures and not whether exposures and doses represent an absolute minimum or Onsite radiation protection supervisors shouki periodi.
whether the licensee has used all possible methods to reduce cally perform and document reviews of the effective-exposures." Thus the use of the word " practicable" in 10 ness of the radiation protection staffin such areas as CFR 20.1101(b) does not imply procedures and engineering radiological work practices, work monitoring, proco-controls that are unproven. (
Reference:
10 CFR 20.1101) dural compliance, and survey adequacy.
Quality assurance audits Question 134: 10 CFR 20.1101(c) requires a periodic (at least annual) review of the radiation protection program as Quality assurance audits shoukt be performed by the defined in 20.1101(a). 10 CFR 20.1101(a) refers to 10 onsite auditing group. Personnel in the auditing group CFR 20.2102 for recordkeeping requirements. (a) Does the should have sufficient radiation protection training or use of the word " audit" in 10 CFR 20.2102(a) require experience so they can determine whether radiation records for all audits that are performed in addition to the protection functions are being performed as required.
periodic review? (b) Are the reviews required by 10 CFR The quality assurance program audits shoukt meet the 20.1101(c) also considered to be audits that are subject to requirements of Appendix B to 10 CFR Part 50.
the quality assurance criteria specified in 10 CFR Part 50, Appendix B, XVIll?
Corporate or contract audits 13 NUREG/CR-6204
1 Questions and Anawers Answer: (a) No. b recordkeepag requirements of 10 CFR 20.2102(a)(2) apply only to audits and reviews per.
Question 381: (a) For nuclear power facilities does confor-formed by the hcensee to comply with 10 CFR 20.1101. If mance with Regulatory Guides 8.8 and 8.10 fully meet the the review is perfonned annually, then only the records of requirements of 20.1101(b) regarding ALARA programs?
that myiew are required.
(b) If not, does the NRC plan to update these Regulatory guides to confonn to new requirements?
(b) No, b requirements of Parts 20 and 50 am separate l
requirements. However, quabty assurance audits of aspects Answer: No, to both questions.-(a) Regulatory Gua 8.8 cf the radiation protection program at nuclear power plants Rev. 3 is now (in 1993) 15 years old, the second proposed pursuant to the requirements of 10 CFR Part 50, Appendix revision to this guide is now 11 years oki, and Regulatory B, XVIII, may padially satisfy the requirements of 10 CFR Guide 8.10 is 16 years old. These guides do not adequately 20.1101(c). (
Reference:
10 CFR 20.1101,10 CFR cover all the_means that the nuclear power industry has 20.2102).
developed and shown to be practical and cost-effective for
= "N occupational doses ALARA. For example, these guides do not recognize the importance of water -
Question 380: Nuclear power plant bcensees are required chemistry contmis and radiation source and flek! controls to meet the quality assurance criteria in 10 CFR Part 50
' for maintaining doses that are ALARA.
Appendix B. Regulatory Guide 1.33 describes a program '.
acceptable to the NRC staff to demonstrate c-- - ' m with (b) b NRC staff has not yet established a schedule for.
10 CFR 50 Appendix B requirements and includes guidance updating these guides, b staff did issue Draft kegulatory.
mganling the documentation, use of procedume'and periodic Guide DO-8004, " Radiation Protection Programs for myiew of radiation protection programs. Does commitment
' Nuclear Power Plants,' to provide guidance on compliance to and confonnance with 10 CFR Part 50 Appendix B and with 10 CFR 20.1101, ' Radiation Protection Programs,"
Regulatory Guide 1.33 fully meet the requirements of 10 including guidance on the ALARA requirements of 10 CFR CFR 20.1101(a) and (c)? Note: b answer to Question 20.1101(b). However, representatives of the' nuclear power 118 provided previously did not clarify if additional require '
industry stated that this guide was not needed and it has monts are imposed on nuclear power plants by 10 CFR been waimlrawn. (
Reference:
20.1101(a) and (c) that are new or different from the previously applicable requirements.
2.3 SUBPART C - OCCUPATIONAL Answer: No See related question 134 and answer, 10 CFR Part 50 Appendix B and 10 CFR 20.!!01(a) and (c)
DOSE LIMITS cre different requirements.10 CFR Part 50 Appendix B establishes quahty assurance requirements for the operations of nuclear power plant safety-related structures systems al 10 CFR 20.1201 - Occupational Dose Limits components. 10 CFR 20.1101(a) requires each license to for Adults develop, <t~~M and implement a radiation protection program commensurate with the scope and extent of Question 2: What are the reqnirements for including dose licensed activities and sufficient to ensure compliance with from non-NRC-licensed sources (x-rays, accelerators, the provisions of Part 20. 10 CFR 20.1101(c) requires NORM) as part of occupational dose?
periodic reviews of that radiation protection program.
Ahhough for nuclear power plants, there is some overlap Answer: b combined total of the doses from licensed between the requirements of 10 CFR 50 Appendix B and the and unlicensed sources (other than backgre - ' and medical requirements of 10 CFR 20.1101(a) asul (c), they clearly are radiation) must be below the Part 20 occupational dose different requirements. For example, some aspects of the limits. b requirement for inclusion'of doses from non-radiation protection program established pursuant to 10 CFR licensed sources is intended to account for occupational 20.1101 (a) may not be considend " safety related" within doses received while working for activities or with materials the meaning of this term in 10 CFR 50 Appendix B. b that are licensed or controlled by organizations other than reference to 10 CFR Psit 50 Appendix B in the answer to the NRC, e.g., states, DOE, etc. Thus licensees must Question 118 was provided in the context of a discussion of record and add the doses from non-licensed sources to the quality assurance audits and was not an irulication that doses from licensed sources to obtain the total dose for '
" commitment to and conformance with Appendix B and companson with the occupational limit. (
References:
10 I
Regulatory Oukie 1.33 fully meet the requirements of CFR 20.1001,10 CFR 20.1002,10 CFR 20.1003,10 CFR-(20.1101(a) and (c)." (Referencesi 10 CFR 20.1101).
20.1201)
NUREO/CR-6204 14
Questions and Answers need to clearly designate the particular areas in a hospital Question 3: What do you do about hot particles?
that are
- restricted areas." (
Reference:
Answer: Until changed by rulemaking, the dose limits in Part 20 (10 CFR 20.1201(a)(2)) apply. Special rulemaking Question 34: What are the applicable radiation limits in a on " hot particles" is still pending. Until rulemakmg is ac-controlled area if the licensee does not allow nwmbers of complished the NRC will continue handling hot particle the public to enter the aren?
enforcement issues in accordance with the stated Enforce-ment Policy published in the Federal Register (55 FR Answer: Occupational dose limits apply to individuals who 31113, 7/31/90) and transmitted to nuclear reactor licensees receive an " occupational dose" in a " controlled area." (See as Attachment 2 to NRC Information Notice 90-48 (8/2/90).
definitions of " occupational dose" and " controlled area" in
(
References:
10 CFR 20.1201, U.S. NRC Enforcement 10 CFR 20.1003.) (
References:
10 CFR 20.1003,10 CFR Policy) 20.1201)
Question 6: What if an NRC licensee hires a DOE em-Question 41: Licensee A questions a new employee about ployee who earlier in the year received an internal exposure outside employment. The employee states that he is only ofless than 5 rems annual effective dose equivalent, but working at that facility. ARet 3 months, the employee starts greater tluun 5 rems committed effective dose equivalent?
working, in the evenings, at another licensed facility (Licensee B). The employee does not tell A about B; Answer: Previous occupational exposures, even those therefore, Licensee A does not take the exposure received received at an unlicensed DOE facility, count against the by the employee at facility B into account when he calcu-limit. - The worker could not be allowed further radiation lates the employees annual total effective dose equivalent exposure for the year (except a planned special exposure).
(TEDE). Will Licensee A be in noncompliance for not Note: There are also beenmi DOE facilities. (
References:
knowing about the dose received by the employee at Licen-10 CFR 20.1201,10 CFR 20.2104) see B7 Iflicensee A was made aware of the exposure at
{
Licensee B aRer-the-fact, must Licensee A go back aral account for this exposure when calculating TEDE7 If Question 31: Are students and volunteers subject to the Licensee A firx!s out about the worker's exposure at Licen-occupational dose limits? For example, nuclear medicine see B after the year's end, and if the sum of the exposures students, or " candy stripers' that transport nuclear medicine exceeded the annual limit, is Licensee A obligated to record patients or perform volunteer work in a nuclear medicine and report the overexposure and deduct it from the 25 rem department.
lifetime PSE limit?
Answer: Occupational dose is defined in revised Part 20 Answer: In order to meet the requirements of 10 CFR as "the dose received by an irxlividual in a restricted area or 20.1201(f), the licensee must establish some means to have in the course of emninymad in which the irmlividual's each employee inform the licensee when that employee is assigned duties involve exposure to radiation...* In the receiving occupational dose from sources outside the licen-question above, the individual's assigned duties do involve see's control. it is not sufficient merely to ask each em-exposure to radiation as a necessary feature of those duties; playee once (as in the example), with no continuing pro-therefore, the students and volunteer are subject to the vision for employee notification. Assuming that Licensee A occupational dose limits. (
Reference:
10 CFR 20.1003,10 made no provision for learmng of the new employees subse-CFR 20.1201) quent concurrent employment in other jobs that resulted in occupational dose, Licensee A would be in noncompliance for not deternumng the dose received on the job at Licensee Question 33: What is the dose limit for visitors entering a B. If Licensee A was made aware of the exposure at Licen-restricted area (e.g., visitors to a hospital, patients' rela-see B aAer-the-fact, Licensee A must go back and account tives, escorted tourists)?
for this exposure when calculating TEDB. If Licensee A finds out about the worker's exposure at Licensee B after Answer: Occupational dose limits apply to all individuals year's end, and if the sum of the exposures exceeded the who enter a " restricted area." This is also the case under annuallimit, Licensee A is obligated to record and report the old Part 20. " Visitors to a hospital, patients' relatives, the overexposure and to deduct it from the 25 rem lifetime escorted tourists" who do not enter a restricted area are not PSE limit. Although the question and preceding answer are subject to the occupational dose limits. Therefore, there is a provided in terms of Licensee A's responsibilities with 15 NUREG/CR-6204
Questions and Answers respect to doses received at Licensee B's facility, Licensee they are doing and regardless of the area they are in outside B has the same responsibilities with respect to doses receiv-a " restricted area." (
References:
10 CFR 20.1003,10 ed at licensee A's facility. (
Reference:
CFR 20.1201).
Question 45: In determmmg the " eye dose equivalent," can credit be taken for shiekling provided by eyeglasses / safety Question 97: 10 CFR 20.1201(b) refers to " doses received glasses?
during accidents, emergencies, and...." Is there any d'f-ference between an " accident" and an " emergency"?
Answer: Yes. (
Reference:
Answer: Yes. An accident is an unexpected and undesir-able event. An emergency is a situation or occurrence of a Question 46: Will determination of the " eye dose equiva-serious nature, developing suddenly and unexpectedly, and lent," at a tissue depth of 300 rug /cm, he included in the demadling immediate action. Thus an accident usually 2
NVLAP personnel dosimetry accreditation program?
results in an emergency, but it is possible to have an emer-gency without an accident (e.g., action taken in an emer-Answer: Not until ANSI N13.11, which defines the testing gency inay prevent an accident). In either case, licensees program used in the NVLAP accreditation program, is must account for doses received in excess of the annual revised to inchule tests for the 300 mg/cm depth and this limits in either an accident or an emergency, or both, in 2
revised standard is adopted by the NVLAP program. (Note:
accordance with 10 CFR 20.1201(b). (
Reference:
10 CFR Requirements under the old Part 20 include the determina-20.1201(b)).
2 tion of the dose to the eye at a tissue depth of 300 mg/cm.
See Instructions for Preparation of NRC Form 5, Item 5.
(
Reference:
Question 100: (a) is any special TLD monitoring of eye dose equivalent required? (b) Do TLDs for eye dose mea-surement need to be physically located near the eye?
Question 77: Representatives of the nuclear power industry cre concerned that the additional terms provided in the Answer: (a) Individual monitoring of the dose equivalent revised rule to describe the "real estate" in and around to the lens of the eye is required if the eye dose is likely to commercial power plants seems to be overlapping. This exceed, in a year,1.5 rem (10% of 15 rem) for an adult or couki lead to confusion. Access to these various areas may 0.15 rem (10% of 1.5 rem) for a minor. Licensees may use also affect the category to which individuals working within any form of monitoring that is capable of measuring these these areas are assigned. At nuclear power plants, either
- doses, the " protected area" or " radiation controlled area" may serve as the " restricted area." Although workers granted (b) The answer to this question depends on the conditions of unescorted access entering the " protected area" may not be exposure, in most cases a licensee will not have to physi-directly monitored for radiation exposure, they nmst be cally place a TLD near the eye. However, there may be considered as " occupationally exposed." At least minimal unusual exposure situations (such as exposure of the eye to
- radiation worker" training is required for these workers a narrow beam of radiation) that wouki make it necessary to consistent with the regulations. " Controlled areas" would place a dosimeter near the eye. [ Note: See Questions 45 typically extend to the " site boundary" or " owner controlled and 46.] (
References:
10 CFR 20.1003,10 CFR 20.1201, area." Does the NRC staff have any conunents on this 10 CFR 20.1502).
matter?
Answer: Each licensee shouki carefully document how the Question 123: In 10 CFR 20.1201(a)(1) does " annual licensees local " area" terms corresporxl to the area terms in limit" for dose (s) mean the limit on doses received in a 10 CFR Part 20 (restricted, controlled, and unrestricted
" year" as defined in 10 CFR 20.1003?
creas). Under both oki and revised Part 20, anyone who enters a restricted area is subject to the occupational dose Answer: Yes. (
References:
10 CFR 20.1201,10 CFR limits and must receive appropriate instructions in accor-20.1003) dance with 10 CFR 19.12. Workers can also be occupa-tionally exposed (arx1, therefore, subject to the occupational dose limits) in controlled and unrestricted areas (i.e., areas outside restricted areas) deperxling (in accordance with the definition of " occupational dose") on the nature of the work NUREO/CR-6204 16
i Questions and Answers l'
Question 172: (a) If the annual limit to the head is five rem and/or neck, and few if any shields protect the head from deep dose equivalent, what is the purpose of the 15 rem eye external radiation. Therefore, few shields wouki satisfy the dose equivalent? (b) llow can a person receive 15 rem eye conditions for credit.1lowever, licensees shoukt use shieki-done equivalent without exceeding the annual TEDE limit?
ing as necessary to minimize the area of exposure and keep doses ALARA. (
Reference:
Answer: (a) h purpose of the 15 rem non-stochastic limit to the lens of the eye is to prevent lens opacities (cataracts). The dose limit to the head (a stochastic limit)
Question 176: 10 CFR 20.1201 (a)(2)(ii) states a limit of end the dose limit to the eye (non-stochastic limit) are "A shallow. dose equivalent of 50 rem (0.50 Sv) to the skin measured at different dephs in tissue, I cm tissue equiva-or to any extremity." (a) Can a person receive 50 rem lent desh for deep dose and 0.3 cm for eye dose; and for shallow dose equivalent to the skin of the lower arm (ex-low penetrating radiation (such as beta or low-energy x-tremity) and 50 rem shallow dose equivalent to the upper rays), doses at different tissue dephs can be significantly arm (non-extremity), without having an overexposure? (b) different.
Can a person receive 50 rem shallow dose equivalent to the I
left upper ann, then the same dose to the right upper arm, (b) b 15 rem eye dose equivalent applies to the exposure without having an overexposure? (c) Can a person receive f
to the lens of the eye arxl is measured at a tissue deph of 50 rem shallow dose equivalent to each extremity dunng 0.3 cm. b 5 rem TEDE limit is the sum of the deep dose one year?
l l
equivalent at a tissue deph of I cm arx! the committed l
cffective dose equivalent. In general, a person can receive Anwr* (a) Yes, as long as the total shallow dose equiva-15 rem to the eye (measured at 0.3 cm) without exceeding lent does not exceed 50 rem in either position. b skin of the 5 rem limit on deep dose equave'ent whec tha head is the extremity is not considered in the shallow-dose equiva-exposed to beta or low-energy pheson radiation, although it lent limit to the skin of the whole body. The annual limits wouki be rare. for an individual to receive 15 rem eye dose are a shallow-dose equivalent of 50 rem (0.50 Sv) to the equivalent without exceeding a deep dose equivalent of 5 skin or to any extremity, rem, (
Reference:
(b) Again, as long as it can be shown that the total shallow dose equivalent does not exceal 50 rem at any one location Question 175: A health care worker serves in a dual on the skin of the whole body, there is no violation. If the nuclear medicine and radiology position, b worker wears two different areas of the skin of the whole body each a dosimeter on the wc.ist arxl a dosimeter at the collar, receives 50 rem total shallow dose equivalent during the During fluoroscopy procedures, which is the pnmary source year, then the limit has not been exceeded, of exposure, the worker wears a lead apron that covers the waist dosimeter, but not the collar dosimeter. Over the (c) Yes. The regulation states "... or to any extremity;"
course of a year, the worker receives a dose of 5.2 rem as therefore, a worker may receive a shallow dose equivalent measural by the collar dosimeter arul 1.7 rem as measured of 50 rem to each of the four extremities. (
Reference:
10 by the waist dosimeter. (a) Has the individual been over-CFR 20.1201,10 CFR 20.1003, Regulatory Guide 8.34) exposed? (b) Can licensees take credit for shielding while monitoring the extemal dose component of the TEDE7 Question 177: (a)If a worker is exposed to an extemal Answer: (a) Yes, the irulividual has received a dose in source such that his head is the maximally exposed area of excess of 10 CFR 20.1201 limits. W bead and neck con-the body, are the doses to the head limiting, since the head stitute part of the "whole body", and in this case, received is not inchuled under the definition of " extremity?" (b) the highest exposure. b collar dosimeter measured a dose What is the annual dose limit to the head, assuming no other of 5.2 rem over the course of a year. If the head and neck internal or external dose?
were not shielded, arul if the collar dosimeter was a mea-surement of the dose to the head and neck, then the dose Answer: (a) Yes. b annual limit for the dose to the head exceeded the limit of 5 rem TEDE.
is the same as the annual limit to the trunk and other por-tions of the whole body, which in the absence of internal (b) b licensee can only "take credit" for shiekling ifit dose, is equivalent to 5 rem deep dose equivalent.
can be shown that the dose monitored behind the shiekling is en accurate measurement of the mmmnm deep dose equiva-(b) b limit is 5 rem TEDE. (
Reference:
10 CFR lent to the individual. Many shields used for radiation pro-20.1201) tection do not cover all of the upper legs, upper arms, 17 NUREG/CR-6204
. =. -.
-~ -
..-~ - -.
Questions and Answers Question 217: How will licensees handle cases where oc-this individual would not be allowed any further exposure cupationally exposed workers inform the bcensee that they -
for the balance of the year." (Reference 10 CFR 20.1201,.
l are concurrently being exposed (and/or momtored) at an-10 CFR 20.2104).
other facility, but refuse to name the other facility? (Note i
that if the worker is under contract, the other facilities may j
be competitors of the licensee).
Question 415: This question refers to the answer to Quest on 41 under $20.1201. This answer leaves open what Answer: ~ Without knowing the occupational dose received is an acceptable frequency for querying monitored workers.
by the worker at the other facility, the Scensee cannot This is only an issue of momtored workers, isn't it? In the L demonstrate compliance with the occupational dose limits interest of workload mmaminatiae, I suggest that an anm=1 for the worker if it permits the worker to receive concur - ~
query /ramindar along with the required annual 10 CFR 19 rently an occupational dose. b heensee cannot allow the dosimetry report is =&9 =*=.
worker to receive any occupational exposure aAer the licensee becomes aware the worker is also receiving an Answer: b requirements of 10 CFR 20.1201(f) and the occupational exposure at another facility which the worker naswer to Question 41 apply to any individual who will refuses to name. See 56 FR 23383, third cohima, and receive an occupational dose, not just those individuals for Question 41 for additional information concerning con-whom individual monitoring is required.. b frequency for current employment. ' (
Reference:
- querying /remmding workers shouki be determined by the CFR 20.2106) bconsee; however, given that the dose limit is annual, the -
frequency shoukt be no less than anm ally. (
Reference:
Question 414: This question refers to the answer to Question 6 $20.1201. This answer does not directly ans-wer the implied question, which is, "if a person is assened Q=*atlan 435: b rule requires that "the assigned deep-a history of 5 rem or more for the current year, is that.
dose equivalent... must be for the part of the body receiving person permitted to receive any occupational dose?"
the highest exposure. (The dose] may be assessed from sur-voys or other radiation measurements for the purpose of Implied in the answer is that if monitoring is not required, -
demonstrating comphance with the occupational dose limits, that person can receive an occupational dose, presumably up if the individual monitoring device was not in the region of to 500 mrem for an adult. Conceptually, this is not consis-highest potential exposure." In the event of a hot particle -
tent with normal protection standards, i.e., "if you don't exposure to a portion of the whole body, it is unlikely that measure it, it is not there" is not a normally accepted the associated deep dose equivalent (DDE) resulting from practice. b Commission allowance for an explicit 100 the hot particle gamma radiation would be appropriately mrem (SECY-90-387, November 26,1990) woukt seem a measured by an individual monitoring device due to the much more reasonable a,proach. Both of these positions locahzed nature of the exposure. Is it required that the rppear to conflict with the answer to Question 113 in the DDE associated with a hot particle exposure be assened third set. Ilopefully, a position similar to that taken for the
- and added to the monitored DDE for the purpose of demon-declared pregnant woman with a pre-existing dose history strating compliance with the occupational dose limits?
will be taken. bt is, an additional sma'l increment of exposure is not biologically significant.
Answer: Yes. Although, for a hot particle on the skin, the j
deep dose equivalent is generally a small fraction of the _
Answer: "If a person is assessed a history of 5 rem or -
shallow dose equivalent, it does need to be assessed.'
more for the current year",' that individual is not permitted
(
Reference:
to receive any additional occupational dose during that year (except a planned special exposure). b answer to Ques-tion 6 does not imply that the individual can receive any Question 436: Licensees are required to " reduce the dose additional occupational dose (except in a planned special that an individual may be allowed to receive in the current exposure). As noted in the preamble to revised Part 20 (56 year by the amount of occupational dose received while i
FR 23369, second column), "the allowance of an additional employed by any other person." How shoukt this provision I rem per quarter following an exposure in excess of the be apphed to dose categories required to be monitored by limits has been deleted" from the final nde published on the current licensee, for which the individual's dose report May 21,1991. b answer to Question 6 is consistent with (e.g., NRC Form 5) from previous employment during the the rule and the answer to Question 113, which states that current year at another licensee's facility indicates "NR"
"...if the 5 rem CEDE was received during the current year, (not required), "ND" (not detectable), or is lea blank? May NUREG/CR-6204 18
,1
Questions and Answers the dose in categories denoted on the dose record as "NR",
with other information as a basis for the prospective intake "ND", or left blank be assumed to be zero, and therefore no assessment. For example, if the uses of radioactive materi-reduction be made to the dose that the individual may be als in a facility are not going to change significantly and allowed to receive in the current year?
bioassays ofindividuals employed in the facility have shown that no one has ever received an intake greater than 10%,
Answer: Yes, for cases in which "NR" or "ND" have then one might reasonably conclude that no one is "likely to been reconled. However, if there is no recorded dose for a receive" an intake in excess of 10% of the limit.
s dose category and no reason for this omission has been
(
Reference:
10 CFR 20.1202) provided (i.e., "NR" or "ND" have not been entered), the licensee should determine if the dose value has been omitted erroneously before assuming it to be zero (e.g., by checking Question 86: Does the term "per unit intake" in Footnote 1 with the licensee that provided the Form 5 with a dose cate-to $20.1202 refer to one event or to the entire monitoring gory left blank). If the licensee cannot determine why there period?
is no recorded dose for a dose category, the licensee has been unable to obtain a complete record of the individual's Answer: h term "per unit intake" does not refer to any dose history for that dose category and the individual's ex-particular time period. However, $20.1202, to which psure must be limited in accordance with 10 CFR Footnote 1 refers, provides a comparison to an annual limit.
20.2104(e)(1). (
Reference:
10 CFR 20.1201,10 CFR Thus, the time period of concern in this footnote is the 20.2104, Regulatory Guide 8.7, Rev.1).
" year" as defined in 10 CFR 20.1003. (
Reference:
10 CFR 20.1202 Footnote 1) 10 CFR 20.1202 - Compliance with the Requirements for Summation of External and Question 101: 10 CFR 20.1202(d) requires licensees to nWnal bm evaluate and, to the extent practical, account for mtakes through wounds or skin absorption. What type of "evalua.
tion" is appropriate for determuung absorption through the Question 9: A licensee monitors a worker for both external skin from skin contamination, and at what " practical level" and internal exposure under $20.1502, but the internal exp -
sure for the year is less than 10% of the dose limit. Does shoukt it be accounted for? For what nuclides, using what criteria can absorption be neglected under a certain thres-the licensee add it to the external exposure?
hoki, such as less than 10K,100K of skin contanunation?
Answer: If both internal and extemal doses were required Answer: b requirement to evaluate and account for to be monitored (see 10 CFR 20.1502 for these require-intakes through wounds or skin absorption is not new. W l
ments), then they must be summed. If only the internal or oki Part 20 has a:milar requirements [10 CFR 20.103(a)(1)].
exterrud dose required monitoring, then they don't have t brefore, tb " type of evaluation" that has been used be-i be summed. (Feferences: 10 CFR 20.1202,10 CFR fore L.uequate, can continue to be used. The statement in 20.1502) the old Part 20 (10 CFR 20.103, Footnote 4) that such intakes shouki "be evaluated and accounted for by techni-ques and procedures as may be appropriate to the circum-Question 38: Can the results of bioassays alone be used t stances" continues to be appropriate guidance for the revis-determine if the licensee must sum internal and external ed Part 20. (
Reference:
doses under Part 20?
Answer: No. Summation is required if the licensee is Question 179: If a licensee implements the revised Part 20 required to monitor for both external and internal doses.
in July,1993, is the licensee required to go back and evalu-h results of bioassays alone cannot be used to determine ate internal dose for the purpose of determining total effec-if the licensee must monitor internal exposures or sum mier-tive dose equivalent for the year?
nal and external dose under 10 CFR Part 20. Monitoring for internal is required for adults "likely to receive" in a Answer: No. b footnote to 10 CFR 20.2104(d), as year an intake greater than 10% of the limit. Determmation amended in 57 FR 57877,12/8/92, states, " Licensees are of what an individual is likely to receive is a prospective not required to partition historical dose between the external acsessment ofintake. Bioassay is a retrospective assessment dose equivalent (s) and the internal committed dose equiva.
of intake. Future intakes are not necessarily the same as lent (s)." As long as all of the licensee's worker's doses are past intakes. However, bioassay data may be used together below the oki limits and/or the workers will not participate 19 NUREGICR-6204
Questions and Answers i
in planned special exposures, the licensee need not reevalu-10 CFR 20.1203 - Determination of External e.te prior doses before implementing the revised Part 20.
Dose from Airborne Radioactive Material However, the licensee must subtract the dose already re-ceived during the year from the new annual dose limits to fir.d the limi s for the remainder of the year, as explained in Question 50: Does the footnote to 10 CFR 20.1203 mean Question 1, Set 1. (
Reference:
20.1202,10 CFR 20.2104) that DAC-hours, and not measurements of external dose (using personal dosimeters), shoukt be used for determuung
- **P ""' ' '
8""**
Question 180: Does the word "also" as used in 20.1202(c) mean intahe by oral ingestion and inhalation, or oral inges-Answer: No, as clarified in draft Regulatory Guide 8.N8, tion and extemal exposure?
the preferred method of determmmg worker exposure to n
88 mea 8ur mm 8 "8m8 Person.
Sa8 8 Answer: In 10 CFR 20.1202(c), the words "... also re-nel dosimeters. However, such dosimeters may not be czives an intake by oral m.gestion,.* mean in addition t capable of measuring the skin dose resulting from certain the ingestion associated with inhalat,on, as discussed in 10 noble gas radionuclides that emit weak beta radiation (e.g.,
i CFR 20.1202(b). All intakes by oral ingestion in excess of Xe-133 and Xe-133m). In such cases it is necessary to 10 perc ent of the applicable ALI must be accounted for,.
calculate the skin dose using measurements of the concen-whetN r the dose from oral ingestion is in conjunction with wie d h @
b which the workers were intakes by mhalation, external doses, or both. (
Reference:
exposed. (
Reference:
10 CFR 20.1203 Footnote) 10 CFR 20.1202, Regulatory Guide 8.34) 10 CFR 20.1204 - Determination of Internal Question 438: In general, the nuclear power industry has concluded that workers are not likely to exceed 10% of the Exposure annual limit on intake, and therefore internal dose monitor-ing would not be required. However, some nuclear power Question 47: Will the NRC provide guidance on prepara-plant licensees plan to continue internal dose monitoring and tion of applications pursuant to 10 CFR 20.1204(c)(2) for record and report monitoring results on a voluntary basis.
approval to adjust DAC or ALI values to reflect the actual (a) If the results of both voluntary monitoring of the com-physical and chemical characteristics of airborne radioactive mitted effective dose equivalent (CEDE) and required moni-materials (e.g., aerosol size distribution or density)?
toring of the deep dose equivalent (DDE) are reported on an individual's NRC Form 5, with appropriate comments in-Answer: The NRC staff is considering developing such dicating that the CEDE monitoring results are not required gu'. dance. Some limited guidance on " adjusting DAC's for (1.e., are vohmtary), are the CEDE and the DDE required particle size" is included in drah Regulatory Guide 8.25, to be summed as the total effective dose equivalent on the Rev.1, Section 3.7; however, the staff recognizes that more NRC Form 57 (b) If so, is the remanung available TEDE extensive guidance, including considerations of other physi-for the current year in which the results were obtained de-cal and chemical characteristics of particles, may be needed.
termined as 5 rems minus the year-to-date DDE plus
(
Reference:
CEDE, or as 5 rems minus the year-to-date DDE only?
(Note: the question assumes that the doses described are the only doses received by the individual in the curren' year.)
Question 76: The Department of Energy (DOE) does not assign a 50-year dose commitment in the year ofintake for Answer: (a) No. If monitoring for DDE is required int its workers exposed to internally deposited radioactive ma-monitoring for CEDE is not required, there is no requirs-terial. The internal dose is assigned on an annual basis.
Will commercial nuclear power plant licensees be required to assess intemal 50-year dose commitment for workers (b) No answer to this question is needed because the coming from DOE facilities? Some radionuclides encoun-answer to (a) is "no".] Note: This question and answer tered at DOE facilities may be beyond the normal assess-rpply to all licensees, not just nuclear power plants, ment methods of commercial nuclear power plants.
(
Reference:
Answer: The statement that DOE does not assign a 50-year dose commitment in the year of intake is not correct.
Although the DOE dose limita are applied to the dose ac-tually received in a year, DOE facilities are required by NUREG/CR-6204 20
Questions and Answers 4
DOB Order 5480.11 to generate and mamtain individual 20.1206(d), the licensee waits 7 months to record the dose occupational dose records that include ' committed effective (March), what year shouki the dose be recorded?
dose equivalent from intakes occurring during the year" and
' committed dose equivalent to organ and tissue of concern Answer: b committed effective dose equivalent should from intakes occurring during the year." DOE Order be recorded in the year the intake was received. If the dose 5480.11 also requires that records of exposure be made exceeded the limits, then it is considered an overexposure at available to the worker upon request of the worker. See the time when the intake occurred, and shoukt be reported related Question 6. (
References:
10 CFR 20.1204, DOE unmediately. (
Reference:
Order DOE 5480.11).
Question 372: When monitoring of internal exposure is Question 83: If a worker who has been exposed e intemal required by 10 CFR 20.1502,10 CFR 20.1204(a) requires sources under Department of Energy Order 5480.11 comes the licensee to take ' suitable and timely" measurements.
to work at an NRC-licensed facility, will the worker = ooe-Wi!! NRC define what is suitable and timely to avoid differ-mitted arx! comnutted effective dose equivalents need to be ences of opinion among inspectors?
cdculated for a fifty-year period by the licensee? DOE Order 5480.11 only requires a one-year dose commitment Answer: No. Some general guidance on what is suitable edculation, and timely will be included in Regulatory Guide 8.9, Rev.1,
" Acceptable Concepts, Mode'n Equations, and Assump-Answer: See answer to Question 76. DOE Order 5480.11 tions for a Bioassay Program." uther than this general requires DOE facilities to generate and maintain records of guidance, the NRC staff has no plans to provide a definition occupational dose including (a) committed effective dose of what is " suitable and timely." ht definition depends on equivalent and (b) committed dose equivalent to organ or the circumstances of the particular exposure. What is tissues of concem, in addition to re:ords of(c) amaial
" suitable and timely' under revised Part 20 is (as before, cffective dose equivalent and (d) scaal dose equivalent to under ok! Part 20) a matter of professionaljudgement in a organ or tissue of concern. (
Reference:
10 CFR 20.1204, good radiation protection program. NRC management will 10 CFR 20.2104, DOE Order 5480.11) resolve any " differences of opinion among inspectors' that are called to its attention. (
References:
10 CFR 20.1204, 10 CFR 20.1502)
Question 121: 10 CFR 20.1204(g) provides that when a mixture of radionuclides in air exists, licensees may dis-I r: gard certain radionuclides in the mixture if the licensee Question 437: The rule provides for disregarding certain uses the total actmty of the mixture in demonstrating com-radionuclides in a mixture of radionuclides in air if three pliance with the dose limits in section 20.1201 and if certain conditions are met. b conditions are:
other conditions are met. How can a licensee both disre-gird certain radionuclides and use the total activity?
'Ibe licensee uses the total activity of the mixture in
+
a.
demonstrating compliance with occupational dose limits and Answer: h term " total activity" in this section refers to monitoring requirements;
" gross activity' measurements that are correlated with other measurements of iudividual radionuclides. For example, b.
h concentration of any radionuclide disregarded is
" gross beta" measurements of air samples might be used for less than 10% ofits derived air concemration (DAC); and deternunmg intakes of a mixture of beta-emitting radio-nuclides when (a) gamma-ray spectrometry of representative c.
h sum of the percentages for all radionuclides dis-r.ir samples has identified radionuclides that account for regarded in the mixture does not exceed 30%.
more than 70% of the activity in the air samples (i.e., the percentage of radionuclides disregarded does not exceed As used in this provision, what is the intent of the phrase 30%) and (b) the concentration of any radionuclide
" total activity of the mixture" and how is it to be applied?
disreganled is less than 10% ofits DAC. (
Reference:
10 Please provide an example that illustrates how this provision CFR 20.1204) may be properly used.
Answer: See the answer to Question 121 under the head-Question 183: If an individual receives an intake of Class ing 10 CFR 20.1204. ht answer states that the term Y material in September and, pursuant to 10 CFR
' total activity" in 10 CFR 20.1204 refers to " gross activity' measurements that are correlated with other measurements 21 FUREG/CR-6204
Questions and Answers l
of irulividue radionuclides; an example of the use of this complying with %e 25 rem lifetime allowance," a previous provision is provided in that answer. (
Reference:
10 CFR intake, in units of MPC-hours, in excess of the oki Part 20 1
20.1204).
limit may be converted to a committed effective dose equi-f valent, in units of rems, by multiplying by a factor of (1.25 j
rem /520 MPC-h). Previous whole-body exposures, in units i
10 CFR 20.1206 - Planned Special Exposures of rem, in excess of the oki Part 20 limit may be assumed to be equal to the deep dose equivalent component of the TEDE (in units of rem). For example, if, under the oki Part Question 8: Under what circumstances are planned specid 29, a worker had received a whole-body dose that was 4 rem greater than the applicable limit and had also received exposures permitted 7 1
an intake that was 100 MPC-hours greater than the applic-Answer: The statement of considerations indicates that the able limit, the TEDE available for planned special exposures
)
of that worker under the revised Part 20 would be (25 intent of the p ana~1 apacial exposure was that it be used l
infrequently in circumstances where the elimination of the (100)(1.25/520)] rem, or 20.8 rem.
j 5(N-18) lifetime cumulative limit might create a severe handicap to A licensee's operation. See Regulatory Guide Although the question refers only to "the 25-rem lifetime allowance" on the TEDE, the 10 CFR 20.1206(e)(2) lifetime 8.N6, for further detailed guidance (
Reference:
10 CFR limit (five times the annual limit) also applies to previous 20.1206) over-exposures involving the lens of the eye, the skin, and the extremities. For purposes of complying with 10 CFR Question 24: Will consultants or vendors be able to rou.
20.1206(e)(2), previous exposures to the lens of the eye in tinely come on site to dojobs under the Planned Special excess of the oki Part 20 limits may be assumed to be equal Exposure section of the revised Part 20 if their annual to the previous overexposures to the whole body (because exposure becomes limiting?
the limit for the whole body applied to the lens of the eye) and a previous overexposure to the skin of the whole lxx!y Answer: No. Planned Special Exposures are not to be or to an extremity may be assumed to be equal to a corres-used " routinely." See definition of Planned Special Expo.
ponding overexposure to b skin of the whole body or to a sure in 10 CFR 20.1003 and requirements for Planned hand, forearm, foot or ankle, respectively, excep that over-Special Exposures in 10 CFR 20.1206. (
References:
10 exposures resulting from beta radiation from hot particles on CFR 20.1003,10 CFR 20.1206) or near the skin need not be included in the overexposures to the skin or extremities, l
Question 63: Must doses received in excess of the limits Note: For all future planned special exposures, the lifetime that were in effect before implementation of the revised Part limit is applicable to each annual limit listed in 10 CFR 20 be subtracted from the 25-rem lifetime allowance for 20.1201(a). (
References:
10 CFR 20.1201,10 CFR planned special exposures to obtain the total remaining dose 20.1206,10 CFR 20.2104, Technical Specifications) evailable for planned special exposures?
Answer: Yes. See 10 CFR 20.1206(e), which limits the Question 109: (a) Can a cardiologist who performs both i
dose from all planned special exposures and all doses in nuclear cardiology and cardiac catheterization use a planned excess of the limits to five times the annual dose limits in special exposure (PSE) to perform an emergency canliac 620.1201(a) < hiring the in<livWal'a Wi nm catheterization on the last day of the licensee's monitoring
, ar if his annual exposure as of December 30 is 4.9 rem?
The following discussion applies to individuals who worked It is expected that he will receive greater than 100 mrem l
c.t facilities of NRC licensees. It does not necessarily apply during the procedure. (b) Couki the same cardiologist per-to individuals who worked at other facilities.
form multiple cardiac catheterization as PSEs routinely during November and December if his annual exposure as of October 31 is 4.9 rem?
The "25-rem lifetime allowance" in the question is five times the annual limit (5 rem) for the total effective dose equivalent (TEDE), which is the sum of the deep dose Answer: (a) Yes, provided all administrative require-equivalent (for external exposures) and the committed ments of 10 CFR 20.1206 are met. (Note, although NRC is effective dose equivalent (for internal exposures). Before implementation of the revised Part 20 there were separate not regulating non-byproduct material, NRC still has regula-limits for internal and external exposure. For purposes of tory authority since the occupational dose has twen dfmed NUREO/CR-6204 22
Questions and Answers to include exposure from
- licensed and unlicensed sources people. The coefficients are not applicable to individual of radiation.') (
Reference:
20.1003 and 20.1206) doses as small as PSEs. How are nuclear power plant licensees expected to comply with this rule?
(b) No.10 CFR 20.1206(a) requires that a PSE be r.uthorized "... only in an exceptional situation when Answer: The requirement in 10 CFR 20.1206(c)(2) to alternativer that might avoid the higher exposure are un-inform the individual, who is to receive the PSE, of the available or impractical." Performing routine occupational estimated doses and associated potential risks is not a t sks for two months is not an exceptional situatian, so the requirement to inform that worker of a precise probability condition in 10 CFR 20.1206(a) is not met, in short, PSEs that the worker may suffer some particular deleterious cannot be used as a general mechanism to increase the an-effect(s) from the estimated radiation dose (s). This require-nual dose limit from 5 rem to 10 rem TEDE, for normal ment consists of a brief refresher of the instruction required situations. Note: The regulations do not prohibit the cardi-by 10 CFR 19.12 with respect to instruction concerning the ologist from performing the procedures, if the canliolo-risks associated with radiation exposures. Regulatory Guide gist's exposure exceeds the annual limit, it shouki be treated 8.29, which is being updated, provides guidance on this sub-as an overexposure rather than a PSE. (
Reference:
10 ject that is acceptable for meeting the requinement of 10 CFR 20.1003 and 20.1206)
CFR 20.1206(c)(2) as well as 10 CFR 19.12. That guide i
includes information concerning the differences between the risk to a particular irxlividual and the risk coefficients ap-l Question 110: Can a radiography licensee consider an plicable to large populations of exposed individuals.
individual's exposure, received during a source retrieval, as
(
Reference:
a planned special exposure if an approved generic procedure for source retrieval is on file? Assume that this procedure addresses all the administrative and recordkeeping require-Question 137: At a nuclear power plant, the individual ments of 10 CFR 20.1206.
asked to approve a planned special exposure (PSE) will need to believe that the altematives are impractical or unavailable Answer: Yes, provided it is an excepional situation when before doing so. But he or she must recognize that ther citernatives that might avoid higher exposures are unavail-NRC inspector who later reviews the PSE report may n'ot r_ble or are impractical. (Reference 10 CFR 20.1206) agree, possibly leading to a notice of violation for an over-exposure. If the irxlividual at the nuclear power plant chooses to request it from the Region, can a decision be Question 135: 10 CFR 20.1206 permits a planned special obtained in advance regarding the acceptability of the exposure (PSE) only if the alternatives that might avoid the licensee's alternatives analysis?
higher exposure are unavailable or impractical. Under cer-tain conditions, the collective dose for a task cook! be re-Answer: Yes. Any licensee may contact the appropriate duced ifit coukt be performed by one worker receiving a supervisor or manager (e.g., a Branch Chief in the Division PSE, rather than by a series of several workers each receiv-of Radiation Safety and Safeguards in an NRC regional ing a dose less than the limit. Under these conditions wouki office) to detennine whether or not the NRC staff agrees the NRC consider the alternative of using the series of that the circumstances in an actual situation meet the workers to be unavailable or impractical?
requirement for an " exceptional situation when alternatives i
that might avoid the higher exposure are unavailable or Answer: No. Reductions in collective dose shouki be ac-impractical." A written description of the circumstances of complished while keeping workers within the dose limits.
the exceptional situation should be provided to the NRC Planned special exposures cannot be justified solely on the regional office when requesting NRC review in advance of a basis that they will reduce collective dose; however, reduc-PSE. However, an NRC decision in advance of a PSE, tion in collective dose may be part of the justification.
based on the information submitted by the licensee, that the
(
Reference:
circumstances appear to meet the regulatory requirements does not preclude a subsequent NRC f'mding, based on addi-tional information obtained during an inspection, that the Question 136: 10 CFR 20.1206 states that workers who circumstances were not as originally described and, there-will receive a planned special exposure (PSE) must be in.
fore, that the PSE was not in accordance with the regulatory formed regarding the risk from the radiation exposure that is requirements conceming PSEs. (
Reference:
10 CFR cxpected to be received. Radiation risk coefficients present-20.1206).
ly available are applicable to large populations and are not recommended for risk assessment for a small number of 23 NUREO/CR-6204
l Questions and Answers Question 191: Is a licensee required to provide dosimeters Controls affect the NRC requirement in 10 CFR 20.1208, to an individual during a planned special exposure (PSE)
" Dose to an embryo / fetus," and the guidance in Regulatory that would only be worn during the PSE?
Guide 8.13, ' Instruction Concerning Prenatal Exposure?"
1 Answer: No, there is no requirement, but the licensee may Answer: ht decision has no effect on either the require-do so. 10 CFR 20.1206 requires that the doses received ment or the guide, which are consistent with that decision, during a PSE be accounted for separately from the doses
(
Reference:
letter from Bill M. Morris, NRC/RES, to received under the limits of 20.1201, and the use of separate William E. Morgan, the Boeing Company, August 2,1991).
dosimeters that are wom only during the PSE is a practical means to account for the PSE dose. (
Reference:
10 CFR For the information of those not familiar with this decision, 20.1206,10 CFR 20.2105,10 CFR 20.2204) the Supreme Court in this case overtumed a U.S. Court of Appeals decision. In its decision, the Supreme Court re-sponded in the negative to the question, "Mr. u employer Question 192: 10 CFR 20.1206(e) says that licensees may exclude a fertile female employee from certainjobs because not authorize PSEs for workers whose doses from previous of its concern for the health of the fetus a woman might PSEs and a!! " doses in excess of the limits
- exceed certain conceive?" b court held that Title VII of the Civil Rights limits. (a) What and whose limits apply? (b) Does the Act of 1964, as amended, forbids sex-slaific fetal-protec-actuallimit (e.g. 3 rem / quarter,1.25 rem / quarter, etc.)
tion policies. b majority of the court concluded with a rpply, or does the equivalent annuallimit apply? (c) Do very strong statement: "It is no more appropriate for the doses from non-licensed souras (e.g., x-ray sources) that courts than it is for individual employers to decide whether were in excess of the facility's limits apply, especially if the a woman's reproductive role is more important to herself facility was not a licensee? (d) It appears that overexpo-and her family than her economic role. Congress has left sures will require the licensee to back-calculate the dose in this choice to the woman as hers to make." (
References:
excess of the limits, particularly when that dose was receiv-20.1208, Regulatory Guide 8.13) ed from an intake of radioactive material. However the Footnote 5 of 10 CFR 20.2106 says that assessments of dose equivalent and records made using units in effect Question 84: Can a female worker legally declare preg-b:Jore the licensee's adoption of this Part need not be nancy if she does not yet have documented medical proof 7 changed. Will the licensee have to, in fact, convert the old doses in excess of the limits to committed effective dose Answer: Yes. h revised Part 20 does not require a equivalent?
woman to have
- documented medical proof" of pregnancy before declaring pregnancy. (
References:
10 CFR Answer: (a) b regulatory limits at the time and place of 20.1003,10 CFR 20.1208).
the overexposure apply, if the individual worked for the Department of Energy (DOE), then the DOE limits apply.
If the individual worked in a foreign country, then that Question 170: Woukt a licensee be found to be in noncom-country's limits apply.
pliance with the limit for the dose to an embiyo/ fetus if, at the time the woman declared her pregnancy, the dose to the (b) b actuallimit applies.
embryo / fetus exceeded 0.5 rem and the embryo / fetus subse-quently received more than 0.05 rem from licensed material (c) Yes. It is the purpose of the regulation to control licen-that was in the body of the woman lefore she declared her sed material in such a manner that the total dose to an pregnancy.
individual, from licensed and non-licensed sources, does not exceed standards prescribed in the regulations.
Answer: No. The intent of 10 CFR 20.1208(d) is that the licensee shouki not be in violation of the limit for the (d) Yes. (
Reference:
10 CFR 20.1206,10 CFR 20.2104, embryo / fetus as a result of doses received by the embryo /
10 CFR 20.1001, Regulatory Guide 8.35) fetus before the woman declared her pregnancy or doses received as a result of intakes before that declaration was made. (
Reference:
10 CFR 20.1208) 10 CFR 20.1208 - Dose to an Embryo / Fetus Question 138: Although it is extremely unlikely, long. lived Question 59: How does the U.S. Supreme Court decision residual radioactive material in the body of a female worker in the case of United Auto Workers (UAW) xs Johnson from her previous employment could deliver a dose exceed-NUREG/CR-6204 24
Questions and Answere ing the limit to a subsequently conceived embryo / fetus. For Question 416: This question refers to the answer to example, a former DOB worker who had been involved in Question 84 under $20.1208. h has also been asserted that an accident couki have a large americium or plutonium body the declared pregnant woman (DPW) declaration can be burden. 10 CFR 20.1208 makes no special provision for prospective. Are there any limits on how frequently or how this eventuality. What action wouki the NRC expect the long a duration a person can declare they are in a DPW, licensee to take?
e.g.,10 years?
Answen h answer to this question is provided in Answen No. There is no limit in 10 CFR Part 20 "on Regulatory Guide 8.36, " Radiation Dose to the Embryo /
how frequently or how long a duration a person can declare Fetus," which indicates that if monitoring of a declared they are in a DPW status." A woman can state that she is pregnant woman is required, the existing body burden must pregnant any time she feels it is necessary for her to do so, be included in deternumng the embryo / fetus dose. If the However, by definition (in Part 20) a DPW has voluntarily licensee determines that the dose to the embryo / fetus has informed her employer, in writing, of her pregnancy and of 4
exceeded 0.5 rem, or is within 0.05 rem of the dose limit by tim estimated date of conception. Furthermore, there can be the ti=: the woman declares her pregnancy, the licensee no " prospective" declaration of pregnancy. In the definition may allow the embryo / fetus to receive an additional 0.05 of a " declared pregnant woman," the words "... informed rem during ti wmairder ofla pregnancy. If the prior her employer of her pregnancy..." mean that the woman body burden alone caused a dose to the embryo / fetus in has informed her employer that she is pregnant, not that she excess of the limit, that dose shoukt be recorded, but the will be, or intends to become, pregnant at some time in the NRC wouki not take enforcement actions for this 'over-future. (
References:
10 CFR 20.1003,10 CFR 20.1208).
exposure" provided that the licensee does not allow the embryo / fetus to receive more than 0.05 rem after the woman has declared her pregnancy. See the answer to the Question 439: If the employer has been informed, in related Question 120. ht answer states that the intent of writing, by a female worker that she is pregnant, ami the 10 CFR 20.1208(d) is that the licensee shouki not be in employer is not the licensee (e.g., tim employer is a contrac-violation of the limit for the embryo / fetus as a result of tor to the licensee), may the employer notify the licensee of doses received by the embryo / fetus before the woman the declaration of pregnancy to establish applicability of declared her pregnancy or doses received as a result of
$20.1208, Dare to an Embryo / Fetus, or must the woman intakes before that declaration was made. (
Reference:
10 herself make the declaration to the licensee?
CFR 20.1208).
Answer: h employer may notify the licensee that the woman has declared her pregnancy in accordance with the Question 382: Do NRC regulations allow a declared preg-definition of a " declared pregnant woman" in 10 CFR nant woman to 'undeclare" her pregnancy? If so, does this 20.1003. However, there is no NRC mhmme to do so, withdrawal of a previous declaration of pregnancy also
(
References:
10 CFR 20.1208,10 CFR 20.1003).
oblige the licensee to withdraw restrictive measures and enhanced monitoring established solely to comply with related embryo / fetus dose limits?
Question 440: In order to terminate a declaration of pregnancy, i.e., due to ternunation of the pregnancy or Answer: Yes, to both questions. Under the regulations otherwise, must the female worker inform the licensee or (which are consistent with the Supreme Court decision in employer in writing?
the case of UAW vs. Johnson Controls), a woman has the right to choose whether or not to declare her pregnancy, Answer:
No. hre is no requirement in the regulation including the right to revoke her declaration. It is the specifying how to termmate a declaration. However, since woman's right to choose, not the declaration of pregnancy, the declaration of pregnancy is required to be in writing, it that is irrevocable. Ente: A woman's withdrawal of her wouki be a good practice to terndnate the declaration in the declaration of pregnancy does not alter the requirement of same manner. (
References:
10 CFR 20.1208,10 CFR 10 CFR 20.2106(e) that the licensee (continue to) mamtain 20.1003).
the records of dose to the embryo / fetus (that were prepared r.s a result of the woman's declaration of pregnancy). See Regulatory Guide 8.7, Rev.1, Section 2.3, concerning Question 441: If the declared preguant woman's estimated reporting of the embryo / fetus dose on request of the moni-date of conception encompasses a previous period of em-tored woman. (
Reference:
ployment at another licensee's facility, what assumptions 25 NUREG/CR-6204
1 Questions and Answers should be made by the current licensee for compliance pur-who receive doses from occupational exposure. (
Reference:
poses under each of the following conditions?
c.
Until records are received from the previous licensee; Question 443: Are licensees required to advise personnel b.
If previous monitoring records are incomplete or other-of the provisions for declaring pregnancy, who enter a re-wise unavailable; and stricted area, but do not " work in or frequent" any restricted area (e.g., visitors on tours)?
If monitoring by the previous licensee of the woman's c.
deep dose equivalent and/or the committed effective dose Answer: No. (
Reference:
equivalent was not required, and therefore dose records were not maiaWn~I, but the woman is likely to have re-ceived dose due to the nature of her employment at the 2.4 SUBPART D - RADIATION previous licensee's facility.
DOSE LIMITS FOR Answer: See the answer to the related Question 406 under INDIVIDUAL MEMBERS OF the heading for Regulatory Guide 8.36.
TM PUBLIC (a) As provided in 10 CFR 20.2104(c), the licensee may accept, as a record of the prior dose to the embryo / fetus, a signed statement from the declared pregnant woman.
10 CFR 20.1301 - Dose Limits for Individual
(" Records from the previous licensee" are not required; Members of the Public however, as indicated in the answer to Question 371, it is considered good health physics practice to verify the infor-mation on prior exposure provided by the irxtividual.)
Question 42: A nuclear medicins technologist becomes contammated with I-131 which results in an internal uptake (b) "the answer to this question is the same as the answer to of iodine. She continues to breast-feed her baby. Is the part (a) of the question if the woman can provide the infor-licensee responsible for controlling the dose to the baby as a mation on the prior dose to the embryo / fetus; that is, the member of the public in an unrestricted area? If so, what licensee may accept, as a record of the prior dose to the are the dose limits?
embryo / fetus, a signed statement from the woman. If the woman cannot provide this information, the licensee should Answer: h licensee is responsible for the licensed
[as indicated in the answer to Question 406(b)] make an material that has internally contaminated the technologist.
effort to make a reasonable estimate of the dose using other b limit for a member of the public applies to the baby.
information that the woman and her previous employer have
(
References:
10 CFR 20.1201 and 20.1301) concerning her exposure.
& licensee is responsible for performing a " survey" to (c) As indicated in the answer to part (b) of the question assess the magnitude of the dose to the baby [10 CFR and in the answer to Question 406, the licensee shouki make 20.1501(a)].
an effort to make a reasonable estimatc of the dose using other information that the woman and her previous em-With respect to the continued breast-feeding of the baby, ployer have concerning her 3xposure. (
References:
10 there are important legal, moral, and ethical considerations CFR 20.1208,10 CFR 20.2104).
(including the rights of the technologist) that are outside the limited scope of 10 CFR Part 20. Both NRC and the licen-see would have to address these considerations if such a Question 442: Is the licensee required to advise personnel situation were actually to arise. (
References:
10 CFR of the provisions for declaring pregnancy, who work in the 20.1201 and 20.1301) controlled area, have been classified as " members of the public," and do not " work in or frequent" any restricted area?
Question 48: In 10 CFR 20.1301(a)(2), does ".. 0.002 rem (0.02 mSv) in any one hour" apply to the dose in any Answer: No. However, it would be a good practice to do single hour or can it apply to the average over a discrete so. A provisions of 10 CFR 20.1208, for limiting dose to pericd of time.
the embryo / fetus, apply only to declared pregnant womea l
Questions and Answers Answer: b phrase "0.002 rem in any one hour" means a material in controlled areas. Note that for members of the cumulative dose of 0.002 rem in any peried of 60 consecu-public the 100 mrem in a year limit applies, b 2 mrem in tive minutes regardless of the dose rates within that 60-min.
an hour limit does not apply in a controlled area. This limit period. It does not mean a dose rate, in units of rems per applies only in an unrestricted area.
hour, obtained by averaging over a time period greater than, or less than, one hour. (
Reference:
(b) Yes.
(c) bre may be " airborne radioactivity areas" within Question 105: How shouki demonstration be made of controlled areas that need to be posted. See the answer to compliance with the 2 mrem in an hour limit [10 CFR Question 27. (
Reference:
10 CFR 20.1301,10 CFR 20.1301(a)(2)]? Is it adequate, for a nuclear power plant, to 20.1201) demonstrate compliance by having effluent control (trip) systenu that prevent effluent releases from exceeding the limits on the instantaneous release rates, and by performing Question 111: Section 20.105(a) of 10 CFR Part 20 priodic surveys during radioactive material storage arxl provides for Commission anthnriv= tion of radiation levels in movements?
unrestricted areas based on a criterion of 500 millirems in one year to an individual in such areas. Does such an auth-Answer: W 2 mrem in an hour limit is not new; it ap-orization for radiation levels in an unrestricted area that pears in the old Part 20 in 10 CFR 20.105(b)(1). Therefore, could ressdt in a dose to a member of the public in excess of methods for complying with this limit that have been accept-100 millirems in a year continue under 10 CFR 20.1301(c)?
able in the past will continue to be acceptable mvler the new In other words is this considered an " exemption" as covered Part 20. W 2 mrem in an hour limit applies to doses in an in 10 CFR 20.1008(d)?
unrestricted area from radiation sources located either inside or outside of that unrestricted area. brefore, compliance Answer: No and No. h nature of the information re-can be achieved by a reasonable combination of appropriate quested under 20.1301(c) is different from that requested j
controls, surveys, and monitoring of sources, and potential under 20.105(a) in that 20.1301(c) requires a demonstration sources. Such controls, surveys and monitoring are not of need for the proposed dose limit and procedures for necessarily limited to the " effluent control trip system" and maintaining doses ALARA. It may be appropriate for an
- periodic surveys during radioactive material storage and applicant to refer to information submitted under 20.105(a) movements" that are stated in the question. For example, as pan of an application suomitted under 10.1301(c).
controls and surveys related to increased turbine shine at
(
References:
10 CFR 20.1301(c),10 CFR 20.1008(d), and BWRs as a result of hydrogen water chemistry must be 20.105(a))
included. (
Reference:
Question 125: 10 CFR 20.1301(a)(2) requirer that the Question 106: (a) Are there no limits on airborne radio-
" dose" in any unrestricted area from extemal sources not cetivity concentrations in the controlled area, other than de exceed 2 mrem in any one hour. Which of the many facto limits for public dose to keep dose rates less than 2
" doses" in new Pad 20 is "the dose" in $20.1301(a)(2),
mrem in an hour? (b) Wouki stack effluents creating temp-orary airbome radioactivity concentrations greater than Answer: The " dose" from external sources in 10 CFR DAC levels in the controlled areas be allowed, as long as 20.1301(a)(2) means the deep dose equivalent or the eye the public dose cri*eria of 10 CFR 20.1301 are met? (c)It dose equivalent or the shallow dose egaivalent. See defmi-appears that theu areas wouki not need to be " posted" or tions of these dose terms in 10 CFR 20.1003. (
References:
controlled, since there are not any 10 CFR Part 20 airbome 10 CFR 20.1301,10 CFR 20.1003).
radioactivity concentration limits for controlled areas. Is this correct?
Question 201: Why is it that releases to sanitary sewers are Answer: (a) hre are no limits on concentrations of not included in the dose limit for members of the public airbome radioactive materials in controlled areas that are while other effluent releases are?
expressed in terms of concentrations. Ilowever, both the occupc.tional dose limits (for individuals who receive an Answer: W practice of having separate limits for dis-cccupational dose in a controlled area) and the dose limits charge to sewers is a practice that has been in place since 10 for an irxlividual member of the public (when in a controlled CFR Part 20 was proposed in 1955. If the dose limit for crea) indirectly limit the concentrations of radioactive individual members of the public included the dose contnbu.
Questions and Answers tion of licensed material into sanitary sewerage, there would Question 205: (a) 10 CFR 20.1301(a)(2) requires that the be no practical way for the licensee to determine the magni-dose in any unrestricted area from external sources does not tude of that dose contribution for the purpose of demonstrat-exceed 2 millirem "in any one hour." Since this is not an ing compliance with the limit because of the remoteness of instantaneous limit, can the licensee operate at levels much the individual being exposed from the point of discharge.
higher than 2 millirem per hour for a very short period of Water released into the sanitary sewer is consideral unavail-time (e.g.,90 millirem /hr for 1 minute, then no dose for able until it passes through the sewage treatment plant.
the rest of the hour)? (b) If so, how is the 2 mrem in any Effluent concentration limits (as in Table 2 of Appendix B) one hour inspectable?
have always been calculated under the premise that a mem-ber of the public lives at the licensee's site boundary and Answer: General response: This requirement in 10 CFR utilizes the air and water available at that point. Release 20.1301(a)(2) is not new, it is essentially the same as the limits are set in Table 3 so that if the releases from the requirement in 10 CFR 20.105(b)(1). Specific response:
sewage treatment facility were the only source of ingestible (a) Yes.
water, tha Ame to the individual wmid be a committed effective dose equivalent of 0.5 rem per year. (
Reference:
(b) The licensee must be able to demonstrate compliance 10 CFR 2n.1301) with the dose limits of 10 CFR 20.1301 and the survey requirements of 10 CFR 20.1501. If an inspector identifies Question 203: Can you have radiation levels in excess of 2 areas where the radiation levels may be in excess of 2 mrem millirem in one hour or 100 millirem per year in a control-in any one hour and the licensee is unable to demonstrate led area if the public is not allowed to enter the area?
compliance with the dose limits for an unrestricted area and with the survey requirements, the licensee may be cited.
Answer: If the public is not allowed to enter for reasons
(
Reference:
10 CFR 20.1301,10 CFR 20.1501) other than limiting radiation exposure, the answer is yes. If the public is not allowed to enter in order to limit radiation exposure and for other reasons, the answer is no. As indi-Question 206: Can a licensee allow radiation levels of 5 cated in the answer to Question 26(a), under the discussion mR or more in om hour in an area without limiting access of " controlled area", when an area meets both the defmition to the area?
of a controlled area and the definition of a restricted area, the area is considered a restricted area for purposes of com.
Answer: If the phrase "... without limiting access to the l
pliance with Part 20. (
Reference:
10 CFR 20.1301) area" is intended to mean an unrestricted area, the answer is no. See Question 205, this Set. (
Reference:
10 CFR l
20.1301,10 CFR 20.1003)
Question 204: (a) Licensees may apply under 10 CFR i
20.1301(c) to operate at a higher annual dose limit of 500 l
millirem to individual members of the public. How long Question 384: Nuclear power plant licensees are required l
will this 500 millirem limit apply to the licensee? (b) Can a to meet the criteria in 10 CFR 50 Appendix 1 and 40 CFR l
licensee apply for an authorization to operate at this higher 190 with regards to maintaining doses to individual mem-limit indefinitely?
bers of the public ALARA. Related Regulatory Guides (e.g.,1.21,1.109, and 4.1) describe programs which are Answer: (a) The 0.5 rem per year limit is interxled to 1,e acceptable to the NRC staff to demonstrate compliance with applied primarily to temporary situations where operation of 10 CFR 50 Appendix I and 40 CFR 190 criteria. Specific the facility, or public exposure to radiation, is not expectal requirements for monitoring, sampling, dose calculation and to result in doses above 0.1 rem over long periods of time, reporting are included in each plant's Technical Specifica-20.1301(c)(1) requires that the licensee specify the expected tions and related Offsite Dose Calculation Manual. Does duration of operation in excess of the limit. %e Commis-compliance with plant Technical Specifications, applicable sion will only approve such applications if the licensee Regulatory Guides, and the radiation standards in 40 CFR provides all of the information specified in 10 CFR 190 fully meet the requirements of 20.130l? ne purpose 20.1301(c), and if the infonnation is acceptable.
in asking this question is to obtam clarification that, al-though the revised 10 CFR 20 introduces new dose limits (b) It is unlikely that the Commission will approve a re-for individual members of the public and new effluent con-quest to operate at the higher limit indefinitely. (
Reference:
centration values in 10 CFR 20 Appendix B, the scope of 10 CFR 20.1301) monitoring, sampling, dose calculation azul reporting are not changed for nuclear power plants by the revised 10 CFR 20 from the previously applicable requirements and guidance.
l l
NUREO/CR4204 28
~
I 4
Questions and Answers Answer: Not necessarily. See the questions and answers Answer: Principally by the control of acceso and, thereby, in sections 10 CFR 20.1301 and 10 CFR 20.1302. General-exposure time, since the licensee can requite members of ly, for nuclear power plants, no major changes are needed the public to exit the controlled area at any titze. (10 CFR in "the scope of monitoring, sampling, dose calculation, and 20.1301(b) provides that if a licensee permits miembers of reporting" that has been adequate for compliance with plant the public to have access to controlled areas, ths limits for Technical Specifications and 40 CFR 190, and for conform-members of the public continue to apply to thoso individ-ance with applicable regulatory guides. However, some uals.) (
Reference:
10 CFR 20.1302) relatively minor changes may be needed. For example, at some plants, changes may be needed for demonstrating compliance with the requirements of 10 CFR 20.1301 as Question 68: This question concerns demonstration of they apply in members of the public in controlled areas, compliance with the dose limits for individual memiers of (See the answer to Question 104.) (
References:
10 CFR the public. Section 20.1302(b), in the revised 10 CFR Part 20.1301,10 CFR 20.1302).
20, permits the licensee to demonstrate compliance by:
1
" Demonstrating by measurement or calculation that the 10 CFR 20.1302 - Compliance with Dose total effective dose equivalent to the individual likely to
*i 'h* hi h**' d I' " 'h* li '"'*d E*'i "
8 Limits for Individual Members of the Public does not exceed the annual dose limit; or emmstrat ng that:
Question 28: How are annual average concentrations
- 8 (AAC) to be calculated, and is it acceptable for nuclear 8"*""***'
pwer plants to use this AAC in lieu of instantaneous limits boundary of the unrestricted area do not exceed the (as currently required by the operating license) which are derived from NUREG-0133?
va ses sp ified in Table 2 of Apperxlix B to gg20.1001
- 20.2401; and Answer: AACs are calculated by multiplying the annual (ii) if an individual were continually present in an effluent release of individual radionuclides by the annual unstr e
- area, se fmm extemal smrces wmW average atmospheric dispersion factor for the most prevalent n t exceed 0.002 rem (0.02 mSv) in an hour and 0.05 dowmvial sector at the controlled / unrestricted area bound-rem (0.5 mSv) in a year.'
j ary. The instantaneous limits, on the other hand, are based on a whole body dose limit of 500 mrem /y and a thyroid Option (1) above woukt rnquire the utility to demonstrate dose limit of 1500 mrem /y for gaseous releases and "E ""#* *' **
- "* " " I'"#
- E"* '* * * " "
Appendix B concentration values for liquid releases. In 0.1301 and the limits to a member of the pubh.c specified both cases, the dose rate or concentration values are applied m 40 CFR 190. This option allows for the use of occupan-on an instantaneous maximum basis at the boundary of the
- I "# " ' " * * * ' "
^IE*
~
unrestricted area. Annual average dispersion estimates are Y
f recent Acdus Cmfonnm.""d used to relate the concentration or dose rate to a release g Anwalawnts, pmWes an rate, arx1, ultimately, to an effluent monitor alarm set point.
example f a S verity IV vi lati n based on option '2 For purposes of maintaining effluent releases ALARA pur-above which does not account for occupancy factors.
suant to 10 CFR Part 50, Appendix 1, power reactor licen-sees are restricted by Technical Specifications to the instan-h m W WM h h he mW W taneous limits. To permit effluent releases at levels corres-g ggg pnding to the AAC desenbed above would not enable a This unnecessary restriction could severely limit availability licensee to meet the Appendix I design objectives.
of power, particularly at BWRs operating with hydrogen
(
Reference:
water chenu. try, without a corresponding reduction m s
actual dose to the public. It is requested that these examples fv lati ns be clarified to ensure consistency with the Question 29: If a licensee controls exposure to members of M8ulath the public using the new Part 20.1302(b)(2) at the boundary of the unrestricted area, how does a licensee ensure that Answer: The enforcement examples in question are members of the pubhc m, side the controlled area do not gg 2'
exceed this limit?
[10 CFR 20.1301(b)(2)] does not allow for use of occupncy factors other than unity 10 CFR 20.1302(b)(2)(i) concerns 29 NUREG/CR-6204
~ --
. _. -. ~. --
- Questions and Answers -
l emuent concentrations, which do not involve occupancy -.
. licensee will need to perform emuent or environmental and 10 CFR 20.1302(bX2Xii) involves the assumption that momtoring if it is only bcensed for r'%y and/or an individual is cane===lly present in the area or, in other, brachytherapy.- (
References:
10 CFR 20.1302, Byproduct wonis,10 CFR 20.1302(bX2Xii) requires the r, ^L-2 of :
Matenal heenses (medical))i en occupancy factor of 1.0. (
Reference:
I Question 102: Under 10 CFR 20.1302(bX2Xii), (a) do the-Question 69: his question concerns redsonctive emuent words, "If an individual were cane===lly present in an un-concentrations. 10 CFR 20.1302(bX2) addresses the====t reatncted ares," mean that under these provisions it should average concentrations, and limits on these concentrations, be a====arl a hypothetical individual is there, or (b) al==ilti j
as they apply to members of the public. The changes pub-
%y gh=l=a hg ggde jg app ly gg (big martn=7 _
j lished as conformmg avaami==da to Part 2 uniformly.
. (
. a) Yes. (b) No. hppla===tal e=I===a*
address violations to these emuent limita as i=*==*aaaans Answer:
values. Whila i' !? elear that sigmficant iaasmataaar==..
Although this question came from a maclear power plant, it concentrations of these limits constitute a' concern to public -
seems unhkely that a nuclear power plant would choose to safety, the description that any release in concentrations
.- use this option [10 CFR 20.1302(bX2)], with its conserva-above the limits of Appendix B, Table 2 constitutes a -.
tive :-
- =, to densonstrate -- f
- with the annual
^*
- Severity level IV Violation and an i=me==e==ar== release
' dose limit in 10 CPR 20.1301(aX1). ' It seems more likely.-
exceeding twice the limit of this table constituting a Severity
> that a nuclear power plant would prefer to use'the option of Ievel III Violation are not consistent with the intent of the 10 CFR 20.1302(bX1) which does not involve the conserva-mle. It is requested that the descriptions of violations be tive assumptions (emuent concentrations 'at the bon-lary of-clanfied with respect to the clear intent of the rule that the the unrestricted area' and an ' individual... continuously.
limits.
present in an unreatncted aren"). Nuclear power plants and limits of Appendix B. Table 2 apply to===i=1 average' other uranium fuel cycle facilities anst meet the more restnctive public dose limits of 40 CFR 190. As nasart in Answer: The examples in the enforcement policy concern-the aeasa===t of considerations (56 FR 23374, third.
ing release of radioactive materials to an unrestricted arm at column), demonstration of comphance with the limits of 40 concentrations in excess of the limits for members of the CFR 190 will be considered to demonstrate comphance with public shouki be understood to refer to the namial average the 0.1-rem annual limit of 10 CFR 20.1301(aX1) for mo t concentrations and not the instantaneous concentrations.
facilities. His demonstration of compliance wouki be con-i bre is no requirement in 10 CFR Part 20 based on the sistent with the option of 10 CFR 20.1302(b)(1). See the instantaneous concentrations (shbough technical specifica-answer to the related Question 68. (
Reference:
10 CFR tions for power reactors do contam such requirements); thus
-20.1302).-
there can be no violation of a Part 20 requirement involving
~
t instantaneous concentrations and, therefore, the question of the severity level of the violation, and the examples used for ~
Queselan 103: 10 CFR 20.1302(bX2Xii) refers to "the dose these severity levels, are not relevant. Nevertheless, the.
from external sources." (a) What arefexternal sources'?
subject examples will be clanfied in a future revision of the -
(b) Are both (1) shine from the facility or from storal -
enforcement policy to make it clear that the subject exam-M matenals and sources, as well as (2) cloud ples refer to the statement a wi L.g annual average con-shine from emuents to be included?.
centrations in 10 CFR 20.1302(bX2Xi). (
Reference:
10 l-CFR 20.1302(b))-
Au m (a) *ExMrnal sources
- are radiation sources og moe body.
Question 72: Will certain materials licensees (such as
~ (b) Yes. ~ (
Reference:
teletherapy and brachytherapy bcensees) be required to con-duct environmental monitoring in unrestricted areas to de-monstrate compliance with the new dose limit for individual Question 104:.10 CFR 20.1302 provides two options for members of the public?
demonstrating w+ k.i.ce with the annual dose limit, in 10 CFR 20.1301, for members of the public.' How does 10 Answer:. Yes. Le licensee must demonstrate ca=aliam CFR 20.1302(bX2), the second option, provide demoni with 10 CFR 20.1301. Licensees must perform radiation stration of comphance with the annual dose limit for surveys in areas adjacent to locations where radioactive members of the public who are in a contmiled aren?
materials are used or stored. It is unlikely, however, that a NUREO/CR-6204 30 l
a i
Questions and Answers Answer: It doesn't. This second option applies to Answer: The words "... access to which can be limited.
l members of the public in unrestricted areas and a controlled
.." in the definition of " controlled aren* mean that access
[
area is not an unrestricted area. However, it would be can he limited at any and all times, regardless of whether or acceptable to demonstrate compliance with the annual dose not access is limited at may particular time. An area desig-l limit for members of the public in a controlled aren [10 CFR nated by a licensee as a contmiled area continues to be a j
20.1301(a) and (b)] by applying the effluent concentration controlled area until that designation is changed; it does not criteria of 10 CFR 20.1302(b)(2)(i) and the external dose change from being a controlled area, and become an unre-criterion of 10 CFR 20.1302(b)(2)(ii) to the ennemllad area, stricted area, simply because access is not being limited at -
{-
rather than to the unrestricted area. (
References:
10 CFR some pasticular time. [See discussions of " Licensee Discro-j 20.1003,10 CFR 20.1302).
tion' and " Controlled Arens' in the answer to Question 26(n).] (
References:
10 CFR 20.1003,10 CFR 20.1302).
Question 207: W dose limits for an individual member of the public as specified in 10 CFR 20.1301 are specified in Question 427: b word " external" in 10 CFR i
terms of rem. Since mm is an absorbed dose, umst an indi-20.1302(b)(2)(ii) refers to any radiation source which could j
vidual be present for the dose limit to apply?
irradiate an individual from outside the body. Since sources include both airborne radioactive materials and contamed Answer: No. If using 10 CFR 20.1302(b)(1) to show com-sources, the dose from airborne radioactive materials could l-pliance with dose limits, occupancy times (time an indivi-be double-counted - as a concentration pursuant to 10 CFR dualis present) may be taken into account. If using the 20.1302(b)G)(i) and as direct radiation pursuant to 10 CFR 4
j method in 10 CFR 20.1302(b)(2)(ii) to demonstrate 20.1302(b)G)(ii). In a situation where the licensee was j
compliance, dose is calculated as if an individual were con-approaching the 50 mrem /yr limit from direct radiation from tinuously presens, regardless of whether an individual is contamed sources, the additional direct radiation component 3
continuously present.' See related Questions 68, Set 2, and from airborne releases may cause this limit to be exceeded, i-102 Set 3. (
Reference:
10 CFR 20.1302,10 CFR 20.1301)
Clearly, this situation coukt be addressed through use of 10 I
CFR 20.1302(b)(1); however, the intent of the revised Part 20 appears to provide viable alternatives to complying with Question 208: la the licensee required to use the most the regulations whenever feasible. Must a licensee who recurato method for determuung compliance with dose elects to use the method of 10 CFR 20.1302(b)(2) for de-i limits or is it allowable to use any one of the acceptable monstrating compliance with the public dose limits " double-methods (assuming the acceptable method yields the lower count
- the dose from airborne radioactive materials?
dose)?
Answer: No. External sources ordinarily include all I
Answer: W licensee may use any one of the acceptable radiation sources outside of the body, such as direct radia-i methods for determining compliance with the dose limit (10 tion from contained sources and direct radiation from CFR 20.1301(b)(1) or G)). See related Question and airborne radioactive materials. To the extent that doses
[
Answer 102 (
Reference:
10 CFR 20.1302) from airborne radioactive materials (e.g., noble gases) are j
accounted for as concentration values pursuant to 10 CFR 20.1302(b)G)(i), they need not be accounted for as external i
Question 417: This question refers to the answer to sources under 10 CFR 20.1302(b)(2)(ii) in deternumng
{
Question 29 under $20.1302. The statement that a licenseu c=alhe with the 50 mrom/yr limit. (However, airborne can require members of the public to exit a controlled area radioactive material does need to be accounted for in deter-at any time is not obvious, based on the published rule. A mining compliance with the limit of 2 mrom in any one controlled area is one to which access can be limited, but hour). (
References:
10 CFR 20.1302,10 CFR 20.1301).
3 that condition might exist only at certain times or under l
certain conditions or the access limits might be of a nature Other than strict prohibition. For instance, it might be a i
control that specifically limits the stay time. Does NRC i
expect procedures to reflect the changing nature of such an i
area, i.e., controlled at one time but unrestricted at other j
times, or is an area that meets the requirements to be designated a controlled area for some portion of time simply a controlled aron all the time? (W latter, I hope),
j 31 NURBO/CR-6204 1-
L l
l Questions and Answers 2.5 SUBPART F - SURVEYS AND utilize a known ratio of the readily detectable radionuclides in a mixture to the more difficult-to-detect radionuclides, to MONITORING infer the total activity and the DAC fraction of a mixture I
from gross counting methods (i.e., without having to do isotopic analysis of each and every sample). Given adequ-10 CFR 20.1501 - Surveys and Monitoring-ate quality control measures, is the use of such " weighted" General or " effective" DACs acceptable for posting, survey and monitoring purposes?
Question 147: 10 CFR 20.1501(b) requires the licensee to Answer: Yes, in general, the " weighted" or " effective" ensure that instmments and equipment used for quantitative radiation measurements are calibrated periodically; DACs can be used for inferring the total activity and the however, there is no corresponding requirement in ok! Part DAC fraction of a mixture from gross counting methods
- 20. Does this new requirement mean that the accuracy and Provided that the method (s) for calculating the " weighted" frequency of such calibrations that have been found or " effective" DACs (which are not described in the ques-acceptable by the NRC in the past will not be acceptable tion) are appropriate, have been validated, and that the uses i
under the revixd Part 207 of these weighted / effective values are not inconsistent with other regulatory requirements, such as 10 CFR 20.1203,10 Answer: No. 'Ibe accepability of calibrr. tion frequency CFR 20.1204,10 CFR 20.1502,10 CFR 20.1902, and the and accuracy is not changed by the inclusion of Footnotes arul Note to Appendix B. The DAC values used fl20.1501(b)in the revised Part 20. (
Reference:
10 CFR in the calculation of the " weighted" or "ebetive" values 20.1501(b)).
(and the DAC values used for any other purpose) must be the values listed in Appendix B to Pan 20 unless the licen-see has obtained approval, under the provisions of 10 CFR '
Question 209: (a) Does the revised Part 20 require that 20.1204(c)(2) or 20.2301, to use other values. (
References:
meters be calibrated? (b) If so, is the calibration frequency 10 CFR 20.1501,10 CFR 20.1203,10 CFR 20.1204,10 specibd7 CFR 20.1502,10 CFR 20.1902, Appendix B).
Answer: (a) Yes,10 CFR 20.1501(b) requires that the licensee insure that instnunents and equipment used for 10 CFR 20.1502 - Conditions Requiring Indi-quantitative radiation measurements are calibrated periodi-vidual Monitoring of Internal and External celly for the radiation measured.
Occupational Dose (b) Part 20 regulations do not define " periodically." How-sver, specific NRC license conditions and other Parts of Question 43: The licensee initially was required to monitor Title 10 (i.e., Parts 34 and 35) may specify the periodicity nternal dose. 'lhe results indicate that monitoring is not for calibration. (
Reference:
10 CFR 20.1501) required, i.e., levels are positive but less than 10% of the allowable limits. Can the measured internal dose values be Question 210: 10 CFR 20.1501(c) r'9" ires a dosimet'Y sums internal and external doses?
processor to be NVLAP accredited. DOE also has an ac-creditation program. Do DOELAP-accredited processors Answer: The licensee was required to monitor internal meet the requirements of 10 CFR 20.1501(c)?
dose [because the licensee had made a prospective determin-ation that the individual (s) was (were) "likely to receive" an Answer: No. (Reference. 10 CFR 20.1501) intake in excess of 10% of the limits]. The internal dose values cannot be ignored regardless of the fact that they are less than 10% of the limits. If the licensee was not required Question 458: Some Pan 50 power reactor licensees have to monitor internal dose because the licensee had made a developed " weighted" or " effective" derived air concentra-prospective determmation that the doses likely would be less tion (DAC) values for ai2 borne mixtures of radionuclides, than 10% of the limits but elected to monitor internal dose on the basis that the mixtures are well known and relatively anyway, the licensee couki choose to " ignore" the measured stable, as demonstrated through periodic analysis of primary values that are less than 10% or to ackl those values to the sources (e.g., reactor coolant and other process fluids),
external doses to obtain the sum of the internal arxl external airbome and removable contammation samples, and waste doses. Nothing in Part 20 prohibits the licensee from streams (i.e.,10 CFR 61 analysis). These weighted DACs NUREO/CR-6204 32
l Questions arul Answers monitoring or summing intemal doses at less than 10% of At fuel cycle and materials facilities using large quantities of the limits; therefore, a licensee can never be in noncompli-unsealed radioactive materials, the nature of the operations aire for summing the internal and external doses.
is such that bioassays are required for workers who are
('wference: 10 CFR 20.1502) likely to receive an intake in excess of ten percent of the applicable ALis without respiratory protection. Because of j
the types and quantities of radioactive airbome particulates l
Question 44: During 1993, the licensee performed a at fuel cycle and materials licensees, it is advisable to not
~
prospective dose evaluation, arul decided not to measure take credit for respiratory protection factors when determ-intemal dose. In 1994, the licensee again evaluates the ining if monitoring (e.g., bioassay) is required. NRC will internal dose and finds that the thresboki for monitoring is consider licensee proposals to allow using respiratory pro-l exceeded and begins monitoring. Nothing in the facility tection factors when determmmg if internal dose monitoring i
(engineering controls or productivity levels) has changed.
is required, if the licensee demonstrates a verification The licensee accounts for the internal dose contribution method that the respiratory protection factor is actually when calculating TME for 1994. Must the licensee go achieved for all workers wearing respirators. Unless au-back and adjust TEDE for 19937 thorized in the license, fuel cycle and materials licensees shoukt understand that the threshold level for monitoring in Answer: Yes, the licensee must go back and adjust the 10 CFR 20.1502(b) is ten percent of the applicable ALis TEDE for 1993, based on the best available data. The ethnut credit for respirators. (
Reference:
10 CFR information included in the question indicates that the 1993 20.1502(b),10 CFR 20.1703) l prospective evaluation was in error and that intemal dose l
should have been measured; therefore, this error needs to be corrected. (
Reference:
Question 75: Representatives of the nuclear power industry have expresmi a concem regarding 10 CFR 20.1502, which requires licmsees to monitor individual intemal or external l
Question 54: Must bioassay be performal for a worker doses for each individuallikely to exceed 10% of the l
who, without respiratory protection, is likely to receive an applicable annual limit. Licensees are required to maintam J
intake in excess of the applicable ALI(s) but who is not records ofindividuals for whom monitoring was required j
likely to receive such an intake with respiratory protection?
under $20.1502 [$20.2106(a)b The handling of intemal doses at less than 10% of the limit is of particular interest.
Answer: A " Note" in the statement of considerations (56 Since a licensee cannot predict future exposures at other FR 23377, column 2) says that *... the concentrations to licensee facilities during the remainder of the year, a ques-be used for evaluating monitoring threshokls are those of the tion arises regarding summing of doses at these small frac-ambient atmosphere before credit is taken for respiratory tions of the limit if a worker transfers to another licensees protective factors." That note is a conservative assumption during the year. The following procedures have been sug-that is appropriate if there will be no *further verification" gested regarding reporting ofinternal doses at nuclear that the assigned respiratory protection factors actually will power plants that are less than 10% of the limit, be achieved.
1.
At nuclear power plants, an entrance bioassay is typi-At nuclear power plants, if the " surveys and bioassays, as cally performed for all incoming radiation workers. Upon sppropriate," required by 10 CFR 20.1703(a)(3)(ii), include departure from the facility, an exit bioassay is typically reasonable measures to verify that the expected degree of performed. If no net internal contandnation is detectable in respiratory protection will be achieved, "the concentrations the exit bioassey, no internal dose assessment is required.
to be used for evaluating monitoring threshokis' may be if internal contamination is detected, an assessment will those that include credit for the protection factors when undoubtedly be made. Any positive result above the LLD is respirators are to be used. Measures to verify that the available for reporting.
expected degree of respiratory protection has been achieved may include (but are not limited to) measurements of nasal 2.
Respiratory protection programs are required, under I
smears from workers who have used respirators and whole 520.1703, to monitor workers to assess intake. Air sampl-body counting, relatively soon after a job, of one or more ing results and bioassay measurements are acceptable me-r:presentative workers among a group of workers who wore thods to perform this monitoring, with the results used to respiratory protective equipment while working on thejob, perform an intake assessment.
and periodic whole-body counting (e.g., anmially) of all workers who wear respiratory protective equipment.
3.
Therefore, if a worker is monitored for potential intem-al exposure, data regarding the results of such monitoring 33 NUREO/CR-6204
Questions and Answers will be available and must be recorded. Since these records (a) Since the nuclear power industry has had few intakes are available, positive results, above LLD, shoukt be report.
approaching the 10% criteria for adding internal and ed to subsequent licensees, even if there is no reason to external doses, is the historical secord of intakes plus the sxpect the worker will exceed 10% of the annualinternal establishment of a corporate (licensee) policy to limit intakes committed effective dose equivalent limit.
- to less than 10% of an ALI sufficient to exchule a nuclear j
power licensee from the requirements for ' monitoring
- Does the NRC have any objections to this procedure?
intakes (10 CFR 20.1502) and adding internal and external
]
.(except for specific intake instances)? -
Answer: No. 'Ihis procedure for nuclear power plants goes beyond the requirements of the revised Part 20 for -
(b) Will the apparent new practice of nurumizmg TEDB j
monitoring, reconting, and reporting internal doses to and allowing some intakes invalidate this historical basis and workers. See the answer to Question 114. (For example, essentially require nuclear power licensees to " monitor * '
I routine entrance and exit bionssays for all workers are not intakes?
required by Part 20). However, the procedure is not inconsistent with the Part 20 requireme. (
References:
10 (c) In determimng whether a worker is likely to exceed the.
CFR 20.1502.10 CFR 20.2106) 10% criteria, on what basis are projections to be made of the future intake of contract workers (for the remamder of -
the year aAer they leave our site)?
Question 81: (a) Are licensees required to provide instruction on the procedures for declaring her pregnancy to Answer: (a) Yes, assuming that the conditions of exposure i
I an occupationally exposed woman if she does not enter a are not expected to change to the extent that they are outside restricted area? (b) Is it necessary to monitor all (occupa-the bounds of that historical record and that procedures will tionally exposed) declared pregnant women?
be put into effect to implement the policy. (However,
" surveys", in acconlance with 10 CFR 20.1501(a), wouki Answer: (a) There are no provisions in the revisel Part still be needed.)
20, or in Part 19, to provide instruction on declarations of pregnancy to women who are occupationally exposed but do (b) Not likely. However, the resulting potential incmase in not enter a restricted area. It is suggested that the licensee, intakes will need to be considered in determining whether or in accordance with good radiation practice, provide instruc-not workers are likely to receive intakes in excess of 10% of tion on this topic to all occupationally exposed individuals, an ALI. The historical record shnuki be useful in evaluating
)
regardless of where they receive exposure, this potentialincrease.
1 (b) No. Only declared pregnant women who are likely to (c) Such projections are not required. As indicated in draA -
receive in one year from sources external to the body a dose Regulatory Guide DO-8010 (" Criteria for Monitoring and in excess of 0.05 rem (20.1502(a)(2)) or who are likely to Methods for Summation ofInternal and External Occupa-1 receive in one year a committed effective dose equivalent in tional Doses"), each licensee makes the determmation excess of 0.05 rem from occupational intakes independently; doses that may have been received, or that (20.1502(b)(2)). (
Reference:
10 CFR 20.1502) may be received in the future, at another licensee's facility
]
are not included in the determmation of the monitormg Question 82: Will workers who enter a restricted area and have been determined to require monitoring under 520.1502(a) require monitoring in the controlled area Question 114: A licensee is required to provide individual (outside the restricted area)?
monitoring for each occupationally exposed individual who is likely to receive, in a year, a dose in excess of 10% of Answer: Yes, if the workers receive ' occupational the applicable limits in 10 CFR 20.1201,10 CFR 20.1207, i
dose (s)* in the controlled area. (
References:
10 CFR or 10 CFR 20.1208. Must a licensee account for the expo-l 20.1003,10 CFR 20.1502),
sure that an individual may receive at another licensee's -
l facility, if that worker transfers to another licensed facility i
during the monitoring year, when determmmg if it is likely Question 98: The following questions concern the that the individual may exceed 10% of the limits? In ad-requirements of 10 CFR 20.142 as applied to nuclear dition, if a new employee already has an exposure in excess power plants.
of 10% of the limits when they start work at the new l
Questions and Answers 4
employer, must the new employer automatically monitor the this refer to? (b) Since the gestation period is 9 months employee?
(ard sinco monitoring woukt begin after the declaration, which may be several months into a pregnancy), why does Answer: No. b licensee is only responsible for evahsat-the regulation use a year? (c) The licensee badges a declar-ing the potential for exposure at its facility. If the licensee ed pregnant woman (whose estimated date of delivery is in makes an evaluation that the dose will not exceed the 10%
January or Februasy) during the current calerdar year. W j
threshoki, the licensee need not reconi or monitor the dose.
licensee then estimates that for the next calendar year, j
If the licensee opts to measure the dose, although its prelim-hatwaan tha start nf tha year arut dativerv. the declared inary evaluation shows that it is not necessary arxl finds that pregnant woman's external doses will be less that 10 percent the threshoki has been exceeded, it must reevaluate its of the applicable embryo / fetus dose limits, is the licensee program and provide monitoring as required. In addition required to badge the woman for the new year? (d) Can the licensee will need to reconsider the requiremerts to sum licensees assume that after delivery, the ' year" time period internal and external doses. (
Reference:
10 CFR 20.1502) is over and that monitoring the woman (to demonstrate compliance with the embryo / fetus dose limits) is no longer required?
Question 126: Individuals performing assigned duties are often exposed to small amourts of radiation from plant Answer: (a) The word " year" is used to indicate a 12-cffluents at licensees' sites under normal operating condi-month period starting in January. (See definition of year in tions. (a) If these individuals are likely to receive, or have 10 CFR 20.1003).
already received, in excess of 10% of an occupational dose 1
limit from external sources, does the licensee have to (b) This requirement is for determmmg whether monitoring j
determine, record, and report doses from the effluents to must be provided, and the term year is used to be consistent comply with the revised Part 207 (b) If so, what are the with other monitoring criteria as specified in 10 CFR monitoring threshokts for the external and internal com-20.1502.
ponents of the dose?
(c) Once a determmation is made to monitor the declared Answer: (a) Yes. In this case, the licensee woukt have to pregnant woman, monitoring is to continue for the entire monitor and record the external dose from the effluents, pregnancy, to determine compliance with the limit of ex-since the individuals are in excess of 10% of the occupa-posure to the embryo / fetus.
tional dose limit from all external sources (20.1502(a)).
However, the licensee is not required to monitor the effluent (d) Yes. Once the woman is no longer a declared pregnant dose separately from other external doses.
woman, the need to provide monitoring will be based on requirements of 10 CFR 20.1502(a)(1). (
Reference:
10 (b) The licensee must monitor and record the internal CFR 20.1502,10 CFR 20.1003) occupational dose only if the individuals are likely to receive in excess of 10% of the applicable ALIs from all occupationalintakes of radioactive material. Note: For Question 212: A licensee makes a prospective determina-nuclear power plants, the preceding answer does not mean tion that adult workers in Department W are not likely to that all workers for whom mor.itoring of external dose is receive doses in excess of 10% of the limits from external required must wear their personal dosimeters at all times sources, so external dosimetry is not required by 20.1502.
while on site. Such workers in controlled areas (outside h workers in Department W complain when their TLD restricted areas) need not wear personal dosimeters to badges are taken away, so the licensee decides to leave them measure external doses from effluents. However, they badged, but nne en daman=trata camnlianca with tha acenna-shouki wear personal dosimeters in a controlled area when rinnat dama limite of the revised Part 20. (a) If an inspector performing work that has the potential for significant finds the TLD badges being worn incorrectly or misused by occupational exposure such as performing a radiation survey Department W workers, can the licensee be cited? (b) of a vehicle loaded with a shipment of radioactive material.
Must the doses be reported to the workers? If recording is
(
Reference:
10 CFR 20.1502) required, must it be kept on Form 5?
Answer: (a) No citation against 10 CFR 20.1502 wouki Question 211: 20.1502(a)(2) and (b)(2) say that monitoring be issued, provided the licensee can provkle documentation is required for declared pregnant women "...likely to re-that adequately supports the evaluation that monitoring of czive, in 1 year,..." a dose in excess of 10 percent of the external dose is not needed. An inspector may bring the cpplicable limits for the embryo / fetus. (a) What year does issue of incorrect wearing of dosimeters to the attention of 35 NUREG/CR-6204 6
Questions azul Answers the licensee, and may h=aae this lack of good practice in Answen No See the answer to related Question 214.
the inspection report.
(
Reference:
(b) No, reporting is not required. If the badges are not used for camaliaa~ with the regulations, the licensee is not Question 216: Will Regulatory Guide 10.8 be revised to required to reconi the results on NRC Form 5 or its equiva-include guidance on monitoring external dose (and demon-lent. (
Reference:
10 CFR 20.1502,10 CFR 20.2106) strating compliance with the annual occupational dose limits) for heahh personnel working in several hospitals simultaneously? [ Note: This is a common practice for Questlan 213: (a) Who is responsible for monitoring a physicians in Hawaii and there is no good mechanism for representative from a service company while the individual licensees to track where the physicians work outside the is on-site at a licensee's facility perfonning duties that may facility]
result in an occupational dose from sources owned / posses-sed by the licensee? (b) Where shoukt the resuhs of the Answen Appendix X to Regulatory Guide 10.8, Rev.2, monitoring be mamtamad?
was developed to provide guidance on how to implement revised Part 20 at a medical facility. This guide will be Answen (a) The individual /organharion that is licensed to revised in its entirety in the future to address the changes in possess the material used is responsible for monitoring the 10 CFR Part 20. (
Reference:
10 CFR 20.1502) representative.
(b) The resuha of the monitoring must be==iaea;a~1 by the Question 375: In supporting a conclusion that individual licensee as required by 10 CFR 20.2106. (
Reference:
10 monitoring of internal occupational dose is not required [10 CFR 20.1502,10 CFR 20.2106)
CFR 20.1502(b)] and, therefore, that summing of internal and external dose is not required [10 CFR 20.1202(a)], what is considered to be acceptable for bioassay (mquency, DAC-Question 214: (a) If the individual had not been monitored hour administrative limit, and whole-body counting at his previous employer while receiving an occupational muumum testing level?
dose (i.e., the dose there had been determmed not likely to exceed 10% of the limits), and the current employer, Licen-Answen Under 10 CFR 20.1502(b), tHe is no required see Z, determines in advance that the worker's annual dose frequency for bioassay, DAC-hour administrative limit, or for both licensees will exceed 10% (although the dose at minimum testing level for whole-body counting either for Licensee Z will not exceed 10%), must Licensee Z monitor individuals for whom monitoring is required or to support a for external dose? (b) If the individual worked for several conclusion that individual monitoring is not required. How-previous employers dunng the year, some who badged and ever, the answer to Question 54 provided a number of some who did not, and Licensee Z rankes a prospective examples of measures that couki be used at nuclear power determination that its own activities will resuh in a dose less plants to verify that the expected degree of respiratory than 10 %, must Licensee Z monitor for external dose?
protection will be achieved so that the concentrations of radionuclides in air aRet credit is taken for respiratory Answen (a) No. The criteria to determine whether protection may be used in makmg the prospective assess-monitoring is required is independent of exposures received ment that individual monitoring for intemal dose is not at any other place of employment prior to or subsequent to required. These measures
- include, (but are not limited to) employment with Licensee Z.
measurements of nasal smears from workers who have used respirators and whole body counting, relatively soon aRer a (b) No. (
Reference:
10 CFR 20.1502,10 CFR 20.2104, job, of one or more workers among a group of workers who Regulatory Guide 8.34) wore respiratory protective equipment while working on the job and periodic whole-body counting (e.g., annually) of all workers who wear respiratory protective equipment."
2 Question 215: An individual works concurrently at Licen-sees W, X, Y, and Z. All four licensees make a prospec-It shouki be recognized that in addition to the bioassay tive determmation that external doses will not exceed 10%
requirements of 10 CFR 20.1502(b), there is the bioassay of the limits at u a n r.cmev-Must any of the licensees requirement of 10 CFR 20.1703(a)(3)(ii), which is related to monitor for external dose?
the use ofindividual respiratory protection equipment. If whole body counting is to be used to verify the effectiveness of the respiratory protection program, it must be able to NUREO/CR.6204 36
- n. ----------- ----
Questions and Answers demonstrate that estimates of intake based on exposure personal dosimeters to measure external doses from efflu-c:lculations (i.e., on air concentrations and on taking credit ents, However, they shouki wear personal dosimeters when for protection factors) are consistent with estimat >s of intake performing work with or near licensed materials that are based on bioassay. The licensee shoukt take into account sources of external occupational exposure (e.g., when the fact that demonstrating effectiveness of the respiratory performing a radiation survey of a vehicle loaded with protection program may have to be based on exposures over radioactive material ready for shipping.) (
Reference:
10 durations much shorter than a year, particularly for materi-CFR 20.1502),
als that are expected to be cleared rapidly from the body.
Some general guidance on air sampling is provided in Regu-NOTE: Questions 444,445, and 446 relate to determmmg latory Guide 8.25, Rev.1, (which states that this guide does whether occupational radiation dose monitoring of an indivi-not apply to reactor facilities), and general guidance on dual is required (i.e., is the individual likely to exceed 10%
bioassay will be provided in Regulatory Guide 8.9, Rev.1.
of an applicable limit?)
(
References:
10 CFR 20.1502,10 CFR 20.1202,10 CFR 20.1703, Regulatory Guide 8.9)
Question 444: In this example, it has been determined that an individual will receive less than 100 mrems in a year while in the controlled area, and the individual has therefore Question 398: Regulatory Guide 8.7 (Section C.2.2) states been classified as a member of the public while in the con-that "if during the course of the year the dose to date for the trolled area. The individual also accesses and performs year exceeds 1 rem CEDE [ committed effective dose equi-work in the restricted area. In evahiating whether the in-valent) or the individual receives an overexposure in another dividual requires monitoring in the restricted area, may the dose category, the CDE [ committed dose equivalent] to the evahiation be limited to only the dose likely to be received maximally exposed organ must be calculated, recorded and in the restricted area, i.e., may the potential dose received reported." If an individual arriving from work at another in the controlled area be disregarded for the purpose of the (previous) licensee's facility within the current year has a evaluation?
CEDE that exceeds 1 rem, does the guidance imply require-ments for monitoring, recording or reporting ofinternal Answer: 'Ihe answer to the question is yes, assuming that dose, even if the present licensee's prospective evaludion the basis for classifying the individual as a member of the shows that the individual is not 'likely to exceed" 10% of public while in the controlled area is the type of work the an annuallimit on intake (ALI)?
individual will do in the controlled area.
Answer: For the situation described in the question, the As emphasized in the answer to Question 26(a), whether the quoted section of the Regulatory Guide 8.7 indicates that the dose to an individual outside a restricted area is an occupa-i previous licensee should have calculated, recorded, and tional dose or a public dose depends on what the individual should report the CDE to the maximally exposed organ.
is doing and not on what area (controlled or unrestricted However, as indicated in Section C.l.1 of Regulatory Guide area) the individual is in when the dose is received. Fur-8.7, in performing the prospective evaluation (urxler 10 thermore, it is possible, and acceptable (as indicated in 4
CFR 20.1502) to determine if monitoring is required "for many previous questions and answers), for the licensee to individuals who received exposure at other facilities in the consider the dose -(other than backgrourxi, etc.) that indivi-current year, the previous dose need not be considered in dual receives in a controlled area to be an occupational prospective evaluation. Only the dose that couki be dose, even though, as stated in the question, the dose the received at the facility performing the evaluation need be indivkhtal receives in the controlled area is less than 100 considered when determinmg the need for monitoring and, mrem per year. Regardless of the magnitude of the dose, therefore, the recordkeeping and reporting requirements."
the dose is an occupational dose if it is received (in accor-(
References:
10 CFR 20.1502, Regulatory Guide 8.7).
dance with the definition of occupational dose) "... in the course of employment in which the individual's assigned duties involve exposure to radiation and to radioactive Question 429: A " Note" added to the answer to Question material...' For example, an individual who performs a 126 clarifies the answer with respect to nuclear power radiation survey, in any area, of a vehicle loaded with radio-plants. Does this clarification also apply to non-power active material prepared for shipment would be receiving an reactor facilities?
occupational dose as a result of exposure to the radiation from the radioactive material on the vehicle regardless of Answer: Yes. As indicated in that " Note", workers at the magnitude of the dose. However, the dose (other than nuclear power plants, for whom individual monitoring is backgramd, etc.) received by a worker performing ofHee required and who are outside restricted areas need not wear work in a controlled area could be considered to be either 37 NUREG/CR-6204
.=-
4 i
4 Questions and Answers an occupational dose or a public done; either choice wouki Answer: (a) Yes. (b) Yes. (
References:
10 CFR.
f be considered to be consistent with the definition of "occu-20.1502,10 CFR 20.2206).
pational dose." See Question 26 and answer for additional information concermng bcensee options with respect to area designations and dose categories. See Question 126 con-Question 461: Does the word " applicable" in the phrase
. cermng the use individual momtoring of occupational doses
" applicable All(s)" in 10 CFR 20.1502(b)(1) mean that the from effluents. (
References:
10 CFR 20.1502,10 CFR atachastic ALI(s) [SALl(s)) shouki be used?
20.1003).
It is noted that 10 CFR 20.1502(b) requires the licensee to monitor the occupational intake and assess the committed Question 445: In this example, it has been detenmned that effective dose equivalent. We believe that the answer to this an individual is not likely to exceed 5 mas shallow dose
. question should be yes, if a licensee is operating under the
{
equivalent from any sources with the possible exception of
'more limiting' dose limit of 5 rem TEDE. b occupa-dose from hot particles. There is a potential that exposure tional dose limits in 10 CFR 20.12f'l apply to the "more.
to an individual fan a hot particle may occur and that the limiting
- of 5 rem TEDE or 50 rrm TODE. If a licensee's dose to the individual from a hot particle, shouki it occur, prospective assessment shows Gat the exposure conditions may potentially exceed 5 rems shallow dose equivalent. In at their facility is most likely to be limited by the 5 rem this circumstance, may the potential done resulting from a TEDE limit, then the ' applicable" ALI is the S ALL This is potential exposure to a hot particle be disreganled for the further shown by the wording used in 10 CFR 20.1502(b);
purpose of the ovahnation on the basis that the dose is not i.e., use of the "comnutted effective dose equivalent" likalg to exceed 10% of the applicable limit? Note that the terminology.
scope of this question is limited to the requirements for individual monitoring ($20.1502) and is not intended to Answer: No, not necessarily. &
- applicable" ALIis the address the general requirements for radiological surveys ALI for the appropriate radionuclide, the appropriate
($20.1501).
cohann (inhalation or ingestion), and, for inhalation ALis, the appropriate " class" (D, W, or Y) When both a sto-Answer: Yes. W fact that an individual has the potential chastic and a non-stochastic inhalation ALI are listed for a to receive a dose does not mean that the individual is likalg particular radionuclide (e.g., for I-131), the " applicable -
to receive the dose. [ Note: It shouki also be recognized All' in 10 CFR 20.1502(b) means the more limiting ALI, that individual monitoring devices (personal dosimeters) are which is listed first (the non-stochastic ALI), not tlw sto-not appropnate for measuring doses from hot particles on or chastic ALI, which is listed second and is shown in paren.
near the skin.] (
Reference:
theses, b statements made by the questioner following the question are not relevant to the question. (
Reference:
Question 446: In this example, an individual has worked at the licensee's facility earlier in the current year and was requimi to be monitored because the individual access *d a 2.6 SUBPART G - CONTROL OF high radiation area. During this period, the individual's monitored dose did not exceed 10% of a limit. Now the EXPOSURE FROM EXTERNAL individual is performing other work at the licensee's facility SOURCES IN RESTRICTED in the restricted area, but ne longer has access to high ruliation area. An evaluation based on the individual's new gg job scope shows that the individual is not likely to exceed 10% of a limit for their entire period of work during b -
year at the licensee's facility. (a) May tim personnel dose 10 CFR 20.1601 - Control of Access to High monitoring of the individual be discontinued on tim basis Radiation Areas that the individual is not likely to exceed 10% of a limit and the imlividual no longer has access to high radiation areas?
(b) If so, trust the individual's dose monitoring results, Question 218: 10 CFR 20.1601(a)(1) says that the control acquired during the period of required monitoring, still be devices must cause the radiation level to be reduced 'upon reported in accordance with $20.2206 " Reports ofImlivi-entry." (a) Must the devices prechide authorized or unau-dual Monitoring *? b purpose of these questions is to thorized entry? (b) At what point must the control devices determine under what conditions required inlividual moni-activate, when a person passes the final 30 cm before, or toring may be discontinued as no longer required, entry itself?
Questions and Answers Answer: (a) 10 CFR 20.1601(a) requires that entrance or that an individual h not ah6 to gain unauthorized or eccess points to a high radiation area have "one or more* of inadvertent access." h NRC staff realizes that tools the listed features to prechule excessive radiation exposure (wrenches, wire cutters, cutter torches) are readily available to an individual. b control device in subparagraph (1) in a nuclear power plant amt that it is virtually impossible to stipulates only that it cause the radiation level to be reduced prevent detemuned willful circumvention of physical so that an individual, upon entry, could not receive 100 barriers. However, physical controls can and should be mrem in an hour within 30 cm of an accessible area of the established so that any such willful acts are detectable (i.e.,
source. This paragraph does not distinguish between they resuh in cut locks or fencing, wall panels removed,
' authorized
- or " unauthorized.*
ete';. For example, the use of a fence to prevent access to a VF tA wouki not satisfy the requirements of 10 CFR (b) b control device must activate "nnnn entrv into the 20.1602 if an individual coukt gain access to the VilRA by crea" at the
- entrance or access point." (
Reference:
10 climbing over the fence. (
References:
10 CFR 20.1601,10 CFR 20.1601)
CFR 20.1602)
Question 219: 10 CFR 20.1601 requires control of access Question 385: Do licensees have discretion regarding the to high radiation areas. It provides an exception for access form and applicability of additional posting and barriers for to hospital areas with patients contammg radioactive materi-individual high radiation areas (HRAs) that are located c.1, "provided that there are personnel in attendance...*
within a larger area posted and barricaded (e.g., with a who will take certain specified precautions. (a) Does a locked door) as an HRA or inside a posted HRA control nursing station within line-of-site of a patient's room satisfy point? If licensees must post and barricade such individual the requirement? (b) Does a nursing station controlling HRAs at each area's entrance, then " double posting" cccess to a ward, but not in the line-of-site, satisfy the results. Double posting has long been a concern due to the requirement?
confusion that it might create for workers. The need to clearly identify to workers areas with high radiation levels Answer: (a) Yes, provided there are personnel in atten-might be accomplished through posted survey maps, " hot dance at all times who will take the necessary precautions to spot
- stickers, or other means. In addition to effectively prevent the exposure of individuals to radiation or radio-accomplishing the need for notifying workers of high radia-active material in excess of the limits established in Past 20, tion areas, these methods may be preferable to posting and and operate within the ALARA provisions of the licensee's barricading each HRA, located as described above, due to radiation protection program, potential dose savings that couki result from fewer entries into the area solely for the purpose of verifying the second-(b) Yes, provided the room is properly posted. (
Reference:
ary postings and barriers. This question is intended to es.
10 CFR 20.1601, Appendix X to Regulatory Guide 10.8) tablish flexibility in implementation, appropriate to the circumstances, to maintain control over access and inform workers in an effective and efficient manner.
Question 373: What are the nummum requirements for height ami access restriction <3 of barriers used to prevent Answer: Power reactor licensee discretion and flexibility entry to locked high radiation areas (HRAs) aml very high with respect to posting and barriers for high radiation areas radiation areas (VHRAs) at nucleas power plants?
is the same under revised Part 20 and applicable Technical Specifications as it has been under old Part 20 and applic-Answer: b NRC has prepared Regulatory Guide 8.3E able Technical Specifications. Existing guidance on control that details control measures that shouki be implemented for and posting of high radiation areas is contained in the Heahh such areas. This regulatory guide provides guidance on the Physics Positions (HPPOS) Data Base (NUREO/CR-5569, following program elements as related to control oflocked Rev.1). b particular question of individual HRAs that HRAs and VHRAs: management controls, procedural are located within a larger posted and barricaded HRA or controls, training, communications and physical controls.
inside a posted HRA control point is addressed in the documents identified as HPPOS-014 and HPPOS-066 in In general, there are no prescriptive, specific nummum NUREO/CR-5569, Rev.1. HPPOS-066 is IE Information height requirements for barriers preventing entry to locked Notice No. 84-82, " Guidance for Posting Radiation Areas,"
HRAs and VHRAs. It is required that physical controls dated November 19,1985. Other related guidance is (such as barriers) provide assurance that inlividuals are not contained in HPPOS-036, HPPOS-234, HPPOS-242, and gaining unauthorized access to locked HRAs. For VHRAs, HPPOS-210. This guidance will continue to be applicable 10 CFR 20.1602 requires " additional measures to ensure under the revised Part 20. Regulatory Guide 8.38 also 39 NUREO/CR-6204
Quations and Answers contains guidance on this subject for nuclear power plants.
Question 92: At power reactor facilities, when the reactor For most material heensees, posting and accas comrol is at poww, very high radiation areas (due to neutron and' requirements contained in 10 CFR Parts 20,34,35, and 36 N 16 gamma radiation fiekis) can exist inside the primary should be adequate. More dotaded information and m=eala==at. At some facilities, these areas inside contain-requirements wouki be contamed in individual heenses and ment are not readily locked, without substantial plant bcense apphcations. (
References:
10 CFR 20.1601,10 modifications to make them lockable. In recognition of this CFR 20.1902).
sieumeian, the following contmle are planned to meet the requirements of 10 CFR 20.1602 as it relates to a PWR or do-inested BWR caneammane at power: When the reactor is Question 430: Question 373 concems the======
at power and entry is not required, the primary contamment reqmroments for height and access restrictions of barriers access hatch (and any other access way) will be locked and '
used to prevent entry to locked high radiation areas (HRAs) posted as a vwy high radiation area. The key control access and very high radiation areas (VHRAs) at nuclear poww and special radiation work permit for entry will be in accor-plants. Dee: thi: qwtie: and answer also apply to non.
dance with, or provide pmtection equivalent to, the gui-power reactors?
dance in draA Regulatory Guide DO-8006. When the reae-tor is at power, and entry is required, a qualified (in accor,
Answer: No. h answer to Question 373 and Regulatory dance with the applicable ANSI s = art =rd) radiation protec-e Guide 8.38 which is referred to in the answer were all writ-tion technician will' accompany and provide contmuous job ten to address conditions at nuclear power plants and are not
. coverage to each (small) group of workers assigned to per-necessarily adaptable to all situations at non-power reactors, form a particular task (e.g., surveillance). Do the preceding materials, or fuel cycle facilities. Furthennore, the answer controls meet the intent of 10 CFR 20.16027 -
)
to Question 373 states that, in general, there are no pro-scriptive, specific nununum height requirements for barriors Answer: Yes. b controls outlined are an example of l
used to prevent entry to locked HRAs and VHRAs.
one way (but not the only way) to comply with 10 CFR
(
Reference:
10 CFR 20.1601,10 CFR 20.1602).
20.1602 in this situation. (
References:
.CFR 20.1602).
l Question 431: Although Question 385 does not refer to any particular class of licensee (e.g., power reactor, non-power Question 220: 10 CFR 2fs.1602 gives requirements for reactor, materials), the answer to the question mentions only control for access to very nigh radiation areas, and has no power reactor licensees and material licensees. Does the exemption clause, 10 CFR 20.1003 defines a very high answer to % question also apply to non-poww reactor or radiation area. (a) Are teletheropy rooms or fixed / field fuel cycle licensees?
radiography facilities, with twure that can deliver in excess of 500 rad in 1 bour at 1 aneter, very high radiation areas?
Answer: Yes, to the extent that the situations described in (b) Do the requirements in 20.1602 apply to teletherapy the answer apply to non-power reactors or fuel cycle licen-rooms or fixed /fiekt radiography facilities?
sees. Ilowever, there may be situations at non-power reac-tors and fuel cycle facilities that are not within the scope of Answw: (a) Yes.
the answer. (
Reference:
(b) Yes. However, this does not prohibit patients from receiving prucribed medical treatment in a teletherapy 10 CFR 20,1602 - Control of Access to Very room (Refwence: 10 CFR 20.1602,10 CFR 20.1003)
High Radiation Areas Question 423: Se=arland Technical Specification (STS) 6.12
- nu Poww reacton pmam andhods fw catml of Question 49: For control of access to very high radiation areas, will physical barriers be needed to prochade unauthor-access to Mgli redimi a areas the are attematim to dw motbods specified m a CFR Part 20. Power reactor licen.
see that have adopted this technical specification are requir-Anmer: Yes. See draA Regulatory Guide 8.N10.
ed to pmvide additional controls fw access to liigh radiation (Refwence: 10 CFR 20.1602) amas 4 dose ntes greater than I d in addition to the controls required for access to high radiation areas with dose rates of I rem /h or less. Providing the additional controls at I rem /h is conservative relative to providing NUREO/CR-6204 40
Questions aml Answers additional controls for areas having dose rates of 500 rads radiation areas; however, these positions continue to be or more in an hour as required for very high radiation areas applicable with respect to posting ami contml of both high by 10 CFR 20.1602. Do licensees that have adoped STS armi very high radiation areas unter 10 CFR 20.1601,10 6.12, ami that are providing the additional controls required CFR 20.1602, amt 20.1902(b) and (c) of the revised Part by this STS for areas with dose rates greater than I rem per
- 20. These position documents emphasize that when a diver hour or less, have to provide additional controls for very enters the pool to perfonn "under pool-surface duties" or high radiation areas in accordance with 10 CFR 20.16027 upon movement of highly radioactive materials stored in the pool, proper health physics controls must be initiated.
Answer: Yes, they do. The alteraative controls for high IE Information Notice No. 90-33, dated May 9,1990, radiation areas in STS 6.12 do not apply to the new require-provides suggestions for radiological control considerations ment in 10 CFR 20.1602 to provide additional controls for that can help nunmuze the possibility of unexpected very high radiation areas. 'Ihe compensatory measures in exposure from radiation sources in spent fuel pools, the STS that provide alternative methods of control for areas
(
References:
10 CFR 20.1602,10 CFR 20.1902,10 CFR i
with dose rates greater than 100 mrem per hour but less 20.1003).
than 1000 mrem per hour do not constitute adequate con-trols ever = cess to very high radiation areas. (
References:
Question 448: If irradiated hardware, suspended (e.g., on a 10 CFR 20.1601,10 CFR 20.1602, Reactor Technical lanyard) in the spent fuel pool, is potentially realing greater Specifications) than 500 rads /bour at one meter (i.e., if it were removed from the pool), does access to this hardware require posting and control as a Very High Radiation Area?
Question 447: Is the spent fuel pool, when containing irradiated fuel, required to be posted and controlled as a Answer: No. See Section 4.2, " Materials," in Regulatory Very High Radiation Area under any of the following cir-Guide 8.38, ' Control of Access to High arxl Very High cumstances:
Radiation Areas in Nuclear Power Plants." Also see Health Physics Position document HPPOS.245 (NUREG/CR-5569, When there are no activities unterway involving the Rev.1.). Although this position document was written to a.
spent fuel pool?
address access controls for spent fuel pool storage pools under the unrevised Part 20 requirements for high radiation b.
When underwater manipulation of irradiated fuel or areas, it also applies to these access controls under the other irradiated hardware is umlerway?
revised Part 20 requirements for both high and very high radiation areas. The essential point is that although move-c.
When diving operations in the spent fuel pool are ment of radioactive material stored in the pool has the underway?
potential to create a high, or very high, radiation area around the pool, those areas are not created until movement d.
Are there other considerations that couki affect require-of the material actually results in a radiation level, in an ments for posting and controlling access to the spent fuel area that is accessible to individuals, that meets the dose pool?
criterion in the definitions of a high, or a very high, radia-tion area. NRC Information Notice No. 90-33, dated May Answer:
9,1990, is also relevant. After providing reviews of a number of events in which sources of unexpected occupa-(a) No.
tional radiation exposures were encountered in activitius associated with spent fuel storage pools, this notice provides (b) No.
suggestions (which are not regulatory requirements) for radiological control considerations that can help minimize (c) The answer deperxts on the particular circumstances of the possibility of unexpected exposures from radiation the diving operations. See discussion under (d) below.
sources in these pools. (
References:
10 CFR 20.1602,10 CFR 20.1601,10 CFR 20.1003).
(d) See Health Physics Positica documents HPPOS-016 and llPPOS-245 (NUREG/CR-5>69, Rev.1.) for additional 10 CFR 20.1603 - Control of Access to Very information concerning access controls for spent fuel pools Illgh Radiation Areas-Irradiators arxl HPPOS-002 for additional information concerning diving operations in a spent fuel pool. These position documents refer to 10 CFR 20.203(c) of Part 20 prior to the Question 130: 10 CFR 20.1603(a), Footnote 2, exemps a 1991 revision with respect to posting and control of high nuclear power plant from the requirements of $20.1603 41 NUREG/CR-6204
1 Questions and Answers unless a non-self-shiekled irradiator is used at the reactor.
A licensee should optimize design and engineering controls,
(:) If the source used for the calibration of high-radiation as well as operating procedures, as a means of ensuring that instruments is non-self-shiekled, and the absorbed dose at I doses from airborne radiciodine are ALARA. However, in meter distance coukt exceed 500 rads in I hour, is the situations where KI has been adnunistered following a sus.
source an irradiator? (b) Do the provisions of $20.1603 (a) pected intake, the licensee may take credit for the protection i
apply?
if bionssays support the effectiveness of the KI in blocking the thyroid.
Answer: (a) No. An 'irradiator," as the term is used in 10 CFR 20.1603, uses gamma radiation to irradiate pro-Finally, ahhough licensees are not authorized to require ducts to change their charactoristics in some way (55 FR their employees to routinely take K1 when working with 50008,12/4/90, Licenses and Radiation Safety Require-radioiodine, nothing in NRC regulations prohibits an in-ments for Large Irradiators, proposed 10 CFR Part 36). A dividual from taking K1 nn = =raly vnknearv h=W radioactive source used for calibrating radiation survey however, the NRC does not recommend the voluntary use instruments is not an 'irradiator.'
of KI in this manner. (Reference 10 CFR 20.1701)
(b) No. However, the provisions of 10 CFR 20.1602 wouki apply. (
Reference:
Question 115: b words, "e.g., containtnent or ventila-tion," have been added to 10 CFR 20.1701. Does this mean that increased emphasis is being placed on glove bags to do 2.7 SUBPART H - RESPIRATORY valve mplacements, repacks, etc. at nuclear power plants?
PROTECTION AND Answer
- No. bse words were added simply to provide CONTROLS TO RESTRICT exampla of " process or other engineering controls."
INTERNAL EXPOSURE IN
(**'*"o e: 1 CFR 20.1701)
RESTRICTED AREAS 10 CFR 20.1702 - Use of Other Controls 10 CFR 20.1701 - Use of Process or other Engineering Controls Question 145: Automated personnel contammation monitors (" portal monitors *) are used at nuclear power plants to detect radioactive surface contammation on the Question 90: Can a licensee require its workers to routine-skin ami clothing of workers. W alarm setpoints for these ly take potassium iodide (KI) when handling large quantities monitors are n=intained very low to detect low levels of of radiciodine ami take credit for the reduction in occupa-surface contanunati n aml bot particles. Implementation of tional dose that results from the use of the Kl?
the " respirator ALARA rule," [10 CFR 20.1702 and 20.1703(b)(1)] may result in intakes of radioactive material Answer: No. Requiring the use of KI for this purpose is by workers that will trigger the alarms on these monitors.
neither a " process or engineering control...to control the W uki the NRC object if, to facilitate compliance with the concentration of [radioiodine] in air" (10 CFR 20.1701).
'new respirator ALARA rule", portal monitor set points Furthermore, because KI blocks uptakas (not intakna), the were raised to a more reasonable level?
use of KI for thyroidal blocking cannot be considered to be Answer: Set points for automated personnel contamina-among the "other controls' required by 10 CFR 20.1702 for limiting intakna h following cautionary note in NRC ti n m nitors are established by, and can be changed by, Information Notice 88-15 (4/18/88) continues to be applic-licensees without NRC approval. NRC has no requirement able under the Revised Part 20:
that licensees use automated personnel monitors nor does it have numerical guidance on set points for these monitor "It is important to stress that the use of potassium iodide is (unless a licensee has canmitted to using automated person-net a substitute for preventive measures; e.g., proper handl-nel e ntammation monitors, with a particular set point m a licen88 *PP cation). However, if a licensee uses these mon.
li ing techniques, control measures, ami emergency proco-dures that protect the individual from exposure to radio-iton arxl the monitor alarms because of an intake (rather active material..
than because of extemal contarnin= Hon), that intake shoukt be evaluated. W question implies that the detection of small intakes of radioactive material using these monitors is NUREG/CR-6204 42
Questions and Answers urulesirable and should be avoided by raising the monitor set Quotion 387: la evaluating the use of respirators to limit points above their current levels. This is not necessarily the intakes, in addition to detennining the total effective dose 4
{
case. At least one nuclear power reactor licensee has recog-equivalent (TEDE), should the evaluation arxl subsequent nizal that the sensitivity of these monitors for detecting decision on whether to use respirators also consider irxlus-intakes can be usal to advantage in internal " passive inter-trial safety hazards associated with wearing respirators?
i nal monitoring program" for workers for whom irs!ividual For example, added effort increasing the probability of heat
)
monitoring for intake is not requiral by 10 CFR 20.1502(b).
stress, limited range of vision while climbing, or difficulty
]
That licensee plans to use these monitors with a setpoint that of maneuvering readily while working in confined spaces results in the reliable detection of internal contamination due to wearing a respirator may pose potentially greater equivalent to s 1% of the All for mixtures of radionuclides safety risks than does the potential dose from uptake of encotmteral in the licensee's plant. (
Reference:
10 CFR airbome radioactive material to which an irulividual might 20.1702) be exposed by not wearing a respirator.
?
Answer: 10 CFR 20.1702 provides for the use of respira-l Qmlion 386: In evaluating whether to require the use of tors consistent with maintaining the TEDE as low as is respirators to limit intakes, it is found that wearing a res-ramnnhlv achievable. A reduction in the TEDE for a j
pirator will likely increase the total effective dose equivalent worker is not ramnably achievable if an atterxiant increase j
(TEDE). Ilowever, the workers request that tlay be allow-in the worker's irxlustrial health arul safety risk would al to wear respirators to limit intakes, despite the results of exceal the benefit to be obtained by the rahietion in the the evaluation. With regard to NRC regulation, what dis-radiation risk associated with the reduction in the TEDE.
cretion may the licensee exercise in this circumstance?
The NRC has never maintained that application of the ALARA principle requires ignoring factors other than a
Answer: 10 CFR 20.1702 provides for the use of respira-radiation that may have an adverse impact on public heahh tors consistent with maintaining the TEDE as low as is and safety. (
References:
10 CFR 20.170~2,10 CFR r~mnnhlv achievable. Assuming that the licensee has pro-20.1703).
vided appropriate training to the workers in question, the licensee may exercise discretion on a case-by-case basis in detennining whether to grant approval to a worker's request Question 38& In regard to Question 91 (previously an-i for using a respirator when the TEDE-ALARA determina-swered in the third set of Q&As), can NIOSH approved tion dictates that respiratory protection not be used. 'the respiratory equipment which makes use of a combination NRC staff realizes that the significant " culture shift"/* para-particulate fdter and ialine sorbent with a protection factor digm shifP (i.e., changing from the traditional operational for particulates be used in a mixed particulate arxl iodine philosophy of not allowing any worker inrakes to one of atmosphere to limit intakes? This practice would seem valid allowing some intakes when this is consistent with the goal for equipment that is NIOSil approved arxl has a protection of maintaining the TEDE ALARA) may not take place factor for particulates, quickly. Furthermore, accegwance of this change will cer-tainly be difficult for some individuals. Therefore, the NRC Answer: ~Yes. However, there is no assigned protection staff realizes that during this transition period licensees will factor far radioialine with this equipment. [The NRC may need reasonable flexibility to allow for individual neals arxl authorize radioialine protection factors for this equipment in i
problems in nutking this shift However, the staff expects accordance with 10 CFR 20.1703(b)(2) as it has previously 1
that over time the transition to ALARA-TEDE will be nuule authorized them in accordance with 10 CFR 20.103(d).]
and this worker accegwance problem will become an excep-(
References:
10 CFR 20.1702,10 CFR 20.1703).
I l
tional occurrence. In the meantime, when assigning a respirator to the requesting worker, the licensee should i
make every reasonable effort to provide the worker with a Question 449: Detectable, minor intakes may result for respirator that minimizes the loss of worker efficiency.
some irxlividuals who do not wear respirators during speci-Note: The NRC staff is aware of existing state OSH A fic radiological work activities for the purpose of maintain-regtdations that requim an employer to provide a worker ing the total effective dose equivalent (TEDE) as low as is with a respirator upon request; compliance with such state reasonably achievable (ALARA), as required by regulation.
regulations is acceptable to the NRC staff. See the answer Such resulting intakes may involve substantial follow-up to the related Question 387. (
Reference:
10 CFR 20.1702, activities in terms of bionssay, internal dose assessment, and s
responses to various monitor alarms (e.g., hand-hekt frisk-ers arxl portal monitors) as the individual continues to per-form work in the restricted area in the period following the 43 NUREG/CR-6204
Questions and Answers i
intake, due to the sensitivity of the monitors and the low planned to be used, the licensee does not need to record monitor alarm set points, established to detect small such ALARA evaluations when the prospective intake is amounts of contamination or hot particles on individuals below the threshokt.
sxiting work areas or the restricted area. In evaluating whether or not to use respirators in a given situation, may 3.
Irrespective of the statements in #1 and #2 above, the thi assessment of costs versus benefits appropriately inchale licensee does need to perform and record such evaluations the resource costs associated with follow-up activities to for situations to which the ALARA provisions of 10 CFR potential intakes, and ultimately be factored into the decision 20.1703 (b)(1) apply, that is to situations in which it is making on wearing respirators?
anticipated that protection factor for the respiratory pro-tection equipment to be provided is less than the multiple by Answer: Yes; however, there is no requirement that these which the peak concentrations of airborne radioactive cc:ts be considered. (
Reference:
materials in the working area are expected to exceed the concentrations specified in Appendix B Table 1. Col. 3.
10 CFR 20.1703 - Use of Individual Respira.
4.
Regardless of the magnitude of the projected external t:ry Protection Equipment d se, the li ensee d es a t need t perf rm r rec nl su h evaluations before requiring the use of respiratory protect on equipment as a precautionary measure in situations in which Question 60: In a respiratory protection program what the is a large unartainty in the inagnitude of the projected e nantrations o%me radioactive matenal to which the records are needed of evaluations that demonstrate comp-liance with the requirement for maintaining the total effec.
w rkers will be exposed (e.g., a newjob with no history of tiva dose equivalent ALARA? For example, must such an previous similar jobs) (
References:
evaluation be made each time an individual is to wear a 10 CM 20.1703) respirator?
Answer: Such records need not be made each time some-Question 78: Under $20.1703(d), licensees ruust notify the ono is to don a respirator. A licensee who performs and NRC Regional Director at least 30 days prior to first using reconis such evaluations in accordance with the following re8Ptratory protection equipment pursuant to $20.1703(a) or guidance will be considered to be in compliance with the (b). All current respiratory pmtection programs have been requirements for such evaluations:
documented under the provisions of 520.103(g) which con-tains equivalent language. Do licensees need to "re-notify" 1.
(a) If the licensee establishes a reasonable threshold NRC if such notification has alre.xty taken place under the
" kl* Part 207 value for prospective deep dose equivalent (rem) for an individual from a task / job belaw which a record of such Answer: Licensees do not need to "re-notify" NRC if such an evaluation is not needed, and notification has taken place under the oki Past 20.
(
Reference:
(b) the licensee establishes a threshold value for pro-spective collective deep dose equivalent (person-rem) from a task / job helow which the record of such an evaluation is not needed, 0"*80*".91: As I ng as n credit is taken for the protec-tion provxted by the respiratory protection equipment, the (c) in situations in which the licensee plans to use kl Part 20, in 10 CFR 20.103(c), allows licensees to use respiratory protection equipment, the licensee does not this equipment without meeting the requirements of 10 CFR need to recon! such ALARA ovaluations for situations 20.103(c)(1) through 20.103(c)(4), inclusive. Has this P ole" in the ok! Part 20 been closed in the revised Part h
in which the projected external dose to any individual is below the threshokls established under 1(a) and 1(b) above for both the projected individual external dose Answer: Yes. 10 CFR 20.1703(a), which contains
[1(a)) and projected collective external dose [1(b)].
requirements smular to those m, 10 CFR 20.103(c), imposes 2.
If the licensee establishes a threshok! value for pro-these requirements "if a licensee uses respiratory protection 89ui ment to limit intakes," regardless of whether the licen-P spective intake of radioactive material (as a fraction of the ALI or as DAC-hours) for an individual from a task / job see makes " allowance for this use of respiratory protective equi ment m estimating exposures of individuals...."
P 1
h which a record of such an evaluation is not needed, in situations in which respiratory protection equipment is not
( efence: 10 CFR 20.1703)
NUREO/CR-6204 44
_~
4 4
i Questions and Answers Answer: Yes, bre is no explicit requirement in 10 CFR
.1 l
Question 124: Do the requirements of 10 CFR 20.1703(a)
Part 20 for a " respirator effectiveness program" other than apply to respiratory protection equipment that is to be used the requirement of 10 CFR 20.1703(a)(3)(ii) for "suiveys 4
only m emergencies?
and bionssays, as appropriate, to evaluate actual intakes."
l 10 CFR 20.1704 specifies that the Commission may impose Answer: Yes, if that equipment is to be used to limit in-additional restrictions to ensure that the respiratory p otec-l takes'of radioactive material. (
Reference:
10 CFR tion program is adequate and to limit the extent to which a 20.1703) licensee may use respiratory protection equipment instead of 7
j process or other engineering controls, b NRC staff does -
not anticipate a need to impose further restrictions on the
?
Question 131: 10 CFR 20.1703(a)(3)(iii) requires that -
use of respiratory protection equipment at nuclear power respirators be tested for operability immediately prior to
- plants pursuant to 10 CFR 20.1704.- Also as indicated in each use. How is this to be done?
the (revised) answer to Question 54, information from a
" respirator effectiveness program" can be used to justify the l
assumption that the concentrations of radionuclides in air to 4
Answer: This requirement is not now. It is essentially the same as the requirement in 10 CFR 20.103(c)(2). For be used for determuung whether or not monitoring is requir-g guidance on respirator operability tests (fit checks), see: (1) ed [ pursuant to 10 CF.R 20.1502(b)] are the concentrations 4
Regulatory Position C.4.C in Regulatory Guide 8.15, (2) that include credit for the assigned protection factors when Section 8.5.2.3 in NUREG-0041, and (3) Section 7.4 and '
respirators are to be used, rather than the concentrations
~
Appendix A7in ANSIZ88.21980 (
Reference:
10 CFR without that credit. See the answer to the related Question 376. (
References:
10 CFR 20.1703,10 CFR 20.1704,10 20.1703).
CFR 20.1502).
I Question 132: How are nuclear power plant licensees to identify the " potential" harant using air sampling techmques Question 418: 'nds question refers to the answer to -
r.s specified in 10 CFR 20.1703(a)(3)(i)? (Air samphng is Question 91 in $20.1703. Please clarify this response, as only useful in harant identification aAar radioactive material indicated below.
{
becomes airborne).
(a) Can NRC envision any purpose by which a licensee can
.i use respiratory protection devices without having an approv-Answer: 10 CFR 20.1703(a)(3)(i), which requires that a i
respiratory protection program include f air sampling ed respiratory protection program, e.g., meeting the provi.
4 sufficient to identify the potential hazard...", uses the -
sions of $20.17037
[
word " potential" with respect to the hazard because aisborne radioactive material is only a " potential" hazard to a worker (b) For instance, work is being conducted where the licen-i until the worker is exposed to it. Before workers enter an see has determmed there is no requirement for respiratory trea contammg airborne radionuclides, the concentrations of protection but workers prefer to use it anyway. Fmm the
!=
these radionuclides shoukt be estimated using air sampling.
workers perspective it is for protection. From the licensees l
This is not a new requirement (see 10 CFR 20.103(c)(2).
viewpoint, it is simply for peace of mind, with the ackled j.
h potential hazard of radioactive material that may be.
benefit of being an ALARA effort. Is this usage subject to i
come, but that has not yet become, airborne can't be iden-620.17037
_ tified by air _ sampling. h potential hazard snust be iden-l tified by other means (e.g., using the experience gained in
%= ian-If the answer to these questions is that I
previous similar activities that cause radioactive material to 320.1703 applies to any conceivable use of respirators then become airborne). Procedures that have been acceptable in this in essence is a directive for all licensees without the past for klentifying potential hazards of airborne radio -
approved equipment or an approved program to discant all.
a active material, or of radioactive material that may become respiratory protection aqMnenant It cannot be used even for airborne, will continue to be acceptable. (
Reference:
10 ALARA purposes at less than DAC levels. It cannot be CFR 20.1703) kept on hand for use in emergency response situations 1-where any protection is useful in initial response conditions.
(Note: As a basic presumption, assume that any use of l
Question 374: In general, do established respirator ef-respirators complies with the basic OSHA guidance for i
fectiveness programs at nuclear power plants meet the intent medical approval.)
of the regulation in providing assurances of the effectiveness of chosen respiratory protection?
?
45 NUREG/CR 6204 I
Questions and Answers Answer: (a) h requirements of 10 CFR 20.1703 must be tation, but it certainly is not evident in the cited regulations.
l met if the respiratory protection equipment is used to limit is there related supporting justification somewhere?
intakes of radioactive material pursuant to 10 CFR 20.1702.
10 CFR 20.1703 does not apply if the respiratory protection Answer: b answer to Question 129 is a statement as to equipment is used for other purposes (e.g., for protection how this requirement will be enforced by the NRC staff egainst harmful dusts, fogs, fumes, mists, gases, smokes, (i.e., in the same way as similar requirements have been sprays, or vapors that are not radioactive); however, OSHA enforced in the past). As irulicated in the answer to regulations (which include a requirement for a nummal Question 129, the requirements of 10 CFR 20.1801 and acceptable respiratory protection program) do apply to most 20.1802 are essentially the same as the requirements of 10 of these uses.
CFR 20.207(a) and 20.207(b) except that 10 CFR 20.1801 and 20.1802 apply to controlled area as well as to restricted (b) Yes, assuming that the equipment will be used to limit areas. The answer is based on the NRC staff's understand-intake, this usage is subject to 10 CFR 20.1703, b use of ing of the intent of these requirements, as reflected in the respiratory protection equipment without meeting the staff's enforcement of the similar requirements of 10 CFR respiratory protection program requirements of 10 CFR 20.207(a) and 20.207(b). (
Reference:
20.1703 (e.g., respirator not properly maintaina1, poor fit of respirator to wearer, untrained or improperly trained respirator user) can be hazardous to the worker, can lead to Question 450: Licensees are required to " secure from a false sense of protection, and cannot be justified on the unauthorized removal or access" licensed materials in stor-Insis of ALARA, worker peace of mixxi, or usefulness in an age, and to " control and maintain constant surveillance" of emergency. (
Reference:
licensed materials not io storage, in controlled or unrestrict.
ed areas. The following questions relate to the security and control of licensed materials in enntrnflal arem nnly, i.e.,
2.8 SUBPART I - STORAGE AND the questions am nd imended to address unrestricial areas:
CONTROL OF LICENSED wouk! the provisions for security and control be met if I
a.
MATERIAL the licensed materials are appropriately labeled or marked (e.g., in accordance with $20.1904) and are located within i
an area to which access is controlled through the use of 10 CFR 20.1801 - Security of Stored Material banin wpu and signs restricting awess by unaudmrized personnel?
Question 129: 10 CFR 20.1801 arxl 20.1802 do not specify Would the provisions for security and control be met if b.
- I*'***"*'""
" " ^ " " " ' * * * "
the quantities of radioactive material below which m,a", above, that was located within a Part 50 licensee unauthon. zed access to, unauthon. zed removal from, or the maintenance of constant surveillance over, are not required in controlled areas. Will these requirements be imposed (a) g g,,,
g on all quantities of licensed matenal, however small and (b) on quantities that are exempt from labeling by 10 CFR radiological caution signs (e.g., " Caution, Radiation Area"),
20.1905(a) and (b)?
MdM um Whkaw W m W h fore the provisions of $20.1801 and $20.1802 would not Answer: (a) No. The requirements of 10 CFR 20.1801 8 PPM and 20.1802 are not new; they are essentially the same as Answer' the requirements of 10 CFR 20.207(a) arxl 20.207(b) e... pt that the revised Past 20 requirements apply to controlled (a) No. To secure the material from unauthorized removal rreas as well as unrestricted areas. NRC will continue to g
g g
enforce these requirements as it has m the past, b is m d
d%
"P"
- E"' I * * * ""** ' '" N'* I C*"'"I (b) No. (
References:
10 CFR 20.1801,10 CFR 201802,
"#*".8"' " "# " "'""' " ' ""'*""'I" * """"
10 CFR 20.1905) removal in accordance with 10 CFR 20.1801 and does not
" maintain constant surveillance" of the material in accor-dance with 10 CFR 20.1802.
Question 419: This question refers to the answer to Question 129 in $20.1801. This is a very useful interpre-NUREGICR-6204 46
Questions and Answers (b) No. This use of barrier ropes and signs within a Part do posting and labeling requirements renmin in effect while 50 licensee security protected area does not necessarily the package is on licensee property outside of the radiologi-secure the licensed material from unauthorized removal cally controlled area?
1 from that aren (in accordance with 10 CFR 20.1801 for -
stored material) and does not provide the constant surveil-(b) Does the shipment have to be posted in the protected -
lance of the material (in accordance with 10 CFR 20.1802 aren?
for material that is not in storage). Individuals who are cuthorized to enter the security protected area are not (c) Does the shipment have to be posted within the owner-necessarily authorized to remove the licensed material and, controlled area?
as indicated in the answer to (a), above, this use of ropes and barriere does not secure the material from unauthorized (d) Once the transporter has taken control of a package and shipping papers are in effect, is the shipment exempt from
- use, posting?
(c) No, not necessarily. Simply posting the area desented in part (a) of the question with a " radiological caution sign *,
Answer: The answer to all four questions is that the post:
such as " Caution, Radiation Area," does not, in the absence ing requirements remam in effect until the transporter has of other measures for access control, result in the creation actually taken possession of the package and is starting to of a " restricted arent and, thereby, make the provisions of transport it. Following are additional responses to three of 10 CFR 20.1801 and 20.1802 inapplicable. However, the the four specific questions:
provisions of 10 CFR 20.1801 and 20.1802 wouki not apply to the area described in part (a), above, if that area is con-(a) 10 CFR 20.1905(d) exengts this package from the '
tained within a radiation area within a restricted aren, access lahahng requirements of 10 CFR 20.1904(a),
to which is adequately controlled. (
References:
-10 CFR 20.1801,10 CFR 20.1802,10 CFR 20.1003,10 CFR (b) Whether or not the package is in a ' protected area," as 20.1904).
defined in 10 CFR 73.2, is not relevant to any requirements in 10 CFR Part 20.
4 2.9 SUBPART J - PRECAUTIONARY (c) Wi=dar or ad da rackasa i$ in "a "="reatmW area' (or ' controlled aren" as defined in 10 CFR Part 20) is PROCEDURES not,eieveo, to cae po,t,,egmrements of 10 CFR 20.1902(e).
10 CFR 20.1902 - Posting Requirernents
(
References:
- 10 CFR 20.1902(e),10 CFR 20.1903,10 CFR 20.1904(a),10 CFR 20.1905(d))
I Question 27: Do licensees have to post controlled areas (outside the restricted area) as airborne radioactivity areas if Question 85: In $20.1902, posting of areas is based upon derived air concentrations (DAC) are exceeded?
" dose equivalent." la this " deep," " shallow,'." lens of eye,'
' total effective" or some combination of the above?
Answer: Yes, if the airborne radioactivity is indoors. If the airborne radioactivity is outdoors, the answer depends Answer: 'Ihese posting requirements are based on tlw on the particular situation. In certain situations the bconsee deep dose equivalent for " radiation areas
- and "high radia-may need to identify and delineate an outdoor airborne tion areas
- and the absorbed dose at a tissue depth of I cm radioactivity area. For example posting woukt be required (1000 mg/cm2) for "very high radiation areas." See the in a small area, accessible to workers, in the immediate answer to Question 74. (
References:
10 CFR 20.1003,10 vicinity of a vent on the outside of a buikling, exhausting air CFR 20.1902) canhiaia= concentrations of radioactive materials in excess of the DACs specified in Appendix B to 10 CFR Past 20.
(
References:
10 CFR 20.1003,10 CFR 20.1902)
Question 221: Since the posti e ? quirements are allin terms of deep dose equivalent, what requirements shouki be followed when posting for low energy beta radiation?
Question 53: (a) When a package is properly labeled for I
transport, shipping papers are still in effect, and a trans-Answer: Unless the beta particle can deliver a dose at a prter has accepted responsibility for control of the package, tissue depth of I cm, the area does not require posting as a 47 NUREO/CR-6204
Questions and Answers radiation area (20.1902(a)), high radiation area (20.1902 indicates that areas that meet the dermition of " airborne (b)), or very high radiation area (20.1902(c)); however, radioactivity area
- because of the presence of noble gases posting for airborne radioactivity area (20.1901(d)) and for are required to be posted.) (
References:
10 CFR 20.1902, areas or rooms in which licensed material is used or stored 10 CFR 20.1003).
(20.1901(e)) needs to be considered for beta emitters. See Questions and Answers 57,74, and 85 for more infomia-tion. (
Reference:
10 CFR 20.1902,10 CFR 20.1901)
Question 459: In the answer to Question 379, the NRC addressed the issue of whether noble gases shotdd be includ-ed in assessing the requirement to post an area as an air-Question 379: Shoukt radioactive noble gas concentrations borne radioactivity area. This question is interxlal to obtain be excludal (a) with regard to evaluating arul posting Air-further clarification with regards to the two separate provi-bome Radioactivity Areas and (b)in determuung Derived sions that require posting of airborne radion(tivity areas.
Air Concentration-hours (DAC-hours)? b definition of b first provision requires posting of areas in which Aisberne Radioactivity Area refers to areas where airborno concentrations of airborne radioactive materials are "in radioactivity concentrations exceed the DAC values or excess of the derived air concentrations (DACs) specified in wherc r.n individual could exceed 12 DAC-hours in a week.
Appendix B." As pointed out previously (in the answer to DAC is defined as the " concentration of a specific radio.
Question 379), Apgundix B inchules DACs for noble gases, nuclide in air which, if breathed...results in an intake of one and therefore nobis gas concentrations should be inchuled in ALI [ Annual Limit on Intakej." b values listed for posting considerations. The secorx! provision requires that radioactive noble gases in the DAC column in 10 CFR 20 posting be established for areas where an individual could Appendix B are identified as " submersion" values that apply
" exceed...an intake of 0.6 percent of the armual limit on to external, rather than internal, exposure. Also, there are intake (ALI) or 12 DAC-hours" in a week. h answer to no ALI values listed in 10 CFR 20 Appendix B for Question 379 states, " radioactive noble gases... (which radioactive noble gases. From this, it appears that radio-have no inhalation ALI) should be exchuled in determining retive noble gas concentrations do not apply to evaluating DAC hours for use in detennining the committed effective and posting Airborne Radioactivity Areas or to DAC-hour dose equivalent (CEDE)." From this it appears that for the determinations.
second provision regarding posting of airborne radioactivity areas, which established precautions to limit internal expo-Answer: (a) Radioactive noble gas concentrations shoukt sures from intakes, one shouki not take into account noble not be excluded with regant to evaluating arxl posting air-gas concentrations because they result in external exposures borne radioactivity areas. See the discussion below.
from submersion. However, noble gas radioactive daugh-ters must be included when determining posting requiro-(b) Radioactive noble gases of the " submersion" class ments under either provision. Is this clarification of the (which have no inhalation ALI) should be exchxled in deter-differences between the two provisions and respective ap-mining DAC hours for use in deternumng the committed plicability of radioactive noble gas concentrations correct?
effective dose equivalent (CEDE). In other words, the DACs for noble gases are based on external dose and Answer: Yes, assuming that it is understood that the "two shouki not be used to assess internal dose, provisions" in the statements preceding the question refer to the two parts of the definition (in 10 CFR 20.1003) of Discamon b following discussion relates to the posting
" airborne radioactivity area", which are separated by the question. Although the definition of DAC in 10 CFR woni "or" bre is only one " provision" that requires 20.1003 does not include concentrations calculated on the posting of airborne radioactivity areas, the " provision" of 10 basis of the external dose resulting from " submersion,"
CFR 20.1902(d). (
References:
10 CFR 20.1902,10 CFR Appendix B clearly states that the DAC values listed in 20.1502,10 CFR 20.1003).
Table 1 of Apperxlix B " relate to one of two modes of i
exposure: either external submersion or the internal com-
)
mitted dose equivalents resulting from inhalation of radio-Question 460: Appendix B contains only one derived air active materials." h defmition of " airborne radioactivity concentration (DAC) value for each radionuclide h crea" refers to "... concentrations - (1) In excess of the DAC provided in Appendix B is derived from the more d: rived air concentrations (DACs) specified in Appendix limiting of the stochastic or the non-stochastic annual limit B...." hs, the definition of " airborne radioactivity area" on intake (ALI). In Regulatory Guide 8.34 (Section 3.3) the includes the DACs in Appendix B that are noble gases arul NRC provides guidance that tlw stochastic DAC should be that are based on " submersion." b preamble to revised used, in preference to the non-stochastic DAC, to calculate Part 20 (56 FR 23379, second and third columns) also the committed effective dose equivalent (CEDE). This NUREO/CR-6204 48
Questions and Answers Regulatory Guide further provides a method for deriving 10 CFR 20.1903 - Exceptions to Posting stochastic DACs for radionuclides that only have the non-Requirements stochastic DAC listed in Appendix B. In addition, Regula-tory Guide 8.7 (Section 2.2) provides guidance that if the CEDE does not exceed I rem, then organ doses, which utihze non-stochastic DACs for calculation, need not be Question 35: Do posting requirements apply to the hospital calculated. Some licensees have concluded, from their pro-room of a hospitalized nuclear medicine patient if the patient spective evaluations of potential internal dose to workers at received less than 30 mci and the dose rate at 1 meter is greater than 5 mrem /hr?
their facility, that workers are not likely to exceed 10% of an ALI (i.e., are not likely to exceed 500 mrem CF.DE).
Answer: No, the hospital room is not regidred to be post-For the situation where the licensee has conchuled that workers are not likely to exceed 10% of an ALI, may the ed pmvidml that the provision of $20.1903(b)(2) is also met.
licensee derive and use stochastic DACs, in lieu of the non-(Note that only one of the three conditions in $20.1903(b)(1) r ehastic DACs listed in Appeudix B, for (a) posting and needs to be met and that one has been met). (
Reference:
(b) exposure control purposes? Such an approach, employ-1 ing the stochastic DACs, woukt allow licensees to more tppropriately assess and control exposures commensurate Question 223: Are radiographers exempt from posting at a with the applicable radiological conditions, than wouk! be the case if the more conservative, non-stochastic DACs temporary field site, under 10 CFR 20.1903(a), since they were used. For example, m evaluating the use of respira-perform radiography in each area less than 8 hours9.259259e-5 days <br />0.00222 hours <br />1.322751e-5 weeks <br />3.044e-6 months <br />, attend tors with regard to keeping the total effective dose eqmva-the material to prevent exposure of individuals in excess of lent (TEDE) ALARA, the use of stochastic DACs, and the limits (i.e., have clear sight over the designated area and respective calculated internal dose projections, wouki pro-are n constant attendance), and control the area (i.e., tell vide a more valid comparison with projected doses from individuals to leave if they come too close to the source)?
external sources of exposure, than would be affonfed Answer: The revised part 20 requirements do not change i
through the use of non-stochastic DACs' this exempion. Radiographers continue to be exempt under Answer: (a) No, with respect to posting of " airborne 20.1903(a); however, industrial radiographers are required -
i rcdioactivity areas" m accordance with the provisions of 10 under 10 CFR 34.42 to conspicuously post areas where CFR 20.1902(d) and the dermition of " airborne radioactivity radiography is being performed. (
Reference:
10 CFR crea" in 10 CFR 20.1003. The use of stochastic DACs in 20.1903, 34.42)
I lieu of non-stochastic DACs listed in Appendix B wouki require an exempion, under the provisions of 10 CFR Question 224: 10 CFR 20.1903(a) gives exemptions to 20.2301 [ applications for exemptions], from the postirg requirements of 10 CFR 20.1902(d) [ posting of airbome
. caution signs" under certain conditions. Since 10 radioactivity areas].
CFR 20.1902 specifies " danger" signs, instead of caution
. grave danger, very high radiation area"), do (b) It is not possible to answer the general question with the exemptions in 10 CFR 20.1903 apply to these " danger" gg respect to " exposure control purposes," without having an explanation of what is meant by this term. However, in Answer: No. The authorization to use only the term regard to the specific example given, the use of a stochastic DACs, and respective calculated internal dose projections'
.dgr" (vice " caution") for a very high radiation area is accepable m evaluating the use of respirators witt. t*%
provides emphasis to the potential hazards. 'Ihere are no exemptions in the code for posting a very high radiation to keepmg the total effective dose equivalent (TEDy) 3 a hi6 radiation area does not mm using u ALARA, when tius results in a more valid comparison with projected doses from extemal sources of exposure than
,, fne exemption would apply to this area if the wouki be afforded through the use of non-stochastic DACs.
conditions of 10 CFR 20.1903(a) are met. (
Reference:
10 CFR 20.1903,10 CFR 20.1902)
Note: See related Question 459 concerning the meaning of the word " applicable" in the phrase " applicable ALIs" in 10 CFR 20.1502. (
References:
10 CFR 20.1902,10 CFR 20.1502,10 CFR 20.1003).
49 NUREG/CR-6204 i
Questions and Answers 10 CFR 20.1904 - Labeling Containers Question 226: (a) Under 10 CFR 20.1904, what is a container? (b) How big can a container be? (c) Can a room be considered a container? (d) is a transportation Question 127: 10 CFR 20.1904(a), Labeling contamers, cask a container when it is not being transported? (e) Are indicates in a parenthetical statement that "the radio, vehicles (e.g., trailer of a tractor-trailer) containers?
nuclides(s) present" may now be intended to be a part of the Answer: (a) In the context of 10 CFR 20.1904, ard m information required to be inchuled on labels. In reply to comments on this rule, the preamble (56 FR 23380, first accordance with Heahh Physics Position (HPPOS) 28, a i
column) provides a special interpretation for nuclear power container is a receptacle in which radioactive material is held or carried, plant licensees as to acceptable methods for compliance for labeling fission and activation product containers. Taken together, the rule and preamble can be understood to mean (b) There is no limit to the size of a container.
that nuclear power plant licensees are required by the revis-ed Part 20 to include the words " activation products" and/or (c) Typically, a room is not consklered a container; it is
" mixed fission products" on all containers in which greater considered an area, and shoukt be posted as such.
than an Appendix C quantity is present - a considerable undertaking which wouki not contribute appreciably to (d) A transportation cask or package in certain circum-radiation protection. Do the words "such as* in the paren.
stances could be a container. If a container is in transport thetical statement mean that this interpretation is incorrect?
and packaged and labeled in accordance with Department of Transportation (DOT) regulations, it is exempt from the Answer: Yes. This interpretation of the rule and preamble labelling requirements of 10 CFR 20.1904. If, however, the is incorrect. The parenthetical statement provides examples container / cask / package is not in transport, it is subject to the of the types of information that may be included on the labelling requirements of 10 CFR 20.1904.
1:. bel; it is not a requirement to imlude all of the information in the parenthetical statement. However,10 CFR 20.1904 (e) Under certain circumstances, the trailer of a tractor-l does require the label to include sufficient information to trailer could be considered a contairer. (Refeme: 10 permit irxlividuals handling or using the containers, or CFR 20.1904, HPPOS 28) working in the vicinity of the containers, to take precautions to avoid or muumize exposures. Simply having only
" Caution, Radioactive Material" or " Danger, Radioactive 10 CFR 20.1906 - Procedures for Receiving Material" on the label is not sufficient. (
Reference:
10 and Opening Packages CFR 20.1904)
Question 36: Part 20 requires that " labelled packages" be Question 128: If a package contammg radioactive maierial monitored. Is it correct to assume that only packages with is to be shipped, and marking the package as low specific White I, Yellow II, or Yellow III labels must be monitored, e.ctivity (LSA) is the only U.S. Department of Transpor-and that markul packages (LSA or radioactive snarkings) tation (DOT) warning requirement, is labeling under 10 are not required to be monitored?
CFR 20.1904(a) required?
Answer: Yes. Based on the statement of considerations, it Answer: No. Although the exemption of 10 CFR is correct to assume that only packages with DOT White I, 20.1905(d) applies to U.S. Department of Transportation Yellow II or Yellow III labels need to be monitored.
(DOT) " labeled" containers, not DOT " marked" containers,
(
Reference:
the Statement of Considerations, in discussing 10 CFR 20.1905(d) [56 FR 23380, secorxl column], states that
" Quantities arxl concentrations not requiring DOT labels Question 108: Can the surveys of radiographic exposure wouki not warrant an NRC labeling requirement." See also devna.s performed under 10 CFR 34.43(b) and (c) be used the answer to Question 36 (10 CFR 20.1906), which indi-to show compliance with 10 CFR 20.1906(f)? If so, is it cates that DOT " marked" packages are not DOT " labeled" sufficient to document the survey once, to satisfy both packages. (
References:
10 CFR 20.1904,10 CFR requirements?
20.1905).
Answer: The survey performed to show compliance with 10 CFR 34.43(c) can be used to show compliance with 10 NUREO/CR-6204 50
Questions arul Answers CFR 20.1906(0 It is sufficient to document the survey the package contains quantities less than a Type A quantity, results one time, the licensee is not required to survey the surface of the package for radiation levels. If the package contains quan-The survey performed to show compliance with 20 CFR tities of radioactive materialin excess of a Type A quantity, j
34.43(b) cannot be used to show compliance with 10 CFR as defined in 10 CFR 71.4 and Appendix A to 10 CFR Part 29.1906(0 The purpose of the survey performed under 10 71, the licensee, in accordance with 10 CFR 20.1906(c),
CFR 20.1906(0 is to ensure the radioactive soun:e is still shall perform monitoring as soon as practicable but not later properly lodged in its shield after transport. (
Reference:
10 than 3 hours3.472222e-5 days <br />8.333333e-4 hours <br />4.960317e-6 weeks <br />1.1415e-6 months <br /> after the package is received et the licensee's CFR 201906(0, 34.43(b), and 34.43(c)).
facility ifit is received during the licensee's normal working hours, or not later than 3 hours3.472222e-5 days <br />8.333333e-4 hours <br />4.960317e-6 weeks <br />1.1415e-6 months <br /> from the beginning of the next working day if it is received after working hours.
Question 227: (a) Must gauge licensees perform a survey of each gauge package (if the package is labeled with a (b) No. The ps.ckage *is received at the licensee facility" DOT label) for contamination and radiation levels upon when it is returned to the storage location at the end of the receipt of the package? (b) What surveys must a licensee day. It is not necessary to survey radiation levels at tempor-perfonn during routine operation where portable gauges are ary job sites. (
Reference:
10 CFR 20.1906,71.4) transported daily from site to site, then returned to a storage location?
Question 229: Will the radiographers have to wipe test the Answer: (a) As a result of amendments to Part 20 sealed source upon receipt (10 CFR 20.1906(b)(1)) even if published on 8/31/92 [57 FR 39353], the licensee is not the manufacturer has performed a recent leak test on the required to survey the gauge package for contamination if source?
the source is in special form an defined in 10 CFR 71.4 and is not required to monitor radiation levels unless the pack-Answer: The requirements of 20.1906 refer to the external age contains quantities of radioactive material that are in surface of package, not the source itself; the requirement to excess of the Type A quantity, as defined in 10 CFR 71.4 wipe test a source is usually a license condition. If the rad Appendix A to Part 71, provided there is not evidence source is not a gas or not in special form, the licensee is of degradation of package integrity.
required to monitor the labeled package (White I, Yellow II or III) for contammation regardless of whether a leak test (b) If there is no evidence of degradation of package inte-has been performed. If the source is in special form as grity, no surveys are required if the package contains less defined in 10 CFR 71.4, the external surface of the package than or equal to a Type A quantity and the source is in does not need to be monitored for contamination.
special form. If the source is not in special form, a contam-(
Reference:
10 CFR 20.1906,71.4) ination survey is required; if the source is greater than a Type A quantity, the external surface of the package must be monitered for radiatSn levels. (
Reference:
10 CFR Question 230: 10 CFR 20.1906(a) gives specific require-20.1906, 71.4) ments for packages contammg radioactive material in excess of Type A quantities; it is not followed by the word "and."
10 CFR 20.1906(b) appears to apply to all packages as con-Question 228: A licensee (e.g., radiographer, moisture taining radioactive matwial, or labeled packages that are density gauge operator, well logger) has a source that the crushed, wet, or damaged. Is it a correct statement that 10 licensse transports to temporary job sites in a licensee-CFR 20.1906(b) requirements have nothmg to do with Type owrnl vehicle. 10 CFR 20.1906(0 exempts the licensee A quantities, and that (a) and (b) are independent require-from doing contammation surveys during routine operations, ments?
but does not exempt the licensee from performing surveys for radiation levels. (a) When must the licensee perform Answer: No. 10 CFR 20.1906(b)(2) correlates radiation such surveys (i.e., when is the package " received")? Is it level monitoring requirements with Type A quantities; only after returning to the storage location at the end of the however,10 CFR 20.1906(a) and (b) are independent re-day? (b) Or is each transport from one temporary site to quirements because 20.1906(a) delineates requirements for another considered a shipment, with a " receipt" at each job making arrangement for r-iving rsulioactive material, and site?
10 CFR 20.1906(b) delineates the mnnienring requirements once the material is received. See Question 227.
Answer: (a) The source should be surveyed at the end of
(
Reference:
10 CFR 20.1906,71.4) the work day, just prior to or immediately after storage. If 51 NUREG/CR-6204
Questions and Answers Question 389: 'Ihe revised 10 CFR 20 includes a new 2.10 SUBPART K - WASTE provisio 2 that allows disposal of licensed material "...by decay in storage..." What criteria should be used in imple-DISPOSAL menting tus provision? Is the NRC planning to develop generic guidance for " decay in storage"?
10 CFR 20.2001 - Waste Disposal - General Answer: See the answer to Question 376 for a discussion of " decay in storage." As indicated in that answer, " decay in storage" is not a practical means of disposal of licensed Question 376: " Decay in storage" is one means of waste material at nuclear power plants (and at some other facili-disposal authorized in the revised Part 20 [10 CFR ties). Therefore, the NRC is providing no criteria to be 20.2001(a)(2)]. How can " decay in storage" be used for used in implementing this provision at nuclear power plants wastes (a) at nuclear power plants and (b) at materials and is not planning to develop (additional) generic guidance for " decay in storage" at nuclear power plants. As noted in facilities?
the statement of considerations for revised Part 20 (56 FR Answer: (a) The inclusion of the " decay in storage" 23380, third column, aal 23381, first column), technically, option in revised Part 20 does not provide any new opions the " decay in storage" option has always been available to for waste disposal at nuclear power plants. See the discus-licensees as an allowed waste disposal opion. This option sion of " decay in storage" in the preamble to revised Part 20 was formally included in the proposed and final rules (56 FR 23380-23381). " Decay in storage" is a practical because the list of disposal options is exclusive and there means of disposal only for radionuclides with short half had been questions as to whether this opion is allowed lives. Wastes from nuclear power reactors usually include under gl20.1-20.601 (in oki Part 20). It should be noted rdonuclides whose half lives are too long for application of that this option does not allow material that has " decayed in the
- decay in storage" option. In any case, wastes that are storage" to be released to an unrestricted area unless it to be released to unrestricted areas after having decayed in meets the requirements of one of the other allowed forms of storage must meet the requirements of one of the other waste disposal in part 20, or the requirements of $35.92, cllowed forms of waste disposal in Part 20, or the require.
" Decay in Storage," of 10 CFR Part 35, or the specific ments of $35.92, " Decay in-storage," of 10 CFR Part 35 or requirements given in any NRC or Agreement State license.
the specific requirements given in the applicable NRC or
(
References:
Agreement State License conditions. However, the require-ments of $35.92 of Part 35 are not applicable to Past 50 licensees.
Question 428: 10 CFR 20.2102(a) requires the use of the units curie, rad, rem, including multiples and subdivisions, (b) As indicated in the answer to part (a) of this question, on records required by Part 20. May a licensee continue to wastes that are to be released to unrestricted areas after use roentgen-based units (e.g., R, mR, R/h, mR/h) in expo-having decayed in storage must meet the requirements of sure control, radiation survey, amt instrument and dosimeter one of the other ellowed forms of waste disposal in Part 20, calibration records without conversion to rad or rem, pro-or the requirements of $35.92, " Decay in Storage," of 10 vided that assessed doses for individuals are recorded in CFR Part 35 or the specific requirements given in the ap-units of rad or rem?
plicable NRC or Agreement State License conditions. For medical licensees (under 10 CFR Part 35), requests for
%r-h The purpose in asking this question is to es-specific license amendments providing exempions from 10 tablish whether or not the units of measurement specified in CFR 35.92 may be considered by the NRC for approval 10 CFR 20.2101(a) - curie, rad, rem, and multiples and based on extraordinary circumstances, in accordance with subdivisions - must appear in all records required by Part 10 CFR 35.19, provided that the licensee demonstrates a 20 or only in those records that specifically deal with activi-real need for the requested exemption. These exempion ty, absorbed dose, or dose equivalent. The intent is to be requests to NRC Regional Offices will be reviewed at NRC scientifically correct in recording exposure rate measure-Headquarters on a case-by-case basis under a technical ments made with radiation survey instruments and estimates assistance request from the Regional Office. See Question of exposure obtained with direct-reading dosimeters and to 389 for additional discussion of decay in storage.
avoid unnecessary changes to existing recordkeeping
(
Reference:
practices. Nuclear fuel cycle, radiography, medical, well-logging, and low-level waste licensees perform hundreds of thousands of radiation surveys each year with instmments that are calibrated for exposure rate and that read out in NUREO/CR-6204 52
Questions and Answers units of pR/h, mR/h, or R/h. husands of workers at required by Part 20, the quantitative relationship between nuclear power plants and licensed radiographers wear exposure (roentgen) and absorbed dose (rad) or dose equi-direct-reading dosimeters that are calibrated for exposure valent (rem) must be clearly documented and understood by and that display mR or R. hse radiation surveys and individuals using these quantities and units in meeting the dosimeters are used to estimate exposure rates and expo-requirements of Part 20. b documentation of this rela-sures for the purpose of controlling individual doses, but tionship may be in the licensee's *radntion protection plan" they are not normally used to assess dose equivalent.
or other radiation protection program document (s), inchad-hrefore, it is not normally necessary to convert roentgen-ing survey procedures; it is not necessary that this relation-based units to rad or rem in records of surveys and dosi-ship (e.g., conversion factor) appear on each form, map, or meter readings. Rather than change the hundreds of forms, log used in 6urveys and calibrations. It may be assumal survey maps, logs and calibration sheets that are used at a that one roentgen equals one rem, or a more accurate con-i facility to reconi exposure control data, radiation surveys, version factor may be used. b relationship between and calibrations, each licensee woukt prefer to continue exposure (roentgen) and absorbed dose (md) or dose equi-j recording radiation levels and exposures in roentgen-based valent (rem) shouki also be included in the instruction units and to explain the relationship of these units to rem in (training) of individuals who make the measurements of n single program document, such as the facility's radiation exposure (in roentgen units), arul records of those measure-j protection plan. An example of such an explanation for a ments, that are required by Part 20.
nuclear power plant is " exposures and exposure rates mea-sured and recorded in roentgen-based units are numerically Note: h answer to Question %(a) has been revised to be equal to or greater than deep < lose equivalent rates in rem-consistent with the answer above. Questions and answers based units for the x-ray and ganuna radiation energies 116 and 117 and answers also discuss dose quantities and normally present in locations other than inside or near open units to be used in records. (
References:
10 CFR 20.2101, reactor plant components." b use of a single program 10 CFR 20.1003; 10 CFR 34.21, 34.24, 34.33; 10 CFR l
statement would pennit a licensee to record what was 39.33).
actually measured in the true units of measurement. 'Ihis epproach to reconfing exposures and exposure rates appears to be consistent with 10 CFR 20.210!(a), which implicitly Question 432: Questions 376 and 389 in section 10 CFR prohibits the use of the SI units becquerel, gray, and sievert, 20.2001 concern the use of the " decay in storage" option of but which does not prohibit the use of roentgen and other 10 CFR 20.2001(a)(2) at nuclear power plants and at mater-cppropriate units when measuring and recording quantities ials facilities. However, it is not clear whether or not these other than activity, absorbed dose, ard dose equivalent. It questions and answers also apply to non-power reactor is also consistent with the use of roentgen-based units in 10 facilities. How can this option be used at non-power reactor CFR Part 34 (il34.21,34.24,34.33) and in 10 CFR Part facilities?
39 (fl39.33).
Answer: As indicated in the statement of considerations for Answer: Yes, except that the " assessed doses for indivi-revised Part 20 (56 FR 23380, third column, and 23381, duals" must be recorded arul reported in terms of dose equi-first column), and in the answers to questions 376 and to valent quantities in units of rem for demonstrating compli-389, technically, the " decay in storage" option has always cnce with the limits of Part 20.
been available to all licensees as an allowed waste disposal i
option. However, this option does not allow material to h.
As indicated in the background to the question,10 CFR ruleased to an unrestricted area unless it meets the require-20.2101(a) prescribes the units to be used for the==ntitia ments of one of the other allowed forms of waste disposal in activity, absorbed dose, and dme equivalent on records 10 CFR Part 20, or the requirements of $35.92, " Decay in required by Part 20. 10 CFR 20.2101(a) also requires that Storage," of 10 CFR Part 35 (for medical licensees, only),
each licensee clearly indicate the units of all quantities on or the specific license conditions given in any NRC or records required by Part 20. b roentgen is a unit for the Agreement State license. (
Reference:
guantity exposure; it is not a unit for the==ntitin absorbed due or dme equivalent. hs the use of this gnantity and unit are not inconsistent with the requirements of 10 CFR 20.2101(a). However, the giantity expmure and its unit roentgen are commonly used as surrogates for the quantity absorbed dose and the unit rad or the gnantitv due equivalent and the unit rem. When this is the case for use of the gnantity exposure and its unit roentgen on records 53 NUREO/CR-6204
Questions arul Answers 10 CFR 20.2003 - Disposal by Release into intended to apply to surveys for contanunation. Note:
There are requirements in 10 CFR 35.70(h) which apply to i
Sinitary Sewerage medical licensees to record the results of surveys for remov-able contammation as disintegrations per minute per 100,
Question 39: Can biological material be defined better in 20.2003? For example, is all organic material biological material? Can animal fats be released to the sewer?
10 CFR 20.2104 - Determination of Prior Occupational Dose Answer: Biological material, in its ordinary meanmg, is material pertammg to living organisms (plants or ammals).
)
The statement of considerations irx!icates that ground-up ammal carcasses are examples of such material. Ammal Question 10: Why does the revised Part 20 still require Form 4?
fats are biological material and, if 'dispersible," can be released to the sewer. (
Reference:
Answer: Form 4 is used as a cumulative record of expo-sures at each liceusee facility and serves as a mechanism for
"""ii"8 '** "* "*** ** ' """": U * **'
d 2.11 SUBPART L - RECORDS must attempt to obtain the information on lifetime cumula-tive occupational radiation dose on Form 4, or equivalent, for all workers requiring monitoring.' Licensees must obtain 10 CFR 20.2101 - Records, General that information for occupational radiation doses received Provisions during the current year and prior to pennitting a Planned Special Exposure. (See 10 CFR 20.2104.) Form 4 is not transmitted to the NRC. Form 5 is a summary of annual Question 116: 10 CFR 20.2101(b) requires the licensee to exposure and may have imre frequent entrien. The data on make a clear distinction among the dose quantities entered several previous Form 5's might be used to prepare a sum-l on the records and gives examples of the following different mary Form 4. The Form 5 will be provided to the NRC dose quantities: total effective dose equivalent, shallow annually for workers in 7 classes oflicensed facilities under dose equivalent, eye dose equivalent, deep dose equivalent, the revised Part 20. (
References:
10 CFR 20.2104,10 committed effective dose equivalent. Does this mean (for CFR 20.2206) example) that the dose rates measured during surveys of external radiation fields must be recorded in terms of one of these dose quantities or (as another example) that the results Question 51: Do 10 CFR 20.2104(a),10 CFR 20.2104(d) of air sampling must be recorded in terms of one of these and Footnote 4 to 20.2104(d) mean that a licensee must quantities?
- backfit" effective dose equivalents (EDE) for irxlividuals who were occupationally exposed before implementation of Answer: No. The examples given refer to dose quantities the revised Part 207 used for doses to individuals, not to dose (or activity) quantities used in surveys of areas. (
Reference:
10 CFR Answer: No. Such backfitting is not required. However, 20.2101) licensees may, if they so desire, make estimates of the EDE and committed EDE based on the occupational dose reconis available for this period. (
References:
Question 117: Does the requirement of 10 CFR 20.2101(a) 10 CFR 20.2104(d),10 CFR 20.2104(d) Footnote 4 )
to use the unit curie (for activity) mean that it will not be permissible to record the results of contamination surveys in units of disintegrations per minute (dpm) or mrad Question 55: 10 CFR 20.2104(e)(1) prorates the 5-rem smearable?
annual limit on the total effective dose equivalent at a rate of 1.25 rems per quarter for each quarter for which records Answer: No. The 10 CFR 20.2101(a) requirement as it were unavailable but includes no similar provir. ions for the l
applies to units of activity (curies) is interxled to apply to other annual limits (individual organs, eye, skin, extremi-l records of quantities of material directly related to the ties). Is similar proration required for doses covered by the explicit requirements of Part 20 (e.g., storage and control, other limits?
f posting and labeling, waste disposal, concentrations in air, ux! individual intakes of radioactive material). h is not NUREO/CR-6204 54
l:
Questions and Answers i
I Answer: Yes. As indicated in the statement of considera.
Question 139: In-vivo measurements for an incoming tions (56 FR 23383, first column), the values for the other worker could indicate that the worker's internal dose, as limits should be reduced by one quarter for each unreported determined and recorded by the preceding licensee, was quarter. - (
References:
10 CFR 20.1201(f),10 CFR incorrect. What action would the NRC expect the current j
20.2104(e)(1))
licensee to take 1
i Answer: b NRC wouki expect the licensee to correct
}
Question 64: b following question relates to the require-the erroneous dose,' document the reasons for that correc-ments of 10 CFR 20.2104(a)(2),10 CFR 20.2104(c), and tion, and inform the worker about this correction.
]
20.2104(d) concerning records oflifetime cumulative on-(
Reference:
10 CFR 20.2104) cupational dose. Assummg that (1) the bcensee has obtain-ed by electronic media, a pnoted report (or reports) con-taming the Form 4 information en an individual's lifetime Qwstion 142: (a)In compliance with 10 CFR j
cumulative dose, (2) the indiviAsJ wha received the dose 20.2104(a)(2), what constitutes an acceptable attempt to signed Form 4, or equivalent, in acconlance with 10 CFR obtam a record of the lifetime dose for a worker? (b) Since 20.2104(d), and (3) there is no other signature attesting to there are no limits for lifetime doses (other than planned the anehanticity of the Form 4 record. Is the licensee in special exposures), and lifetime dose reports to workers are comphance with the requiraraaa#= in 10 CFR 20.2104 not required, why must bcensees go to the expense of ob-4 concerning records of lifetime cumulative occupational taining and recording these doses?
dose?
4 Answer: (a) b licensee should request this information Answer: Yes. As stated in Regulatory Guide 8.7, Section from the worker Alternatively, the beensee also may re-l C.I.3, to demonstrate s?=+ with the requirement of quest this information from the worker's most recent em-10 CFR 20.2104(a)(2) (to =*earnpe to obtain the records of player for work involving radiation exposure or the :
lifetime cumulative occupational radiation dose), the indi-worker's current employer if the individual is not employed e
' vidual to be monitored may provide a wntten estimate of the by the bcensee. If this request is derved, the licensee need 1
cunnlative lifetime dose or an up-to.date NRC Form 4 make no further efforts to obtam the information; however,
{
signed by the individual. This information does not need to the individual will not be available for a planned special be venfied so long as the individual does not participate in a exposure.
i planned special exposure. However, in the unkkely event j
that it was the individual who providad the licensee with the (b) As explained in the Statement of Consklerations (56 FR 1
report by electronic media, Regulatory Guide 8.7, Section 23383,23384) the requiroment to attempt to obtain the '
C.I.3, also states that "Akhough not required by the regula-records oflifetime cumulative doses follows one of the tions, it is considered good health physics practice to verify provisions of the guidance to Federal agencies on occupa-i the information provided by the individual." (
Reference:
10 tional radiation protection. Also, as stated in SECY-88-315 CFR 20.2104)
(available in the NRC Public Document Room), the record.
keepag and reporting requirements of the resised Part 20 are consistent with implementing an NRC staff recommen-Qweelan 113: If an NRC licensee employs an individual dation to establish a registry of radiation workers and their i
formerly employed at a DOE lab and that individr.al's DOE radiation doses. Such a registry will be of value in analyz-lab dose record shows a CEDE of more than 5 rems (but ing doses received by workers at several sites during the i
within DOE limits) must the NRC heensee consider this an year, in tracking exposure trends, and will facilitate epidem-overexposure and reduce this individual's planned special iological studies of potential radiation-induced health effects.
1 exposure allowance accordingly?
(
Reference:
Answer: No, b ' limits
- referenced in 20.2104(a)(2) and 20.1206(e) are the limits in'effect and appbcable to the Question 143: 10 CFR 20.2104(c) states in three places l
individual at the time of the exposure. It should be noted that hcensees may accept or obtam dose data from the most that if the 5 rem CEDE was received during the current -
recent employer. b most recent employer may not be the
^
year, this individual would not be allowed any further ex-bcensee at whose facility the worker was most recently posure for the balance of the year. (
References:
10 CFR exposed. Will it be permissible to accept or obtain the data 20.2104 and 20.1206(e)). '
from the most recent facility at which the worker was exposed? (Small contractors oAen do not have the data.
t 3
)
55 NUREO/CR-6204
?
Questions armi Answers Nuclear power plant licensees in general wouki much prefer 20 (e.g., shallow dose equivalent to the skin of 35 rems in to continue receiving data from the most recent licensee).
the current quarter and year to date), is the individual un-available for further exposure in that dose category for the Answer: Yes. (
Reference:
remamder of the year? (4) If the individual has received a planned special exposure (PSE) at the previous workplace in the current quarter, how should the PSE dose be accounted Question 371: 10 CFR 20.2104(c)(1) states that a licensee for as prior occupational dose by the present licensee under tr y accept, as a record of the occupational dose that the the *okl* Part 207 Shouki the PSE dose be subtracted from individual received during the current year, a written signed the available current quarter dose for that dose category?
statement from the individual. If this was done and the l
st:.tement is false, wouki a resulting exposure greater than 5 (b)In the case of a worker whose dose was monitored rem in the year be considered an overexposure aru! a viola-earlier in the year at a licensee that has nnt implemented the tion?
revised Part 20 and is now inprocessing at a licensee that has implemented the revised Part 20: if the individual has Answer: The exposure wouki be an ' overexposure" (an received recorded internal dose (in terms of rem) or internal occupational dose in excess of the annual limit). However, exposure (in terms of MPC-hrs) or internal uptake (in tenns as indicated in the statement of considerations for the of organ burden), how shouki this data be considered with revised Part 20 (56 FR 23384, first column) if the individual regard to revised Part 20 requirements (i.e., TEDE, CEDE, d:liberately falsifies the staterrmat, the licensee wouki not be or CDE)?
penahzed for a resulting overexposure. Furthermore, the st:ff believes that the licensee shouki not be penahzed for Answer: (a) (1) DDE. (2) Yes, the individual is "unavail-flise information provided by the irulividual even if the able for any further exposure in that dose category for the flisification was not deliberate. However, as indicated in remamder of the quarter" because the individual has already Regulatory Guide 8.7, Rev.1, although not required by the exceeded the applicable dose limit for the quarter. (3) The regulations, it is considered good health physics practice to indivklual is unavailable for further exposure in that dose vsrify the information on prior exposure provided by the category for the remainder of the quarter (because the in-J individual. Such verifications shouki reduce the likelihood dividual has exceeded the applicable dose limit for the quar-of overexposure resulting from false information on prior ter), but is available for further exposure in that dose cate.
exposures. If an individual deliberately provides falso infor-gory for the remainder of the year after the end of the mation on the prior dose, that individual woukt be in poten-quarter. (4) The PSE dose shoukt be accounted for as oc-tial violation of the revised regulations covering the 'delib-cupational dose received during the quarter and should be crate misconduct" (56 FR 40664,8/15/91) that caused the subtracted from the available current quarter dose for the licensee to be in violation of the regulatory limit.
dose category.
(
Reference:
(b) CEDE. (
Reference:
Question 390: During 1993, there may be radiation work-era transiting between licensees that have, and have not, Question 408:
implemented the revised Part 20. (a) In the case of a j
worker whose dose was monitored earlier in the year at a Mgnmd licensee that has implemented the revised Part 20 and is now in processing at a licensee that han not implemented the 10 CFR 20.2104 states that for each irdividual for whom revised Part 20: (1) Shoukt "whole body dose" be taken as monitoring is required, the licensee must: 1.) Determine the " total effective dose equivalent" (TEDE) or as the "doep the occupational radiation dose for the current year; and 2.)
dose equivalent" (DDE) recorded by the previous licensee?
Attempt to obtain the records of lifetime cumulative oc-(2) If the individual has received dose in excess of an 'okl*
cupational radiation dose. " Records of lifetime cumulative Part 20 limit for the current quarter, but less than the res-occupational radiation dose" refers to occupational dose pective revised Part 20 limit for the year (e.g., shallow dose records prior to the current year. These records are only equivalent to an extremity of 20 rems for both the current used when implementing the planned special exposure quarter and year to date), is the individual unavailable for option. Some licensees may use prior year's TEDE to con-any further exposure in that dose category for the remamder trol an individual's lifetime dose in compliance with NCRP-of the quarter? (3) If the individual has received done in 91 woummiations or average annual exposure in com-cxcess of the " implied annuallimit" of the "ok!" Part 20, pliance with ICRP-60 recommendations. However, other but less than the respective annual limit in the revised Part prior year's dose quantities such as stallow dose equivalent NUREG/CR-6204 56
a Questions and Answers (SDE) and lens (eye) dose equivalent (LDE) are not useful dose limits include limits for the eye, shallow, and extremity to licensees and provide no additional protection to ialivi-doses mal the " occupational dose" in 10 CFR 20.2104(a)(1) duals. Therefore, it was reasonable ami compliant to obtain includes the eye, shallow, and extremity doses. b recom-only TEDE for prior years. Can a licensee seek only to mendation in the Statement of Considerations (which is not obtain the TEDE occupational dose quantity for prior years an explicit requirement in the regulation) that, in establish-to comply with the 20.2104(a)(2) requirement to " attempt to ing administrative controls, the licensee should reduce the obtain the records of lifetime cumulative occupational values for limits other than the TEDE by one quarter of l
radiation dose *?
their annual limit for each unreported quarter provides a mdhod, acceptable to the NRC staff, for licensees to Answer: Yes, provided the licensee does not intend to demonstrate compliance with those limits when records of ruthorize planned special exposures for the irdividuals for those doses are missing for a portion of the year.
whom the licensee attempts to obtain only the TEDE. For planned special exposures, the provisions of 10 CFR (c) A licensee is required to determine a particular occupa-20.1206(e) that limit " lifetime" exposures apply to all tional dose received by a new employee earlier in the cur.
occupational doses having annual limits in 10 CFR rent year only if the licensee makes the prospective deter-20.1201(a) (TEDE, organ dose, eye dose, skin dose and mination that individual monitoring will be required, pur-extremity dose), not just the TEDE. The reasons for this suant to 10 CFR 20.1502, for the prospective occupational requirement other than for use in cases of planned special dose. If the licensee determines that inlividual monitoring exposures are given in the answer to Question 142(b).
for eye or shallow or extremity dose are not required for a
(
Reference:
10 CFR 20.2104) particular individual (because, at the licensee's facility, those doses are not likely to exceed 10 percent of the limits for those doses), the licensee is not required to determine Question 420: 'lhis question refers to the answer to the prior eye or shallow or extremity doses. (
References:
Question 55 in 520.2104. (a) Despite the quoted reference, 10 CFR 20.2104,10 CFR 20.1003).
920.2104 only refers to occupational radiation dose (why radiation when the defined term is occupational dose?),
which is defined in terms of " dose." (b) The defmition of 10 CFR 20.2105 - Records of Planned Special dose does not include eye, shallow, or extremity doses
- Qosures What is the regulatory basis for including eye, shallow, and extremity doses within the scope of $20.2104 where it is so explicitly not included? A simple discussion in the State Question 112: A licensee authorizes a " planned special ment of Considerations does not seem to be an adequate lusts for rewriting a regulation. (c) Are the dose histories exposure" in accordance with 10 CFR 20.1206 and the of these three organs (eye, skin, extremity) so high as t doses to the involved individuals are fortuitously much necessitate the paperwork to track these for new employees?
lower than anticipated. In retrospect, a planned special etWion m u tb dosa b I suspect that for the vast majority of workers, these are mi as "
" doses on the Form 5 rather than negligible compared to TEDE.
recorded as planned special exposure doses?
Anmer:
Answer: No. Following a planned special exposure, the individual doses must be recorded in accordance with 10 (a) " Dose" aal " radiation dose" are synonymous (see " Dose or radiatmn dose" in $20.1003); therefore, " occupational CFR 20.2105 (no matter how small) and may not be record-ed as routine doses on the Form 5. (
References:
10 CFR dose" and " occupation radiation dose" are synonymous.
20.1206 and 20.2105).
(b) Contrary to the statement in the question, " dose or radiation dose" is biaadly dermed in Part 20 as "a generic term that means absorbed dose, dose equivalent, effective 10 CFR 20.2106 - Records of Individual dose equivalent, committed dose equivalent, committed Monitoring Results effective dose equivalent, or total effective dose equivalent, as defmed in other paragraphs of... [10 CFR 20.1003)."
The " eye dose equivalent" and the " shallow dose equiva.
Question 399: The NRC Form 5 (Item No. 8) provides for lent" (the quantity used in the limits for the skin and for the entry of multiple NRC license numbers. Sonw licensees extrernities) are both " dose equivalent" quantities and, there-may hoki multiple licenses and provide common monitoring fore, are " doses" as dermed in Part 20. The occupational (e.g., a single set of dosimeters) for personnel working 57 NUREG/CR-62M
4 Questions and Answers under any or all of the licenses, in such cases, it is pro-Answer: Yes, if the sxposure data are reported to the posed that only a single NRC Form 5 wouki be generated NRC by electronic transmission, the Form 5 exposure for each individual, listing all licenses under which they report prepared from the data base and provided to the were monitored under 20.1502. Is this acceptable to satisfy worker need not be signed (" signature on fue" is accept-regulatory requirements?
able). However, if the exposure data are provided to the NRC on Form 5, rather than by electronic transmission, the Answer: Yes, in general. For one nuclear power station, form must be signed. As noted in the question, the signa-it is acceptable for the licensee to provide a single NRC ture block on Form 5 is not opional. (References. 10 CFR Form 5 for an individual who works at one or more units at 20.2106,10 CFR 20.2206, Regulatory Guide 8.7, Rev.1).
the station. However, a nuclear utility that has two or more power stations shouki not use a single NRC Form 5 for an individual who works at two or more different stations; a Question 402: NRC Form 5 (Item No. 21, " Comments")
separate form should be used for each station at which the implies that dose from a " hot particle" shouki be added to individual works. (
References:
10 CFR 20.2106,10 CFR the shallow dose equivalent, maximum extremity (SDE, ME 20.2206, Regulatory Guide 8.7).
- Block 14). However, I&E Notice 90-48 states that " hot particle exposure will not be added to skin doses from sources other than hot particles." (a) Should hot particle Question 400: NRC Form 5 (Item No.10B) includes the doses be added to the shallow dose equivalent as implied?
symbol "V", which is not defined in Regulatory Guide 8.7, (b) If so, shoukt this dose be subtracted from the applicable Revision 1. (a) Does the "V" signify
- vapor" as used in dose category with regard to remauung available shallow Federal Guidance Report No.117 (b) If so, how is this lung dose equivalent (skin or extremity) for the year? Based on clearance class to be applied in operational air sampling and our understanding of the intent ofI&E Notice 90-48, we internal dosimetry programs?
believe that " hot particle" doses shouki not be subtracted from the remaining available shallow dose equivalent (skin Answer: (a) *V" in Item 10B of Form 5 is an abbreviation or extremity) for the year.
for the lung clearance class " vapor" in Appendix B to 10 CFR 20.1001 - 20.2401. " Vapor" is listed as a lung clear.
Answer: The intent of the " hot particle" example in the ance " class" for only two elements, sulfur and nickel.
instmetions for Item 21 on Form 5 is simply to give one an (However, the " water" inhalation class for hydrogen-3 example of how this space on the form might be used.
indicates water vapor.)
bre is no intention to imply that hot particle doses shouki be added to other doses. W question of adding hot particle (b) h " vapor" inhalation class should be used when the skin doses to other skin doses was ackfressed in IE Informa-radionuclides are present in the form of a vapor in the air tion Notice 90-48, " Enforcement policy for Hot Particle and the associated air sampling shouki be appropriate for Exposures," and the enforcement policy enclosed with that sampling the radionuclides in this form. (
References:
10 notice, and in Health Physics Position (HPPOS) 246 (in CFR 20.2106,10 CFR 20.2206, Regulatory Guide 8.7).
NUREG/CR-5569, Rev.1). W NRC policy and staff positions in these documents have not been changed by revised Part 20 or the instmetions for Form 5 in Regulatory Question 401: NRC Form 5 (Item No. 20) provides for the Guide. Answers to the specific questions are as follows:
signature of the licensee's authorized representative respon-(a) As indicated in HPPOS-246, licensees may choose sible for the data arxl is not noted as " optional" as is the whether or not to add a hot particle dose to other skin or licensee signature block on NRC Form 4. Appendix A of extremity doses. However, in either case, the record shouki Regulatory Guide 8.7, Rev.1, " Instructions for Recording be clear as to the amount of the hot particle dose. In and Reporting Occupational Radiation Exposure Data,"
determining whether or not an overexposure has occurred, provkles for the licensee to sign the transmittal letter for the NRC will consider the hot particle dose alone, without electronic transmission of exposure data to the NRC and adding it to other doses, thereby certify the database. if a letter certifying the database is maintained on file, can the licensee so noto NRC (b) h hot particle dose shouki not be subtracted from the Form 5's which are generated from the database, e.g.,
remauung available shallow dose equivalent (skin or ex-
" signature on file," rather than signing each individual NRC tremity) for the year. (
References:
10 CFR 20.2106,10 Form?" In particular, this woukt facilitate the providing of CFR 20.2206, Regulatory Guide 8.7).
individual exposure reports annually to each worker, as required by 10 CFR Part 19.
Questions and Answers Quesilon 403: NRC Fonn 5 (ltem No.10) provides for can recalculate the reported doses using the new models and listing of specific radionuclides in intakes that contribute to weighting factors. Another reason, of benefit to licensees, the recorded committed effective dose equivalent (CEDE).
is to make it possible for a licensee to determine the CDE to When detennining the CEDE only significantly irradiated the maximally exposed organ for an individual who has organs need be included in the calculations [10 CFR organ doses reported from previous employers. For exam-20.1202(b)(3)). An organ is considered to be significantly ple, consider an individual, who, during a year, was em-irradiated if the product of the weighting factor and com-ployed by licensee A and received a CDE of 20 rem to the mitted dose equivalent, per unit intake, is greater than 10%
lung, then was employed by licensee B and received a CDE of the maximum weighted value of committed dose equiva-of 20 rem to the bone, and finally was employed by licensee lent (CDE), por unit intake [ Footnote 1 to 20 CFR C and received a CDE of 20 rem to the thyroid. NRC 20.1202(b)(3)]. Similarly, an isotope need not be consider.
Fonn 5 does not provide a space for recon!ing which organ ed to be in an airborne mixture if the concentration of any is the maximally exposed organ (unless the " Comments
- radionuclide is less than 10% of its DAC, and the sum of space is used for this purpose). In the absence of informa-the percentages of the disregarded radionuclides is less than tion on which organ was maximally exposed and on the 30% [10 CFR 20.1204(g)]. Given these two examples of intakes of individual radionuclides, the total CDE to the cut off levels, can a licensee disregard the contribution a maximally exposed organ in this example woukt be consi-radionuclide makes to the CEDE, with regani to recording dered to be the total of these three 20-rem doses (to different a
i cnd reporting specific radionuclides, ifit is less than 10% of organs), or a total of 60 rem, which wouki appear to be a the total CEDE resulting from uptake of a mixture, arxl the potential violation of the organ dose limit. With the in-sum of the disregarded radionuclides is less than 30%? In dividual radionuclide intake information, the CDE to the this way insignificant doses, the addition of which imply maximally exposed organ couki be recalcula:ed and very greater precision than exists for internal dosimetry, can be likely would be below the limit. The NRC will also use the disregarded without compromising sound radiological intake data from some of the earlier reports to the NRC practices.
under revised Part 20 to recalculate the doses to ensure that the reported doses are reasonably consistent (within a factor Answer: No. 'Ihe statements conceming significantly of 2 or so). Finally, the recordkeeping and reporting re-irradiated organs [in 10 CFR 20.1202(b)(3) and Footnote 1]
quirements of revised Part 20 are consistent with imple-apply to compliance with requirements for summation of menting an NRC staff recommendation to establish a regis-external and internal dose and are not relevant to cutoffs of try of radiation workers and their radiation doses. Such a j
radionuclides used in intake calculations. The statement in registry will be of value for a number of reasons, one of 1
l the quedon concerning the provisions of 10 CF?
which is to facilitate epidemiological studies of potential l
20.1204(g) is incorrect; it dees not in:lude the necessary radiation-induced health effects. The inclusion of the condition of 10 CFR 20.12M(g)(1) concerning use of the radionuclide intake data in the dose records provides a
" total activity" in demonstrating compliance. [See the better basis for these studies than records of dose alone.
answer to Question 121 for clarification of 10 CFR
(
References:
10 CFR 20.2106,10 CFR 20.2206, 20.1204(g).] There is no basis in the regulations for the Regulatory Guide 8.7).
proposed cutoffin the calculation of the CEDE. (Refer-ences: 10 CFR 20.2106,10 CFR 20.2206, Regulatory Guide 8.7).
10 CFR 20.2107 - Records of Dose to Indi-vidual Members of the Public Question 404: NRC Form 5 (Item No.10) provides for reporting of individual radionuclides involved in an intake.
How does the NRC plan on using this data (i.e., what is the Question 391: (a) Are records maintained by nuclear power plants that satisfy the requirements of 10 CFR Part 50, NRC's purpose in collecting this data)?
Appendix I, and related regulatory guidance sufficient to demonstrate compliance with the requirements of 20.21077 Answer: NRC Form 5 (ltem 10) provides for recording /
(b) If not, what additional records are required?
reporting of ialividual radionuclides involved in an intake because 10 CFR 20.2106, records of individual monitoring Answer: (a) Not necessarily.
results, requires that the records mehide, when applicable, the estimated intake or body burden of radionuclides. There (b) For example, additional records may be needed to de-are several reasons for mclusion ofintake information on monstrate compliance with the limits for individual members Form 5. One reason is that if the internal dose models and of the public in controlled areas. See the answer to the weighting factors are changed at some future date, the NRC 59 NUREG/CR-6204
Questions ami Answen 1o related Question 384 and answers (
References:
10 CFR -
10 CFR 20.2203 - Reports of Exposures, 20.2107).
Radiation levels; etc-a 10 CFR 20.2110 - Foran of Records Question 122: The conforming anumhnent to 10 CFR 50.73(aX2) states that reports subautted in accordance with 10 CFR 50.73(a)(2Xviii) also meet the e#1uent release Q=atian 141: 10 CFR 20.2110 requwes adequate safe,
reporting requiremanen of 10 CFR 20.2203(aX3). However, '
- guards against tampering with and loss of records. - For data 10 CFR 20.2203(aX3) requires reporting of concentrations stored in electronic systems, what safeguards are accep-in an unrestricted area of.10 times any apphcable limit in table?
Part 20 while 10 CFR 50.73(aX2Xviii) requires reposts of 4
airborne or liquid enluent releases that exceed 20 times the; Auswer: 'Ihe NRC does not have, and has no plans to apphcable concentration limits in Table 2, Appendix B.
develop, prescriptive requirements or gmd-e on safe-Why is the nadtiple ten in one case and twenty in the other? -
guards for electronic systems to prevent tampering with or loss of records.~ However, the Electric Power Research Answer:; The two reporting requirements are consistent in :
Institute (EPRI) has published a report, 'Ouidelines for
. terms of public dose. The anmaal dose limit for a member Quahty Records in Electronic Media for Nuclear Facilities of the public is 100 mrem. 10 CFR 20.2203(aX3) requires
' (NCIO-10),* Report No. EPRI NP4295 (May 1989) that reporting above a threshold of ten times this applicable may be helpful in meeting this' requirement in 10 CFR
. limit, or 1000 mrom. : 'Ihe concentrations in Table 2,1
~
4 20.2110. The NRC staff has taken no position in regard to Appendix B, correspond to an annual dose of 50 mrem; this EPRI document. The abstract of this report includes the therefore,' the requironwat in 10 CFR 50.73(a)(2)(viii) for '
statement that the guidehnes'in the report " provide a con-reporting at 20 times these concentrations corresponds to a sistent approach to the electronic creation, storage, retrie-
' reporting threshold in terms of annual dose, of 20 x 50 -
val, control and approval of quahty records, a subject here-mrem, or 1000 mrem, which is the same dose threshold as tofore not addressed by industry standards and regulations.'
that in 10 CFR 20.2203(a)(3). (
References:
10 CFR
(
Reference:
10 CFR 20.2110) 20.2203, 50.73)'
' 2,12 SUBPART M - REPORTS 10 CFR 20.2206 - Reports 'of Individual Monitoring 10 CFR 26.2202 - Notification of Incidents Question 383: Reports of planned special exposures (PSEs) are required by 10 CFR 20.2204 to be submitted within 30 Question 56: : Woukt areas periodically patrolled, but not days of the PSE to the NRC Regional OHice. ~ Complete constantly manned, be considered to fall within the excep-records of PSEs are required to be mamenmad in accordance tion in 10 CFR 20.2202(a)(2) and 20.2202(b)(2) for "loca-with 10 CFR 20.2105 and the monitoring results for PSEs ~
tions where personnel are not normally stationed durmg.
shouki be recorded on NRC Form 5 or equivalent in accor-routine operations, such as bot-cells or process enclosures?"
dance with the guidance in Regulatory Guide 8.7, Revision l
I For example, would these exceptions apply "if a hallway or
- 1. (a) Are the PSE dose reports also required to be submit.
cubicle in the reactor auxthary becomes an airborne radio-ted to NRC annually in accordance with 20.22067 (b) If so, activity area and auxibary equipment operators make their is only the NRC Form 5 equivalect required to be subnut-
~
rounds periodically during their shiA?"
ted, or does the other information reqmred by 10 CFR.
20.2105 also have to be included? (c) Shoukt separate NRC Answer: No, the exception wouki not apply to these areas Form 5s, i.e., one for routine dose and one for PSE dose,'
~
that are 'penodically patrolled
- or otherwise normally ac-be subautted for each apphcable individual??
cessible to personnel. ' However, for nuclear power plants at power, prunary contamments are examples of " locations Answer: (a) Yes.
. where personnel are not normally stationed." (
References:
- 10 CFR 20.2202(a)(2),10 CFR 20.2202(b)(2))
(b) Only the information on Form 5. 7he information required by 10 CFR 20.2105 does not have to be included in the reports required by 10 CFR 20.2206. (c) Two separate NURBO/CR4204 60
.j
Questions and Answers 1
1 forms, one for routine dose and one for PSE dose should be 20.1502. However, it is not intended that related radio-submitted for each individual who had both routine and PSE nuclide intake data will also be recorded azul reported be-doses. Separate reports are needed because completion of cause of the resources which would be needed to track and item 9B on Form 5 requires indicating whether the reported transfer the specific radionuclide data to the NRC Form 5 or occupational exposure is for routine exposure or for PSE.
equivalent. For example, the licensee may only have track-In other words, the design of the Form 5 does not allow ed Derived Air Concentration hours (DAC-hrs), using the both routine exposures and PSEs to be reported on the same appmpriate most restrictive DAC, without assessing specific form. (
References:
10 CFR 20.2206,10 CFR 20.1206,10 radionuclide intakes. Accordingly, the " Intake" section of CFR 20.2204, Regulatory Guide 8.7) the NRC Form 5 would be noted as "NR" for "not requir-ed," and no specific radionuclide data woukt be recorded.
However, the " Instructions and Additional Infonnation Question 392: What monitoring period should be used in Pertinent to the Completion of NRC Form 5," items 10A-D cnnual individual monitoring reports submitted, in accor-require that intake data be recorded "...for each radio-dance with 10 CFR 20.2206, following the first year of nuclide that resulted in an internal exposure recorded for the revised 10 CFR Part 20 implementation, if the period of individual." The issue is that these instructions should not implementation did not encompass the full year? For be considered applicable for recording and reporting per-example, if a licensee implements the revised 10 CFR Part formed that is not required. This approach to the partial 20 on July 1,1993, is the licensee required to provide recording arxl reporting of occupational dose data, when ennual individual monitoring reports early in 1994 that done on a voluntary basis, appears to be consistent with the cover the entire year, or only for the final six months of the flexibility that is implied in the revised Part 20 and related year during which monitoring was provided to individuals regulatory guidance. Note that Regulatory Guide 8.34, under 10 CFR 20.1502?
Section C.I.4, states "the results of monitoring provided when not required by 10 CFR 20.1502 are not subject to Answer: This annual report should cover the entire year,
[the] dose recording requirements."
preferably using the format of Regulatory Guide 8.7, Rev.1 (Form 5) for the entire year. However, if it is impractical Answer: Yes. The instructions for Form 5 do not apply to to use this format for the portion of the year under 10 CFR recording and reporting that is not required by Part 20 and 20.120.601, the format previously used for reports in that is being done voluntarily. NRC encourages licensees to compliance with 10 CFR 20.403 (" termination reports")
report CEDE vohmtarily when monitoring is performed may be used for that portion of the year. (
Reference:
10 even though not required. If the intake information is CFR 20.2206).
omitted when reporting voluntarily, licensees shoukt foot-note the CEDE entry with a notation in the comments section that " monitoring was not required." (
Reference:
10 Question 393: Is it acceptable for regulatory purposes that CFR 20.2206).
occupational dose data that are being provided on a vohm-tary basis (i.e., the results of dose momtoring provided that is not required by cegulation) be reconled and reported only Question 394: (a) Are the results of dose monitoring of in part? The purpose in asking this question is to establish minors and declared pregnant woman performed in accor-whether or not the revised Part 20 provides the flexibility dance with 20.1502 required to be reported to NRC as part for licensees to record and report the results of " monitoring of the annual reporting of individual monitoring results? (b) prformed but not required" without also incurring implied if so, are the records of dose to the embryo / fetus, which requirements with regards to NRC Forms 4 and 5, or equi-may differ from records of dose to the declared pregnant velents. The intent is to be able to provide useful informa-woman, required to be submitted as part of the annual re-tion, that is not required by the regulation, on a voluntary porting of individual monitoring results? It would seem that insis to the worker arxt/or the NRC without unduly taxing embryo / fetus dose records are not required to be included in available licensee resources. The specific example outlined the annual report, because the embryo / fetus dose records below is provided to illustrate the more general issue of are developed in accordance with 20.1208, " Dose to the flexibility in recording and reporting occupational dose in.
Embryo / Fetus," and not 20.1502, " Conditions Requiring formation that is not necessary for compliance with regula.
Individual Monitoring of External and Intemal Occupational tory requirements.
Dose," which is the base reference for the annual reporting requirement.
Some licensees intended to voluntarily record and report the calculated Committed Effective Dose Equivalent (in rem),
Answer: (a) Yes. For a declared pregnant woman, the even when internal monitoring is not required by 10 CFR dose to be reported in accordance with 10 CFR 20.1502 is 61 NUREG/CR-6204
Questions arx! Answers the dose to the woman herself, not the dose to the embryo /
2.13 10 CFR 20 APPENDICES fetus.
(b) No. See Section 2.3 of Regulatory Guide 8.7, Rev.1, 10 CFR Part 20 Append A ix concerning reporting of embryo / fetus dose. (
Reference:
10 CFR 20.2206,10 CFR 20.1502,10 CFR 20.1208).
Question 452: The following questions refer to the selec-Question 395: If an individual is monitored several times ti n and use of a half-mask face piece, as desenhed in A perxlix A " Protection Factors for Respirators":
P during a year by the same licensee (e.g., during two moni.
toring periods separated in time), how should the monitoring period (s) be designated in the annual individual monitoring
- a. Footnote "g" of Appendix A states that "this type of report required by 10 CFR 20.2206 (i.e., on the NRC Form respirat r is n t satisfact ry for use where it might be 5 or equivalent)? Due to the possible limitations in the p saible (e.g., if an accident or emergency were to occur) format and structure in licensee's computerized occupational f r ambient airborne concentrations to reach instantaneous dose recordkeeping systems, it seems that there shouki be values greater than 10 times the pertinent values in table 1, firxibility m meeting the intent of the requirements. Al.
column 1 of Appendix B...," i.e., the derived air concentra-timatives might include the following:
tions (DACs) for inhalation. Is this provision interxled to apply to the work activity in progress for which the respi-
- e. Issue one NRC Form 5 or equivalent with a single moni-rator is being used, or is it more broadly applicable to the toring period that begins on the first day of the year and type f facility or licensed activiry? For example, is the ends on the last day of the year.
statement intended to exclude the use of a half-mask face piece respirator at a nuclear power plant? We believe that
- b. Issue one NRC Form 5 or equivalent with single moni-the use of half-mask face piece respirators shoukt be permit-toring period that begins on the first day of the first moni-ted with the same limitations as are applied to other respira-toring period and ends on the last day of the last monitoring tor types because the use of a half-mask face piece may period.
offer advantages over, for example, a full face piece respira-tor in some applications by keeping the overall total effec-
- c. Issue a separate NRC Form 5 or equivalent for each tive dose equivalent ALARA. This wouki appear to be in individual monitoring period (i.e., issue two or more NRC keeping with the intent of $20.1703, Use ofIndividual Form 5s for the same individual in the same year).
Rpiratory Protection Equipment, which states that "...
the licensee may select respiratory protection equipment Would any or all of these approaches be acceptable in with a lower protection factor only if such a selection wouki meeting the intere of the regulatory requirements? Would result in keeping the total effective dose equivalent other approaches be acceptable? If so, please describe.
ALARA."
Answer: All three options are acceptable (option B is
- b. Footnote "g" requires that "... the mask is to be tested preferable) provided that the separate "mor.itoring f r fit pri r t use each time it is donned..." for the use of period (s)" in the question fall within the year used to de-half-mask face pieces. Is a negative pressure test an accep-monstrate compliance.10 CFR 20.2206 requires an annual table method to adequately test the respirator prior to use?
report of monitoring for individuals for whom monitoring Such a qualitative test method wouki seem to be acceptable was required by 10 CFR 20.1502 during that year (emphasis because it appears that there wmdd be no practical method added). 10 CFR 20.1502 requires monitoring sufficient to t acc mplish a quantitative test in the field prior to each demonstrate compliance with the limits. The year as defin-
"8**
ed in 10 CFR 20.1003 is the period of time used to demon-strate compliance. Thus, the time period for reporting Answer:
under 10 CFR 20.2206 must be the year as defined in 10 CFR 20.1003 that is used to demonstrate compliance.
(a) This provision is intended to apply to situations in which
(
Reference:
the ambient airborne concentrations are likely "... to reach instantaneous values greater than 10 times the pertinent values in table 1, column 3 of appendix B..." The state-ment is not interxled to exchxle the use of a half-mask face piece at a nuclear power plant or other licensee facility.
,~
i 1
I Questions and Answers i
}
(b) Yes. See NUREG-0041, Section 8.5.2.3, for four one. Values of this factor greater than one were selected as l
. acceptable testing methods for field testing of respirator values indicating 'a significard contribution from external ~
l operation (isoamyl acetate, irritant smoke, negative pressure exposure." (
References:
Part 20 Appendix B Footnote 2)
I test, and positive pressure test). (
Reference:
Appendix A).
4 Question 23: Will all of the libraries of reference data and j
the procedures for gamnwray spectrometry software or j
10 CFR Part 20 Appendix B appendices that contain 10 CFR Part 20 MPCs have to be l
changed?
Question 13: Why was a 2-hour half-life chosen as a time Answer: Yes. ' (
Reference:
Part 20 Appendix B) of reference for noble gases or short-lived radionuclides, as l
' used in 10 CFR Part 20, Appendix B and its footnotes?
j Question 71: "Ihe ' Class" column of 10 CFR 20 Appendix Answer: As indicated in Footnote 2 to Appendix B, the B covers inhalation, but does not refer to ingestion. When -
radionuclides that have half-lives of less than 2 hours2.314815e-5 days <br />5.555556e-4 hours <br />3.306878e-6 weeks <br />7.61e-7 months <br /> "might there are two ALis for ingestion, how do tbse relate to the j
include a significant contribution from external exposure."
" Class," since they really were based upon the f value for j
'Significant contribution from external exposure" in this gut absorption? (Note: b f value is the fractional uptake footnote means that the contribution to the dose equivalent from the smallintestine to blood).
from external irradiation exceeds that from inhalation. Two I
hours is the half-life value below which the contribution to Answer: b ALis for ingestion do not relate to the j.
the dose equivalent from external exposure exceeds that
' Class," which refers to the retention time in the pulmonary from inhalation for virtually all radionuclides, region of the lung. bre are two situations for which there j
are two ALis for ingestion. One is when the ALI is deter-
'l
}
A more detailed explanation is provided below. For a given mined by the non-stochastic dose to an organ. In this case, 2
radionuclide, the ratio of the dose from external irradiation the organ or tissue to which the limit applies is shown, and -
j.
to that from internal irradiation (from inhalation) depends on the ALI for the stochastic limit is shown in parentheses (for the half-life of the radionuclide, the characteristics of the example, see ingestion ALI for beryllium-10)..h other radiations emitted in the decay of the radionuclide, th case (and the case presumably in question) is when different f values were used to calculate the ingestion ALIs. For -
f physical and chemical properties of the' radioactive material t
j contaming the radionuclides, and the physiological response example, see the entry for cobalt-60, for which the ingestion of the body to intakes of this material. However, consider.
ALis are 500 (on the first line) and 200 (on the second line).
{
ing the effect of half-life alone, and in general, the value of These ingestion ALI values have no relationship to the this ratio increases as the half-life decreases, b Statement corresponding " Class" on the same line (W on the first line from the 1983 Meeting of the ICRP includes the following and Y on the second line). Rather, as explained in Faderal j
paragraph:
Mlanca Report No.11, these different ingestion ALis are i
based on two different f values: f = 0.05 for ALI = 500, i
'In ICRP Publication 30 the values of DAC for occupational and f = 0.3 for ALI = 200. As shown in Ful-al thst-exposure to short-lived nuclides (other than isotopes of a-Da-t Na- % Table 3, f = 0.05 for " oxides, by-g j
noble gases) are based on the dose equivalent to organs and droxides and trace inorganic," and f = 0.3 for ' organic tissues as the resuk ofinhalation. b Conunission wishes complexed and other inorganics." For inhalatian of cobalt-4
{
to draw attention to the fact that there is an additional 60, f, = 0.05 for both " oxides, hydroxides, halides and contribution to these dose equivalents from external irradi.
nitrates' (class Y), and "all others" (class W).
4 ation. In situations where short-lived materials are widely j
' distributed in the workplace, this additional contribution b following information on Federal Guidance Report No.
may be greater than that due to inhalation by a factor that 11 is provided for those not familiar with this document:
increases from about i to 100 as the half-life of the radio-b title of this report is " Limiting Values of Radionuclide nuclide decreases from 1 day to 10 min. Such contributions latake and Air Concentre' ion and Dose Conversion Factors i
shouki be assessed as part of the external irradiation.-
of inhalation, Submersion and Ingestion." b report is subtitled " Derived Guides for Control of Occupational-Actually, for radionuclides with half-lives of roughly 2 Exposure and Exposure-to-Dose, Conversion Factors for I
hours, the values of this factor fall within the range of about General Application, Based on 1987 Federal Radiation -
i 1 to 10. bs, for virtually all radionuclides with half-lives Protection Guidance." b report was published by the less than 2 hours2.314815e-5 days <br />5.555556e-4 hours <br />3.306878e-6 weeks <br />7.61e-7 months <br />, the value of this factor is greater than U.S. Environmental Protection Agency (EPA) as report 3
63 NUREO/CR-6204 '
Questions and Answers number EPA-520/1-88-020 on Sepember 1,1988. & ALI tables. Some very short-lived daughters oflong-lived radio-and DAC values in this report are used in Appendix B of nuclides are not included in either "old" or " revised" Part the revised Part 20. (Referencec: 10 CFR 20 Appendix B, 20 (e.g., the 2.55-min barium-137m daughter of 30-year hieral riste Repnrt No. I1).
h tables in Appendix B of "old" and " revised" Part 20 are Question 146: h term "not present," which is defined in consistent with respect to treatment of daughter radio-paragraph 5 of the Note (concerning mixtures of radio-nuclides in the dose modeling used to derive the ALis and nuclides) following Appendix B of the oki Part 20, is not DACs listed in the tables. When a listed radionuclide has a dermed in the corresporxling " Note" in the revised Part 20.
radionuclide daughter, the value in the table for that parent Does this definition from the old Part 20, which indicates radionuclide takes into account the dose frorn the daughter when a radionuclide may be considered as not present in a radionuclide produced in the body from the decay of the mixture, continue to apply in the revised Part 20?
parent following intake of the parent (unless n " submersion" value is listed for the parent). However, the value in the Answer: No. Nothing in the oki Part 20 (6520.120.601) table for a parent radionuclide does not take into account rpplies in the revised Part 20 (ll20.1001-20.2401). This any simultaneous intake of the daughter radionuclide. hs dermition of "not present" is not included in the revised Part the ALIs and DACs for daughter radionuclides need "to be 20; however,10 CFR 20.1204(g) stipulates the conditions considered separately" from their parent radionuclides "with under which licensees may disregard certain radionuclides regard to the posting ard other requirements of Part 20."
in a mixture when determining internal dose. See the ans-(
Reference:
4 wer to the related Question 121 for clarification of 10 CFR 20.1204(g). (
References:
Appendix B,10 CFR 20.1204)
Question 425: It appears that some of the oral ingestion ALIs in Appendix B of 10 CFR 20 are sometimes associated Question 396: b Appendix B tables of the revised Part with the wrong chemical forms; is this the case?
20 include ALIs and DACs for daughter radionuclides, in contrast to the Appendix B tables in the "ok!" Part 20, Answer: No, See the answer to Question 71 in section 10 which do not include these daughter radionuclides. For CFR Part 20, Appendix B which indicates that the " Class" example, ALis and DACs for rubidium-88 arxl cesium-138 column of 10 CFR Apperxlix B applies to inhalation only; it r.re listed. Are the listed ALis and DACs expected to be does not refer to ingestion. In other words, neither the D, considered separately with regard to posting and other W, and Y classes nor the chemical forms (compounds) in requirements in the revised Part 20?
the " Class" column refer to the ingestion ALis. (
Reference:
Answer: Yes. However, the statements preceding the question itself may reflect misunderstandings; these possible misunderstandings are addressed in the following discus-Question 426: Are the noble gas (" submersion") DACs sion.
based on a dose of 5 rem per year or 50 rem per year? Is the submersion dose calculated at a depth of 1000 mg/cm2
& Appendix B tables of both "ok!" and " revised" Part 20 or 7 mg/cm'?
r do inchule many " daughter radionoclides." h tables of
" revised" Part 20 include more radionuclides, and therefore Answer: hre is no one particular dose or one particular raore daughter radionuclides, than the tables of "okl* Part depth. b method for calculating submersion doses is
- 20. Although rubidium-88 and cesium-138 (daughters of explained in Fedeml Guidance Report No.11 on pages 10, krypton-88 and xenon-138, respectively) are not inchxled in 18,181, and 182. When air concentration is limited by "ok!" Part 20, they do need to be " considered separately submersion dose, the DAC for a particular radionuclide is with regard to posting and other requirements.. " of "ok!"
the maximum concentration of that radionuclide in air that, 1
Part 20; the relevant concentrations for rubidium-88 and for a 2,000-hour exposure, will result in a dose that is equal cesium-138 are those listed at the end of Appendix B for to or less than each of the applicable limits (5 rem effective "Any single radionuclide not listed above with decay mode dose equivdent,15-rem eye dose equivalent,50-rem dose other than alpha emission or spontaneous fission arxl with equivalent to other organs and tissues, shallow dose equiva-radioactive half-life less than two hours." & "okl* Part 20 lent of 50 rem to the skin). ht is, the DAC for a particu-does include the rubidium-87 daughter of krypton-87 and the lar radionuclide depends on which of the applicable dose cesium-135 daughter of renon-135, as well as many other limits is the most restrictive with respect to the concentra-i daughters whose parent radionuclides are listed in the tion of that particular radionuclide. b dosimetric axxlel NUREO/CR-6204 64
i Questions and Answers I
used to calculate the DACs considers shiekling of organs by provides an example of the proper use of this provision of overlying tissues and the degradation of the photon spectmm Part 20; Question 403 and answer in section 10 CFR through scatter and attenuation by air. The dose from beta 20.2106 which concerns the relevance of 10 CFR 2
particles is evaluated at a depth of 7 mg/cm for skin, and at 20.1202(b)(3) and 20.1204(g) to a cutoff levels for radio-a depth of 3 rnm for the lens of the eye. The worker is nuclides contributing to the CEDE; and Question 146 and casumed to be immersed in pure parent radionuclide, and no answer in section 10 CFR 20 Appendix B which indicates radiation from airborne progeny is considered. In most that the definition of the term "not present" in oki Part 20 cases, the concentration limit for submersion is based on does not apply to the revised Part 20. (
References:
10 external irradiation of the body; it does not take into account CFR 20 Appendix B,10 CFR 20.1202,10 CFR 20.1204).
either absorbed gas within the body or the inhalation of radioactive decay products. An exception to the proceding statement is Ar-37, for which direct exposure of the lungs 2.14 10 CFR 19 - NOTICES, by inhaled activity limits (stochastically) the concentration in air. The skin dose is limiting for Ar-39, Kr-85, and Xe.
INSTRUCTIONS, AND l
131m; the eye dose is limiting for Kr-83m. Note: There REPORTS TO WORKERS:
i are typographical errors in the discussion of submersion INSPECTION AND doses on page 10 of Fulm1 rW-De Nn. I t in the fifth sentence of the paragraph beginning "Some air-INVESTIGATIONS borne radionuclides...", the word " effective" should be added before the words " dose equivalent rate". In equation (ab), the subscript "E" shouid be the subscript "T
- 10 CFR 19.12 - Instructions to Workers 4
(
Reference:
Question 95: 10 CFR 19.12 requires training (instmetion)
Question 453: Note 2 of Appendix B provides criteria for of workers who enter a restricted area. Do individuals re-i determining the appropriate derived air concentation ceiving occupational doses in controlled areas need training?
(DAC) for a mixture of radionuclides where "the identity of each radionuclide in the mixture is not known, but it is Answer: Yes. They need training, but it is not specifically known that certain radionuclides are not present in the required by 10 CFR 19.12 since this section addresses only 4
mixture." In $20.1204, Determination of tnternal Exposure, individuals working in or frequenting any portion of a re-provisions are made to disregard the concentration of any stricted area. The obvious intent of the training (instruction) radionuclide that is less than 10% ofits DAC so long as the requirement of Part 19 is that individuals who are permitted j
sum of the percentages for all of the radionuclides disre-to receive occupational doses within the occupational limits garded in the mixture does not exceed 30%. Can this ap-will receive appropriate training. Although not explicitly proach of disregarding certain radionuclides be applied t stated in 10 CFR Parts 19 or 20, individuals who are to re-the determination of the appropriate DAC, as outlined in ceive an occupational dose in any area shouki receive ap-note 2 to Appendix B; in other words, can radionuclides that propriate training. (
Reference:
are not present in the mixture in concentrations greater than or equal to 10% ofits DAC be disregarded so long as the sum of the percentages for all of the radionuclides disre-Question 411: Under 10 CFR 19.12, what is the minimum garded in the mixture does not exceed 30%? This question training that licensees must provide to visitors who will is intended to affirm a practical approach to truncating the enter a restricted area (where the occupational dose limits analysis of radionuclide mixtures by disregarding radio-
,pp y)7 y
nuclides that are not present nr may only be present in insignificant concentrations relative to other radionuclides in Answer: 10 CFR 19.12, " Instructions to Workers,' re-a mixture.
quires that training (instruction) be provided to "all indivi-4 duals working in or frequenting any portion of a restricted Answer: No. This wouki be a misapplication of the pro-area." Frequenting an area means to pay frequent visits to visions of 10 CFR 20.1204(g), which applies to the deter-the area or to be in the area often. Therefore,10 CFR mination of internal exposure under specified circumstances, 19.12 does not apply to infrequent visitors who will not be not to the choice of the appropriate DAC for a mixture. See working in the restricted area. However,10 CFR 19.12 the following related questions and answers: Question #121 does apply to visitors or other individuals (a) who will be and answer in section 10 CFR 20.1204 which clarifies the working in the restricted area nr (b) who are expected to be 4
meaning of ' total activity" in 10 CFR 20.1204(g) and in the area often. (Thus,10 CFR 19.12 does require in-65 NUREO/CR-6204 i
Questions and Answers struction of anyone working in a restricted area, even if that other appropriate record, on file to document compliance.
work is infrequent.) Licensees have the responsibility to
(
Reference:
10 CFR 19.13) determine which individuals are frequent visitors and which c_re not. Although not required by 10 CFR 19.12, in accor-dance with good radiation protection practice, infrequent Question 377: Are licensees required by 10 CFR 19.13 to visitor (s) shouki be provided with a tramed escod who will report to individuals the results of monitoring performed but provide the visitor (s) with the information needed for pro-not' required under 10 CFR 20.1502? 10 CFR 19.13 states tection from any potential radiological hazards. (
Reference:
that! radiation exposure data shall be reported to the indivi-10 CFR 19.12) dual, and that "the information reported shall include data and reSults obtained ruirmant tn ('nmmietinn remilatinna.
nrdern nr ficanca ennrlitinnn. as shown in records maintainad Question 422: This question refers to Question 95 under 10 by the licensee rurmant en ('nmmluinn ramlatiana-From CFR Part 19 and Question 81 under 10 CFR 20.1502, this, it appears that the results of monitoring performed but Clearly there is a significant population of occupationally not required by NRC regulations is not required to be exposed persons in unrestricted areas of whom the licensee reported to individuals.
has no knowledge. Even among their own employees, the licensed operation may be a small segment of the whole Answer: No. The results of monitoring performed but not organization where license management treats the rest of the required by NRC regulations are not required to be reported organization as general public. So presumably, the general to individuals. (
References:
10 CFR 19.13,10 CFR principle of educating occupationally exposed persons has a 20.1502).
dose threshold, e.g., something like the public dose limit; is this correct?
Question 378: If a worker formerly nwnitored at the Answer: No. There is no such thresboki. It is incorrectly licensee's facility as a " declared pregnant woman," requests cssumed that any dose received by an individual while that her exposure records be forwarded to her current em-working is an occupational dose. ISee the discussion of this ployer, shouki related embryo / fetus dose records also be point in the answer to Question 26 (a)
- Occupational Dose forwarded if not specifically requested?
vs. Public Dose."] A licensee may have an organization in 7
which most of the workers are members of the public; these Answer: No. Regulato y Guide 8.7, Res.1, includes the workers do not need and are not required to receive the kind following statement in Section 3.2. " Licensees should be 1
of training outlined in 10 CFR 19.12. Workers who do sensitive to the issue of personal privacy with regard to receive an occupational dose (and therefore are not mem-embryo / fetus dose. If requested by a monitored woman, a bers of the public) shouki receive such training, whether letter report may be provided to document prior embryo /
required by 10 CFR 19.12 or not. For workers who must fetus dose." Otherwise, the embryo / fetus dose records receive such training, there is no " dose thresbok!"; how-shouki not be provided. (
Reference:
10 CFR 19.13,10 cver, the extent of the instruction of these workers should be CFR 20.1208).
commensurate with the potential radiological health protec-tion problems for these workers. (
Reference:
Question 409: In complying with the 10 CFR 19.13(c) report request, is it acceptable to report on a Form-4 dose received in the current year as one monitoring period and 10 CFR 19.13 - Notification and Reports to dose received in prior years as another monitoring period Individuals even if the prior years monitoring period exceeds one year?
Answer: Yes. However, it shouki be recognized that this Question 37: Is it necessary to document that employees rep rt shouki include records of doses received during P anned special exposures, accidents, and emergency con-l have been advised of their annual doses? Is it sufficient to ditions as shown in the records maintained m accordance let employees see the results of the monitoring? Does j
posting doses on a bulletin board in a common area, each wah 10 CFR 20.2!06. If there have been no planned month, fulfill this requirement?
special exposures or overexposures, a statement to that effect shouki be provided. (
Reference:
Answer: See 10 CFR 19.13(a), which has not been revised. The licensee must provide a writt-n rannre to each worker. The licensee may keep a copy of the report, or NUREG/CR-6204 66
Questions and Answers Question 421: This question refers to the answer to preceding year, is an additional, duplicative report still Question 37 in ' Conforming Changes: 10 CFR Part 19
- I required to be issued in accordance with gl9.13(b)?
sincerely hope that the NRC will encourage licensees to simply file a memo to the effect that these reports were In providing annual dose reports to workers in accor-e.
done. Otherwise, the volume of paper will be ridiculous.
dance with gl9.13(b), are reports of dose to the worker's embryo / fetus, maintained in accordance with 10 CFR Answer: A filed memorandum to the effect that each 20.2106, also required to be provided to the worker with the worker has been advised of his or her dose in acconlance report?
with 10 CFR 19.13(a) is an acceptable way of documenting compliance with that requirement. Another acceptable way f.
In providing dose reports to a worker in accordance of documenting compliance is to file copies of the reports with $19.13(e), at the request of the worker at the time of provided to employees (as irulicated in the answer to termmation of employment, are reports of dose to the Question 37). (
Reference:
worker's embryo / fetus, maintained in accordance with 10 CFR 20.2106, also required to be provided to the worker with the report?
Question 454: What is the specific scope of the reports required to be provided to workers in accordance with the Answer:
various provisions of 10 CFR Part 19.137 The provisions in question are as follows:
(a) Yes; the monitoring period covered by 10 CFR 19.13(b) is limited to the previous year. See related Ques-c.
Part 19, il9.13(b) requires that licensees provide tions 392-395, inclusive, concerning reports required by 10 reports to workers annually of dose as shown in records CFR 20.2206 and Questions 37, 377, arxl 378 concerning maintained by the licensee. Is the monitoring period cover-the requirements of 10 CFR 19.13(b).
ed by this section limited to the preceding year only? This would appear to be the case basrd on the comments made (b) Yes, the scope of the information on NRC Fonn 5 (or by the NRC staff in the statements of consideration (56 FR equim!ent) fulfills the information requirements of 10 CFR l
23386, column 2) which states, "a copy of the annual report 19.13 (a) [and 10 CFR 19.13(b). However, in accordance to NRC couki also be given to the individual worker to with 10 CFR 19.13(a), the transmittal of the information by satisfy the revised reporting requirement in 619.13..." The the licensee to the individual must contain the following annual report referred to is the report submitted in accor-statement (which is not on Form 5): This report is fumish-dance with Part 20, $20.2206, which is limited to the ed to you under the provisions of the Nuclear Regulatory monitoring period of the preceding year.
Commission regulation 10 CFP. Part 19. You shouki pre-serve this report for further reference.
b.
If the licensee provides workers with an NRC Form 5 (or equivalent), does the scope of this information fulfill the (c) 10 CFR 19.13(b) applies to all workers who were ie-requirements of Part 19, 519.13(a) to provide certain in-quired to be monitored during the preceding year, not just formation to workers? The purpose in asking this question those who continue to be monitored at the end of tlw year.
is to confirm that, although $19.13(a) was not revised as a conforming amendment to the revised Part 20, the corn-(d) No, an additional duplicative report need not be issued, ments made by the NRC (as described in item "a", above) provided that it was made clear to the worker that the report also apply, i.e., "a copy of the annual report to NRC could he or she was given at time of termination of employment rJso be given to the individual worker to satisfy the revised was a 'complde and final report" from the licensee for that reporting requirement in $19.13." If the NRC Form 5 (or worker for that year, equivalent) is not sufficient to comply with 619.13 (a), what additional information is required to be provided to the (e) No, not unless requested by the worker. See the worker?
answer to Question 378 in the section headed 10 CFR 19.13).
c.
Does this provision [i.e., f19.13(b)) apply to all work-crs who were monitored during the preceding year by the (f) Yes, if the worker has requested this information.
licensee, or only to workers who continue to be monitored
(
References:
10 CFR 19.13,10 CFR 20.2106).
by the licensee at the end of the year?
d.
If the workers were given a complete and final dose report at the time of termmation of employment during the 67 NUREO/CR-6204
Questions and Answers 2.15 10 CFR 50 - DOMESTIC wmply with the revised EPA PAG manual. (
Reference:
- '""^"^ """*D LICENSING OF PRODUCTION AND UTILIZATION Question 17: Will QA Category I requirements discussed p
gg in Regulatory Guide 1.26 have to be changed due to offsite dose requirements of 0.5 rem being changed to 0.1 rem in the revised Part 20?
10 CFR Part 50 Answer: b revised Part 20 does not change the QA Category I requirements. W 0.5 rem bench-mark is for Question 14: Are Design Basis Accident criteria (doses) design considerations; therefore, it will likely remain the changed by the revised Part 207 same. (
Reference:
Answer: No, only those conforming changes included in the Federal Register notice will be effective when the Question 20: Pertaining to Question 19, will 10 CFR 50 revised Part 20 is implemented. Ok! dose criteria used for Appeixlix I and Technical Specifications have to be modified Design Basis Accident will retain their original definitions to reflect a total effective dose equivalent (TEDE)?
unless they are specifically changed in a licensing action.
(
References:
10 CFR 50 Appendix A,10 CFR Part 100)
Answer: Appendix I, and the corresponding Technical Specifications, will not have to be modified as a result of the revised Part 20; however, the staffis considering whether Question 15: Will the reporting criteria of 10 CFR 50.72 Appendix I design objectives need to be recast as effective ml 50.73 have to be changed?
dose equivalent. (
References:
10 CFR 50 Appendix I, Reactor Technical Specifications)
Answer: h necessary changes have been already been made. See " Conforming Amendments," in the May 21, 1991 Federal Register notice on 10 CFR Part 20 et al. (56 Question 456: FS ARs for Part 50 power reactor licensees FR 23473). Licensee's procedures may have to be changed typically contain multiple references to current 10 CFR Part accontingly. (
References:
10 CFR 50.72,10 CFR 50.73) 20 concepts and terminology, primarily with regard to describing aspects of the radiation protection program.
Updating of these references wouki be editorial in nature, Question 16: Will the Emergency Action Levels (EAL) as without any health and safety benefit, but would neverthe-part of the Emergeay Plans have to be changed if baaed on less divert resources from potentially more significant
{
the old Part 20 methodology?
matters. Additionally, these changes wouki be submitted to I
the NRC as part of the FSAR Update process, involving Answer: 'Ihe EALs e not related to Part 20. Appendix NRC staff review, an additional expenditure of resources.
1 of NUREG-0654 contains the descriptions for the four May licensees forego such editorial changes to the FSAR, emergency classific lions; unusual event, alert, site area that have no health and safety significance? Note that emergency, and general emergency. Example initiating programmatic changes required to implement the revised corxlitions are also found in this appendix. No reference is Part 20 will still be accomplished through new or revised made to the use or applicability of Part 20 in either the procedures and training. Additional clarification of the regulations pertinent to emergency classifications nor in the NRC staff's expectations would be useful for Part 50 licen-guidance, in the class descriptions, reference is made to sees to more appropriately efficiently allocate resources to EPA protective action guide (PAG) exposure levels.
their revised Part 20 implementation efforts.
EPA has revised its PAG manual. EPA recommends the Answer: Yes; power reactor licensees do not need to use of committed effective dose equivalent to replace the provide updates that are purely editorial and have no heahh whole body dose for the plume PAG. The numerical values and safety significance. 10 CFR 50.71(e) requires each for the plume PAG remain the same. It is therefore expect-power reactor licensee to update the licensee's FS AR and to ed that the licensees will have to revise, if necessary, their submit the changes to the NRC. The only FSAR changes emergency dose calculation methodology to classify an (resulting from the revised Part 20) that need to be nuule emergency and recommend protective actions in onler to are: (a) significant changes in commitments identified in the FSAR regarding the radiation protection program; (b)
l Questions and Answers i
\\
changes in the facility described in the FSAR; and (c) changed is currently underway. (
Reference:
Regulatory changes that involve an unreviewed safety question or Guides) technical specification change pursuant to 10 CFR 50.59.
'Ihe NRC staff does not expect that implementation of Regulatory Guide 8.25 revised Part 20 will result in significant changes to power reactor facilities or in unreviewed safety questions at these facilities. Changes in reactor technical specifications are Question 405: Regulatory Guide 8.25 (Section C.I.7) not required by the revised Part 20; however, the staff does states that "to determine whether the concentration exceeds expect that some power reactor licensees will voluntarily the DAC o er the short term, the sample collection time request changes in technical specifications as a result of should not exceed one hour. Shorter sample collection r; vised Part 20, such as changes in ESF-related process times may be used if desired, but they are not required."
monitor alarm set points (which may have been based on the a.) Does this section mean to imply that the duration of a old Part 20). (
Reference:
work zone air sample shoukt not exceed one hour if it may be used to determine whether an area needs to be posted or otherwise controlled? b.) Under what circumstances does 2.16 REGULATORY GUIDES this mm har rule apply?
Answer: (a) No. The one-hour criterion applies only for Regulatory Guides - General sampling used "to determine whether the concentration exceeds the DAC nver the shM term" (emphasis added).
Qintion 12: How will the revised Regulatory Guides be (b) The one-hour criterion is guidance; it is not a " rule "
used in determining acceptability of a licensee's implemen-8ee answer to (a) regarding the circumstances of applica-t: tion of the revised Part 207 tion. (
References:
Regulatory Guide 8.25,10 CFR 20.1902).
Answer: In determining the acceptability of a licensee's implementation of the revised Part 20, new regulatory guides will be used in the same way existing guides have Regulatory Guide 8.36 been used in determinmg acceptability of a licensee's implo-mentation of the oki Part 20 in cases in which there is no licensee commitment to the guide in a license application.
Question 406: Regulatory Guide 8.36, " Radiation Dose to As stated in virtually every guide, Regulatory Guides are the Embryo / Fetus," (Section C.I.3) states that "the deter-not regulations and compliance with them is not required, mination of external dose shouki include all occupational unless the guide has been made a specific condition of a exposures of the declared pregnant worker since the estimat-license (a common practice for materials licensees who are ed date of conception."(a) If declared pregnant worker has licensed by NRC's Office of Nuclear Material Safety arxl received occupational dose during this pregnancy while 5:_feguards). Also, as indicated in every guide, alternatives working for a previous licensee, is it intended that the dose to methods described in the guide may be acceptable, from the previous licensee be obtained and inchuled in
(
Reference:
Regulatory Guides) esti:nating and limiting the embryo / fetus dose for the ges-tation period? (b) If this is the intention, what shoukt be done if applicable dose records are not svailable because the Regulatory Guide 1.109 worker had not declared pregnancy or was not monitored (i.e., was not likely to exceed 10% of a limit) at her pre-vious workplace? In the absence of other data, shouki the Question 21: Is it time to update Regulatory Guide 1.109 previous dose be assumed to be zero?
and its corresponding codes due to the updated dose conver-sion factors in the revised Part 207 Answer: (a) Yes.
Answer: Perhaps, but such an update coukl only be a (b) The licensee shouki make an effort to make a reasonal%
partial update at this time. 'Ihe full updating couki only estimate of the dose using other information that the worbr cecur if and when Appealix Iis recast as an effective dose and her previous employer have concerning her exposure, equivalent. The evahiation of whether Appendix I shouki be Even when the worker was not monitored, a well-trained worker and her employer should be able to provide sone information concerning her exposure.
s Questions and Answers (c) No. Neithir shoukt it be assumed to be the maxmmm mrem /yr limit). Will changes in the Technical Specifica-possible dose. See answer to question (b). (
Reference:
tions and ODCMs be required as a msuit of the explicit Regulatory Guide 8.36).
100-mrem /yr limit in the revised Part 207 -
Regulatory Gini L.7, Rev. l' Answer: W insta=*ananus release rate limits for airborne releases will not be changed because they are imposed on li-
- as a control to ensure that hcensees meet Appendix Question 451: May the codes "ND" (not detectable), "NR-I requir===*. However, the instantananus release rata (not required), and "NC' (not W ") be used mor, for liquid effluents, to the extent that they directly reference Appendix B concentration values, will need to be changed.
generally in the radiation dose data blocks on the NRC Forms 4 and 5 than is imphed by the instmetions on the The cormsponding bases and certain alarm set-points will forms? h purpose in asking this question is to clarify the have to be changed by bcense amendment. (Reference-guidance for filling out the fonns provided in the regulatory Reactor Technical Specifications) position and in the instructions on the reverse side of the I
NRC Forms 4 and 5. % Form 5 instructions appear to limit the use of the 'NR" and *NC' codes to the committed -
Question 19: Current computer codes, such as LADTAP effective dose equivalent (CEDE) and the comnutted dose and GASPAR, calculate individual organ doses for compari-equivalent (CDE), 'ND* is not referenced in the Form 5 son against individual organ dose limits in 10 CFR 50 A Pendix I and/or Technical Specifications. Will the codes i
P instructions, and the NRC Form 4 instructions do not appear to refer to any of these codes.lWe believe that the have to be modified to convert whole body and organ doses references to the codes in the guidance and instructions on to efhetive dose equivalents?
the forms are as examples for emphasis, and that the intent of the guidance is that "NR' and 'ND" are appropnate for
' Answer: Appendix I is not changed by the revised Part 20.
use, as applicable, in any of the dose blocks, and are not.
brefore, until Appendix I is changed, licensees must spe:ifically limited for use by the manner in which referene, continue to show compliance with technical specifications ed er described in the guidance However, we do note that based on Appendix ! and exprenal in terms of organ and "NC' may only be applicable to the CDE (e.g., if the whole body doses. (Reference Reactor Technical CEDE were less than I rem).
Specifications).
Answer: Yes. As indicated in the second paragraph of regulatory position 1.1 of the guide, 'NR" shouki be enter.
Question 52: Since the techr.ical specification 'exemp-i ed in the blocks on Forms 4 and 5 to indicate the areas for tions" for nuclear power reactors already apply to locking of which monitoring was not required and "ND'should be high radiation areas, does this ' exemption
- continue to entered on these forms to indicate "where monitoring was apply pursuant to 10 CFR 20.1008(d) if a 45-cm (18-inch) provided but not measurable [6etectable)". As indicated in survey distance is specified (in technical specifications) regulatory position 2.2 of the guide, the use of "NC' is ap-versus the rule's 30-cm distance (10 CFR 20.1601(a))?
l propriate only for items 16 and 18 on NRC Forms 4 and 5 for cases in which the CEDE does not exceed I rem and Answert The provisions of power reactor technical 1
there are no overexposures in any done category within the 8Pecifications for control of high radiation areas are not monitoring year. (
References:
Regulatory Guide 8.7, Rev.
- exemptions" from the regulations. by are akernative 1; 10 CFR 20.2104,10 CFR 20.2106).
inethods of control provided in accordance with the provi-sions of 10 CFR 20.203(c)(5). Under the revised Part 20 these technical specifications will continue to apply to the
"'"' I hi h '"dii " *"" (but not very high radiation 8
2.17 TECHNICAL areas) until they are changed. These technical specifications SPECIFICATIONS rekt to a high radiation area a defined in Part 20. When revised Part 20 is implemented, the revised definition of a,
high radiation area, using the 30-cm distance, will apply.
Reactor Technical Specifications m to determine the bauxlanes of the high radiation area, the 30-cm (12-in.) distance will be used. However, within the boundaries of that aren the less-restrictive 45-cm (18-in.)
Question 18: For power reactors, the Technical Specifica, distance specified in the technical specifications will be used tion instantaneous release rate limits are based on oki Part to determine whether the radiation exposure is less than, 20 doses and concentrations (relative to an implied 500 equal to, or greater than 1,000 mR/h, the exposure rate used NUREG/CR-6204 70
)
4 4
4, 4
i
)
Questions and Answers i
i in the technical specifications to define the degree of control i
required. Changes in the technical specifications to be pro-Question 397: After implementation of the revised 10 CFR posed by the NRC staff will include a change from 45 cm to Pan 20, should nuclear power plant licensees report total 30 cm for the specified distance. (
References:
20.1601, 10 effective dose equivalent (TEDE) or deep dose equivalent j
CFR 20.1602, Reactor Technical Specifications)
(DDE) as the 'whole body dose
- for annual reports submit-ted in accordance with reactor technical specifications and Regulatory Guide 1.167 j
Question 61: Will the annual reports that are required by j
power reactor technical specifications (reports that tabulate Answer: Deep dose equivalent. (
Reference:
Reactor occupational exposures gneter than 100 mrem /yr according Technical Specifications, Regulatory Guide 1.16).
j to work and job functions) still be required after the revised j.
Part 20 is implemented.
3 Question 433: Question 397 concerns a reporting require--
l Answer: Yes. bre are no plans to change this require-ment in " reactor technical specifications." Does this ques-ment of the Technical Specifications. However, the reports tion, and the answer provided, apply to non-power reactors?
i on occupational exposures required by the ok! Part 20 in 10
]
CFR 20.407 (statistical summary reports) and 10 CFR Answer: No. Question 397 and its answer refer to report-
]
20.403 (termmation reports),' will no longer be required.
ing requirements contamed in technical specifications for l
These statistical summary and termmation reports are being power reactors, but not in technical specifications for non-i replaced by the revised " reports of individual monitoring" power reactors. Question 397 also refers to Regulatory
}
required by 10 CFR 20.2206. (
Reference:
Reactor Guide 1.16, " Reporting of Operating Information - -
Technical Specifications,10 CFR 20.2206)
Appendix A Technical Specifications," which applies only j
to nuclear power plants.- (
Reference:
Reactor Technical Specifications).
Question 79: Many existing reactor Technical Specifica-tions require commercial power plant licensees to provide statistical personnel dose summary to NRC annually. b Question 455: Part 50 license standard technical speci-
]
oki Part 20 contamed provisions for such reports, but no fications define " Dose Equivalent I 131" as "...that concen.
corresponding requirement carried over to the revised rule.
tration of I.131 (microcurie / gram) which alone would j
}
Why?
produce the same thyroid dose as the quantity and isotopic mixture of I 131,1 132, I-133, I-134, and 1 135 actually i
Answer: 'Ibe statement above confuses Technical present..." and the thyroid dose conversion factors used for j
Specification requirements with Part 20 Requirements.
this calculation shall be those listed in NRC Regulatory 3
Guide 1.109.* (a) After implementation of the revised 10 -
}
Under the oki Part 20, power reactor licensees (and other CFR Part 20, should licensees continue to use the Regula.
l licensees) wm required, by Part 20, to submit both annual tory Guide 1.109 thyroid dose conversion factors or shoukt
' statistical summary" reports (in accordance with 10 CFR they use the thyroid dose conversion factors in EPA Federal
{
20.407) and 'termmation" reports (in accordance with 10 Guidance Report No.11? (b) Will this be addressed in j
CFR 20.408). In addition to these two Part 20 reporting NRC's forthcoming generic letter on changes to technical requirements, power reactor licensees are required by their specifications related to the revised Part 207 j
Technical Specifications to submit arumal reports that in-4 clude a tabulation of workers receiving exposures greater Answer:(a) Licensees must continue to use the thyroid dose j
than 100 mrom/y and their associated collective dose ac-conversion factors (DCFs) that are referenced in their i
cording to work and job functions.
technical specifications (TS). A TS amendment would be
{
needed to allow the use of other technically acceptable Under the revised Part 20, the statistical summary and ter-values. It shouki be noted that in the absence of such regu-mination reports of the ok! Part 20 are eliminated and latory requirements, the NRC has allowed licensees to use i
replaced by a new annual report on the results ofindividual scurces ofintake-to-dose conversion factors other than -
[
monitoring of occupational exposure (10 CFR 20.2206).
'lhe revised Part 20 has no e&ct on the annual report re-quired by Technical Specifications. bre are no plans to (b) b use of Federal Guidance Report No.11 thyroid change this reporting requirement in the Technical Specifi-DCFs is not planned to be included in the generic letter on J
cations. (
References:
10 CFR 20.2206, Reactor Technical changes to power reactor technical specifications to incor-Specifications) porate the revised Part 20 but will be addressed in a forth-4 71 NUREO/CR-6204 w.
,n
Questions and Answers coming health physics position document (which will be and uranium 23P (U-238) in the oxide (insoluble) fonn, the mado publicly available). (
Reference:
Reactor Technical DACs are lower than the MPCs by factors of 30 and 5, Specifications).
respectively. Similarly, alarm setpoints for both airborne -
and waterborne releases for most materials licensees woukt i
have to be modified.' It should also be noted that for air-Power Reactor Technical S w& =" and Materials borne releases, the allowable concentrations for insoluble i
Licenses
'Ih-232 and U-238 have been reduced by factors of about.
170 and 80, respectively. For wate: borne releases, the allowable release concentrations for sohible Th-232 and Question 22: Alarm setpoints for many radiation monitors U-238 have been reduced by factors of about 70 and 130, are based on 10 CFR 20 Appendix B concentrations. Will respectively. For these reasons, it is anticipated that mim.
these new changes require numerous ODCM changes, set-erous procedural changes will have to be made for licensees point change requests, and procedure changes?
handling significant quantities of source and special nuclear material.
Answer: Separate answers are provided for reactor and materials licensees because these answers are somewhat diffent.
2.18 OTHER QUESTIONS Reactnr beansana-Alarm setpoints for airborne effluent monitors are not likely to change. These monitors are Question 87: Will the numbering sequence of the revised typically set up to detect an effluent concentration which regulation be changed once the "ok!" Part 20 expires?
wouki yiekt a whole body dose rate of 500 mrem /y or a thyroid dose rate of 1500 mrom/y (or fraction thereof) in an Answer: No. (
Reference:
~ None) unrestricted area on an instantaneous basis, as required by the Technical Specifications. Since other limiting conditions
. cre also contained in Technical Specifications to restrict Question 88: Will each NRC region boki orientation.
i annual doses to the public to much smaller values than those meetings for licensees on the revised regulation? When implied above, and since short-term operational flexibility is and where might these occur?
i necessan, it is unlikely that changes wouki need to be made in the alarm setpoints for misborne effluent monitors.
Answr
'I"b are no plans to hoki such orientation
-l meetings. However, the NRC is providing " orientation
- Alarm setpomis for waterborne effluent momtors are likely information by publishing Regulatory Guides and the new to require change, since they are based on 10 CFR 20 xa, oki Part 20 comparison in NUREG-1446, by making Appendix B concentrations, as required by the Tecluncal doctunented questions and answers on revised Part 20 Spectfications. Because Apperxlix B concentration values publicly available, by publishing information in the NMSS differ for many radionuclides between the revised and oki Newsletter, and by NRC staff participation in topical versions of Part 20, liquid effluent monitor alarm setpoints meetings concerning revised Part 20. (
Reference:
None) may have to be changed.
For reactors, the extent of staff involvement and licensee Question 89: Is it possible to obtain copies of revised NRC cfforts m adjusting and documenting alarm setpoints will
. inspection modules" for inspection for compliance with the depend on whether the licensee has implemented NRR revised regulation? How may these bo obtained?
1 Genene Letter 89-01. (
References:
10 CFR 20 Appendix B, Reactor Technical Specifications, NRR Genenc Letter h
All " inspection modules" (inspection procedures 89-01) in the NRC Inspection Manual) are available from the NRC Public Document Room,2120 L Street N.W., Lower Level, Maamriala Licensama-Area monitor alarm setpoints for most Washington, DC 20555; Telephone (202) 634-3273. In-materials beensees that are currently required to conduct spection procedures have not yet been revised to' reflect the continuous air monitoring will m all likelihood require revised Part 20, but will be revised during 1992.
change. 'Ihis is especially true for those facilities that
(
Reference:
None)
I handle significant quantities of source and special nuclear material since the new DACs for these types of material are lower or more restrictive than the oki MPCs. It shouki be Question 457: Some licensees have established adminis-noted that for commonly occurring thorium-232 (Th-232) trative dose control levels or guidelines, below regulatory
' NUREG/CR.6204 72 1--
- Questions and Answers dose limits, as a tool to support supervisory and nunage-ment involvement in dose muumintion. Procedures com-monly describe certain review actions to be taken at succes-sive dose levels, with a higher level of management involve-ment at higher dose levels. If an administrative dose control Irvel or guideline is exceeded without all of the described actions being taken, but no regulatory limit is exceeded, is th fact of exceeding the control level or guideline a viola-tion of NRC regulations?
Answer: Exceeding an administrative dose control level or guideline that is below the limits of 10 CFR Part 20 is not a violation of 10 CFR Part 20. This is genomily true with respect to other parts of the NRC regulations, akhough it is subject to exceptions; for example, for medical licensees,10 -
CFR 35.25(a)(2) specifies requirements for a " supervised individual" including following % written radiation safety and quality management procedures established by the licensee". Such procedures might include adnunistrative dose control levels or guidelines and failure to follow such procedures couki be a violation of 10 CFR 35.25(a)(2).
Furthermore, exceeding an administrative dose control level or guideline couki be a violation of procedural requirements in the plant technical specifications at a nuclear power plant or a violation of specific license conditions in a material '
license. (
Reference:
Other) l l
l l
73 NURBO/CR 6204 l
E APPENDIX A NUMERICAL LIST OF QUESTIONS Qwstim 10 Page 54 AND ANSWERS Q/A Set i PDR-9112190258 Regulatory Reference 10 CFR 20.2104, Determmation of Prior Occupational Dose -
Question 1 Page 3 Question iI Page 12 Q/A Set 1 PDR-9112190258 Q/A Set 1 PDR-9112190258 Regulatory Reference 10 CFR 20.1003, Definitions Regulatory
Reference:
10 CFR 20.1101, Radiation Protection Programs Question 2 Page 14 Q/A Set 1 PDR-9112190258 Question 12 Page 69 Regulatory
Reference:
10 CFR 20.1001, Purpose Q/A Set 2 -
PDR-9;05010117 RegulatonReference RegulatoryGuides Q/A Set 1 PDR-9112190258 Question 13 Page 63 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose
'Q/A Set 1 PDR-9112190258 Limitsfor Adults Regulatory Reference 10 CFR 20 Appendix B, Annual Limits on Intake (ALIs) and Derived Air Concentrations Question 4 Page 3 (DACs) of Radionuclides for Occupational Exposure; Q/A Set 1 PDR-9112190258 Efiluent Concentrations; Concentrations for Release to Regulatory
Reference:
10 CFR 20.1001, Purpose '
Sewage Question 5 Page 3 Question 14 Page 68 Q/A Set 1 PDR-9112190258 Q/A Set 1 PDR-9112190258 Regulatory
Reference:
10 CFR 20.1001, Purpose Regulatory Reference 10 CFR 50 Appendix A, General Design Criteria for Nuclear Power Plants Question 6 Page 15 4
Q/A Set 1 PDR 9112190258 Question 15 Page 68 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Q/A Set i PDR-9112190258 Limits for Adults Regulatory Reference 10 CFR 50.72, Maintenance of Records, Making ofReports Question 7 Page 12 Q/A Set 1 PDR-9112190258 Question 16 Page 68 Regulatory
Reference:
10 CFR 20.1101, Radiation Q/A Set 1 -
PDR-9112190258 Protection Programs Regulatory
Reference:
10 CFR 50.47,Pennits - Emergency Plans Question 8 Page 22 Q/A Set 1 PDR-9112190258 Question 17 Page 68 Regulatory
Reference:
10 CFR 20.1206, Planned Special Q/A Set i PDR-9112190258 Exposures Regulatory
Reference:
10 CFR 50 Appendix B, Quality Asurance Criteria for Nuclear Power Plants and Fuel Question 9 Page 19 Reprocessing Plants Q/A Set 1 PDR 9112190258 Regulatory
Reference:
10 CFR 20.1202, Compliance with Question 18 Page 70 Requirements for Summation of External and Internal Doses Q/A Set 1 PDR-9112190258 Regulatory
Reference:
TechnicalSpecifications 75 NUREG/CR-6204
Appendix A Question 19 Page 70 Question 29 Page 29 Q/A Set 1 PDR-9112190258 Q/A Set 1 PDR-9112190258 Regulatory
Reference:
Technical Specifications Regulatory
Reference:
10 CFR 20.1302, Compliance with Dose Limits for Individual Members of the Public Question 20 Page 68 Q/A Set 1 PDR-9112190258 Question 30 Page11 Regulatory
Reference:
10 CFR 50 Appendix I, Numerical Q/A Set 1 PDR-9112190258 Guides for Design Objectives and Limiting Conditions for Regulatory
Reference:
10 CFR 20.1008, Implementation Operation to Meet the Criterion "As Low as is Reasonably Achievable" for Radioactive Material in Light-Water-cooled Question 3i Page 15 Nuclear Power Reactor Efiluents Q/A Set 2 PDR-9205010117 i
Regulatory
Reference:
10 CFR 20.1201, Occupat onal Dose Question 21 Page 69 Limits for Adults Q/A Set 1 PDR-9112190258 Regulatory
Reference:
Regulatory Guides Question 33 Page 15 Q/A Set i PDR-9112190258 Question 22 Page 72 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Q/A Set 2 PDR-9205010117 Limits for Adults Regulatory
Reference:
Technical Specifications Question 34 Page 15 Question 23 Page 63 Q/A Set 1 PDR-9112190258 Q/A Set 1 PDR-9112190258 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Regulatory
Reference:
10 CFR 20 Appendix B, Annual Limits for Adults Limits on Intake (ALIs) and Derived Air Concentrations (DACs) of Radionuclides for Occupational Exposure; Question 35 Page 49 Ef!1uent Concentrations; Concentrations for Release to Q/A Set i PDR-9112190258 Sewage Regulatory
Reference:
10 CFR 20.1903, Exceptions to Posting Requirements Question 24 Page 22 Q/A Set 1 PDR 9112190258 Question 36 Page 50 Regs ory
Reference:
10 CFR 20.1206, Planned Special Q/A Set 1 PDR-9112190258 Exposures Regulatory
Reference:
10 CFR 20.1906, Procedures for Receiving and Opening Packages Question 25 Page 4 Q/A Set 1 PDR-9112190258 Question 37 Page 66 Regulatory
Reference:
10 CFR 20.1003, Definitions Q/A Set 1 PDR-9112190258 Regulatory
Reference:
10 CFR 19.13, Notifications and Question 26 Page 4 Reports toIndividuals l
Q/A Set 4 PDR-9209230012 l
Regulatory
Reference:
10 CFR 20.1003, Definitions Question 38 Page 19 Q/A Set 1 PDR-9112190258 i
Question 27 Page 47 Regulatory Referwee: 10 CFR 20.1202, Compliance with I
Q/A Set 2 PDR 9205010117 Requirements for Summation of External and Intemal Doses Regulatory
Reference:
10 CFR 20.1902, Posting Requirements Question 39 Page 54 Q/A set i PDR-9112190258 Question 28 Page 29 Regulatory
Reference:
10 CFR 20.2003, Disposal by Q/A Set 1 PDR-9112190258 Releaseinto Sanitary Sewerage Regulatory
Reference:
10 CFR 20.1302, Compliance with Dose Limits for Individual Members of the Public Question 40 Page 7 Q/A Set 1 PDR 9112190258 Regulatory
Reference:
10 CVR 20.1003, Defmitions NUREG/CR-6204 76
d Appendix A Question 4i Page 15 Question 51 Page 54 Q/A Set 1' PDR-9112190258 Q/A Set 1 PDR-9112190258 Regulatory r:ference: 10 CFR 20.1201, Occupational Dose Regulatory
Reference:
10 CFR 20.2104, Deternunation of -
Limits for Adults Prior OccupationalDose i
Question 42 Page 26 Question 52 Page 70 Q/A Set 1 PDR-9112190258 Q/A Set i PDR-9112190258 l
Regulatory
Reference:
10 CFR 20.1301, Dose Limits for RegulatoryReference TechnicalSpecifications--
IndividualMembers of the Public Question 53 Page 47 Question 43 Page 32 Q/A Set 2 PDR-9205010117 Q/A Set 1 PDR-9112190258 Regulatory Reference 10 CFR 20.1902, Posting Regulatory
Reference:
10 CFR 20.1502, Conditions Requirements l
Requiring Individual Monitoring of External and Internal 1
Occupational Dose Question 54 Page 33
. Q/A Set 1 PDR-9112190258 i
Quest on 44 Page 33 Regulatory Reference 10 CFR 20.1502, Conditions.,
Q/A Set 1 PDR-9112190258 Requiring Individual Monitoring of External and Internal Regulatory
Reference:
10 CFR 20.1502, Conditions Occupational Dose Requiring Individual Monitoring of Extemal and Intemal Occupational Dose Question 55 Page 54 Q/A Set 1 PDR-9112190F8 Question 45 Page 16 Regulatory Reference 10 CFR 20.2104, Determination of Q/A Set 1 PDR-9112190258 Prior OccupationalDose Regulatory
Reference:
10 CFR 20.1201, OccupationalDose j
Limits for Adults Question 56 Page 60 i
Q/A Set 1 PDR-9112190258 i
Question 46 Page 16 Regulatory Reference 10 CFR 20.2202, Notification of 1
Q/A Set l PDR-9112190258 Incidents Regulatory
Reference:
10 CFR 20.1201, Occupational Dose 4
Limits for Adults Question 57 Page 7 Q/A Set 1 PDR-9112190258 Question 47 Page 20 Regulatory
Reference:
10 CFR 20.1003, Defmitions Q/A Set 1 PDR-9112190258 i
Regulatory
Reference:
10 CFR 20.1204, Determination of Question 58 Page11 laternalExposure Q/A Set 1 PDR-9112190258 Regulatory
Reference:
10 CFR 20.1008, Implementation 1
Question 48 Page 26
'~
Q/A Set 1 PDR-9112190258 Question 59 Page 24 Regulatory
Reference:
10 CFR 20.1301, Case Limits for.
Q/A Set 1 PDR-9112190258 4
Individual Members of the Public Regulatory Reference 10 CFR 20.1208, Dose to an Embryo / Fetus Question 49 Page 40 Q/A Set 1 PDR 9112190258 Question 60 Page 44 Regulatory
Reference:
10 CFR 201602, Control Access to Q/A Set 1 PDR-9112190258
[
VeryHighRadiation Areas Regulatory
Reference:
10 CFR 20.1703, Use ofIndividual Respiratory Protection Equipment 3
Question 50 Page 20 Q/A Set i PDR-9112190258 Question 61 Page 71 Regulatory
Reference:
10 CFR 20.1203, Determination of Q/A Set 1 PDR-9112190258 j
External Dose From Airbome Radioactive Material Regulatory
Reference:
Technical Specifications 77 NUREO/CR-6204
Appendix A Question 62 Page 12 Question 74 Page 8 i
Q/A Set 1 PDR-911219025S Q/A Set 2 PDR-9205010117 Regulatory Refeence: 10 CFR 20.1101, Radiation Regulatory Reference 10 CFR 20.1003,Defmitions Protection Programs Quetion 75 Page 33 Question 63 Page 22 Q/A Set 2 PDR-9205010117 Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 CFR 20.1502, Conditions Regulatory
Reference:
10 CFR 20.1206, Planned Special Requiring Individual Monitoring of External and Internal Exposures Occupational Dose Question 64 Page 55 Question 76 Page 20 Q/A Set 5 PDR-9306110303 Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 CFR 20.2104, Determination of Regulatory
Reference:
10 CFR 20.1204, Determination of Prior Occupational Dose Intemal Exposure Question 65 Page11 Question 77 Page 16 Q/A Set 2 PDR-9205010117 Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 CFR 20.1008, Implementation Regulatory
Reference:
10 CFR 20.1201, OccupationalDose Limits for Adults Question 66 Page 7 Q/A Set 2 PDR-9205010117 Question 78 Page 44 Regulatory
Reference:
10 CFR 20.1003,Defmitions Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 t FR 20.1703, Use ofIndividual Question 67 Page 8 Respiratory Protection Equipment Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 CFR 20.1003, Defmitions Question 79 Page 71 Q/A Set 2 PDR-9205010117 Question 68 Page 29 Regulatory
Reference:
Technical Specifications Q/A Set 2 PDR-9205010ll7 Regulatoiy
Reference:
10 CFR 20.1302, Compliance with Question 80 Page 8 Dose Limits for Individual Members of the Public Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.1003, Defmitions Question 69 Page 30 Q/A Set 2 PDR-9205010117 Question 81 Page 34 Regulatory
Reference:
10 CFR 20.1302, Compliance w;th Q/A Set 2 PDR-9205010117 Dose Limits for Individual Members of the Public Regulatory
Reference:
10 CFR 20.1502, Conditions RequSg Individual Monitoring of Extemal and Intemal Question 71 Page 63 Occupational Dose Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 CFR 20 Appendix B, Annual Question 82 Page 34 Limits on Intake (ALIs) and Derived Air Concentrations Q/A Set 2 FDR-9205010117 (DACs) of Radionuclides for Occupational Exposure; Regulatory
Reference:
10 CFR 20.1502, Conditions Efiluent Concentrations; Concentrations for Release to Req siring Individual Monitoring of Extemal and Intemal Sewage Occupational Dose Question 72 Page 30 Question 83 Page 21 Q/A Set 2 PDR-9205010117 Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 CFR 20.1302, Compliance with Regulatory
Reference:
10 CFR 20.1204, Determination of Dose Limits for Individual Members of the Public IntemalExposure Question 73 Page11 Question 84 Page 24 Q/A Set 2 PDR-9205010117 Q/A Set 2 PDR-9205010117 Regulatory
Reference:
10 CFR 20.1004, Units of Radiation Regulatory
Reference:
10 CFR 20.1208, Dose to an Dose Embryo / Fetus NUREG/CR-6204 78
Appendix A Question 85 Page 47 Question 97 Page 16 Q/A Set 2 PDR-9205010117 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1902, Posting Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Requirements Limits for Adults Question 86 Page 19 Question 98 Page 34 Q/A Set 2 PDR-9205010117 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1202, Compliance with Regulatory
Reference:
10 CFR 20.1502, Conditions Requirements for Summation of External and Intemal Doses Requining Indisidual Monitoring ofExtemal and Internal Occupational Dose Question 87 Page 72 Q/A Set 2 PDR-9205010117 Question 99 Page 12 Regulatory
Reference:
None Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1101, Radiation Question 88 Page 72 Protection Programs Q/A Set 2 PDR-9205010117 Regulatory
Reference:
None Question 100 Page 16 Q/A Set 3 PDR-9207300261 Question 89 Page 72 Regulatory
Reference:
10 CFR 20.1201, Occupatic.,al Dose Q/A Set 2 PDR-9205010117 Limits for Adults Regulatory
Reference:
None Question 101 Page 19 Question 90 Page 42 Q/A Set 3 PDR-9207300261 Q/A Set 2 PDR-9205010117 Rep bory
Reference:
10 CFR 20.1202, Compliance with Regulatory
Reference:
10 CFR 20.1701, Use ofProcess or Requirements for Summation of Extemal and Internal Doses Other Engineering Controls Question 102 Page 30 Question 91 Page 44 Q/A Set 3 PDR-9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1203, Determination of Regulatory
Reference:
10 CFR 20.1703, Use ofIndividual Extemal Dose From Airbome Radioactive Material Respiratoiy Protection Equipment Question 103 Page 30 Question 92 Page 40 Q/A Set 3 PDR 9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1302, Compliance with Regulatory
Reference:
10 CFR 20.1602, Control Access to Dose Limits for Individual Members of the Public Very High Radiation Areas Question 104 Page 30 Question 93 Page 8 Q/A Set 3 PDR 9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1302, Compliance with Regulatory
Reference:
10 CFR 20.1003, Dermitions Dose Limits for Individual Members of the Public Question 94 Page 8 Question 105 Page 27 Q/A Set 3 PDR-9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1003, Definitions Regulatory
Reference:
10 CFR 20.1301, Dose Limits for IndividualMembers of the Public Question 95 Page 65 Q/A Set 3 PDR-9207300261 Question 106 Page 27 Regulatory
Reference:
10 CFR 19.12, Instructions to Q/A Set 3 PDR-9207300261 Workers Regulatory
Reference:
10 CFR 20.1301, Dose Limits for IndividualMembers of the Public Question 96 Page 8 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1003, Dermitions 79 NUREO/CR-6204
Appendix A Question 108 Pagc50 Question 118 Page 13 Q/A Set 2 PDR-9205010117 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
19 CFR 20.1906, Procedures for Regulatory
Reference:
10 CFR 20.1101, Radiation Receiving and Opemng Packages Protection Programs j
Question 109 Page 22 Question 119 Page 9 Q/A Set 2 PDR-9205010117 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.1206, Planned Special Regulatory
Reference:
10 CFR 20.1003, Definitions Exposures Question 120 Page 24 Question 110 Page 23 Q/A Set 3 PDR-9207300261 Q/A Set 2 PDR 9205010117 Regulatory
Reference:
10 CFR 20.1208, Dose to an Regulatory
Reference:
10 CFR 20.1206, Planned Special Embryo / Fetus Exposures Question 121 Page 21 Question 1I1 Page 27 Q/A Set 3 PDR-9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1204, Detennination of Regulatory
Reference:
10 CFR 20.1301, Dose Limits for Internal Exposure Individual Members of the Public Question 122 Page 60 Question 112 Page 57 Q/A Set 3 PDR-9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.2203, Reports of Regulatory
Reference:
10 CFR 20 2l05, Records of Planned Exposures, Radiation Levels, and Concentrations of Special Exposures Radioactive Material Exceeding the Limits Question 113 Page 55 Question 123 Page 16 Q/A Set 3 PDR-9207300261 Q/A Set 3 PDR-9207300261 Regulatoiy
Reference:
10 CFR 20.2104, Detennina !on of Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Prior Occupational Dose Limits for Adults Question 114 Page 34 Question 124 Page 45 Q/A Set 3 PDR-9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1502, Conditions Regulatory
Reference:
10 CFR 20.1703, Use ofIndividual Requiring Individual Monitoring of External and Intemal Respiratory Protection Equipment Occupational Dose Question 125 Page 27 Question i15 Page 42 Q/A Set 3 PDR-9207300261 Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1301, Dose Limits for Regulatory
Reference:
10 CFR 20.1701, Use ofProcess or IndividualMembers of the Public Other Engineering Controls Question 126 Page 35 Question i16 Page 54 Q/A Set 5 PDR-9306110303 j
Q/A Set 3 PDR-9207300261 Regulatory
Reference:
10 CFR 20.1502, Conditions i
Regulatory
Reference:
10 CFR 20.2101, Records - General Requiring Individual Monitoring of External and Intemal Provisions Occupational Dose Question 117 Page 54 Question 127 Page 50
)
Q/A Set 3 PDR-9207300261 Q/A Set 4 PDR-9209230012 1
Regulatory
Reference:
10 CFR 20.2101, Records - General Regulatory
Reference:
10 CFR 20.1904, Labeling l
Provisions Containers NUREO/CR-6204 80
Appendix A Question 128 Page 50 Question 139 Page 55 Q/A Set 4 PDR-9209230012 Q/A Set 4 PDR-9209230012 Regulatory
Reference:
10 CFR 20.1904, Labeling Regulatory
Reference:
10 CFR 20.2104, Detennination of Containers Prior Occupational Dose Question 129 Page 46 Question 141 Page 60 Q/A Set 4 PDR 9209230012 Q/A Set 4 PDR-9209230012 Regulatory
Reference:
10 CFR 20.1801, Security ofStored Regulatory
Reference:
10 CFR 20.2110, Form ofRecords Material Question 142 Page 55 Question 130 Page 41 Q/A Set 4 PDR-9209230012 Q/A Set 4 PDR-9209230012 Regulatoiy
Reference:
10 CFR 20.2104, Determination of Regulatory
Reference:
10 CFR 20.1603, Control Access to Prior Occupational Dose Very IIigh Radiation Areas - Inadiators Question 143 Page 55 Question 131 Page 45 Q/A Set 4 PDR-9209230012 Q/A Set 4 PDR-9209230012 Regulatory
Reference:
10 CFR 20.2104, Determination of Regulatory
Reference:
10 CFR 20.1703, Use ofIndividual Prior Occupational Dose Respiratory Protection Equipment Question 144 Page 9 Question 132 Page 45 Q/A Set 4 PDR-9209230012 Q/A Set 4 PDR 9209230012 Regulatory
Reference:
10 CFR 20.1003, Dermitions Regulatory
Reference:
10 CFR 20.1703, Use ofIndividual Respiratory Protection Equipment Question 145 Page 42 Q/A Set 4 PDR-9209230012 Question 133 Page 13 Regulatory
Reference:
10 CFR 20.1702, Use of Other Q/A Set 5 PDR-9306110303 Controls Regulatory
Reference:
10 CFR 20.1101, Radiation Protection Programs Question 146 Page 64 Q/A Set 4 PDR-9209230012 Question 134 Page 13 Regulatory
Reference:
10 CFR 20 Appendix B, Annual Q/A Set 4 PDR 9209230012 Limits on Intake (ALis) and Derived Air Concentrations Regulatory
Reference:
10 CFR 20.1101, Radiation (DACs) of Radionuclides for Occupational Exposure; Protection Programs EfIluent Concentrations; Concentrations for Release to Sewage Question 135 Page 23 Q/A Set 4 fDR-9209230012 Question 147 Page 32 Regulatory
Reference:
10 CFR 20.1206, Planned Special Q/A Set 4 PDR 9209230012 Exposures Regulatory
Reference:
10 CFR 20.1501, Sun'eys and Monitoring - General Question 136 Page 23 Q/A Set 4 PDR-9209230012 Question 148 Page 9 Regulatory
Reference:
10 CFR 20.1206, Planned Special Q/A Set 4 PDR-9209230012 Exposures Regulatory
Reference:
1o mt 20.1003, Dermitions Question 137 Page 23 Question 149 Page 9 Q/A Set 4 PDR-9209230012 Q/A Set 5 PDR-9306110303 RegulatoryIbference: 10 CFR 20.1206, Planned Special Regulatory
Reference:
10 CFR 20.1003, Defmitions Exposures Question 150 Page 10 Question 138 Page 24 Q/A Set 5 PDR-9306110303 Q/A Set 4 PDR-9209230012 Regulatory
Reference:
10 CFR 20.1003, Dermitions Regulatory
Reference:
10 CFR 20.1208, Dose to an Embryo / Fetus 81 NUREG/CR-6204
Appendix A Question 172 Page 17 Question 204 Page 28 Q/A Set 6 PDR-9310070005 Q/A set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1201, occupational Dose Regulatog
Reference:
10 CFR 20.1301, Dose Limits for Limits for Adults IndividualMembers of the Public Question 175 Page 17 Question 205 Page '28 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Regulatory
Reference:
10 CFR 20.1301, Dose Limits for Limits for Adults IndividualMembers of the Public Question 176 Page 17 Question 206 Page 28 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Regulatory
Reference:
10 CFR 20.1301, Dose Limits for Limits for Adults IndividualMembers of the Public Question 177 Page 17 Question 207 Page 31 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Regulatory
Reference:
10 CFR 20.1302, Compliance with Limits for Adults Dose Limits for Individual Members of the Public Question 179 Page 19 Question 208 Page 31 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005, Regulatory
Reference:
10 CFR 20.1202, Compliance with Regulatory
Reference:
10 CFR 20.1302, Compliance with Requirements for Summation of Extemal and Internal Doses Dose Limits for Individual Members of the Public Question 180 Page 20 Question 209 Page 32 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1202, Compliance with Regulatory
Reference:
10 CFR 20.1501, Surveys and Requirements for Summation of Extemal and Intemal Doses Monitoring-General Question 183 Page 21 Question 210 Page 32 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1204, Detennination of Regulatory
Reference:
10 CFR 20.1501, Surveys and Internal Exposure Monitoring - General Question 191 Page 24 Question 211 Page 35 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1206, Planned Special Regulatory
Reference:
10 CFR 20.1502, Conditions Exposures Requiring Individual Monitoring of Extemal and Internal Occupational Dose l
Question 192 Page 24 Q/A Set 6 PDR-9310070005 Question 212 Page 35 Regulatory
Reference:
10 CFR 20.1206, Planned Special Q/A Set 6 PDR-9310070005 Exposures Regulatory
Reference:
10 CFR 20.1502, Conditions Requiring Individual Monitoring oiExternal and Intemal Question 201 Page 27 Occupational Dose Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1301, Dose Limits for Question 213 Page 36 Individual Members of the Public Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1502, Conditions Question 203 Page 28 Requiring Individual Monitoring of External and Internal Q/A Set 6 PDR-9310070005 Occupational Dose Regulatory
Reference:
10 CFR 20.1301, Dose Limits for Individual Members of the Public NUREG/CR-6204 82
Appendix A Question 214 Page 36 Question 226 Page 50 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory Reference 10 CFR 20.1502, Conditions Regulatory
Reference:
10 CFR 20.1904, Labeling Requiring Individual Monitoring of External and Internal Containers Occupational Dose Question 227 Page 51 Question 215 Page 36 Q/A Set 6 PDR-9310070005 Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1906, Procedures for Regulatory
Reference:
10 CFR 20.1502, Conditions Receiving and Opening Packages Requiring Individual Monitoring of External arxi Internal Occupational Dose Question 228 Page 51 Q/A Set 6 PDR-9310070005 Question 216 Page 36 Regulatory
Reference:
10 CFR 201906, Procedures for Q/A Set 6 P9R-9310070005 Receiving and Opening Packages Regulatory
Reference:
10 CFR 20.1502, Conditions Requiring Individual Monitoring of Extemal and Internal Question 229 Page 51 Occupational Dose Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1906, Procedures for Question 217 Page1F Receiving and Opening Packages Q/A Set 6 PDR-931007000.1 Regulatory
Reference:
10 CFR 20.1502, Conditions Question 230 Page 51 Requiring Individual Monitoring of Extemal and Internal Q/A Set 6 PDR-9310070005 Occupational Dose Regulatory
Reference:
10 CFR 20.1906, Procedures for Receiving and Opening Packages Question 218 Page 38 Q/A Set 6 PDR-9310070005 Question 371 Page 56 Regulatory
Reference:
10 CFR 20.1601, Control Access to Q/A Set 5 PDR-9306110303 Iligh Radiation Areas Regulatory
Reference:
10 CFR 20.2104, Detennination of Prior Occupational Dose Question 219 Page 39 Q/A Set 6 PDR-9310070005 Question 372 Page 21 Regulatory
Reference:
10 CFR 20.1601, Control Access to Q/A Set 5 PDR-9306110303 Iligh Radiation Areas Regulatory
Reference:
10 CFR 20.1204, Determination of Internal Exposure Question 220 Page 40 Q/A Set 6 PDR-9310070005 Question 373 Page 39 Regulatory
Reference:
10 CFR 20.1602, Control Access to Q/A Set 5 PDR-9306110303 Very High Radiation Areas Regulatory
Reference:
10 CFR 20.1601, Control Access to High Radiation Areas Question 221 Page 47 Q/A Set 6 PDR-9.310070005 Question 374 Page 45 E
Regulatory
Reference:
10 CFR 20.1902, Posting Q/A Set 5 PDR-9306110303 Requirements Regulatory
Reference:
10 CFR 20.1703, Use ofIndividual Respiratory Protection Equipment Question 223 Page 49 Q/A Set 6 PDR-9310070005 Question 375 Page 36 Regulatory
Reference:
10 CFR 20.1903, Exoptions to Q/A Set 5 PDR-9306110303 Posting Requirements Regulatory
Reference:
10 CFR 20.1502, Conditions Requiring Individual Monitoring of Extemal and Internal Question 224 Page 49 Occupational Dose Q/A Set 6 PDR-9310070005 Regulatory
Reference:
10 CFR 20.1903, Exceptions to Posting Requirements 83 NUREG/CR-6204
Appendix A Question 376 Page 52 Question 387 Page 43 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.2001, Waste Disposal-Regulatory Reference. 10 CFR 20.1702, Use of Other GeneralRequirements Controls Question 377 Page 66 Question 388 Page 43 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 19.13, Notifications and Regulatory
Reference:
10 CFR 20.1702, Use of Other Reports toIndividuals Controls Question 378 Page 66 Question 389 Page 52 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 19.13, Notifications and Regulatory
Reference:
10 CFR 20.2001, Waste Disposal-Reports toIndividuals General Requirements Question 379 Page 48 Question 390 Page 56 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.1902, Posting Regulatory
Reference:
10 CFR 20.2104, Determination of Requirements Prior OccupationalDose Question 380 Page 14 Question 391 Page 59 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 i
Regulatory
Reference:
10 CFR 20.1101, Radiation Regulatory
Reference:
10 CFR 20.2107, Records of Dose to Protection Programs IndividualMembers ofthe Public Question 381 Page 14 Question 392 Page 61 Q/A Set 5 PDR 9306110303 Q/A Set 5 PDR.9306110303 Regulatory
Reference:
10 CFR 20.110l, Radiation Regulatory
Reference:
10 CFR 20.2206, Reports of Protection Programs IndividualMonitoring Question 382 Page 25 Question 393 Page 61 Q/A Set 5 PDR 9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.1208, Dose to an Regulatory
Reference:
10 CFR 20.2206, Reports of Embryo / Fetus Individual Monitoring Question 383 Page 60 Question 394 Page 61 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.2206, Reports of Regulatory
Reference:
10 CFR 20.2206, Reports of IndividualMonitoring Indi5idualMonitoring Question 384 Page 23 Question 395 Page 62 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR 9306110303 Regulatory
Reference:
10 CFR 20.1301, Dose Limits for Regulatory
Reference:
10 CFR 20.2206, Reports of IndividualMembers of the Public IndividualMonitoring Question 385 Page 39 Question 396 Page 64 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.1601, Control Access to Regulatory
Reference:
10 CFR 20 Appendix B, Annual High Radiation Areas Limits on Intake (ALIs) and Derived Air Concentrations (DACs) of Radionuclides for Occupational Exposure; l
Question 386 Page 43 Effluent Concentrations; Concentrations for Release to Q/A Set 5 PDR-9306110303 Sewage Regulatory
Reference:
10 CFR 20.1702, Use of other Controls NUREO/CR-6204 84
Appendix A Question 397 Page 71 Question 408 Page 56 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulaton
Reference:
Technical Specifications Regulatory
Reference:
10 CFR 20.2104, Determination of Prior OccupationalDose Question 398 Page 37 Q/A Set 5 PDR-9306110303 Question 409 Page 66 Regulatory
Reference:
10 CFR 20.1502, Conditions Q/A Set 5 PDR-9306110303 Requiring Individual Monitoring of External and Internal Regulatory
Reference:
10 CFR 19.13, Notifications and Occupational Dose Reports to Individuals Question 399 Page 57 Question 411 Page 65 Q/A Set 5 PDR-9306110303 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.2106, Records of Regulatory
Reference:
10 CFR 19.12, Instructions to Individual Monitoring Results Workers Question 400 Page 58 Question 412 Page 10 Q/A Set 5 PDR-9306110303 Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.2106, Records of Regulatory
Reference:
10 CFR 20.1003, Dermitions individualMonitoring Results Question 413 Page 10 Question 401 Page 58 Q/A Set 7 PDR-9311050284 Q/A Set 5 PDR-9306110303 Regulatory
Reference:
10 CFR 20.1003, Defmitions Regulatory
Reference:
10 CFR 20.2106, Records of IndividualMonitoring Results Question 414 Page 18 Q/A Set 7 PDR-9311050284 Question 402 Page 58 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Q/A Set 5 PDR-9306110303 Limits for Adults Regulatory
Reference:
10 CFR 20.2106, Records of Individual Monitoring Results Question 415 Page 18 Q/A Set 7 PDR-9311050284 Question 403 Page 58 Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Q/A Set 5 PDR 9306110303 Limits for Adults Regulatory
Reference:
10 CFR 20.2106, Records of IndividualMonitoring Results Question 416 Page 25 Q/A Set 7 PDR-9311050284 Question 404 Page 59 Regulatory
Reference:
10 CFR 20.1208, Dose to an Q/A Set 5 PDR-9306110303 Embryo / Fetus Regulatory
Reference:
10 CFR 20.2106, Records of Individual Monitoring Results Question 417 Page 31 Q/A Set 7 PDR-9311050284 Question 405 Page 69 Regulatory
Reference:
10 CFR 20.1302, Compliance with Q/A Set 5 PDR-9306110303 Dose Limits for Individual Members of the Public Regulatory
Reference:
Regulatory Guide 8.25, Air Sampling in the Workplace Question 418 Page 45 Q/A Set 7 PDR-9311050284 Question 406 Page 69 Regulatory
Reference:
10 CFR 20.1703, Use ofIndisidual Q/A Set 5 PDR-9306110303 Respiratory Protection Equipment Regulatory
Reference:
Regulatory Guide 8.36 Radiation Dose to the E nbryo/ Fetus Question 419 Page 46 Q/A Set 7 PDR-9311050284 Question 407 Page 3 Regulatory
Reference:
10 CFR 20.1801, Security of Stored Q/A Set 5 PDR-9306110303 Material Regulatory
Reference:
10 CFR 20.1001, Purpose 85 NUREG/CR-6204
Appendix A Question 420 Page 57 Question 430 Page 39 Q/A Set 7 PDR-9311050284 Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.2104, Determination of Regulatory
Reference:
10 CFR 20.1601, Control Access to
(
Prior Occupational Dose liigh Radiation Areas i
l Question 421 Page 67 Question 431 Page 39 Q/A Set 7 PDR-9311050284 Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 19.13, Notifications and Regulatory
Reference:
10 CFR 20.1601, Control Access to Reports to Individuals fligh Radiation Areas Question 422 Page 66 Question 432 Page 53 Q/A Set 7 PDR-9311050284 Q/A Set 7 PDR 9311050284 Regulatory
Reference:
10 CFR 19.12, Instructions to Regulatory
Reference:
10 CFR 20.2001, Waste Disposal-Workers General Requirements Question 423 Page 40 Ques
- ion 433 Page 7 I Q/A Set 7 PDR-9311050284 Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.1602, Control Access to Regulatory
Reference:
Technical Specifications VeryIlighRadiation Areas Question 434 Page11 Question 425 Page 64 Q/A Set 7 PDR-9311050284 Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.1003, Defmitions Regulatory
Reference:
10 CFR 20 Appendix B, Annual 5
Limits on Intake (ALIs) and Derived Air Concentrations Question 435 Page 18 (DACs) of Radionuclides for Occupational Exposure; Q/A Set 7 PDR-9311050284 Efiluent Concentrations; Concentrations for Release to Regulatory
Reference:
10 CFR 20.1201, Occupational Dose Sewage Limits for Adults Question 426 Page 64 Question 436 Page 18 Q/A Set 7 PDR 9311050284 Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20 Appendix B, Annual Regulatory
Reference:
10 CFR 20.1201, Occupationa! Dose Limits on Intake (ALIs) and Derived Air Concentrations Limits for Adults (DACs) of Radionuclides for Occupational Exposure; Ef!!uent Concentrations; Concentrations for Release to Question 437 Page 21 Sewage Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.1204, Determination of Question 427 Page 31 Intemal Exposure Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.1302, Compliance with Question 438 Page 20 Dose Limits for Individual Members of the Public Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.1207, Occupational Dose Question 428 Page 52 Limits for Minors Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.2103, Records of Surveys Question 439 Page 25 Q/A Set 7 PDR-9311050284 Question 429 Page 37 Regulatory
Reference:
10 CFR 20.1208, Dose to an Q/A Set 7 PDR-9311050284 Embryo / Fetus Regulatory
Reference:
10 CFR 20.1502, Conditions Requiring Individual Monitoring of External and Internal Question 440 Page 25 Occupational Dose Q/A Set 7 PDR-9311050284 Regulatory
Reference:
10 CFR 20.1208, Dose to an Embryo / Fetus NUREO/CR-6204 86
Appendix A Question 441 Page 25 Question 451 Page 70 Q/A Set 7 PDR-9311050284 Q/A Set 7 PDR 9311050284 Regulatory
Reference:
10 CFR 20.1208, Dose to an Regulatory
Reference:
Regulatory Guide 8.7, Rev.1, Ernbryo/ Fetus Instructions for Recording and Reportmg Occupational Exposure Data Question 442 Page 26 Q/A Set 7 PDR 9311050284 Question 452 Page 62 Regulatory
Reference:
10 CFR 20.1208, Dose to an Q/A Set 7 PDR-9311050284 Embryo / Fetus Regulatoiy
Reference:
10 CFR 20 Appendix A Protection Factors for Respirators
- Question 443 Page 26 Q/A Set 7 PDR-9311050284 Question 453 Page 65 Regulatory
Reference:
10 CFR 20.1208, Dose to an Q/A Set 7 PDR-9311050284 Embryo / Fetus Regulatory
Reference:
10 CFR 20 Appendix B, Annual Limits on Intake (ALis) and Derived Air Concentrations Question 444 Page 37 (DACs) of Radionuclides for Occupational Exposure; Q/A Set 7 PDR-9311050284 Efiluent Concentrations; Concentrations for Release to Regulatory
Reference:
10 CFR 20.1502, Conditions Sewage Requiring Individual Monitoring of External and Internal Occupational Dose Question 454 Page 67 Q/A Set 7 PDR-9311050284 Question 445 Page 38 Regulatory
Reference:
10 CFR 19.13, Notifications and Q/A Set 7 PDR-9311050284 Reports toIndividuals Regulatory
Reference:
10 CFR 20.1502, Conditions Requiring Individual Monitoring of External and Internal Question 455 Page 7i Occupational Dose Q/A Set 7 PDR-9311050284 Regulatory
Reference:
Technical Specifications Question 446 Page 38 Q/A Set 7 PDR-9311050284 Question 456 Page 68 Regulatory
Reference:
10 CFR 20.1502, Conditions Q/A Set 7 PDR-9311050284 Requiring Individual Monitoring of External and Internal Regulatory
Reference:
Technical Specifications Occupational Dose Question 457 Page 72 Question 447 Page 41 Q/A Set 7 PDR-9311050284 Q/A Set 7 PDR-9311050284 Regulatory
Reference:
FSAR Regulatory
Reference:
10 CFR 20.1602, Control Access to Very High Radiation Areas Question 458 Page 32 Q/A Set 7 PDR-9311050284 Question 448 Psge 41 Regulatory
Reference:
10 CFR 20.1501, Surveys and Q/A Set 7 PDR-9311050284 Monitoring - General Regulatory
Reference:
10 CFR 20.1602, Control Access to VeryIligh Radiation Areas Question 459 Page 48 Q/A Set 7 PDR-9311050284 Question 449 Page 43 Regulatory
Reference:
10 CFR 20.1902, Posting Q/A Set 7 PDR-9311050284 Requirements Regulatory
Reference:
In CFR 20.1702, Use of Other Controls Question 460 Page 48 Q/A Set 7 PDR-9311050284 Question 450 Page 46 Regulatory
Reference:
10 CFR 20.1902, Posting Q/A Set 7 PDR-9311050284 Requirements Regulatory
Reference:
10 CFR 20.1801, Security ofStored Material 87 NUREG/CR-62M
Appendix A Question 461 Page 38 Q/A Set 7 PDR 9311050284 Regulatory Reference 10 CFR 20.1502, Conditions Requiring Individual Monitoring of External and Internal.
OccupationalDose I
. 1 1
I l
i NURBO/CR4204 88 O
APPENDIX B REGULATORY REFERENCES 10 CFR 20.1502, Conditions Requiring Individual Monitoring of Extemal and Intemal Occupational Dose CITED IN TEXT 10 CFR 20.1601, Control Access to High Radiation Areas 10 CFR 19.12, bstructions to Worken 10 CFR 20.1602, Control Access to Very High Radiation Amas 10 CFR 19.13, Notifications and Reports to Individuals 10 CFR 20, Standards for Protection Against Radiation 10 CFR 20.1603, Control Access to Very High Radiation Areas -Irradiators 10 CFR 20.!001 Purpose 10 CFR 20.1701, Use of Process or Other Engmeenng Controls 10 CFR 20.1002, Scope 10 CFR 20.1303, Definitions 10 CFR 20.1702, Use of Other Controls -
10 CFR 20.1004, Units of Radiation Dose 10 CFR 20.1703, Use ofIndividual Respiratory Protection Equipment 10 CFR 20.1008, Implementation 10 CFR 20.1704, Further Restrictions on the Use of 10 CFR 20.1009 Repoding, Recording, and Application Respiratory Protection Equipment Requirements: OMB. Approval 10 CFR 20.1801, Security of Stored Material 10 CFR 20.1101, Radiation Protection Programs 10 CFR 20.1802, Control of Material not in Storage 10 CFR 20.1201, Occupational Dose Limits for Adults 10 CFR 20.1901, Caution Signs 10 CFR 20.1202, Comphance with Requirements for Summation of Extemal and Internal Doses 10 CFR 20.1902, Posting Requirements 10 CFR 20. ! 203, Detennination of External Dose From 10 CFR 20.1903, Exceptions to Posting Requirements Airbome Radioactive Material 10 CFR 20.1904, Labeling Containers 10 CFR 20.1204, Determination ofInternal Exposure 10 CFR 20.1905, Exemptions to Labeling Requirements 10 CFR 20.1206, Planned Special Exposures 10 CFR 20.1906, Procedures for Receiving and Openmg 10 CFR 20.1207, Occupational Dose Limits for Mmors Packages 10 CFR 20.1208, Dose to an Embryo / Fetus 10 CFR 20.2001, Waste Disposal - General Requirements 10 CFR 20.1301, Dose Limits for Individual Members of 10 CFR 20.2003, Disposal by Release into Sanitary the Public Sewerage 10 CFR 20.1302, Compliance with Dose Limits for 10 CFR 20.2101, Records - General Provisions IndividualMembers of the Public 10 CFR 20.2102, Records of Radiation Protection 10 CFR 20.1501, Surveys and Monitoring - General Pmgrams 89 NUREO/CR-6204
I Appendix B 10 CFR 20.2103, Records of Surveys 10 CFR 50 Appendix A, General Design Criteria for Nuclear Power Plants 10 CFR 20.2104, Detemunation of Prior Occupational Dose 10 CFR 50 Appendix B, Quality Assurance Criteria for Nuclear Power Plants and Fuel Reprocessing Plants 10 CFR 20.2105, Records of Planned Special Exposures 10 CFR 50 Appendix I, Numerical Guides for Design 10 CFR 20.2106, Records ofIndividual Monitoring Results Objectives and Limiting Conditions for Operation to Meet the Criterion "As Low as is Reasonably Achievable" for 10 CFR 20.2107, Records of Dose to Individual Members Radioactive Material in Light Water-Cooled Nuclear Power of the Public Reactor Efiluents 10 CFR 20.2110, Form ofRecords 10 CFR 71.4, Packaging and Transportation of Radioactive Material Definitions 10 CFR 20.2202, Notification ofIncidents 10 CFR Part 100, Reactor Site Criteria 10 CFR 20.2203, Reports of Exposures, Radiation Levels, and Concentrations of Radioactive Material Exceedmg the Byproduct Material licenses (medical)
Limits DOE Order 5480.11, Radiation Protection for Occupational 10 CFR 20.2204, Reports of Planned Special Exposures Workers 10 CFR 20.2206, Reports ofIndividual Monitoring EPA PAG Maaual 10 CFR 20 Appendix A, Protection Factors for Respirators FSAR, Final Safety Analysis Report 10 CFR 20 Appendix B, Annual Limits on Intake (ALis)
Federal Guidance Report No. I1 and Derived Air Concentrations (DACs) of Radionuclides for Occupational Exposure; Efiluent Concentrations; HPPOS-028, Further Guidance on Labeling Requuements" Concentrations for Release to Sewage in Health Physics Positions Data Base, NUREG/CR-5569, Rev.1 i
10 CFR 34.21, Limits on Levels of Radiation for l
Radiographic Exposure Devices and Storage Containers NRR Generic Letter 89-01 10 CFR 34.24, Radiation Survey Instmments NUREG-1301, Offsite Dose Calculation Manual Guidance.
Standard Radiological Efiluent Control for Pressurized 10 CFR 34.33, Personnel Monitoring Water Reactors 1
(
10 CFR 34.42, Posting NUREG-1302, Offsite Dose Calculation Manual Guidance.
Standard Radiological Efiluent Control for Boiling Water 10 CFR 34.43, Radiation Surveys Reactors 10 CFR 39.33, Radiation Detection Instmments Regulatory Guide 1,16, Reporting of Operating Information, Appendix A - Technical Specification, Rev. 4 10 CFR Past 50, Domestic Licensing of Production and Utilization Facilities Regulatory Guide 8.13, Instruction Concernmg Prenatal l
Radiation Exposure, Rev. 2 l
10 CFR 50.47, Permits - Emergency Plans i
Regulatory Guide 8.25, Air Sampling in the Workplace 10 CFR 50.72, Maintenance of Records, Making of Reports Regulatory Guide 8.34, Monitoring Criteria and Methods to 10 CFR 50.73, License Event Report System Calculate Occupational Radiation Exposure Regulatory Guide 8.35, Planned Special Exposures NUREG/CR-6204 90
Appmuhx B Regulatory Guide 8.36, Radiation Dose to the Eminyn/ Fetus Regulatory Guide 8.7, Rev.1, Instmetions for Recordmg and Reporting Occupational Exposure Data Regulatory Guide 8.9, Interpretation of Bioassay Measurements Regulatory Guide 10.8 Appendtx X, Guidance on Complying with New Part 20 Requirements (for medical use programs)
Regulatory Guides Technical Specifications U.S. NRC Enforcement Policy 91 NUREO/CR 6204
APPENDIX C 1
QUESTIONS AND ANSWERS BY 10 CFR 20.1003, nefinitions (continued)
Question 74 Page 8 REGULATORY REFERENCE Que,tio,77 page 16 Question 80 Page 8 10 CFR 19.12,Inatructions to Workers Question 82 Page 34 Question 66 Page 7 Question 84 Page 24 Question 95 Page 65 Question 85 Page 47 Question 411 Page 65 Question 92 Page 40 Question 422 Page 66 Question 93 Page 8 Question 94 Page 8 10 CFR 19.13,Notificatlans and Reports to Individuals Question %
Page 8 Question 37 Page 66 Question 100 Page 16 Question 377 Page 66 Quation 104 Page 30 Question 378 Page 66 Question 109 Page 22 Question 409 Page 66 Question 119 Page 9 Question 421 Page 67 Question 123 Page 16 Question 454 Page 67 Question 125 Page 27 Question 144 Page 9 10 CFR 20, Standards for Protection Against Radiation Question 148 Page 9 Question 452 Page 62
. Question 149 Page 9 Question 150 Page 10 10 CFR 20.1001, Purpose Question 176 Page 17 Question 2 Page 14 Question 206 Page 28 Question 4 Page 3 Quation 211 Page 35 Question 5 Page 3 Question 220 Page 40 Question 99 Page 12 Quation 379 Page 48 Question 192 Page 24 Question 412 Page 10 Ouestion 407 Page 3 Question 413 Page 10 Question 416 Page 25 10 CFR 20.1002, Scope Question 417 Page 31 Question 2 Page 14 Question 420 Page 57 Question 4 Page 3 Question 428 -
Page52 Question 5 Page 3 Quation 434 Page 11 Question 439 Page 25 10 CFR 20.1003, Definitions Question 440 Page 25 Question 1 Page 3 Question 444 Page 37 Question 2 Page 14 Question 447 Page 41 Question 4 Page 3 Question 448 Page 41 Question 5 Page 3 Quation 450 Page 46 Question 24 Page 22 Question 459 Page 48 Question 25 Page 4 Question 460 Paget8 Question 26 -
Page 4 Question 27 Page 47 10 CFR 20.1004, Units of Radi=slan Dose Question 31 Page 15 Question 73 Page 11 Question 34 Page 15 Question 40 Page 7 Question 57 Page 7 Question 66 Page 7 Question 67 Page 8 93 NURBO/CR-6204
~
Appendix C 10 CFR 20.1008, Implementation 10 CFR 20.1202, Compliance with Requirements for Question 30 -
Page 11 -
Summation of External and Internal Doses J
Question 58 Page 11 Question 9 Page 19 -
Question 65 Page 11 Question 38 Page 19 Question 111 '
Page 27 Question 86 Page 19.
- Question 101 Page 19 10 CFR 20.1009,' Reporting, Recording, and Application Question 179 Page 19 Requirements: OMB Approval Question 375 Page 36 Question 180 =
Page 20 Question 65 Page 11 Question 438 Page 20 =
.10 CFR 20.1101, Radiation Protection Programs -
. Question 453 Page 65 -
- Question 7 Page 12 Question 11 Page 12 10 CFR 20.1203, Determination of External Dose From.
Question 26 Page 4 -
Alstorne Bmaamreive Material Question 60 Page 44.
Question 50 Page 20 Question 62
- Page 12 '
Question 4581 Page 32 Question 99 Page 12 Question 118 Page 13 10 CFR 20.1204, Determination of Internal Exposure Question 133 Page 13 Question 47
' Page 20 Quation 134 Page 13
' Question 76 -
Page 20
. Question 380 Page 14
- Question 83 Page 21 Question 381 Page 14 Question 121 Page 21 -
Question 146 Page 64
-l 10 CFR 20.1201, Occupational Dose Ilmits for Adults
~ Question 1831 Page 21 l
Question 2 Page 14 Question 372 Page 21 j
Question 3 Page 15 Question 437 Page 21
.i Question 6 Page 15 Question 453 Page 65 Question 26 Page 4 Question 458 Page 32
.j Question 31 Page 15 Question 33 Page 15 -
10 CFR 20.1206, Planned Special Exposures Question 34 Page 15 Question 8 Page 22 Question 41 Page 15 Question 24 Page 22 Question 42 '
Page 26 Question 63 Page 22
{
Question 45 Page 16 Question 66 Page 7 J
Question 46 Page 16 Question 109 Page 22 Question 55 Page 54 Question 110 Page 23 Question 63 Sge 22
. Quation 112 Page 57 Question 66 Page 7 Question 113.
Page 55 Question 77.
age 16 Question 135 Page 23 J
Question 97 Page 16 Question 136 Page 23 Question 100 Page 16 Question 137 Page 23 ~
Question 106 Page 27 Question 191 Page 24 Question 123 Page 16 -
Question 192 Page 24 Question 172 Page 17 Question 383
- Page 60.
Question 175 Page 17 j
Question 176 Page 17 10 CFR 20.1207, Occupational Dose Limits for Minors l
Question 177 Page 17 Question 26 Page 4 i
(
Question 217 Page 18 Question 66 Page 7 Question 413 Page 10 Question 414 Page 18 10 CFR 20.1208, Dose to an Embryo / Fetus '
Question 415 Page 18 Question 26 Page 4 Question 435 Page 18 Question 58
- Page 11 Question 436 Page 18 Question 59 Page 24 Question 66 Page 7
- NUREG/CR-6204 94
Appendix C 10 CFR 20.1208, Dose to an Embryo / Fetus (continued) 10 CFR 20.1502, Conditions Requiring Individual Question 84 Page 24 Monitoring of External and Internal Occupational Dose Question 120 Page 24 Question 9 Page 19 Question 138 Page 24 Question 43 Page 32 Question 378 Page 66 Question 44 Page 33 Question 382 Page 25 Question 54 Page 33 Question 394 Page 61 Question 75 Page 33 Question 416 Page 25 Question 81 Page 34 Quest:on 439 Page 25 Question 82 Pags 34 Question 440 Page 25 Question 98 Page 34 Question 441 Page 25 Question 100 Page 16 Question 442 Page 26 Question 114 Page 34 Question 443 Page 26 Question 126 Page 35 Question 211 Page 35 10 CFR 20.1301, Dose Limits for Individual Members of Question 212 Page 35 the Public Question 213 Page 36 Question 26 Page 4 Question 214 Page 36 Quettion 42 Page 26 Question 215 Page 36 Question 48 Page 26 Question 216 Page 36 Question 105 Page 27 Question 372 Page 21 Question 106 Page 27 Question 374 Page 45 Question 111 Page 27 Question 375 Page 36 Question 125 Page 27 Question 377 Page 66 Question 201 Page 27 Question 394 Page 61 Question 203 Page 28 Question 398 Page 37 Question 204 Page 28 Question 429 Page 37 Question 205 Page 28 Question 444 Page 37 Question 206 Page 28 Question 445 Page 38 Question 207 Page 31 Question 446 Page 38 Question 384 Page 28 Question 458 Page 32 Question 427 Page 31 Question 459 Page 48 Question 460 Page 48 10 CFR 20.1302, Compliance with Dose Limits for Question 461 Page 38 Individual Members of the Public Question 28 Page 29 10 CFR 20.1601, Control Access to Iligh Radiation Areas Question 29 Page 29 Question 52 Page 70 Question 68 Page 29 Question 74 Page 8 Question 69 Page 30 Question 218 Page 38 Question 72 Page 30 Question 219 Page 39 Question 102 Page 30 Question 373 Page 39 Question 103 Page 30 Question 385 Page 39 Question 104 Page 30 Question 423 Page 40 Question 207 Page 31 Question 430 Page 39 Question 208 Page 31 Question 431 Page 39 Question 384 Page 28 Question 448 Page 41 Question 417 Page 31 Question 427 Page 31 10 CFR 20.1602, Control Access to Very High Radiation Areas 10 CFR 20.1501, Surveys and Monitoring - General Question 49 Page 40 Question 147 Page 32 Question 52 Page 70 Question 205 Page 28 Question 57 Page 7 Question 209 Page 32 Question 92 Page 40 Question 210 Page 32 Question 220 Page 40 Question 458 Page 32 Question 373 Page 39 95 NUREG/CR-6204
Appendix C 10 CFR 20.1602, Control Access to Very fligh Radiation 10 CFR 20.1901, Caution Signs Areas (Continued)
Question 221 Page 47 Question 423 Page 40 Question 430 Page 39 10 CFR 20.1902, Posting Requirements Question 447 Page 41 Question 27 Page 47 Question 448 Page 41 Question 53 Page 47 Question 85 Page 47 10 CFR 20.1603, Control Access to Very Iligh Radiation Question 221 Page 47 Areas - Irradiators Question 224 Page 49 Question 130 Page 41 Question 379 Page 48 Question 385 Page 39 10 CFR 20.1701, Use of Process or Other Engineering Question 405 Page 69 Controls Question 447 Page 41 Question 90 Page 42 Question 458 Page 32 Question 115 Page 42 Question 459 Page 48 Question 460 Page 48 10 CFR 20.1702, Use of Other Controls Question 145 Page 42 10 CFR 20.1903, Exceptions to Posting Requirements Question 386 Page 43 Question 35 Page 49 Question 387 Page 43 Question 53 Page 47 Question 388 Page 43 Question 223 Page 49 Question 449 Page 43 Question 224 Page 49 10 CFR 20.1703, Use of Individual Respiratory 10 CFR 20.1904, Labeling Containers Protection Equipment Question 53 Page 47 Question 54 Page 33 Question 127 Page 50 Question 60 Page 44 Question 128 Page 50 Question 78 Page 44 Question 226 Page 50 Question 91 Page 44 Question 450 Page 46 Question 124 Page 45 Question 131 Page 45 10 CFR 20.1905, Exemptions to Labeling Requirements Question 132 Page 45 Question 53 Page 47 Question 374 Page 45 Question 128 Page 50 l
Question 375 Page 36 Question 129 Page 46 Question 386 Page 43 i
Question 387 Page 43 10 CFR 20.1906, Procedures for Receiving and Opening Question 388 Page 43 Packages Question 418 Page 45 Question 36 Page 50 l
Question 108 Page 50 l
10 CFR 20.1704, Further Restrictions on the Use of Question 227 Page 51 Respiratory Protection Equipment Question 228 Page 51 l
Question 374 Page 45 Question 229 Page 51 Question 230 Page 51 10 CFR 20.1801, Security of Stored Material Question 129 Page 46 10 CFR 20.2001, Waste Disposal - General Requirements l
Question 419 Page 46 Question 376 Page 52 Question 450 Page 46 Question 389 Prge 52 Question 432 Page 53 l
10 CFR 20.1802, Control of Material not in Storage Question 129 Page 46 10 CFR 20.2003, Disposal by Release iato Sanitary Question 450 Page 46 Sewerage Question 39 Page 54 NUREG/CR-6204 96
Appendix C 10 CFR 20.2101, Records - General Provisions 10 CFR 20.2107, Records of Dose to Individual Members Question %
Page 8 of the Public Question 116 Page 54 Question 391 Page 59 Question 117 Page 54 Question 428 Page 52 10 CFR 20.2110, Form of Records Question 141 Page 60 10 CFR 20.2102, Records of Radiation Protection Programs 10 CFR 20.2202, Notification oUncidents Question 134 Page 13 Question 56 Page 60 10 CFR 20.2104, Determination of Prior Occupational 10 CFR 20.2203, Reports of Exposures, Radiation Dose levels, and Concentrations of Radioactive Material Question 6 Page 15 Exceeding the Limits Question 10 Page 54 Question 122 Page 60 Question 51 Page 54 Question 55 Page 54 10 CFR 20.2204, Reports of Planned Special Exposures Question 63 Page 22 Question 191 Page 24 Question 64 Page 55 Question 333 Page 60 Question 83 Page 21 Question i13 Page 55 10 CFR 20.2206, Reports of Individual Monitoring Question 139 Page 55 Question 10 Page 54 Question 142 Page 55 Question 61 Page 71 Question 143 Page 55 Question 79 Page 71 Question 179 Page 19 Question 383 Page 60 Question 192 Page 24 Question 392 Page 61 Question 214 Page 36 Question 393 Page 61 Question 371 Page 56 Question 394 Page 61 Question 390 Page56 Question 395 Page 62 Question 408 Page 56 Question 399
- Page 57 Question 414 Page 18 Question 400 Page 58 Question 420 Page 57 Question 401 Page 58 Question 436 Page 18 Question 402 Page 58 Question 441 Page 25 Question 403 Page 58 Question 451 Page 70 Question 404 Page 59 Question 446 Page 38 10 CFR 20.2105, Records of Planned Special Exposures '
Question 112 Page 57 10 CFR 20 Appendix A, Protection Factors for Question 191 Page 24 Respirators Question 452 Page 62 10 CFR 20.2106, Records of Individual Monitoring Results 10 CFR 20 Appendix B, Annual Limits on Intake (ALis)
Question 75 Page 33 and Derived Air Concentrations (DACs) of Radionuclides Question 212 Page 35 for Occupational Exposure; Emment Concentrations; Question 213 Page 36 Concentrations for Release to Sewage Question 217 Page 18 Question 13 Page 63 Question 390 Page 57 Question 22 Page 72 Question 400 Page 58 Question 23 Page 63 Question 401 Page 58 Question 71 Page 63 Question 402 Page 58 Question 146 Page M Question 403 Page 58 Question 425 Page 64
- Question 404 Page 59 Question 426 Page 64 Question 451 Page 70 Question 453 Page 65 Question 454 Page 67 Question 458 Page 32 t
97 NUREO/CR-6204
Appendix C 10 CFR 34.21, Limits on levels of Radiation for 10 CFR 71.4, Packaging and Transportation of Radiographic Exposure Devices and Storage Containers Radioactive Material-Definitions Question 428 Page 52 Question 227 Page 51 Question 228 Page 51 10 CFR 34.24, Radiation Survey Instruments Question 229 Page 51 Question 423 Page 52 Question 230 Page 51 10 CFR 34.33, Personnel Monitoring 10 CFR Part 100, Reactor Site Criteria Question 428 Page 52 Question 14 Page 68 10 CFR 34.42, Posting Byproduct Material Licenses (Medica 0 Question 223 Page 49 Question 72 Page 30 10 CFR 34.43, Radiation Surveys DOE Order 5480.11, Radiatlan Protection for Question 108 Page 50 Occupational Workers Question 76 Page 20 10 CFR 39.33, Radiation Detection Instruments Question 83 Page 21 Question 428 Page 52 EPA PAG Manual 10 CFR Part 50, Domestic IJcensing of Production and Question 16 Page 68 Utilization Facilities Question 456 Page 68 FSAR, Final Safety Analysis Report Question 456 Page 68 10 CFR 50.47, Permits - Emergency Plans Question 16 Page 68 Federal Guidance Report No.11 Question 71 Page 63 10 CFR 50.72, Maintenance of Records, Making of Reports HPPOS-028, "Further Guidance on Labeling Question 15 Page 68 Requirements" in Health Physics Positions Data Base, NUREG/CR-5569, Rev.1 3
10 CFR 50.73, License Event Report System Question 226 Page 50 Question 15 Page 68 Question 122 Page 60 NRR Generic IAtter 89-01 Question 22 Page 72 10 CFR 50 Appendix A, General Design Criteria for Nuclear Power Plants NUREG-1301, Offsite Dcse Calculation Manual Question 14 Page 68 Guidance. Standard Radiological Emuent Control for Pressurized Water Reactors 10 CFR 50 Appendix B, Quality Assurance Criteria for Question 80 Page 8 Nuclear Power Plants and Fuel Reprocessing Plants Question 17 Page 68 NUREG-1302, Offsite Dose Calculation Manual Question 3%
Page 64 Guidance. Standard Radiological Emment Control for Boiling Water Reactors 10 CFR 50 Appendix I, Numerical Guides for Design Question 80 Page 8 Objectives and Limiting Conditions for Operation to Meet the Criterion "As Low as is Reasonably None Achievable" for Radioactive Material in Light-Water-Question 87 Page 72 Cooled Nuclear Power Reactor Emuents Question 88 Page 72 Question 20 Page 68 Question 89 Page 72 Other Question 457 Page 72 NUREO/CR-6204 98 l
Appendix C Regulatory Guide 1.16, Reporting of Operating In-Regulatory Guide 8.9, Interpretation of Bloassay formation, Appendix A - Technical Specification, Rev. 4 hieasurements Question 397 Page 71 Question 375 Page 36 Regulatory Guide 8.13, Instruction Concerning Prenatal Regulatory Guide 10.8 Appendix X, Guidance on Radiation Exposure, Rev. 2 Complying with New Part 20 Requirements (for medical Question 59 Page 24 use programs)
Question 219 Page 39 Regulatory Guide 8.25, Air Sampling in the Workplace Question 405 Page 69 Regulatory Guides Question 12 Page 69 Regulatory Guide 8.34, Monitoring Criteda and Methods Question 21 Page 69 to Calculate Occupational Radiation Exposure Question 176 Page 17 Technica' Specifications Question 180 Page 20 Question 18 Page 70 Question 214 Page 36 Question 19 Page 70 Question 20 Page 68 Regulatory Guide 8.35, Planned Special Exposures Question 22 Page 72 Question 192 Page 24 Question 52 Page 70 Question 61 Page 71 Regulatory Guide 8.36, Radiation Dose to the Question 63 Page 22 Embryo / Fetus Question 79 Page 71 Question 406 Page 69 Question 397 Page 71 Question 423 Page 40 Regulatory Guide 8.7, Rev.1, Instructions for Recording Question 433 Page 71 and Reprting Occupational Exposure Data Question 455 Page 71 Question 383 Page 60 Question 398 Page 37 U.S. NRC Enforcement Policy Question 399 Page 57 Question 3 Page 15 Question 400 Page 58 Question 401 Page 58 Question 402 Page 58 Question 403 Page 58 Question 404 Page 59 Question 436 Page 18 Question 451 Page 70 99 NUREO/CR-6204
't 9
NUREG/CR4204 ORNI1TM-12690 Dist. Category AN INTERNAL DISTRIBUTION 1-34.
Tim Borges 35.
Dan Carter l
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Po-Yung Lu 37.
R.S. Stafford 38.
Dan O'Connor.
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ORNL Patent Office 41.
Central Research Library 42.
Document Research Section -
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EXTERNAL DISTRIBUTION '
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Given distribution as shown in category AN (NTIS-10) i
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NRC FOAM 335 U.S. NUCLE AR CEGULAToAY CoMMISSloN
- 1. hEPoRT NUMBEk Nc$1102, ed N
22oi. m BIBLIOGRAPHIC DATA SHEET (see instruct,oan on the <=rw/
NUREG/CR-6204 2, TITLE AND SU8 TITLE ORNL/TM-12690 Questions and Answers Based on Revised 10 CFR Part 20 3.
DATE REPORT PUBLISHED
)
g uoNrn vtAR May 1994
- 4. FIN oR GR ANT NUM8E R L2416
- 5. AUTHOR {S)
- 6. TYPE OF REPORT T. Borges R.S. Stafford, P.Y. Lu, Oak Ridge National Laboratory Technical D. Carter, U.S. Nuclear Regulatory Commission
- 7. PE RioD Covt REo tinews-e oeresi 8.
F R ANlZ ATioN - N AME AND ADDR ESS tor NMC. provw Ow.non, Cornee or ne.non, U.2, akener neeukterv Comnueuen, and metime enkhwea;it contrereer. Perm Oak Ridge National Laboratory Oak Ridge, TN 37831-6050
- 9. SPONSORING ORGANIZATION - NAME AND ADOR ESS (se knC. troe "same as eeove";if contoursor. provide NAC O won, prime or Aspen, ul Nuemar Aspuserery CommJouen, and memne ea>>went Division of Regulatory Applications Office of Nuclear Regulatory Research U.S. Nuclear Regulatory Commission Washinton DC 20555-0001
- 10. SUPPLEMENTARY NOTES II. ABSTRACT uoo sem or mesJ NUREG/CR-6204 is a collection of questions and answers that were originally issued in seven sets and which pertain to revised 10 CFR Part 20.
The questions came from both outside and within the NRC. The answers were compiled and provided by NRC staff within the offices of Nuclear Reactor Regulation, Nuclear Material Safety and Safeguards, Nuclear Regulatory Research, the Office of State Programs, and the five regional offices. Although all of the questions and answers have been reviewed by attorneys in the NRC Office of the General Counsel, they do not constitute official legal interpretations relevant to revised 10 CFR Part 20.
The questions and answers do, however, reflect NRC staff decisions and technical options on aspects of the revised 10 CFR Part 20 regulatory requirements. This NUREG is being made available to encourage communication among the public, industry, and NRC staff concerning the major revisions of the NRC's standards for' protection against radiation.
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