ML20155G222
| ML20155G222 | |
| Person / Time | |
|---|---|
| Issue date: | 10/09/1998 |
| From: | Rathbun D NRC OFFICE OF CONGRESSIONAL AFFAIRS (OCA) |
| To: | Inhofe J, Schaefer D HOUSE OF REP., SENATE, ENVIRONMENT & PUBLIC WORKS |
| References | |
| FRN-63FR13372, RULE-PR-72 CCS, NUDOCS 9811060244 | |
| Download: ML20155G222 (2) | |
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NUCLEAR REGULATORY COMMISSION WASHINGTON, D.C. 20556 0001 4e*****,o October 9, 1998 The Honorable James M. Inhofe, Chairman Subcommittee on Clean Air, Wetlands, Private
~ Property and Nuclear Safety Committee on Environment and Public Works United States Senate Washington, DC 20510
Dear Mr. Chairman:
The U.S. Nuclear Regulatory Commission (NRC) has sent, to the Office of the Federal Register, for publication, the enclosed final rule to amend its 10 CFR Part 72 regulations for independent Spent Fuel Storage installations (ISFSis), and the Monitored Retrievable Storage (MRS) Installation.
This final rule: (1) amends ISFSI and MRS design-basis accident dose limits in 10 CFR 72.106(b) to confcrm to the dose calculational methodology currently used in 10 CFR Part 20; and (2) makes a minor change to 10 CFR 72.104(a), so that it will match the U.S.
Environmental Protection Agency's regulations in 40 CFR 191.03(a).
This action is needed to make Part 72 limits for design-basis accidents consistent with Part 20 dose calculational methodology, and to afford Part 72 licensees the flexibility provided by Part 20 dose methodology, when performing design-basis accident analyses.
This final rule is the same as the proposed rule (63 FR 13372; March 19,1998) except for the radiation exposure limits in 10 CFR 72.104(a), which are now expressed in metric units, as well
- as in English units. All public comments were addressed in the final rule.
Sincerely,
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Av.~ }f h-Dennis K. Rathbun, Director Office of Congressional Affairs jj
Enclosure:
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Federal Register Notice cc: Senator Bob Graham
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- NUCLEAR REGULATORY COMMISSION 2
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October 9, 1998 The Honorable Dan Schaefer, Chairman l
L Subcommittee on Energy and Power j_
Committee on Commerce United States House of Representatives Washington,' DC 20515
Dear Mr. Chairman:
l The U.S. Nuclear Regulatory Commission (NRC) has sent, to the Office of the Federal L
Register, for publication, the enclosed final rule to amend its 10 CFR Part 72 regulations for Independent Spent Fuel Storage Installations (ISFSis), and the Monitored Retrievable Storage (MRS) installation.
This final rule: (1) amends iSFSI and MRS design-basis accident dose limits in 10 CFR 72.106(b) to conform to the dose calculational methodology currently used in 10 CFR Part 20;
- and (2) makes a minor change to 10 CFR 72.104(a), so that it will match the U.S.-
Environmental Protection Agency's regulations in 40 CFR 191.03(a).
This action is needed to make Part 72 limits for design-basis accidents consistent with Part 20 dose calculational methodology, and to afford Part 72 licensees the flexibility provided by Part 20 dose methodology, when performing design-basis accident analyses.
This final rule is the same as the proposed rule (63 FR 13372; March 19,1998) except for the radiation exposure limits in 10 CFR 72.104(a), which are now expressed in metric units, as well as in English units. All public comments were addressed in the final rule.
Sincerely, v, M J
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Oennis K.
athbun, Director Office of Congressional Affairs
Enclosure:
Federal Register Notice cc: Representative Ralph Hall
[7590-01-P]
NUCLEAR REGULATORY COMMISSION 10 CFR Part 72 RIN: 3150-AF84 I
Minor Revision of Design Basis Accident Dose Limits for Independent Spent Fuel Storage and Monitored Retrievable i
Storage Installations i
l AGENCY: Nuclear Regulatory Commission.
ACTION: Final rule.
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SUMMARY
- The Nuclear Regulatory Commission (NRC)is amending its regulations governing the dose limits agd the dose calculational methodology used in design basis accident analyses for Independent Spent Fuel Storage Installations (ISFSis) and Monitored Retrievable Storage Installations (MRS). This final rule amends ISFSI and MRS design basis accident dose limits to conform to the dose calculational methodology currently used in the regulations that specify standards for protection against radiation and make a mincr change to match the Environmental Protection Agency's (EPA) regulations. This action will ensure that limits for design basis accidents at ISFSI and MRS installations are consistent with the dose methodology specified in NRC radiation protection regulations, and will allow licensees the flexibility provided by that dose methodology when performing design basis accident analyses.
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EFFECTIVE DATE: (30 days after date of publication in the Federal Register).
FOR FURTHER INFORMATION CONTACT: Naiem S. Tanlous, Office of Nuclear Material Safety and Safeguards, U.S Nuclear Regulatory Commission, Washington, DC 20555-0001, telephone (301) 415-6103, E-mail: INTERNET:NST@nrc. gov SUPPLEMENTARY INFORMATION:
Background
Paragraph (b) of 6 72.106 establishes the dose limit for a design basis accident at an -
independent spent fuel storage installation (ISFSI) or a monitored retrievable storage installation (MRS). The dose limit in 72.106(b) is based on the dose calculational methodology contained in International Commission on Radiological Protection Publication Number 2 (ICRP-2,1959). The ICRP-2 methodology was subsequently revised in ICRP Publication Numper 26 (ICRP-26,1977), and was incorporated into 10 CFR Part 20 when Part 20 was revised in 1991.
The calculational methodology in the revised Part 20 no longer quantifies dose in terms 4
of whole body dose and ;ndividual organ dose. Instead, the dose is quantified as a risk equivalent dose. In this manner, the doses absorbed by the whole body and the individual organs can be summed to a single quantity relating to risk.
Under the Part 20 calculational methodology, deep-dose equivalent (Ha), which applies to the external whole-body exposure, is defined in 10 CFR 20.1003 as the dose equivalent at a 2
tissue depth of 1 cm (1000 mg/cm ). The committed dose equivalent (CDE)(Huo) is defined in 10 CFR 20.1003 to mean the dose equivalent to organs or tissues of reference (T) that will be received from an intake of radioactive material by an individual during the 50-year period 2
4 following the intake. The committed e//ective dose equivalent (CEDE) (Huo) is defined in
~ 10 CFR 20.1003 as the sum of the products of the weighting factors applicable to each of the.
body organs or tissues that are irradiated and the committed dose equivalent to these organs or' tissues (He,3o = [w Hr,3a). The totaleffective dose equivalent (TEDE) is the sum of the deep-r dose equivalent (for' external exposure) and the committed effective dose equivalent (for internal exposures).
1 The ICRP-26 methodology was not incorporated into Part 72 at the time Part 20 was revised. Part 72 contains two regulations setting dose limits: Q 72.104, which sets dose limits during normal operations and ant'icipated occurrences; and 72.106, which sets dose limits for
' design basis accidents
' The main objective of this final rule is to revise 72.106(b) to incorporate the Part 20 methodology. A second objective of the rule is to make a minor word change to Q 72.104(a) to match the language used by EPA in 40 CFR 191.03(a).
On March 19,1998 (63 FR 13372), the NRC published the notice of proposed rulemaking that would amend ISFSI and MRS design basis accident dose limits to conform to the dose calculational methodology currently used in 10 CFR Part 20, and to make a minor
- change to 72.104(a) to match EPA's regulation in 40 CFR 191.03(a). The public comment period expired May 4,1998.
Discussion At present, 72.106, Controlled area of an ISFSI or MRS in part provides:
.(b) Any individual located on or beyond the nearest boundary of the controlled area shall not receive a dose greater than 5 rem to the whole body or any organ l.
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from any design basis accident. The minimum distance from the spent fuel or high level radi,oactive waste handling and storage facilities to the nearest boundary of the controlled area shall be at least 100 meters.
i This 0.05 Sv (5 rem) limit to the whole body or any organ is amended in the final rule to i
conform with the Part 20 dose calculational methodology. The amended limit becomes the more limiting of the TEDE of 0.05 Sv (5 rem), or the sum of the deep dose equivalent and the committed dose equivalent to any individual organ or tissue (other than the lens of the eye) of 0.5 Sv (50 rem). The amendment also includes a separate dose limit for the lens of the eye of 0.15 Sv (15 rem); and for the skin or any extremity, a shallow dose equivalent of 0.5 Sv (50 rem). The use of separate dose limits for the lens of the eye, skin, and extremities will conform with the dose calculational methodology used in Part 20 and will ensure that no observable effects (e.g., induction of cataracts in the lens of the eye) will occur as a result of cny accidental radiation exposure.
This final /ule makes 9 72.106 consistent with Part 20 dose calculational methodology.
This rule also provides Part 72 licensees flexibility when performing design basis accident 1
enalyses because they would be able to use organ weighting factors to calculate the dose to the maximally exposed organ. In addition, Part 72 licensees will no longer need to comply with one calculational methodology for their radiation protection programs (i.e., the revised Part 20 methodology) and another methodology for their design basis accident analyses.
This final rule does not revise 6 72.104(a) to incorporate ICRP-26 methodology because doing so would render this regulation incompatible with the EPA's regulation at 40 CFR 191.03(a) which is applicable to ISFSI and MRS licensees. However,40 CFR 191.03(a) phrases the standard in terms of dose limits to the whole body and any critical organ; whereas, G 72.104(a) phrases the standard in terms of dose limits to the whole body and any organ. This 4
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final rule makes 72.104(a) more consistent with 40 CFR 191.03(a) by inserting the word criticalbef. ore the word organ. The critical organ (listed in Table 1 of ICRP-2) associated with an intake of radioa::tive material is considered to be that organ of the body whose damage by j
the radiation results in the greatest damage to the body.
This final rule adopts the term " Lens dose equivalent" in Q 72.106 which replaces the term " Eye dose equivalent". This new term was added to Part 20 in an NRC final rule published on July 23,1998 (63 FR 39477).
Public Comments on the Proposed Rule The NRC received two public comments: one from the Nuclear Energy institute (NEI),
l an organization that represents the nuclear energy industry, and the other from TSW Enterprises, a private company. Both commenters supported the proposed rule. NEl, while expressing ' isappointment that NRC was not amending 9 72.104(a) because this would create d
incompatibility with EPA's regulation, urged the NRC to proceed with the revisions as proposed.
TSW Enterprises also supported the proposed rule and suggested that in 72.104(a) the radiation exposure limits be expressed in metric units as well as English units in accord with the Commission's policy cn the use of metric units (61 FR 31169). The Commission agrees with this suggestion and this change is made in the final rule.
Criminal Penalties For purposes of Section 223 of the Atomic Energy Act (AEA), the Commission is issuing the find rule under one or more of sections 161b,161: or 161o of the AEA. Willful violations of
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the rule will be subject to criminal enforcement.
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EnvironmentalImpact: Categorical Exclusion 1
The NRC has determined that this final rule is'the type of action described in categorical l
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exclusion 10 CFR 51.22(c)(2). Therefore, neither an environmentalimpact statement nor an environmental assessment have been prepared for this regulation.
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Paperwork Reduction Act Statement This final rule does not contain a new or amended information collection requirement subject to the Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et seq.). Existing requirements were approved by the Office of Management and Budget, approval number 3150-0132.
Public Protection Notification 4
If an information collection does not display a currently valid OMB control number, the NRC may not conduct or sponsor, and a person is not required to respond to, the information collection.
Regulatory Analysis To determine whether the amendments to 10 CFR Part 72 are appropriate, the NRC staff considered the following two alternatives:
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- 1. The No-Action Alternative. This alternative is not acceptable to the NRC for the l
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l following, reasons. Section 72.106(b) would continue to be inconsistent with Part 20. Part 72 1
licensees would demonstrate compliance with the dose limits in Part 20 using the 1977 dose calculational methodology of ICRP-26 for their radiation protection programs as required by 1
@@ 72.24(e) and 72.44(d). However, Part 72 licensees would continue t'o use the 1959 dose calculational methodology of ICRP-2 in addressing radiation dose from a design basis accident l
as required in 72.106(b). Thus, licensees would not be able to take advantage of the i
flexibility provided by the dose calculational methodology used in Part 20 when performing design basis accident analyses. Therefore, this alternative was not pursued.
- 2. Amendments of 10 CFR Part 72. In this option, the staff considered preparing a proposed rule to amend the dose limiting design objective in @ 72.106(b) to 5 rem TEDE. This is consistent with the intent of the existing 9 72.106(b), and updates the dose calculational methodology to that which is used for demonstration of compliance with Part 20. Updating the dose calculationg! methodology also would increase the organ dose limit, CDE, from 5 rem to l
C0 rem; allow for the use of risk-based weighting factors for each organ or tissue to determine l
l the 50-year CEDE; and provide licensees with additional flexibility in conducting and submitting design basis accident analyses to demonstrate compliance with the requirements in 9 72.106(b).
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In addition to the increased flexibility provided to licensees, they would no longer need to l
comply with one calculational methodology for their radiation protection programs (i.e., the revised Part 20 methodology) and another methodology for their design basis accident j
analyses.
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. Moreover, design basis accident analyses for ISFSis and MRS installations would use I
.the same dose calculational methodology as design basis accident analyses for a geologic repository operations area (6 60.136(b)). This alternative was chosen by the NRC.
This constitutes the regulatory analysis for this final rule. As discussed above, this rule does not impose any new requirements. L Therefore, there will be no additional cost burden to -
Part 72 licensees or the Federal Government.
Regulatory Flexibility Certification As required by the Regulatory Flexibility Act of 1980,5 U.S.C. 605(b), the Commission certifies that this rule will not have a significant economic impact upon a substantial number of small entitles. The final rule will provide licensees with additional flexibility in conducting and i
submitting design basis accident analyses to demonstrate compliance with the requirements in 6 72.106(b). : In addition, the licensees would no longer need to comply with one calculational
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methodology forJheir radiation protection programs.(i.e., the revised Part 20 methodology) and another methodology for their design basis accident analyses.
The final rule will not impose any additional obligations on entities that may fall within the
' definition of "small entities" as set forth in Section 601(3) of the Regulatory Flexibility Act; or within the definition of "small business" as found in Section 3 of the Small Business Act,
'15 U.S.C. 632; or within the size standards adopted by the NRC on April 11,1995 1
(60 FR 18344).
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Small Business Regulatory Enforcement Fairness'Act in accordance'with the Small Business Regulatory Enforcement Fairness'Act of 1996,
- -the NRC has determined that this action is not a " major rule" and has verified this determination t
with the Office of Information_ and Regulatory Affairs, Office of Management and Budget.
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. 4 Backfit Analysis 1
The NRC has determined that the backfit' rule, 72.62, does not apply to this final rule, and a'backfit analysis is not required, because these amendments do not involve any provisions that would impose backfits as defined in 72.62(a). This final rule does not constitute a backfit under 72.62, because it does not require a change to existing structures, systems, l
components; procedures, or organization. Further, the rule will not result in a more stringent outcome than the existing rule, and therefore, current licensees who are in compliance with the existing rule will got be required to make any changes or take any action. ~ New applicants and license renewal applications will be able to take advantage of some additional flexibility in the dose calculations that is afforded by this rule.-
1 Agreement State implementation issues i
Under the " Policy Statement on Adequacy and Compatibility of Agreement State i
Programs" approved by the Commission on June 30,1997, (62 FR 46517), this rule is classified 1
. as a compatibility Category "NRC." This rule is not required for compatibility and addresses areas of exclusive NRC authority. This area of regulations cannot be relinquished to 9
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e Agreement States pursuant to the Atomic Energy Act and, as such, States should not adopt this regulatiori.
List of Subjects in 10 CFR Part 72 Criminal penalties, Manpower training programs, Nuclear materials, Occupational safety and health, Reporting and recordkeeping requirements, Security measures, Spent fuel.
For the reasons set out in the preamble and under the authority of the Atomic Energy
' Act of 1954, as amended; the Energy Reorganization Act of 1974, as amended; and 5 U.S.C.
553, the Commission is adopting the following amendments to 10 CFR Part 72.
1 PART 72 -- LICENSING REQUIREMENTS FOR THE INDEPENDENT STORAGE OF SPENT NUCLEAR FUEL AND HIGH-LEVEL RADIOACTIVE WASTE a
- 1. The authority citation for Part 72 continues to read as follows:
AUTHORITY: Secs. 51,53,57,62,63,65,69,81,161,182,183,184,186,187,189, 68 Stat. 929, 930, 932, 933, 934, 935, 948, 953, 954, 955, as amended, sec. 234, 83 Stat. 444, as amended (42 U.S.C. 2071,2073,2077,2092,2093,2095,2099,2111,2201,2232,2233, 2234,2236,2237,2238,2282); sec. 274, Pub. L.86-373,73 Stat. 688, as amended (42 U.S.C.
2021); sec. 201, as amended,202,206,88 Stat.1242, as amended, 1244,1246 (42 U.S.C.
5841,5842,5846); Pub. L. 95 601, sec.10,92 Stat. 2951 as amended by Pub. L. 102-486, sec. 7902,106 Stat. 3123 (42 U.S.C. 5851); sec.102, Pub. L.91-190,83 Stat. 853 (42 U.S.C.
4332); secs.131,132,133,135,137,141, Pub. L.97-425,96 Stat. 2229,2230,2232,2241, 10
sec.148, Pub. L.100-203,101 Stat.1330-235 (42 U.S.C.10151,10152,10153,10155,10157, p
10161,1,0168).
Section 72.44(g) also issued under secs 142(b) and 148(c), (d), Pub. L. 100-203,101
- Stat.1330-232,1330 236 (42 U.S.C.10162(b),10168(c), (d)). Section 72.46 also issued under sec.189,68 Stat. 955 (42 U.S.C. 2239), sec.134, Pub. L.97-425,96 Stat. 2230 (42 U.S.C.
l 10154). Section 72.96(d) also issued under sec.145(g), Pub. L.100-203,101 Stat.1330 235 i
(42 U.S.C.10165(g)). Subpart J also issued under secs. 2(2),2(15),2(19),117(a),' 141(h),
Pub. L.97-425, 96 Stat. 2202, 2203, 2204, 2222, 2224 (42 U.S.C.10101,10137(a),10161(h)).
Subparts K and L are also issued under sec.133,98 Stat. 2230 (42 U.S.C.10153) and sec. 218(a), 96 Stat. 2252 (42 U.S.C.10198).
- 2. In 72.104, the introductory sentence of paragraph (a) is revised to read as follows:
l 6 72.104 Criteria for radioactive materials in effluents and direct radiation from an ISFSI or MRS.
l (a) During normal operations and anticipated occurrences, the annual dose equivalent l
l to any real individual who is located beyond the controlled area must not exceed 0.25 mSv 0
(25 mrem) to the whole body,0.75 mSv (75 mrem) to the thyroid and 0.25 mSv (25 mrem) to any other critical organ as a result of exposure to:
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- 3. In @ 72.106, paragraph (b) is revised to read as follows:
6 72.106 Controlled area of an ISFSI or MRS.
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-(b) Any individuallocated on or beyond the nearest boundary of the controlled area may not receive from any design basis accident the more limiting of a total effective dose equivalent
-of 0.05 Sv (5 rem), or the sum of the deep-dose equivalent and the cobmitted dose equivalent to any individual organ or tissue (other than the lens of the eye) of 0.5 SV (50 rem).
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The lens dose equivalent shall not exceed 0.15 Sv (15 rem) and the shallow dose equivalent to L-s, kin or to any extremity shall not exceed 0.5 Sv (50 rem). The minimum distance from the spent fuel or high-level radioactive waste handling and storage facilities to the' nearest boundary
.i of the controlled area must be at least 100 meters.
9 Dated at Rockville, Maryland, this 2 V day of -
1998.
For the Nuclear Regulatory Commission.
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b L. Joseph Ca lla
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Executive Dii r for Operations.
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RELEASE TO PDR g y[:I' i 1 11/03^98 - P:\\DISRTLIS.DMS