ML023380395
| ML023380395 | |
| Person / Time | |
|---|---|
| Site: | Pilgrim |
| Issue date: | 11/22/2002 |
| From: | Entergy Nuclear Generation Co |
| To: | Office of Nuclear Reactor Regulation |
| References | |
| -RFPFR | |
| Download: ML023380395 (40) | |
Text
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Emergency Plan Implementing Number I
PNPS Procedure Manual I
N/A RType H8.24 TABLE OF CONTENTS J
Number EP-IP-100 EP-IP-100.1 EP-IP-200 EP-IP-201 EP-IP-202 EP-IP-210 EP-IP-220 EP-IP-225 EP-IP-229 EP-IP-230 EP-IP-231 EP-IP-240 EP-IP-250 EP-IP-251 EP-IP-252 EP-IP-253 EP-IP-254 EP-IP-259 EP-IP-300 EP-IP-310 EP-IP-315 EP-IP-330 Effective Revision Date Title Emergency Classification and Notification Emergency Action Levels (EALs)
On-Call Emergency Director Emergency Plant Manager Company Spokesperson Control Room Augmentation TSC Activation and Response Severe accident Management Support TSC/OSC Equipment Operation OSC Activation and Response Onsite Radiation Protection Emergency Security Organization Activation and
Response
EOF Activation and Response Offsite Radiation Protection Facilities Support Relocation of the EOF Communications Support EOF Equipment Operation Offsite Radiological Dose Assessment Radiation Monitoring Team Activation and Response Personnel Monitoring Team Activation and Response Core Damage 20 0
10 3
3 8
11 0
5 4
6 10 9
5 8
3 3
4 4
5 4
4 11/22/2002 Page 1 of 2 Revision 80 08/29/02 08/29/02 08/29/02 08/29/02 02/07/01 08/29/02 11/15/00 02/15/02 07/25/00 08/08/01 08/29/01 08/29/02 02/07/01 12/26/00 08/29/02 07/13/00 05/20/02 09/17/01 05/01/01 11/22/02 05/24/00 12/10/01 Revision 80 Page 1 of 2 11/22/2002
I Emergency Plan Implementing Number. N PNPS Procedure Manual Nb
/
RType H8.24
.U TABLE OF CONTENTS Title Protective Action Recommendations Evacuation/Assembly Search and Rescue Emergency Exposure Controls Transport of Contaminated Injured Personnel Transition and Recovery Effective Revision Date 9
5 3
7 3
5 10/03/01 09/17/01 02/12/01 11/22/02 05/24/00 02/07/01 11/22/2002 Page 2 of 2 Revision 80 Number EP-IP-400 EP-IP-410 EP-IP-420 EP-IP-440 EP-I P-501 EP-IP-520
- K,.."
Revision 80 Page 2 of 2 11/22/2002
RTYPE H8.24 PILGRIM NUCLEAR POWER STATION Procedure No. EP-IP-310 RADIATION MONITORING TEAM ACTIVATION AND RESPONSE Stop Think
- Act Review SAFETY RELATED EP-IP-310 Rev. 5
REVISION LOG REVISION 5
Pages Affected 5,8,11,13 14 REVISION 4 Pages Affected All 8
Date Originated 10102 Description Delete references to specific brands and types of instruments as some equipment was replaced. This will prevent need to revise Procedure for future changes to vendorslsuppliers.
Revise title of EP-IP-251 in Attachment 4 (Document Cross-Reference).
Date Originated 9100 Description Revise Procedure to reflect PNPS 1.3.4-1 format. Revision bars are not shown for reformatting.
Correct editorial reference to "Rad Lab and RMT Coordinator."
EP-IP-310 Rev. 5 Page 2 of 15
TABLE OF CONTENTS PaQe 1.0 PURPOSE.....................................................................................................................
4
2.0 REFERENCES
4 3.0 DEFINITIONS.......................................................................................................
4 4.0 DISCUSSION.......................................................................................................
4 5.0 RESPONSIBILITIES...............................................................................................
4 6.0 PROCEDURE.......................................................................................................
5 6.1 RMT ACTIVATION.........................................................................................
5 6.2 EQUIPMENT CHECKS AND INVENTORY....................................................
5 6.3 OFFSITE MONITORING..............................................................................
6 6.4 SURVEYS......................................................................................................
7 6.5 TEAM DEACTIVATION................................................................................
9 S
7.0 RECORDS..................................................................................................................
10 8.0 ATTACHMENTS....................................................................................................
10 ATTACHMENT 1 - RMT EQUIPMENT CHECKLIST........................................................
11 ATTACHMENT 2 - RMT VEHICLE/COMMUNICATIONS CHECKLIST............................
12 ATTACHMENT 3 - RMT SAMPLE/SURVEY SHEET........................................................
13 ATTACHMENT 4 - DOCUMENT CROSS-REFERENCE..................................................
14 ATTACHMENT 5 - IDENTIFICATION OF COMMITMENTS.............................................
15 EP-IP-310 Rev. 5 Page 3 of 15
1.0 PURPOSE j
This Procedure provides instructions to Radiation Monitoring Team (RMT) members assigned to the Emergency Operations Facility (EOF). The RMTs will ascertain the radiological conditions in the environment during an emergency situation. The survey results obtained will help to determine and verify the protective action recommendations for the general public.
2.0 REFERENCES
[1]
EP-PP-01, "PNPS Emergency Plan" 3.0 DEFINITIONS None 4.0 DISCUSSION None 5.0 RESPONSIBILITIES
[1]
The Rad Lab and RMT Coordinator is responsible for:
(a)
Dispatching and directing the Radiation Monitoring Teams.
(b)
Reporting directly to the Offsite Radiological Supervisor all survey and sample results obtained by the Radiation Monitoring Teams.
[2]
The Radiation Monitoring Teams are responsible for:
(a)
Directly monitoring radiological conditions in the environs as directed by the Rad Lab and RMT Coordinator.
EP-IP-310 Rev. 5 Page 4 of 15
6.0 PROCEDURE 6.1 RMT ACTIVATION When the Emergency Operations Facility (EOF) is to be activated, upon arrival the Radiological Monitoring Teams shall:
[1]
Obtain team assignments and designation from the Rad Lab and RMT Coordinator.
If the Rad Lab and RMT Coordinator is not present, pair up in RP Technician/Driver Teams.
[2]
Sign in on the EOF Manpower status board.
[3]
Obtain an RMT procedure packet from the procedure cabinet.
[4]
When all checks and inventories according to Section 6.2 have been completed, report to the Rad Lab and RMT Coordinator for the dispatch briefing.
NOTES
- 1.
The key to the Field Logistics area is located in the key box outside the door. The combination to the padlock is 000.
- 2.
The keys to the RMT vehicles are located in the key box inside the security area.
6.2 EQUIPMENT CHECKS AND INVENTORY
[1]
Instrument Checks (a)
Obtain a set of instruments.
(b)
Perform the necessary instrument checks. Conduct physical checks, calibration checks, battery checks, and source checks as appropriate.
(c)
Verify operability of each type of air sampler.
(d)
Record the equipment checks as listed on Attachment 1 (RMT Equipment Checklist).
[2]
Field Kit Checks (a)
Obtain an RMT field kit from the Field Logistics area.
(b)
If the seal on the kit has been broken, then inventory the field kit.
(c)
Obtain a package of silver zeolite cartridges from the cabinet in the Field Logistics area.
EP-IP-310 Rev. 5 Page 5 of 15
(d)
Synchronize watches with the EOF clock.
(e)° Distribute thermoluminescent dosimetry (TLD) and self-indicating dosimetry (SID) to each team member.
(f)
Record name and Social Security number on the TLD. Don the TLD.
(g)
Zero and don the SID.
(h)
Record the results of the field kit inventory on Attachment I (RMT Equipment Checklist) (inventory is "SAT" if seal is intact).
[3]
Vehicle Checks (a)
Obtain a set of keys for an RMT vehicle.
(b)
Perform the vehicle checks in accordance with Attachment 2 (RMT Vehicle/Communications Checklist).
[4]
Communications Checks (a)
Obtain a portable radio from the Field Logistics area.
(b)
Verify communications with the EOF by testing the equipment listed on (RMT Vehicle/Communications Checklist).
NOTE RMTs are not to proceed from the EOF without a full briefing by the Rad Lab and RMT Coordinator or Offsite Radiological Supervisor.
6.3 OFFSITE MONITORING
[1]
Continuously observe radiation levels while traveling.
[2]
While operating inside a radiation field, periodically check the SID reading. If it becomes necessary to re-zero the SID, ensure the final and new initial values are reported to the Rad Lab and RMT Coordinator.
[3]
Boundary information on the leading edge, trailing edge, and outer edges of the plume should be relayed to the Rad Lab and RMT Coordinator when available.
EP-IP-310 Rev. 5 Page 6 of 15
6.4 SURVEYS
[1]
Surveys taken in the early stages of an accident will be primarily involved with plume assessment and tracking.
NOTE Radiation and airborne surveys reported to the EOF for use in dose assessment should be centerline values. Survey data reported to the EOF is recorded on Attachment 3 (RMT Sample/Survey Sheet).
[2]
Radiation Surveys (a)
Using the dose rate meter, perform and record the survey at waist level with the beta window closed.
(b)
Using the dose rate meter, perform and record the survey at waist level with the beta window open.
(c)
Using the dose rate meter, perform and record the survey at ground level with the beta window open.
(d)
Report radiation levels to the Rad Lab and RMT Coordinator. Record all information on Attachment 3 (RMT Sample/Survey Sheet).
[3]
Airborne Surveys (a)
Load a silver zeolite cartridge, arrow pointing in the direction of the air flow, into the sample apparatus.
(b)
Place the air sampler 3 to 4 feet off the ground.
NOTE Exceeding a 2 SCFM flow rate may give erroneous iodine concentration levels.
(c)
Draw a 20 cu. ft. air sample (2 SCFM for 10 minutes) unless otherwise directed by the EOF.
(d)
Continue to monitor radiation levels while sampling. Record and report any significant changes.
(e)
After the sample has been obtained, record the start time, stop time, and sample flow rate on Attachment 3 (RMT Sample/Survey Sheet).
EP-IP-310 Rev. 5 Page 7 of 15
(f)
Proceed to an area of low background for counting of the sample. Monitor and report radiation levels while tracking plume boundaries.
(g)
Particulate Filter Field Analysis (1)
Determine background using a count rate meter with an HP-210 probe (or equivalent).
(2)
Count the particulate filter.
(3)
Store the particulate filter in a sealed petri dish. Mark the dish with the appropriate sample number and record all information on Attachment 3 (RMT Sample/Survey Sheet).
(h)
Iodine Cartridge Field Analysis (1)
Connect the Nal probe to the E-600 (or equivalent).
(2)
Turn the function switch to the scaler position.
NOTE Avoid using the E-600 in high background locations (e.g., 2 to 5 mR/hr). Contact Rad Lab and RMT Coordinator if background count rates exceed 40,000 cpm for a 1-minute count time.
Rad Lab and RMT Coordinator should recommend another counting location (i.e., one with a lower background).
(3)
Perform a 1-minute background count by pressing the,*, button located on the E-600 handle.
(4)
Place the iodine cartridge in a sample bag and record its dose rate.
(5)
Place the sample bag next to the detector ensuring that the flow arrow is pointing away from the face of detector.
(6)
Count the sample for 1 minute by pressing the -,*,, button.
(7)
Remove and label the sample. Record all information on Attachment 3 (RMT Sample/Survey Sheet).
(8)
Perform another background count by pressing the -*- button. Notify the EOF if background has changed by more than a factor of two. Recount the sample and verify background as directed ýby the EOF.
(i)
Record all data on Attachment 3 (RMT Sample/Survey Sheet) and report the results to the Rad Lab and RMT Coordinator.
EP-IP-310 Rev. 5 Page 8 of 15
6.5 TEAM DEACTIVATION When told to deactivate by the Rad Lab and RMT Coordinator, the RMTs shall:
[1]
Return to the EOF and transfer all samples to the Rad Lab and RMT Coordinator.
NOTE Vehicle air cleaners could have high dose rates.
[2]
Survey the RMT vehicles. Pay particular attention to the wheel wells, air cleaner, and door handles.
[3]
Remove any anti-contamination clothing (as applicable) and perform a whole body frisk.
[4]
Report any contamination found to the Rad Lab and RMT Coordinator and await further instructions.
[5]
Debrief with the Rad Lab and RMT Coordinator. Ensure at least the following is done:
(a)
All survey records are turned in.
(b)
All checks and inventories are turned in.
(c)
Any procedural problems are reported.
(d)
Any equipment problems are reported.
(e)
All applicable exposure records are correct and current.
[6]
Inventory and restock the field kits.
[7]
Clean out the RMT vehicles and refill the fuel tank.
EP-IP-310 Rev. 5 Page 9 of 15
7.0 RECORDS The following documents are generated as a result of the implementation of this Procedure:
RMT Equipment Checklist RMT Vehicle/Communications Checklist RMT Sample/Survey Sheet The completed documents are to be turned in to the Rad Lab and RMT Coordinator in the EOF.
8.0 ATTACHMENTS ATTACHMENT 1 - RMT EQUIPMENT CHECKLIST ATTACHMENT 2 - RMT VEHICLE/COMMUNICATIONS CHECKLIST ATTACHMENT 3 - RMT SAMPLE/SURVEY SHEET ATTACHMENT 4 - DOCUMENT CROSS-REFERENCE ATTACHMENT 5 - IDENTIFICATION OF COMMITMENTS EP-IP-310 Rev. 5 Page 10 of 15
ATTACHMENT 1 Sheet 1 of I I
RMT EQUIPMENT CHECKLIST DATE:
Ion Chamber Type:
Serial No.:
Cal Due:
Source Check:
Beta Corr. Factor:
Analyzer with Nal probe Type:
Serial No.:
Cal Due:
Efficiency:
HP-210 Probes (2)
Serial No.:
Cal Due:
Air Sampler Type:
Serial No.:
f.*
'l fli.-
Dose Rate Meter Type:
Serial No.:
Cal Due:
Source Check:
Count Rate Meter Type:
Serial No.:
Cal Due:
Source Check:
Serial No.
Cal Due:
Air Sampler Type:
Serial No.:
Cal Due:
Instrument Check(s):
(SAT/UNSAT)
Kit Inventory:
(SAT/UNSAT)
Comments:
EP-IP-310 Rev. 5 Page 11 of 15 TEAM:
TEAM MEMBERS:
I I I I I I
ATTACHMENT 2 Sheet 1 of 1 RMT VEHICLE/COMMUNICATIONS CHECKLIST TEAM:
Vehicle No.:
Fuel Level (fill if < 1/2)
Vehicle Lights Spotlights Emergency (Strobe) Lights Power Inverter Spare Tire Winch Condition of Tires Battery Parallel DATE:
(Check)
(Operates)
(Operates)
(Operates)
(Operates)
(Check)
(Operates)
(Sat/Unsat)
(Operates)
Communications Vehicle Radio Portable Radio Cellular Telephone (Operates)
(Operates)
(Operates)
Vehicle Check:
Sat/Unsat)
Communications Check:
(Sat/Unsat)
COMMENTS:
EP-IP-310 Rev. 5 Page 12 of 15
ATTACHMENT 3 Sheet 1 of 1 RMT SAMPLE/SURVEY SHEET TEAM:
Sample No.:
Detailed Location:
DATE:
Radiation Survey Survey Time:
Dose Rate (Closed Window waist high):
Dose Rate (Open Window waist high):
Dose Rate (Open Window 2" off ground):
Airbor Sample Start Time:
Sample Stop Time:
Sample Flow Rate:
Cartridge Dose Rate:
Frisker
Background:
Particulate Filter Count Rate:
Initial E-600/Nal
Background:
Iodine Cartridge Count Rate:
Final E-600/Nal
Background:
A)
B) mR/hr C) mR/hr D) mR/hr ne Activity Survey E)
F)
G)
CFM H) mR/hr I) cpm J) cpm K) cpm L) cpm M) cpm COMMENTS:
Note if survey/sample was not taken at plume centerline or large variances in background occurred while sampling.
EP-IP-310 Rev. 5 Page 13 of 15 I
ATTACHMENT 4 Sheet I of 1 DOCUMENT CROSS-REFERENCE This Attachment lists those documents, other than References, which may be affected by changes to this Procedure.
Document Number Document Title EP-IP-251 Offsite Radiation Protection EP-IP-310 Rev. 5 Page 14 of 15
ATTACHMENT 5 Sheet 1 of I IDENTIFICATION OF COMMITMENTS This Attachment lists those external commitments (i.e., NRC commitments, QA audit findings, and INPO inspection items) implemented in this Procedure.
EP-IP-310 Rev. 5 Page 15 of 15 I
RTYPE H8.24 PILGRIM NUCLEAR POWER STATION Procedure No. EP-IP-440 EMERGENCY EXPOSURE CONTROLS Stop Think Act Review SAFETY RELATED EP-IP-440 Rev. 7
REVISION LOG REVISION 7
Pacqes Affected 5
7 11 REVISION 6
Pa-ges Affected All 3,13,14 10,12 11 12 Date Originated 10102 Description Correct the TEDE definition.
Add TEDE in Step 6.2[2] to clarify dose category.
Replace reference to SAM-1 1 with Nal equipped E-600 or equivalent.
Date Originated 5101 Description Reformat to reflect PNPS 1.3.4-1. Revision bars are not shown for reformatting.
Add "Dose Card" to title of Attachment 1.
Change "Boston Edison Medical Director" to "Entergy Medical Department".
Change "Chemical Engineer" to "Core Damage Engineer".
Add reference to supplies of KI stored with the Medical Department.
Clarify verbiage of instruction to individual regarding continued administration of KI.
EP-IP-440 Rev. 7 Page 2 of 21
TABLE OF CONTENTS Page 1.0 P U R P O S E.....................................................................................................................
4
2.0 REFERENCES
4 3.0 D EFINITIO N S......................................................................................................
4 4.0 D IS C U S S IO N................................................................................................................
5 5.0 R ESPO NSIBILITIES.................................................................................................
6 6.0 PRO CEDU RE......................................................................................................
6 6.1 DOSES < THE LOWER EMERGENCY EXPOSURE LIMITS........................ 6 6.2 DOSES > THE LOWER EMERGENCY EXPOSURE LIMITS........................ 7 6.3 EMERGENCY EXPOSURE DOCUMENTATION...........................................
8 6.4 POSTEXPOSURE EVALUATION....................................................................
10 6.5 ADMINISTRATION OF POTASSIUM IODIDE (KI).........
10 7.0 R E C O R D S..................................................................................................................
13 8.0 ATTACHMENTS 13 ATTACHMENT 1 - EXAMPLE - EMERGENCY WORKER EXPOSURE "RECORD/DOSE CARD 14 ATTACHMENT 2 - EMERGENCY RADIOLOGICAL CONTROLS FORM......................... 15 ATTACHMENT 3 - EMERGENCY VOLUNTEER ACKNOWLEDGMENT FORM.............. 16 ATTACHMENT 4 - HALOGEN CONCENTRATION WORKSHEET..!.....................................
17 ATTACHMENT 5 - POTASSIUM IODIDE ADMINISTRATION FORM..............................
18 ATTACHMENT 6 - DOCUMENT CROSS-REFERENCE..................................................
20 ATTACHMENT 7 - IDENTIFICATION OF COMMITMENTS............................................
21 EP-IP-440 Rev. 7 Page 3 of 21
1.0 PURPOSE This Procedure provides guidelines and administrative controls for radiation exposure received by PNPS controlled emergency workers during the course of a declared emergency.
2.0 REFERENCES
[1]
Environmental Protection Agency, EPA-400-R-92-001, Manual of Protective Action Guides and Protective Actions for Nuclear Incidents
[2]
EP-PP-01, "PNPS Emergency Plan"
[3]
International Atomic Emergency Agency (IAEA), Technical Report No. 152, Evaluation of Radiation Emergencies and Accidents
[4]
National Council on Radiation Protection (NCRP) Report 39, Basic Radiation Protection Criteria 15]
National Council on Radiation Protection (NCRP) Report 55,:Protection of the Thyroid.
Gland in the Event of Releases of Radioiodine
[6]
The Food and Drug Administration Approved Patient Package Insert for Commercially Packaged Potassium Iodide 3.0 DEFINITIONS
[1]
Corrective Action - Includes surveillance and/or assessment actions and plant operations necessary to minimize further deterioration of the 'level of plant safety or to mitigate the consequences of the accident, if failure to perform these actions could result in a significant increase in offsite exposures.
[2]
Emergency Exposure - Radiation exposure received by an emergency worker conducting accident mitigating or life saving actions during aldeclared emergency.
EP-IP-440 Rev. 7 Page 4 of 21
Emerqency Exposure Limits Dose Limit*
Activity All Protecting valuable property.
Life saving or protection of large populations.
Life saving or protection of large populations.
Conditions Lower dose not practical.
Lower dose not practical.
Only on a voluntary basis to persons fully aware of the risks involved.
- EPA TEDE values for nonpregnant adults from exposure anid intake during an emergency situation in rem. Workers performing services during emergencies should limit dose to the eyes to three times the listed value and dose to any other organ (including skin and body extremities) to ten times the listed value.
[4]
Emergqency Worker - An individual who holds an emergency response function as indicated by the PNPS Emergency Plan during a declared emergency.
i
[5]
Life Savingq Action - Actions related to the search for and rescue of injured persons, or corrective or protective actions to mitigate conditions which could result in imminent injury or substantial overexposure to an individual.
[6]
Total Effective Dose Equivalent (TEDE) - Sum of the external Deep Dose Equivalent (DDE) and the internal Committed Effective Dose Equivalent (CEDE).
4.0 DISCUSSION None EP-IP-440 Rev. 7 Page 5 of 21
[3]
5 10 25
> 25
5.0 RESPONSIBILITIES
[1]
The Emergency Director (ED), or the Emergency Plant Manager (EPM) when delegated, is responsible for the authorization of:
(a)
Individual dose in excess of the lower emergency exposure limits.
(b)
The administration of potassium iodide (KI).
[2]
The Onsite and Offsite Radiological Supervisors are responsible for:
(a)
Tracking dose received by the emergency workers during the course of the emergency.
(b)
Ensuring that proper emergency exposure guidelines are followed by emergency workers.
(c)
Evaluating, recognizing, and recommending the need for KI.
6.0 PROCEDURE 6.1 DOSES < THE LOWER EMERGENCY EXPOSURE LIMITS,
[1]
Individual exposure received over the course of the emergency shall be recorded and documented in accordance with Section 6.3.
[2]
From the time an emergency is declared, ERO personnel are considered emergency workers. Emergency workers are allowed to receive the following exposure over the course of the emergency, exclusive of previous exposure and without special authorization:
(b) 15 rem to the eyes.
(c) 50 rem to the skin, thyroid, and extremities.
[3]
Radiation exposures to emergency personnel shall be maintained, when possible, within the PNPS administrative exposure guides.
[4]
In order to maintain personnel exposures as low as possible, methods used during normal Station operation to control and minimize exposures,isuch as ALARA (As Low As Reasonably Achievable), shall remain in force during an emergency condition to the degree consistent with timely implementation of emergency measures.
[5]
To assure adequate protection of minors and the unborn during emergencies, the performance of emergency-activities should be limited to nonpregnant adults.
EP-IP-440 Rev. 7 Page 6 of 21
6.2 DOSES > THE LOWER EMERGENCY EXPOSURE LIMITS *
[1]
Individual exposure received over the course of the emergency shall be recorded and documented in accordance with Section 6.3.
[2]
Prior ED/EPM approval must be given for all emergency exposures anticipated to exceed 5 rem TEDE or to cause an individual to have accumulated greater than 5 rem TEDE over the course of the emergency.
[3]
Pre-Exposure Evaluation: Consideration of the following guidelines shall be given prior to authorizing doses greater than the lower exposure limits:
(a)
The risk of not performing the task shall be evaluated against the anticipated exposure.
(b)
Dosimetry equipment capable of measuring the anticipated maximum exposure and type of radiation shall be worn by personnel receiving emergency exposures.
I (c)
Personnel shall not enter any area where dose rates are unmonitored or immeasurable.
(d)
Where practical, all attempts shall be made to keep emergency exposures ALARA (for example, use of protective clothing, respiratory protection, thyroid blocking agent).
[4]
Personnel undertaking any emergency operation in which the dose will exceed 25 rem to the whole body shall be identified by signature on the Emergency Volunteer Acknowledgment Form (Attachment 3) and should:
(a)
Do so only on a voluntary basis.
"(b)
Be more than 45 years of age.
(c)
Be made fully aware of the risks involved, including the numerical levels of dose at which acute effects of radiation exposure will be incurred and numerical estimates of the risks of delayed effects.
EP-IP-440 Rev. 7 Page 7 of 21
6.3 EMERGENCY EXPOSURE DOCUMENTATION ký/;
[111 Emergency exposure documentation for ERO personnel shall be maintained by the Onsite and Offsite Radiological Supervisors (as applicable). individual exposures will be recorded on Attachment 1 or other similar form to ensure adequate documentation and tracking during the course of the emergency.
[2]
Activities in support of emergency efforts which involve emergency exposure must include a radiological briefing and will be documented through a Radiation Work Permit (RWP) or on an Emergency Radiological Controls Form (Attachment 2).
[3]
Radiological controls determined to be necessary for a task conducted during the emergency are documented on Attachment 2 as follows:
(a)
Task Assiqnment: The task, number, location, and date are copied from the OSC Team Task Assignment Sheet or completed as appropriate (for tasks such as RMT dispatch).
(b)
Task Exposure (Individual) Estimate: The maximum expected dose to any single member of the team. Team members are instructed to either contact the team coordinator or to return prior to exceeding this dose. Consideration shall be given to the benefit of performing the task versus the exposure to be received by personnel when this value has been determined.
I (c)
Task Dose Rate Limit: The maximum expected whole body dose rate. Team members are to fall back to an area of lower dose rate and contact the team coordinator or return when this limit is encountered.
(d)
Dosimetry: Describes any requirements beyond a TLD and SID. A TLD and SID are automatic requirements for all tasks involving radiological controls.
(e)
PCs and Respiratory Protection: Denotes the necessary protective clothing and equipment required for the task.
EP-IP-440 Rev. 7 Page 8 of 21 NOTE Although it is preferable to document radiological controls prior to dispatching individuals on emergency related tasks, radiological controls and precautions may, be provided verbally and documented as soon as possible thereafter.
NOTE Prior ED/EPM approval must be given for all emergency exposures anticipated to cause an individual to have accumulated greater than 5 rem over the course 6f the emergency.
I
(f)
Sugqgested Route: Best or preferred route to the task site or the sequence to follow for tasks conducted at multiple locations.
(g)
Anticipated Conditions: Radiation, contamination, and airborne conditions.
Values need not be provided for tasks which could be hindered by stopping to conduct contamination and airborne surveys. When air sampling is required, ensure guidance is provided regarding:
(1)
Sample location(s).
(2)
Sample volume (collection time and flow rate).
(3)
Analysis or counting method to be used.
(4)
Actions for high exposure rates on collected samples.
(h)
Survey Equipment and Maps: Describes any radiological equipment and logs or maps used to conduct surveys performed as part of or during the task.
(i)
Special Instructions: Describes any additional radiological information or instructions necessary to the task.
[4]
Task Exposure: The task exposure section is used to identify the individuals assigned to and track exposure received during conduct of the task. Current emergency dose will be checked against the task exposure estimate prior to teamldispatch to ensure no exposure limits are exceeded without proper authorization.
NOTE Although it is preferable to document authorization prior to tasks which allow extended exposure, authorization may be granted verbally and documented as soon as possible thereafter.
[5]
Extended Exposure: The extended exposure section provides authorization by the Emergency Director (or Emergency Plant Manager for onsite ERO personnel when delegated) prior to activities which would result in doses greater than the lower emergency limits.
(a)
If the task exposure estimate exceeds 5 rem or the task exposure will result in an individual's emergency exposure exceeding 5 rem, an extended limit must be determined and authorized.
(b)
Extended emergency exposures for life saving or protection of large populations anticipated to exceed 25 rem must include additional briefing and documentation in accordance with the Emergency Volunteer Acknowledgment Form (Attachment 3).
EP-IP-440 Rev. 7 Page 9 of 21 N
6.4 POSTEXPOSURE EVALUATION
[1]
EPA-400 specifies that emergency exposures received during an emergency are considered a once-in-a-lifetime exposure and are not added to occupational exposure accumulated under nonemergency conditions.
[2]
10CFR20 specifies doses received during emergencies must be subtracted from the limits for Planned Special Exposures that the individual may receive during the current year and during the individual's lifetime.
[3]
Individuals receiving doses beyond the lower exposure limits'shall be restricted from further occupational (nonemergency) radiation exposure pending the outcome of exposure evaluations and medical surveillance.
[4]
The Entergy Medical Department shall be contacted for follow-up care and further evaluation, as required.
6.5 ADMINISTRATION OF POTASSIUM IODIDE (KI)
[1]
The Emergency Director or the Emergency Plant Manager shall be responsible for authorizing the administration of KI to PNPS emergency workers.
NOTE KI is 90% effective in blocking the uptake of radioiodine by the thyroid if administered within the first hour of uptake, and is 50% effective if administered within 4 hours4.62963e-5 days <br />0.00111 hours <br />6.613757e-6 weeks <br />1.522e-6 months <br /> after uptake.
Almost no benefit will be obtained if KI is administered 10 to 14 hours1.62037e-4 days <br />0.00389 hours <br />2.314815e-5 weeks <br />5.327e-6 months <br /> after exposure; therefore, it shall not be administered after such a duration.
[2]
KI should be considered as a potential dose reducing option for any situation in which airborne radioactive iodine is present (an additional ALARA option).
[3]
Dose Determination: KI should be administered to emergency workers if by calculation, measurement, or estimation the total dose to the thyroid will exceed 50 rem.
i (a)
The isotopic halogen concentrations must be determin!ed before a thyroid dose can be estimated. Concentrations can be determined by direct measurement of each isotope or by estimations based on a known 1-131 concentration.
(1)
Concentration estimations can be determined as follows:
By the use of the Halogen Concentration Worksheet (Attachment 4).
0 Through the use of the Excel spreadsheet file SAMPLE. SAMPLE is loaded on the TSC core damage compute'r and the EOF dose assessment computers.
EP-IP-440 Rev. 7 Page 10 of 21
(2)
When estimated concentrations are used, the estimations should be confirmed by direct measurement as soon as practical.
(3)
The sample data and calculation sections are used to determine 1-131 activity if an Nal equipped E-600 (or equivalent) is used to analyze the 1-131 concentration. Otherwise, the 1-131 concentration can be entered directly.
(4)
Accident type is determined by the Reactor or Core Damage Engineer in the TSC. If the accident type is unknown, assume a gap release.
(b)
Thyroid dose can be estimated from isotopic concentrations (in tCi/cc) as follows:
(1)
Direct Calculation Thyroid Dose, = Concentration, x DCFP x-x e"-j. t +
DCF (rem
- cm3 Isotope D
'Ci *'hr )(hr
- 1) 1-131 1.3E+06 3.59E-031 1-132 7.7E+03 3.01 E-01:
1-133 2.2E+05 3.33E-02, 1-134 1.3E+03 7.88E-01'
,1 1-135 3.8E+04 1.05E-01 Te-132 2.9E+05 8.86E-03, Where t = exposure period in hours.
Total thyroid dose is the sum of the individual doses from each of the isotopes above.
(2)
Through the use of the Excel spreadsheet file titled SAMPLE. SAMPLE is loaded on the TSC core damage computer and the EOF dose assessment computers.
(3)
Through the use of the dose assessment computer application titled DAPAR. DAPAR is loaded on computers in the Control Room and the EOF.
EP-IP-440 Rev. 7 Page 11 of 21
[4]
Issuing KI: The Onsite Radiological Supervisor or the Offsite Radiological Supervisor, as applicable, shall:
NOTE The Emergency Director or the Emergency Plant Manager is responsible for authorizing the administration of KI to PNPS emeraencv workers.
(a)
Ensure approval and documentation are recorded on the Potassium Iodide Administration Form (Attachment 5).
Indviual wo aveknwnCAUTION Individuals who have known allergies to iodide shall NOT be issued KI.
(b)
Notify those who are to receive KI to report to a designated location for distribution.
(c)
Issue one 130 mg KI tablet to each individual who is to receive KI. KI is stored in the OSC Medical locker and in the EOF Medical locker. Additional supplies are also located in the Medical Department.
(d)
Contact the Entergy Medical Department and request follow-up care and further guidance concerning KI administration.
(e)
Instruct individuals to take one 130 mg KI tablet daily for 10 days or as directed by the Entergy Medical Department and record each issuance on the Potassium Iodide Administration Form (Attachment 5).
EP-IP-440 Rev. 7 Page 12 of 21
7.0 RECORDS
[1]
The following documents may be generated by the implementation of this Procedure:
(a)
Emergency Worker Exposure Record (b)
Emergency Radiological Controls Form (c)
Emergency Volunteer Acknowledgment Form (d)
Halogen Concentration Worksheet (e)
Potassium Iodide Administration Form
[2]
Completed documents shall be collected by the Onsite Radiological Supervisor or the Offsite Radiological Supervisor, as applicable, who reviews and submits all records to the Emergency Preparedness Superintendent.
8.0 ATTACHMENTS ATTACHMENT 1 - EXAMPLE - EMERGENCY WORKER EXPOSURE RECORD/DOSE CARD ATTACHMENT 2-EMERGENCY RADIOLOGICAL CONTROLS FORM ATTACHMENT 3 - EMERGENCY VOLUNTEER ACKNOWLEDGMENT FORM ATTACHMENT 4 - HALOGEN CONCENTRATION WORKSHEET ATTACHMENT 5 - POTASSIUM IODIDE ADMINISTRATION FORM ATTACHMENT 6 - DOCUMENT CROSS-REFERENCE ATTACHMENT 7 - IDENTIFICATION OF COMMITMENTS EP-IP-440 Rev. 7 Page 13 of 21
I ATTACHMENT 1 Sheet 1 of I EXAMPLE - EMERGENCY WORKER EXPOSURE RECORD/DOSE CARD LAST FIRST M I.
NAME:
SLOT #
SID SERIAL #
DATE:
AVAILABLE DOSE SID SID TASK TOTAL TASK #
IN OUT DOSE DOSE EP-IP-440 Rev. 7 Page 14 of 21
EMERGENCY RADIOLOGICAL CONTROLS FORM ATTACHMENT 2 Sheet 1 of 1 Location:
Date Task Exposure Task Dose Rate Dosimetry (rLD and S1D a minimu)
(Individual) Estimate:
'Limit:
Protective Clothing & Respiratory Protection:
0- None L
Cotton Liners 0
Lab Coat 0i Full Face Part Other (see below)
Rubber Gloves El Full PCs LI Full Face Part/lod LIOhr(seblw Shoe Covers Rubbers SCBA Suggested Route:
Anticipated Conditions:
Enroute At Location Radiation (mR/hr)
Contamination Airborne Survey Equipment and Maps:
Special Instructions (attach additional pages if necessary):
Team Member Name Current SID Dose SID Dose Task Dose Emergency Dose In Out Task Requires an Individual's Emergency Exposure to Exceed 5 Rem:
E3 No Q] Yes Extended Limit:i Authorization Time:
EP-IP-440 Rev. 7 Page 15 of 21 Tak No:
I
A EMERGENCY VOLUNTEER ACKNOWLEDGMENT FORM TTACHMENT 3 Sheet 1 of 1 A
S I
I1LT...
jLocation:
-ealthEffectsassociated wflth'Whole Body'Absorbed DoesL>-'<o..
"p 6Rdved Withina FeW Hours.(AcMte Dose)
Dose (Pad)
% Precursory Effectsb
% Early Fatalitiesc 50 2
100 15 1
140 5
150 50 200 85 t
15 250 98 300 50 400 85 460 I
95 a Risks will be lower for protracted exposures.
b Forewarning symptoms of more serious health effects associated with large doses of radiation.
c Supportive medical treatment may increase the dose at which these frequencies occur by approximately 50 percent.
Age at Exposure (years)
Approximate risk of premature death Average years of life lost if (deaths per 1000 persons exposed) premature death occurs (years) 20 to 30 9.1 1
24 30 to 40 7.2 i
19 40to50 5.3 I
15 50 to 60 3.5 11 I have been briefed on the radiological consequences and hazards associated with the authorized emergency exposure, and I have volunteered to perform the task described.
Name:
Signature:
Date:
Signature:
Signature:
Signature:
Date:
Date:
Date:
Note:
Detailed information for the above tables is located in Appendix B and Appendix C of EPA-400 EP-IP-440 Rev. 7 Page 16 of 21 Pnroiiiate k
Averaierendividuals from25 Rem Acute Exposure...,ý--
Name:
Name:
Name-I Task:
C ATTACHMENT 4 Sheet 1 of I HALOGEN CONCENTRATION WORKSHEET Halogen Concentration Worksheet Calculations Performed By Name:
Date:
S Dw Gross Sample Count Rate (CPM)
A.
Background Count Rate #1 (CPM) B.
Background Count Rate #2 (CPM) C.
Meter Efficiency (%)
D.
Sample Duration (min)
E.
Sample Flow (scfmn)
F:
Time After Shutdown (hrs)
G:_
Accident Type (G or M)
H:
0 O4 (4
0 1.45 2.09 2.31 1.95 0.01 12.63 1
1.45 2.05 1.63 1.76 0.01 12.54 2
1.44 2.00 0.96 1.59 0.01 12.47 3
1.44 1.94 0.52 1.44 0.01 12.41 4
1.43 1.89 0.26 1.30 0.01 12.34 5
1.43 1.83 0.13 1.17 0.01 12.28 6
1.43 1.78 0.06 1.06 0.01 12.21 7
1.42 1.73 0.03 0.96 0.01 12.15 8
1.41 1.68 0.01 0.87 0.01 12.08 16 1.35 1.32 0.00 0.38 001 11.58 24 1.30 1.04 0.00 0.17 0.01 11.11 48 1.14 0.51 0.00 0.01 0.01 9.79 72 1.01 0.25 0.00 0.00 0.01 8.62 96 089 0.12 0.00 0.00 001 7.60 120 0.78 0.06 0.00 0.00 0.00 6.70 144- 0.69 0.03 0.00 0.00 0.00 5.90 168 0.61 0.01 0.00 0.00 0.00 5.20
- Mix ratio assumes end of core life source term.
EP-IP-440 Rev. 7 Page 17 of 21
(
/
i
ATTACHMENT 5 Sheet 1 of 2 POTASSIUM IODIDE ADMINISTRATION FORM I SSN:
1-131 Concentration (1iCi/cc area)
Duration Of Exposure:
jCi/co Hours Projected Thyroid Dose (Estimated):
______Rem Respiratory Protection Worn: LJ Yes LJ No Protection Factor:
Determined by:
Approved by:
Time:
Onsite/Offsite Radiological Supervisor i,
Time:
ED/EPM I have read and understand the precautions in Attachment 4 and understand that taking KI is voluntary. I also verify to the best of my knowledge I have no known allergies to iodide Signature of Individual Taking KI:
I KI Administration Record
-2&
D~t~;
- 4
)ie 4
2
{sigbbd By, 4~~
EP-IP-440 Rev. 7 Page 18 of 21 Name:
(Last)
(MI)
(First)
I
ATTACHMENT 5 Sheet 2 of 2 I
POTASSIUM IODIDE ADMINISTRATION FORM !(CONT.)
THE FOOD AND DRUG ADMINISf INDICATIONS THYROID BLOCKING IN A RADIATION EMERGENCY ONLY.
DIRECTIONS FOR USE Use only as directed by State of local public health authorities in the event of a radiation emergency.
Tablets DOSE ADULTS AND CHILDREN 1YEAR OF AGE OR OLDER: One (1) tablet once a day. Crush for small children.
BABIES UNDER 1 YEAR OF AGE:
One-half (1/2) tablet once a day. Crush first.
Take for 10 days unless directed otherwise by State or local public health authorities Store at controlled room temperature between 150 and 30' C (590 to 86* F). Keep container tightly closed and protect from light.
WARNING Potassium iodide should not be used by people allergic to Iodine.
Keep out of the reach of children In case of overdose or allergic reaction, contact a physician or the public health authority.
DESCRIPTION Each THYRO-B LOCKS TABLET contains 130 mg of potassium iodide. Other ingredients. magnesium stearate, microcrystallne cellulose, silica gel, sodium thiosulfate FRATION APPROVED PACKAGE INSERT HOW POTASSIUM IODIDE WORKS Certain forms of iodine help your thyroid gland work right.
Most people get the iodine they need from foods, like iodized salt or fish The thyroid can "store" or hold only a certain amount of iodine.
i THYRO-BLOCK TABLETS (POTASSIUM IODIDE TABLETS, USP)
(pronounced poe-TASS-e-um EYE-oh-dyed)
(abbreviated: KI)
TAKE POTASSIUM IODIDE ONLY WHEN PUBLIC HEALTH OFFICIALS TELL YOU. IN A RADIATION EMERGENCY, RADIOACTIVE IODINE COULD BE RELEASED INTO THE AIR. POTASSIUM IODIDE (A FORM OF IODINE) CAN HELP PROTECT YOU.
IF YOU ARE TOLD TO TAKE THIS MEDICINE TAKE IT ONE TIME EVERY 24 HOURS DO NOT TAKE IT MORE OFTEN MORE WILL NOT HELP YOU AND MAY IN-CREASE THE RISK OF SIDE EFFECTS. DO NOT TAKE THIS DRUG IF YOU KNOW YOU ARE ALLERGIC TO IODINE. (SEE SIDE EFFECTS BELOW.)
In a radiation emergency, radioactive iodine may be released in the air. This material may be breathed or swallowed It may enter the thyroid gland and damage it. The damage would probably not show itself for years. Children are most likely to have thyroid damage If you take potassium iodide, it will fill up your thyroid gland This reduces the chance' that harmful radioactive iodine will enter the thyroid gland i
WHO SHOULD NOT TAKE POTASSIUM IODIDE The only people who should not take potassium iodide are people who know they are allergic to iodine. You may take potassium iodide even if you are taking medicines for a thyroid problem (for example, a thyroid hormone or anti-thyroid drug).
Pregnant and nursing women and babies and children may also take this drug HOW AND WHEN TO TAKE POTASSIUM IODIDE Potassium Iodide should be taken as soon as possible after public health officials tell you You should take one dose every 24 hours2.777778e-4 days <br />0.00667 hours <br />3.968254e-5 weeks <br />9.132e-6 months <br /> More will not help you because the thyroid can "hold" only limited amounts of iodine Larger doses will increase the risk of side effects You,will probably be told not to take the drug for more than 10 days SIDE EFFECTS Usually, side effects of potassium iodide happen when people take higher doses for a long time You should be careful not to take more than the recommended dose or take it for longer than you are told Side effects are unlikely because of the low dose and the short time you will be taking the drug Possible side effects inclhde skin rashes, swelling of the salivary glands, and "iodism" (metallic taste, burning mouth and throat, sore teeth and gums, symptoms of a head cold, and sometimes stomach upset and diarrhea)
A few people have ant allergic reaction with more serious symptoms These could be fever and joint pains, or swelling of parts of the face and body and at times severe shortness of breath requiring immediate medical attention Taking iodine may rarely cause overactivity of the thyroid gland, underactivity of the thyroid gland, or enlargement of the thyroid gland (goiter)
I WHAT TO DO IF SIDE EFFECTS OCCUR If the side effects are severe or if you have an allergic reaction, stop taking potassium iodide Then, if possible, call a doctor or public health authority foi instructions HOW SUPPLIED THYRO-BLOCK TABLETS (Potassium Iodide Tablets, UPS) bottles of 14 tablts (NDC 0037-0472-20). Each white, round, scored tablet contains 130 mg potassium iodide.
WALLACE LABORATORIES I Division of CARTER-WALLACE. INC Cranbury, New Jersey 08512 IN-0472-O1 I
Rev 2/85 EP-IP-440 Rev. 7 Page 19 of 21
ATTACHMENT 6 I Sheet I of 1 DOCUMENT CROSS-REFERENCE This Attachment lists those documents, other than source documents, which may be affected by changes to this Procedure.
Document Number Document Title EP-IP-230 OSC Activation and Response EP-IP-231 Onsite Radiation Protection EP-IP-251 Offsite Radiation Protection EP-IP251 T
-ff EP-IP-440 Rev. 7 Page 20 of 21
ATTACHMENT 7 Sheet 1 of 1 IDENTIFICATION OF COMMITMENTS This Attachment lists those external commitments (i.e., NRC commitments, and INPO inspection items) implemented in this Procedure.
QA audit findings, EP-IP-440 Rev. 7 Page 21 of 21 Reference Document Commitment Affected Section(s)/Step(s)
NRC Inspection Finding Describe or reference by Procedure the All 84-05-16/85-19-01 program for exposure control during emergencies. Improve program for evaluation/control of re-entry team radiation exposure.