ML17334A978
| ML17334A978 | |
| Person / Time | |
|---|---|
| Site: | Cook |
| Issue date: | 07/10/1986 |
| From: | INDIANA MICHIGAN POWER CO. (FORMERLY INDIANA & MICHIG |
| To: | |
| Shared Package | |
| ML17334A977 | List: |
| References | |
| NUDOCS 8607150189 | |
| Download: ML17334A978 (59) | |
Text
ATTACHMENT 2 TO AEP:NRC:0856 0
PROPOSED CHANGES TO THE DONALD C.
COOK NUCLEAR PLANT UNIT NOS. I AND 2 TECHNICAL SPECIFICATIONS Bb07150189 860710 PDR ADOCK 05000315 P
INSTRUMENTATION CHLORINE DETECTION SYSTEM LIMITING CONDITION FOR OPERATION 3.3.3.11 The chlorine detection
- system, with its alarm setpoint adjusted to actuate at a chlorine concentration of less than or equal to 5 ppm, shall be OPERABLE.
APPLICABILITY: All MODEST ACTION:
a.
With the chlorine detection system of either unit inoperable, within 1 hour1.157407e-5 days <br />2.777778e-4 hours <br />1.653439e-6 weeks <br />3.805e-7 months <br /> initiate and maintain operation of both the Unit 1 and Unit 2 control room emergency ventilation systems in the isolation mode of operation, as defined in the Bases.
b.
The provisions of Specifications 3.0.4 are not applicable.
SURVEILLANCE RE UIREMENTS 4.3.3.11 The chlorine detection system shall be demonstrated OPERABLE by performance of a CHANNEL FUNCTIONAL TEST at least once per 31 days and a CHANNEL CALIBRATION at least once per 18 months.
D.
C.
COOK - UNIT 1 3/4 3-69 Amendment No.
i
PLANT SYSTEMS 3 4.7.5 CONTROL ROOM EMERGENCY VENTILATION SYSTEM LIMITING CONDITION FOR OPERATION 3.7 '.1 The control room emergency ventilation system shall be OPERABLE with:
a.
Two independent heating and cooling systems, b.
Two independent pressurization
- fans, c.
One charcoal adsorber and HEPA filter train, and d.
The control room pressure boundary.
APPLICABILITY: All MODES.
ACTION:
MODES 1, 2,
3, and 4:
a.
With one heating and cooling system inoperable, restore the inoperable system to OPERABLE status within 7 days or be in at least HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
b.
With one pressurization fan inoperable, restbre the inoperable fan to OPERABLE status within 7 days or be in at least HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
c.
With the filter train inoperable, restore the filter train to OPERABLE status within 72 hours8.333333e-4 days <br />0.02 hours <br />1.190476e-4 weeks <br />2.7396e-5 months <br /> or be in at least HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
d.
With the control room pressure boundary inoperable, restore the control room pressure boundary to OPERABLE status within 72 hours8.333333e-4 days <br />0.02 hours <br />1.190476e-4 weeks <br />2.7396e-5 months <br /> or be in at least HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
MODES 5 and 6:
e.
With any of the following: (1) both heating and cooling systems; (2) both pressurization fans; (3) the filter train; (4) the control room pressure boundary; inoperable, suspend all operations involving CORE ALTERATIONS or positive reactivity changes.
D.
C.
COOK - UNIT 1 3/4 7-19 Amendment No.
PLANT SYSTEMS SURVEILLANCE RE UIREMENTS 4.7.5.1 The control room emergency ventilation system shall be demonstrated OPERABLE:
At least once per 12 hours1.388889e-4 days <br />0.00333 hours <br />1.984127e-5 weeks <br />4.566e-6 months <br /> by verifying that the control room air temperature is < 120 F.
0 At least once per 31 days on a STAGGERED TEST BASIS by initiating flow through the HEPA filter and charcoal adsorber train and verifying that the system operates for at least 15 minutes.
At least once per 18 months or (1) after any structural maintenance on the HEPA filter or charcoal adsorber
- housings, or (2) following painting, fire or chemical release in any ventilation zone communicating with the system by:
1.
Verifying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm +
10%.
Verifying that the HEPA filter banks remove
> 99% of the DOP when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
Verifying within 31 days after removal that a laboratory analysis of a carbon sample from either at least one test canister or at least two carbon samples removed from one of the charcoal adsorbers demonstrates a removal efficiency of > 95%
for radioactive methyl iodide when the sample is tested in accordance with ANSI N510-1980 (130 C,
95% R.H.).
The carbon samples not obtained from test canisters shall be prepared by either:
a)
Emptying one entire bed from a removed adsorber tray, mixing the adsorbent thoroughly, and obtaining samples at least two inches in diameter and with a length equal to the thickness of the bed, or D.
C.
COOK - UNIT 1 3/4 7-20 Amendment No.
PLANT SYSTEMS SURVEILLANCE RE UIREMENTS continued b)
Emptying a longitudinal sample from an adsorber tray, mixing the adsorbent thoroughly, and obtaining samples at
- least two inches in diameter and with a length equal to the thickness of the bed.
Subsequent to reinstalling the adsorber tray used for obtaining the carbon sample, the system shall be demonstrated OPERABLE by also verifying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm +
10%.
4.
Verifying a system flow rate of 6000 cfm + 10% during system operation in the recirculation/cleanup
- mode, when tested in accordance with ANSI N510-1980.
d.
After every 720 hours0.00833 days <br />0.2 hours <br />0.00119 weeks <br />2.7396e-4 months <br /> of charcoal adsorber operation by either:
Verifying within 31 days after removal that a laboratory analysis of a carbon sample obtained from a test canister demonstrates a removal efficiency of > 95% for radioactive methyl iodide when the sample is tested in accordance with ANSI N510-1980 (130 C, 95% R.H.); or 2.
Verifying within 31 days after removal that a laboratory analysis of at least two carbon samples demonstrates a removal efficiency of > 95% for radioactive methyl iodide when the samples are tested in accordance with ANSI N510-1980 (130 C,
95% R.H.) and the samples are prepared by either:
a)
Emptying one entire bed from a removed adsorber tray, mixing the adsorbent thoroughly, and obtaining samples at least two inches in diameter and with a length equal to the thickness of the bed, or b)
Emptying a longitudinal sample from an adsorber tray, mixing the adsorbent thoroughly, and obtaining samples at least two inches in diameter and with a length equal to the thickness of the bed.
Subsequent to reinstalling the adsorber tray used for obtaining the carbon sample, the system shall be demonstrated OPERABLE by also verifying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-'1980 while operating the ventilation system at a flow rate of 6000 cfm +
10%.
D.
C.
COOK - UNIT 1 3/4 7-21 Amendment No.
PLANT SYSTEMS SURVEILLANCE RE UIREMENTS Continued e.
At least once per 18 months by:
Verifying that the pressure drop across the combined HEPA filters and charcoal adsorber banks i.s ( 6 inches Water Gauge (W.G.) while operating the ventilation system at a flow rate of 6000 cfm + 10%.
2.
a)
Verifying that on a Safety Injection Signal from Unit 1, the system automatically initiates operation in the recirculation/cleanup mode.
b}
Verifying that on a Safety Injection Signal from Unit 2, the system automatically initiates operation in the recirculation/cleanup mode.
3.
Verifying that the system maintains the control room at a positive pressure of > 1/16 inch W.G. relative to the outside atmosphere at a system flow rate of 6000 cfm + 10% while operating in the recirculation/cleanup mode.
4.
Verifying that the system maintains the machine room and the P250 computer room at a positive pressure with respect to the outside atmosphere, in conjunction with testing required by Specification 4.7.5.1.e.3.
5.
Verifying that the combination of filtered makeup and unfiltered inleakage is within limits, as defined in the Bases, which will maintain the control room habitable under radiological accident conditions, in conjunction with testing required by Specification 4.7.5.1.e.3.
f.
After each complete or partial replacement of a HEPA filter bank by veri.Eying that the HEPA filter banks remove > 99% of the DOP when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
g.
After each complete or partial replacement of a charcoal adsorber bank by veri.fying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
D.
C.
COOK - UNIT 1 3/4 7-22 Amendment No.
t
INSTRUMENTATION BASES 3 4.3.3.9 RADIOACTIVE LI UID EFFLUENT INSTRUMENTATION The radioactive liquid effluent instrumentation is provided to monitor and
- control, as applicable, the releases of radioactive materials in liquid effluents during actual or potential releases.
The alarm/trip setpoints for these instruments shall be calculated in accordance with NRC approved methods in the ODCM to ensure that the alarm/trip will occur prior to exceeding the limits of 10 CFR Part 20.
The OPERABILITY and use of this instrumentation is consistent with the requirements of General Design Criteria specified in Section 11.3 of the Final Safety Analysis Report, for the Donald C.
Cook Nuclear Plant.
3 4.3.3.10 RADIOACTIVE GASEOUS EFFLUENT INSTRUMENTATION The radioactive gaseous effluent instrumentation is provided to monitor and
- control, as applicable, the releases of radioactive materials in gaseous effluents during actual or potential releases.
The alarm/trip setpoints for these instruments shall be calculated in accordance with NRC approved methods in the ODCM to ensure that the alarm/trip will occur prior to exceeding the limits of 10 CFR Part 20.
This instrumentation also includes provisions for monitoring the concentrations of potentially explosive gas mixtures in the waste gas holdup system.
The OPERABILITY and use of this instrumentation is consistent with the requirements of General Design Criteria specified in Section 11.3 of the Final Safety Analysis Report for the Donald C.
Cook Nuclear Plant.
3 4.3.3 11 CHLORINE DETECTION SYSTEM The OPERABILITY of the detection system ensures that sufficient capability is available to promptly detect and initiate protective action in the event of an accidental chlorine release.
In the event chlorine is detected, the control room ventilation system would be manually placed in the isolation mode of operation.
This is accomplished by closing isolation dampers on the normal air intake and the toilet room exhaust.
The pressurization fans are not run, to minimize the amount of contaminated outdoor air which enters the control room.
The emergency air intake damper cannot be closed from the control room beyond the setting for the recirculation/cleanup mode.
- Thus, the recirculation damper is maintained closed so that contaminated air entering via the emergency intake passes through the charcoal adsorbers prio'r to entering the control room.
D.,C.
COOK - UNIT 1 B 3/4 3-5 Amendment No.
PLANT SYSTEMS BASES 3 4.7.5 CONTROL ROOM EMERGENCY VENTILATION SYSTEM The OPERABILITY of the control room emergency ventilation system ensures that 1) the ambient air temperature does not exceed the allowable temperature for continuous duty rating for the equipment and instrumentation cooled by this system and 2) the control room will remain habitable for operations personnel during and following all credible accident conditions.
The OPERABILITY of this system in conjunction with control room design provisions is based on limiting the radiation exposure to personnel occupying the control room to 5 rem or less whole body, or its equivalent.
This limitation is consistent with the requirements of General Design Criteria 19 of Appendix "A", 10 CFR 50.
The 1980 version of ANSI N510 is used as a testing guide.
This standard, however, is intended to be rigorously applied only to systems which, unlike the control room ventilation systems, are designed to ANSI N509 standards.
For the specific case of the air-aerosol mixing uniformity test required by.
ANSI N510 as a prerequisite to in-place leak testing of charcoal and HEPA filters, the air-aerosol uniform mixing test acceptance criteria were not rigorously met.
For this reason, a statistical correction factor will be applied to applicable surveillance test results unless future air-aerosol mixing tests justify the adequacy of filter leak testing methods.
In,the event chlorine gas is detected, or if the chlorine detector of either unit is inoperable, the control room ventilation system is placed in the isolation mode of operation.
This is accomplished by closing isolation dampers on the normal air intake and the toilet room exhaust.
The pressurization fans are not run, to minimize the amount of contaminated outdoor air which enters the control room.
The emergency air intake damper cannot be closed from the control room beyond the setting for the recirculation/cleanup mode.
- Thus, the recirculation damper is maintained closed so that contaminated air entering via the emergency intake passes through the charcoal adsorbers prior to entering the control room.
In the event of a radiological accident, such as a LOCA, the control room ventilation system would be aligned automatically in the recirculation/cleanup mode of operation.
This occurs automatically in both units in the event of a safety injection signal from either unit.
Upon system actuation the normal air intake and toilet room exhaust are automatically closed via isolation dampers.
Both of the redundant pressurization fans start, drawing outdoor makeup air for pressurization purposes through the emergency intake damper.
This damper is preset to a position sufficient to allow the required pressurization, while limiting outdoor air intake to an amount which will ensure control room habitability, as described below.
The operators are instructed to shut off one of the redundant fans after assuring they both started.
This is to assure that iodine residence time requirements are met, so as to provide filter efficiencies consistent with those assumed in the accident analyses.
Figure 1, and its accompanying Table 1, provide a graphic representation of the control room ventilation system under normal, radiological, and toxic gas conditions.
D.
C.
COOK - UNIT 1 B 3/4 7-5 Amendment No.
PLANT SYSTEMS BASES In the recirculation/cleanup
- mode, the ventilation system is sized to provide pressurization of ) 1/16 inches W.G. relative to the outside atmosphere.
The machine room and P250 computer room are intended to be at pressures which are positive with respect to the outside atmosphere, but which may be less positive than the control room.
The lower pressure requirement is because these rooms would not be expected to be entered or exited as often as the control room during an accident.
Pressure in the F250 computer room would always be slightly higher than the machine room because of the small pressure drop associated with air passage through the transfer openings.
Therefore, a positive pressure measurement in the machine room will ensure a
positive pressure in the computer room.
Technical Specifications require verification that the combination of filtered and unfiltered inleakage is within limits which will maintain the control room habitable under radiological accident conditions.
Acceptable combinations of inleakage are those that limit doses to control room personnel to 5 rem whole-body, 30 rem thyroid, or 30 rem to the skin under an assumed accident duration of 30 days.
These combinations are derived from Figures 1
and 2.
Dose lines on,these figures may be extrapolated linearly to accommodate larger values of filtered or unfiltered inleakage.
For purposes of using these figures, filtered air inleakage is taken to be that air which is brought in through the filter unit to provide makeup for pressurization purposes.
Unfiltered makeup air is defined as the sum of air which is measured to leak past the normal air intake isolation damper, when it is in the closed position, and a nominal 10 cfm which accounts for opening and closing of the control room doors during the course of an accident.
To use the whole body and skin dose curves, the total makeup air flow rate is obtained by summing the filtered and unfiltered values obtained as described
- above, and verifying that the 30-day dose resulting from this total is 'below the limits shown.
For the thyroid dose, a point on Figure 3 is found which corresponds to the appropriate filtered and unfiltered leakage combination.
The 30-day dose associated with this point must be below the 30 rem thyroid dose limit.
D.
C.
COOK - UNIT 1 B 3/4 7-5a Amendment No.
a O
FIGURE 11 CONTROL ROOM VENTILATlONSYSTEM P-250 ROOM F
P AIR CONDITIONING SYSTEM C
F P
x EMERGENCY AIRFLOW C
H P
RECIRCULATION DAMPER M
HV-ACRDA 3 MEASURIN G
CLEANUP SYSTEM STATION NORMAL INTAKE DAMPER HV ACRDA-I MACHINE ROOM TOILET EXHAUST DAMPER HV-ACRDA-4 EMERGENCY INTAKE DAMPER HV-ACROA-2 lll Y'l-OZ 1
0 1 ~Z illg 0
< cv OZy 1 X Ul 1 Z
Z illY Oc 0 1-OZ 1N gf O-LEGEND CONTROL ROOM TOILET (UNIT +2 ONLY)
SACKDRAFT DAMPER DAMPER VORTEX DAMPER M MOTOR OPERATED PARALLEL BLADE DAMPER ENTRIFUGAL MOTOR-FAN M OPERATED BUTTERFLY DAMPER CHARCOAL C
ADSORBER HEPA FILTER p
PREFILTER COILING COILS MEDIUM F
EFFICIENCY FILTER I
TRANSFER OP E NING
Table 1'ontrol Room Ventilation E ui ment 0 eratio Normal Operation:
EeeEui ment Condition Damper ACRDA-1 Damper ACRDA-2 Damper ACRDA-3 Damper ACRDA-4 Pressurization Fans Open Open to recirculation/cleanup setting Closed Closed or open Not running Toxic Gas (Isolation):
~Eui ment Condition Damper ACRDA-1 Damper ACRDA-2 Damper ACRDA-3 Damper ACRDA-4 Pressurization Fans Closed Open to recirculation/cleaup setting Closed Closed Not running Radiological (Recirculation/Cleanup)
~Eui ment Condition Damper ACRDA-1 Damper ACRDA-2 Damper ACRDA-3 Damper ACRDA-4 Recirculation Fans Closed Open to recirculation/cleanup setting Open Closed 1 running D.
C.
COOK - UNIT 1
~
~
B 3/4 7-5c Amendment No.
t7 O
A0O I
26 CONTROL ROOM BETA SKIN AND GAMMA BODY DOSE 24 Note:
skin dose limit = 30 rem 22 20 18 16 14 CO0O 10 BE T A SKIN DOS DOSE LIMIT-WHOLEBODY DOSE IIIIIIII
~ I ~IIIIII
~II~ I ~ ~ I ~IIIIIIIII
~ ~IIIIIIII
~ ~ ~IIIIIII
~IIIIIIIIIIIIIIII
~ I ~IIIIII
~IIIIIIIIIII
~III~IIIIII
~ I ~ II~III II I
I ~ IIIIIIII
~III~ I ~ IIIIII~IIII~ II~ I ~IIII~ EI ~III GAMMA WHOLE BODY DOSE WWWW WW&W WWWW WWWW
&WWW WWWW W&WW WWWW 200 400 600 800 1000 1200 1400 1600 1800 2000 MAKEUP'AIR FLOW RATE (ctm) 0
U O
CONTROL ROOM THYROID DOSE 30 25 20 E
lU m
15 0
CI 10 D
ERR U
I 60c 1
50cfm+
~1 11 1
40cfmI
~ 1 30cfm 1 20cfm RQS SSSSSSSSSSQSSSSS SSI OSE LIMIT THYROID
,t 1
IIIII r
1 NFILTERED NLEAKAGE 11 illll 11 Iill" Ill 1
IIIII 1
Illl 11 Illl fm.l" 11 1 1 10cfm +
R0 200 400 600 800 1000 1200 1400 FILTFRED MAKEUP AIR FLOW RATE (cfm) 1600 1800 2000
PLANT SYSTEMS BASES 3 4.7.6 ESF VENTILATION SYSTEM The OPERABILITY of the ESF ventilation system ensures that radioactive materials leaking from the ECCS equipment within the pump room following a LOCA are filtered prior to reaching the environment.
The operation of this system and the resultant effect on offsite dosage calculation was assumed in the accident analyses.
3 4.7.7 SEALED SOURCE CONTAMINATION The limitations on sealed source removable contamination ensure that the total body or individual organ irradiation does not exceed allowable limits in the event of ingestion or inhalation of the probable leakage from the source material.
The limitations on removable contamination for sources requiring leak testing, including alpha emitters, is based on 10 CFR 70.39(c) limits for plutonium.
Quantities of interest to this specification which are exempt from the leakage testing are consistent with the criteria of 10 CFR Parts 30.11-20 and 70.19.
Leakage from sources excluded from the requirements of this specification is not likely to represent more than one maximum permissible body burden for total body irradiation if the source material is inhaled or ingested.
D.
C.
COOK - UNIT 1 B 3/4 7-5f Amendment No.
INSTRUMENTATION CHLORINE DETECTION SYSTEM LIMITING CONDITION FOR OPERATION 3.3.3.11 The chlorine detection system, with its alarm setpoint adjusted to actuate at a chlorine concentration of less than or equal to 5 ppm, shall be OPERABLE.
APPLICABILITY: All MODES.
ACTION:
With the chlorine detection system of either unit inoperable, within 1 hour1.157407e-5 days <br />2.777778e-4 hours <br />1.653439e-6 weeks <br />3.805e-7 months <br /> initiate and maintain operation of both the Unit 1 and Unit 2 control room emergency ventilation systems in the isolation mode of operation, as defined in the Bases.
b.
The provisions of Specifications 3.0.4 are not applicable.
SURVEILLANCE RE UIREMENTS 4.3.3.11 The chlorine detection system shall be demonstrated OPERABLE by performance of a CHANNEL FUNCTIONAL TEST at least once per 31 days and a
CHANNEL CALIBRATION at least once per 18 months.
D.
C.
COOK - UNIT 2 3/4 3-67 Amendment No.
PLANT SYSTEMS 3 4.7.5 CONTROL ROOM EMERGENCY VENTILATION SYSTEM LIMITING CONDITION FOR OPERATION 3.7.5.1 The control room emergency ventilation system shall be OPERABLE with:
a.
Two independent heating and cooling systems, b.
Two independent pressurization
- fans, c.
One charcoal adsorber and HEPA filter train, and d.
The control room pressure boundary.
APPLICABILITY: All MODES.
ACTION:
MODES 1, 2,
3, and 4:
With one heating and cooling system inoperable, restore the inoperable system to OPERABLE status within 7 days or be in at le'ast HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
b.
With one pressurization fan inoperable, restore the inoperable fan to OPERABLE status within 7 days or be in at least HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
c.
With the filter train inoperable, restore the filter train to OPERABLE status within 72 hours8.333333e-4 days <br />0.02 hours <br />1.190476e-4 weeks <br />2.7396e-5 months <br /> or be in at least HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
d.
With the control room pressure boundary inoperable, restore the control room pressure boundary to OPERABLE status within 72 hours8.333333e-4 days <br />0.02 hours <br />1.190476e-4 weeks <br />2.7396e-5 months <br /> or be in at least HOT STANDBY within the next 6 hours6.944444e-5 days <br />0.00167 hours <br />9.920635e-6 weeks <br />2.283e-6 months <br /> and in COLD SHUTDOWN within the following 30 hours3.472222e-4 days <br />0.00833 hours <br />4.960317e-5 weeks <br />1.1415e-5 months <br />.
MODES 5 and 6:
e.
With any of the following: (1) both heating and cooling systems; (2) both pressurization fans; (3) the filter train; (4) the control room pressure boundary; inoperable, suspend all operations involving CORE ALTERATIONS or positive reactivity changes.
D.
C.
COOK - UNIT 2 3/4 7-14 Amendment No.
PLANT SYSTEMS SURVEILLANCE RE UIREMENTS 4.7.5.1 The control room emergency ventilation system shall be demonstrated OPERABLE:
At least once per 12 hours1.388889e-4 days <br />0.00333 hours <br />1.984127e-5 weeks <br />4.566e-6 months <br /> by verifying that the control room air temperature is < 120 F.
0 At least once per 31 days on a STAGGERED TEST BASIS by initiating flow through the HEPA filter and charcoal adsorber train and verifying that the system operates for at least 15 minutes.
At least once per 18 months or (1) after any structural maintenance on the HEPA filter or charcoal adsorber
- housings, or (2) following painting, fire or chemical release in any ventilation zone communicating with the system by:
1.
Verifying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm +
10'.
Verifying that the HEPA filter banks remove > 99% of the DOP when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
Verifying within 31 days after removal that a laboratory analysis of a carbon sample from either at least one test canister or at least two carbon samples removed from one of the charcoal adsorbers demonstrates a removal efficiency of > 95%
for radioactive methyl iodide when the sample is tested in accordance with ANSI N510-1980 (130 C, 95% R.H.).
The carbon samples not obtained from test canisters shall be prepared by either:
a)
Emptying one entire bed from a removed adsorber tray, mixing the adsorbent thoroughly, and obtaining samples at least two inches in diameter and with a length equal to the thickness of the bed, or D.
C.
COOK - UNIT 2 3/4 7-15 Amendment No.
PLANT SYSTEMS SURVEILLANCE RE UIREMENTS continued b)
Emptying a longitudinal sample from an adsorber tray, mixing the adsorbent thoroughly, and obtaining samples at least two inches in diameter and with a length equal to the thickness of the bed.
Subsequent to reinstalling the adsorber tray used for obtaining the carbon sample, the system shall be demonstrated OPERABLE by also verifying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
4.
Verifying a system flow rate of 6000 cfm + 10% during system operation in the recirculation/cleanup
- mode, when tested in accordance with ANSI N510-1980.
After every 720 hours0.00833 days <br />0.2 hours <br />0.00119 weeks <br />2.7396e-4 months <br /> of charcoal adsorber operation by either:
1.
Verifying within 31 days after removal that a laboratory analysis of a carbon sample obtained from a test canister demonstrates a removal efficiency of > 95% for radioactive methyl iodide when the sample is tested in accordance with ANSI N510-1980 (130 C,
95% R.H.); or Verifying within 31 days after removal that a laboratory analysis of at least two carbon samples demonstrates a removal efficiency of > 95% for radioactive methyl iodide when the samples are tested in accordance with ANSI N510-1980 (130 C, 95% R.H.) and the samples are prepared by either:
a)
Emptying one entire bed from a removed adsorber tray,'ixing the adsorbent thoroughly, and obtaining samples at least two inches in diameter and with a length equal to the thickness of the bed, or b)
Emptying a longitudinal sample from an adsorber tray, mixing the adsorbent thoroughly, and obtaining samples at least two inches in diameter and with a length equal to the thickness of the bed.
Subsequent to reinstalling the adsorber tray used for obtaining the carbon sample, the system shall be demonstrated OPERABLE by also verifying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
D.
C.
COOK - UNIT 2 3/4 7-16 Amendment No.
PLANT SYSTEMS SURVEILLANCE RE UIREMENTS Continued e.
At least once per 18 months by:
Verifying that the pressure drop across the combined HEPA filters and charcoal adsorber banks is ( 6 inches Water Gauge (W.G.) while operating the ventilation system at a flow rate of 6000 cfm + 10$.
2.
a)
Verifying that on a Safety Injection Signal from Unit 1, the system automatically initiates operation in the recirculation/cleanup mode.
b)
Verifying that on a Safety Injection Signal from Unit 2, the system automatically initiates operation in the recirculation/cleanup mode.
3.
Verifying that the system maintains the control room at a positive pressure of > 1/16 inch W.G. relative to the outside atmosphere at a system flow rate of 6000 cfm +
10% while operating in the recirculation/cleanup mode.
4.
Verifying that the system maintains the machine room and the F250 computer room at a positive pressure with respect to the outside atmosphere, in conjunction with testing required by Specification 4.7.5.1.e.3.
5.
Verifying that the combination of filtered makeup"and unfiltered inleakage is within limits, as defined in the Bases, which will maintain the control room habitable under radiological accident conditions, in conjunction with testing required by Specification 4.7.5.1.e.3.
f.
After each complete or partial replacement of a HEPA filter bank by verifying that the HEPA filter banks remove > 99% of the DOP when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
g.
After each complete or partial replacement of a charcoal adsorber bank by verifying that the charcoal adsorbers remove > 99% of a halogenated hydrocarbon refrigerant test gas when they are tested in-place in accordance with ANSI N510-1980 while operating the ventilation system at a flow rate of 6000 cfm + 10%.
D.
C.
COOK - UNIT 2 3/4 7-16a Amendment No.
3 4.3 INSTRUMENTATION BASES 3 4.3.3.8 FIRE DETECTION INSTRUMENTATION OPERABILITY of the fire detection instrumentation ensures that adequate warning capability is available for the prompt detection of fires.
This capability is required in order to detect and locate fires in their early stages.
Prompt detection of fires will reduce the potential for damage to safety-related equipment and is an integral element in the overall facility fire protection program.
In the event that a portion of the fire detection instrumentation is inoperable, the establishment of frequent fire patrols in the affected areas is required to provide detection capability until the inoperable instrumentation is restored to OPERABILITY.
Use of containment temperature monitoring is allowed once per hour if containment fire detection is inoperable.
3 4.3.3.9 RADIOACTIVE LI UID EFFLUENT INSTRUMENTATION The radioactive liquid effluent instrumentation is provided to monitor and
- control, as applicable, the releases of radioactive materials in liquid effluent during actual or potential releases.
The alarm/trip setpoints for these instruments shall be calculated in accordance with NRC approved methods in the ODCM to ensure that the alarm/trip will occur prior to exceeding the limits of 10 CFR Part 20.
The OPERABILITY and use of this instrumentation is consistent with the requirements of General Design Criteria specified in Section 11.3 of the Final Safety Analysis Report for the Donald C.
Cook Nuclear Plant.
3 4,3.3.10 RADIOACTIVE GASEOUS EFFLUENT INSTRUMENTATION The radioactive gaseous effluent instrumentation is provided to monitor and
- control, as applicable, the releases of radioactive materials in gaseous effluents during actual or potential releases.
The alarm/trip setpoints for these instruments shall be calculated in accordance with NRC approved methods in the ODCM to ensure that the alarm/trip will occur prior to exceeding the limits of 10 CFR Part 20.
This instrumentation also includes provisions for monitoring the concentrations of potentially explosive gas mixtures in the waste gas holdup system.
The OPERABILITY and use of this instrumentation is consistent with the requirements of General Design Criteria specified in Section 11.3 of the Final Safety Analysis Report for the Donald C.
Cook Nuclear Plant.
3 4 3
3 11 CHLORINE DETECTION SYSTEM The OPERABILITY of the detection system ensures that sufficient capability is available to promptly detect and initiate protective action in the event of an accidental chlorine release.
In the event chlorine is detected, the control D.
C.
COOK - UNIT 2 B 3/4 3-3 Amendment No.
3 4.3 INSTRUMENTATION BASES room ventilation system would be manually placed in the isolation mode of operation.
This is accomplished by closing isolation dampers on the normal air intake and the toilet room exhaust.
The pressurization fans are not run, to minimize the amount of contaminated outdoor air which enters the control room.
The emergency air intake damper cannot be closed from the control room beyond the setting for the recirculation/cleanup mode.
- Thus, the recirculation damper is maintained closed so that contaminated air entering via the emergency intake passes through the charcoal adsorbers prior to entering the control room.
3 4 3 4 TURBINE OVERSPEED PROTECTION This specification is provided to ensure that the turbine overspeed protection instrumentation and the turbine speed control valves are OPERABLE and will protect the turbine from excessive overspeed.
Protection from turbine excessive overspeed is required since excessive overspeed of the turbine could generate potentially damaging missiles which could impact and damage safety related components, equipment or structures.
B 3/4 3-4 Amendment No.
PLANT SYSTEMS BASES The 1980 version of ANSI N510 is used as a testing guide.
This standard, however, is intended to be rigorously applied only to systems which, unlike the control room ventilation systems, are designed to ANSI N509 standards.
For the specific case of the air-aerosol mixing uniformity test required by ANSI N510 as a prerequisite to in-place leak testing of charcoal and HEPA filters, the air-aerosol uniform mixing test acceptance criteria were not rigorously met.
For this reason, a statistical correction factor will be applied to applicable surveillance test results, unless future air-aerosol mixing tests justify the adequacy of filter leak testing methods.
In the event chlorine gas is detected, or if the chlorine detector of either unit is inoperable, the control room ventilation system is placed in the isolation mode of operation.
This is accomplished by closing isolation dampers on the normal air intake and the toilet room exhaust.
The pressurization fans are not run, to minimize the amount of contaminated outdoor air which enters the control room.
The emergency air intake damper cannot be closed from the control room beyond the setting for the recirculation/cleanup mode.
- Thus, the recirculation damper is maintained closed so that contaminated air entering via the emergency intake passes through the charcoal adsorbers prior to entering the control room.
In the event of a radiological accident, such as a LOCA, the control room ventilation system would be aligned automatically in the recirculation/cleanup mode of operation.
This occurs automatically in both units in the event of a safety injection signal from either unit.
Upon system actuation the normal air intake and toilet room exhaust are automatically closed via isolation dampers.
Both of the redundant pressurization fans start, drawing outdoor makeup air for pressurization purposes through the emergency intake damper.
This damper is preset to a position sufficient to allow the required pressurization while limiting outdoor air intake to an amount which will ensure control room habitability, as described below.
The operators are instructed to shut off one of the redundant fans after assuring they both started.
This is to assure that'odine residence time requirements are met, so as to provide filter efficiencies consistent with "those assumed in the accident analyses.
In the recirculation/cleanup
- mode, the ventilation system is sized to provide pressurization of > 1/16 inches W.G
~ relative to the outside atmosphere.
The machine room and F250 computer room are intended to be at pressures which are positive with respect to the outside atmosphere, but which may be less positive than the control room.
The lower pressure requirement is because these rooms would not be expected to be entered or exited as often as the control room during an accident.
Pressure in the F250 computer room would always be slightly higher than the machine room because of the small pressure drop associated with air passage through the transfer openings.
Therefore, a
positive pressure measurement in the machine room will ensure a positive pressure in the computer room.
D.
C.
COOK - UNIT 2 B 3/4'-4a Amendment No.
PLANT SYSTEMS BASES Figure 1, and its accompanying Table 1, provide a graphic representation of the control room ventilation system under normal, radiological, and toxic gas conditions.
Technical Specifications require verification that the combination of filtered and unfiltered inleakage is within limits which will maintain the control room habitable under radiological accident conditions.
Acceptable combinations of inleakage are those that limit doses to control room personnel to 5 rem whole-body, 30 rem thyroid, or 30 rem to the skin under an assumed accident duration of 30 days.
These combinations are derived from Figures 1
and 2.
Dose lines of these figures may be extrapolated linearly to accommodate larger values of filtered or unfiltered inleakage.
In these figures, filtered air inleakage is taken to be that air which is brought in through the filter unit to provide makeup for pressurization purposes.
Unfiltered makeup air is defined as the sum of air which is measured to leak past the normal air intake isolation damper, when it is in the closed
- position, and a nominal 10 cfm which accounts for opening and closing of the control room doors during the course of an accident.
To use the. whole-body and skin dose curves, the total makeup air flow rate is obtained'y summing the filtered and unfiltered values obtained as described
- above, and verifying that the 30-day dose resulting from this total is below the limits shown.
For the thyroid dose, a point on Figure 3 is found which corresponds to the appropriate filtered and unfiltered in-leakage combination.
The 30-day dose associated with this point must be below the 30 rem thyroid dose limit.
D.
C.
COOK - UNIT 2 B 3/4 7-4b, Amendment No.
O FIGURE 11 CONTROL ROOM VENTILATIONSYSTEM CRH P-250 ROOM F
P AIR CONDITIONING SYSTEM F
P X
EMERGENCY AIRFLOW C
H P
RECIRCULATION DAMPER M
HV-ACRDA-3 G
CLEANUP SYSTEM STATION MEASU NORMAL INTAKE DAMPER HV-ACADA I MACHINE ROOM TOILET EXHAUST DAMPER HV ACADA 4 EMEAGENCY INTAKE DAMPER HV-ACRDA-2 QJr Of-OZ I
OZE
~Z Illg 0
~<c OZy 1 X EU I Z
Z III Or Of-OZ IA gf O
LEGEND CONTROL ROOM 7 0 I LE T (UNIT W2 ONLY)
SACKDAAFT DAMPER DAMPEA VORTEX DAMPER M MOTOR OPERATED PARALLEL BLADE DAMPER ENTRIFUGAL MOTOR-FAN M OPERATED BUTTERFLY DAMPER CHARCOAL C
ADSOABER HEPA FILTER PREFILTER COILING COILS MEDIUM F
EFFICIENCY FILTER I
TRANSFER OPENING S
O8 0
Table 1'ontrol Room Ventilation E ui ment 0 eratio Normal Operation:
~Eui ment Condition Damper ACRDA-1 Damper ACRDA-2 Damper ACRDA-3 Damper ACRDA-4 Pressurization Fans Open Open to recirculation/cleanup setting Closed Closed or open Not running Toxic Gas (Isolation):
~Eui ment Condition Damper ACRDA-1 Damper ACRDA-2 Damper ACRDA-3 Damper ACRDA-4 Pressurization Fans Closed Open to recirculation/cleaup setting Closed Closed Not running Radiological (Recirculation/Cleanup)
Fcutui ment Condition Damper ACRDA-1 Damper ACRDA-2 Damper ACRDA-3 Damper ACRDA-4 Recirculation Fans Closed Op'n to recirculation/cleanup setting Open Closed 1 running D.
C.
COOK - UNIT 2 B 3/4 7-4d Amendment No.
U O
OO0 I
CRH 26 24 CONTROL ROOM BETA SKIN AND GAINMA BODY DOSE Note:
skin dose limit = 30 rem 22 20 18 16 14 f12 0O 10 BETA SKIN DOS DOSE LIMIT-WHOLEBODY DOSE IIII~IIIIIII
~ I ~ II~ SS<llll ~ SS<SSISI
~ Ill<<<S<ll<S<lllllll
~ SS<sll ~ <<Ill<ISIS<~IIIIIII
~Illllllllllllllllllll<l
~ <<<I<<<<<<<<<<<<<<<<<<<<<<
~ <<<<<Ill I ~ I ~
SS ~ < ~
'AMMA WHOLE BODY DOSE WWWW WWMW WMWW MMMM WWWW WWWW WWW~
200 400 600 800 1000 1200 1400 1600 1800 2000 MAKEUP AIR FLOW RATE (cpm) 0
U O
C4H FIGURE 3:
CONTROL ROOM THYROID DOSE
~3 Q
Qg9 ft 0
30 25 20 E
L lU cn 15 0O 10 0
200 400 600 800 1000 1200 1400 1600 1800 2000 FILTERED MAKEUP AIR FLOW RATE (cfm)
DOSE LIMIT-THYROID raaaeeaeaaeaaaeaaaaaeeaaaeaeeaaaeaeaeaaeaaaepeaeaaag+eeeereaaea+eaaaaeaaaaaaaaaaa 00
%11%
r 0
UNFILTERED INLEAKAGE lail ygl olL1 lg11 yO 1
60ctm i" i1 0
50cfm+
y4 yO g1 40cfm 30cfm ~
20cfm 10ctm ~
ATTACHMENT 3 TO AEP:NRC:08560 WESTINGHOUSE ELECTRIC CORPORATION CONTROL ROOM HABITABILITYANALYSIS
ATTACHMENT 3 TO AEP:NRC:08560 WESTINGHOUSE ELECTRIC CORPORATION CONTROL ROOM HABITABILITYANALYSIS
Westinghouse Water Reactor Electric Corporation Dlylslons Box 355 Pins0urgh Pennsylvania l5230 0355 AEP-85-629 May 16, 1985 NS-OPLS-OPL-85-235 Ref 1: Telecon 3/18/85
- 3. Feinstein (AEP)
K. Rubin (W),
L. Tomasic (W)
Mr. M.
P. Alexich, Vice President tI Director, Nuclear Operations American Electric Power Service Corporation One Riverside Plaza
- Columbus, Ohio 43216 Ref 2:
LER Submittal 85-007 3/25/85 AMERICAN ELECTRIC POWER SERVICE CORPORATION D.
C.
COOK UNITS 1
AND 2 CONTROL ROOM DOSE EVALUATION
Dear Mr. Alexich:
In response to the referenced request from American Electric Power Service Corporation (Ref. 1), Westinghouse has reviewed the AFP control room dose calculations, documented in Ref. 2, and we find the methodology and the resulting doses to be conservative.
This conclusion is based upon a comparison of the methodology and results of the AEP dose calculations to the methodology and results of analyses performed by Westinghouse.
Parametric values for the major calculational parameters used by Westinghouse are provided in Table l.
Dose conversion factors are provided in Table 2.
The resulting doses are summarized in Table 3 and presented graphically in Figures 1
and 2.
All of the calculated doses are within the guidelines of GDC-19 and SRP 6.4.
- Hence, no protective clothing or eye protection will be required.
Ver tr ly
- ours, KB/anj A.
Su
, Manager Great La es Area Projects Department
cc:
H.
W.
J.
V.
R.
R.
B.
P. Alex)eh, 1L/lA G. Sm)th, 1L/lA G. Felnste/n, 1L/1A Vanderburg, 1L/lA W. Jurgensen, 1L/lA Shoemaker, 1L/lA
- Svensson, 1L/lA
NS-OPLS-OPL-85-235 TABLE 1
PARAMETERS USED IN EVALuATING THE CONTROL ROOM OOSES OUE TO A LOCA FOR THE 0.
C.
COOK NUCL'EAR PLANT General Core power level, HWt Full-power operation, effective full-power days (EFPO)
(Based on a three-region equilibrium cycle core at end of life) 3391 900 Source Term The core iodine and noble gas inventories are based upon a standard Westinghouse 3565 HWt core and have been adjusted downward to reflect a power level of 3391 HWt.
Fifty percent of the core iodine is assumed to be uniformly distributed in the lower containment at time zero (TIO-14844/Regulatory Guide 1.4).
I-l31 I-132 I-133 I-134 I-135 4.7 x 10 curies 7
6.9 x 10 7
9.5 x 10 7
1.1 x 10 8 8.9 x 10 7 Iodine Plate-out Factor 0.5 Iodine species Elemental Organic Particulate 0.91 0.04 0.05 100 percent of the core noble gas is released to containment.
Kr-85m Kr-85 Kr-87 Kr-88 2.6 x 10 curies 7
6.3 x 10 5
4.7 x 10 6.7 x 10 7
0242n/KR/3-85
NS-OPLS-OPL-85-235 TABLE 1
(2 of 4)
PARAMETERS USEO IN EVALUATING THE CONTROL ROOM OOSFS DUE TO A LOCA FOR THE. 0.
C.
COOK NUCLEAR PLANT Xe-131m Xe-133m Xe-133 Xe-135m Xe-135 Xe-138 6.7 x 10 5
2.8 x 10 7
1.8 x 10 8 3.8 x 10 7
4.0 x 10 7
1.5 x 10 8 Activit Release Parameters Free volume of containment, ft3 Volume of upper containment, ft3 Volume of lower containment, ft3 Volume of ice beds 1.23 x 10 6 7.47 x 10 5
3.65 x 10 5 1.22 x 10 5
Containment leak rate 0-24 hr, percent/day
>24 hr.
0.25 0.125
- Control, HVAC and Com uter Rooms 3
Free volume, ft Unfi 1 tered infi 1trati on rate, ft /min 3
Filtered intake rate, ft /min 3
3 Internal recirculation rate, ft /min Iodine removal efficiency for charcoal adsorber (elemental and methyl), percent HEPA filter efficiency for particulates, percent 62,356 10 to 60 200 to 800 5400 95 99 0242n/KR/3-85
NS-OPLS-OPL-85-235 TABLE 1
(3 of 4)
PARAMETERS USEO IN EVALUATING THE CONTROL ROOM OOSFS DUE TO A LOCA FOR THE 0.
C.
COOK NUCLEAR PLANT Containment S ra Parameters 3
Sprayed volume (upper containment), ft Spray fall height, ft
-1 Elemental iodine spray,
- lambda, hr Flemental iodine OF (includes the combined effects of sprays and the ice condenser)
-1 Particulate iodine spray
-50 lo 200 4.8
-100 Ice Condenser Parameters Elemental iodine removal efficiency 0-10 min.
0 10-20 min.
>20 min.
0.3 Flow rates, cfm 0-10 min. (average)
>10 min.
416,000 (from lower to upper containment) 41,800 (recirculated between lower and upper containment)
Miscellaneous Parameters 3
Atmospheric dispersion factors at the control room air intake, sec/m
-4 The 0-24 hour x/g of 8.26 x 10 is adjusted for wind speed, wind direction and occupancy according to the following table:
Oi rection
~Occu anc Over all Factor 0-8 hr.
8-24 hr.
1-4 days 4-30 days
.67
.5
.33
.88
.75
.5
.6
.59
.23
.066 0242n/KR/3-85
NS-OPLS-OPL-85-235 TABLE 1
(4 of 4)
PARAMETERS USED IN EVALUATING THE CONTROL ROOM DOSES DUE TO A LOCA FOR THE D.
C.
COOK NUCLEAR PLANT The overall x/l} factors are as 0-8 hr 8-24 24-96 96-720 fol 1ows:
-4 3
8.26 x 10 sec/m 4.87 x 10 1.9 x 10 5.45 x 10 Breathing rate, m /sec 3
3.47 x 10 Dose conversion factors See Table 2
Finite cloud gamma dose'eduction factor*
28
- K. G. Murphy, K.
M. Campe, "Nuclear Power Plant Control Room Ventilation System Design for Heeting GDC 19," 13th AEC Air Cleaning Conference.
0242n/KR/3-85
NS-QPLS-OPL-85-235 TABLE 2 DOSE CONVERSION FACTORS USED IN ACCIDENT ANALYSIS*
Nuclide Total Body 3
rem-m Ci-s Beta Skin 3
rem-m Ci-s Thyroid
~rem/C1 I-1 31 I-132 I-133 I-134 I-135 NA
.NA NA NA NA NA NA NA NA NA 1.49E+6 1.43E+4 2.69E+5 3.73E+3 5.60E+4 Kr-85m Kr-85 Kr-87 Kr-88 3.71E-2 5.11E-4 1.88E-l 4.67E-1 4.63E-2 4.25E-2 3.09E-1 7.52E-2 NA NA Xe-131m Xe-133m Xe-133 Xe-135m Xe-135 Xe-138 2.91E-3 7.97E-3 9.33E-3 9.91E-2 5.75E-2
'2.80E-1 1.51E-2 3.15E-2 9.70E-3 2.25E-2 5.90E-2 1.31E-l NA NA NA NA NA NA
+"Calculation of Annual Doses to.Han from Routine Releases of Reactor Effluents for the Purpose of Evaluating Compliance with 10 CFR Part 20 Appendix I,"
USNRC Regulatory Guide 1.109, Rev. 1, October 1977.
0242n/KR/3-85
E
NS-OPLS-OPL-85-235 TABLE 3 P
30-OAY DOSES TO CONTROL ROOM PERSONNEL OUE TO A DESIGN BASIS LOCA Th roid Doses Rem*
Unfiltered Inleaka e
CFH Filtered Hakeu
- CFH 10 20 30 40 50 60 200 5.9 8.9 11.8 14.7 17.8 20.6 400 8.5 11.3 14.2 17.0 19.9 22.7 800 13.1 15.8 18.4 21.1 23.8 26.4 Beta Skin and Ganma Bod Doses Rem Hakeu Air Flow Rate CFM 200 300 400 500 600 700 800 g Skin*
9.5 10.4 10.9 11.3 11,7 11.9 12.1
~Boy 11,7 13.4 14.5 15.3 16.0 16.5 16.9 Y Body Ad]usted for Finite Cloud"*
.42
.48
.52
.55
.57
.59
.60
- Dose Guideline
= 30 Rem
- Dose Guideline
=
5 Rem 0242n/KR/3-85
.4
0" 50 FIGURE 1
Conti-oI Room Thyroid Dose 25 20 E
15 CD 10 60 cfm 50 40 cfm
~ ~ o
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~ ~ ~
~ os
~ ~
~ ~
~ oo
~
~ ~ ~
cfm 20 cfm cfm
~
~ ~
rrrr
~ ~
~
~ ~ o ~
~
~ oo
~ ~ o 0
200 400 600 Makeup Air'low Rate(cfm) 800 I/I I
CDD II/I I
CO I
IoO GJ
I
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it I.
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