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{{#Wiki_filter:INDIANA8MICHIGANELECTRICCOMPANYP.O.BOX16631COLUMBUS,OHIO43216June27,1986AEP:NRC:0678VDonaldC.CookNuclearPlantUnitNos.1and2DocketNos.50-315and50-316LicenseNos.DPR-58andDPR-74NUREG-0737,SECTIONII.B.3POST-ACCIDENTSAMPLING,SYSTEMMr.HaroldR.Denton,DirectorOfficeofNuclearReactorRegulationU.S.NuclearRegulatoryCommissionWashington,D.C.20555
{{#Wiki_filter:INDIANA8MICHIGANELECTRICCOMPANYP.O.BOX16631COLUMBUS, OHIO43216June27,1986AEP:NRC:0678V DonaldC.CookNuclearPlantUnitNos.1and2DocketNos.50-315and50-316LicenseNos.DPR-58andDPR-74NUREG-0737, SECTIONII.B.3POST-ACCIDENT
: SAMPLING, SYSTEMMr.HaroldR.Denton,DirectorOfficeofNuclearReactorRegulation U.S.NuclearRegulatory Commission Washington, D.C.20555


==DearMr.Denton:==
==DearMr.Denton:==
PerItemIofourletterAEP:NRC:0678S,datedFebruary19,1986,attachedisacompleteanddetaileddescriptionofthePost-AccidentSampling(PAS)SystemrelativetotherequirementsofNUREG-0737,SectionII.B.3.AsaresultoftheevaluationcompletedbyNUSCorporation,wearerequestingexemptionsfromNUREG-0737,SectionII.BE3forthefollowing:1.Undilutedbackupgrabsamplesforin-linemonitoring.2.Heat-tracingcontainmentairsamplelinetopreventplate-outofiodine.3.Transportingcontainmentatmospheresampleforhydrogenanalysis.OurscheduleforclosingoutNUREG-0737,SectionII.B.3(MPA5F-12)isdependentontheNRC'sresponsetotheaboverequestsforexemption.Pursuanttotherequirementsof10CFR170.12(c),wehaveenclosedanapplicationfeeof$150.00forreviewofthisexemptionrequest.ThisdocumenthasbeenpreparedfollowingCorporateprocedureswhichincorporateareasonablesetofcontrolstoinsureitsaccuracyandcompletenesspriortosignaturebytheundersigned.Verytrulyyours,M.P.AlexichVicePresident'lgSIcmAttachmentcc:JohnE.DolanW.G.Smith,Jr.-BridgmanR.C.CallenG.BruchmannG.CharnoffNRCResidentInspector-Bridgman8g07010188860+2PDRADQCK05000318P ie*A1PEJlJ AttachmenttoAEP:NRC:0678V0DEC.COOKPLANTPASPROGRAMAsaresultofNUREG-0578,NUSCorporationwascontractedinMay1980todesignandfabricateapost-accidentsampling(PAS)systemfortheDonaldC.CookNuclearPlant.InOctober1980,duringfabrica-tionofthePASpanels,NUREG-0737wasissued.NewrequirementsandclarificationsforthePASsystemwereincludedinItemII.B.3.whichhadnotbeenoriginallyincorporatedinthePASpaneldesign.Theserequirementsspecificallyincludedchlorideanalysisofreactorcoolantsamples.Duetosizeconstraintsandstipulatedinstallationdeadlines,in-linechlorideanalysiscouldnotbeincorporatedintothePASsamplingequipment.FabricationandtestingoftheequipmentwerecompletedinAugust1981.TheequipmentwasshippedinSeptember1981.ClarificationstoNUREG-0737ItemII.B.3wereissuedinJune1982addingnewrequire-mentstothePASsystem.Tocomplywiththeserequirements,severalmodificationstothePASsystemwereinitiated.Aftercompletionofthesemodifications,NUSwascontractedin1985toprovideverificationandcompliancetestingofthePASsystem.ThistestworkwascompletedinMay1986.TheresultsofthistestworkandreviewofthePASsystemtomeettheintentofNUREG-0737haveresultedinarequestforthefollowingexemptionsfromNUREG-0737:  
PerItemIofourletterAEP:NRC:0678S, datedFebruary19,1986,attachedisacompleteanddetaileddescription ofthePost-Accident Sampling(PAS)Systemrelativetotherequirements ofNUREG-0737, SectionII.B.3.Asaresultoftheevaluation completed byNUSCorporation, wearerequesting exemptions fromNUREG-0737, SectionII.BE3forthefollowing:
'1)Exemtionfromundilutedbackurabsamlesforin-lineIn-linemonitoringforpHanddissolvedoxygenandin-linedegassingfoidissolvedhydrogenarepreferabletoandmoreaccuratethangrabsampleanalyses.Toinsurethefunctionalcapabilityofthesein-lineapparatus,apreventivemainten-anceprogramisperformedsemi-annually.Also,routineuseofthesesystemsisnecessitatedbytheplanttrainingprogram.Iffailureshouldoccurduringlong-termpost-accidentconditions,thecapabilityexiststoflushallsamplelinesandreplacethefailedcomponents.2)Exemtionfromheat-tracincontainmentairsamlelinetorevent.late-outofiodine.ThePAScontainmentairsamplesareanalyzedforisotopicnoblegasesandhydrogenonly.Isotopiciodinesandnon-volatilefissionproductsareanalyzedinthereactorcoolantandcontainmentsumpforassessmentofcoredamage.Therefore,heat-tracingofthecontainmentairsamplelineisnotnecessaryandwouldservenopurpose.3)Exemtionfromtransortincontainmentatmosheresamleforhdroenanalsis.ThePASsystemhasthecapabilitytoobtainandanalyzeanundilutedcontainmentatmospheresampleforhydrogenusinganin-linegaschromatograph.Otherwise,containmentatmospheresamplesaredilutedandtransportedtothecountingfacility fornoblegasanalysis.Analysisofthedilutedsampleforhydrogenwouldnotbewithintherangeofthelaboratorygaschromatograph.PASSYSTEMDESCRIPTIONTheD.C.CookPlantPASsystemconsistsofaliquidandgassamplepanel(LGSP),anUndilutedLiquidSampleStation(ULSS),andrelatedcontrolpanels.Thesamplecollectionstationsarelocatedonelevation587'ftheauxiliarybuilding.Thesampleanalysisfacilitiesarelocatedonelevation609'ftheauxiliarybuildingapproximately220'romthePASsamplingpanellocations.Grabsamplesfromeithersamplingstationareremovedbylead-shieldedsyringeandtransportedinashieldedcontainertotheanalyticalfacilities.Timeandmotionstudieshavebeenconductedtoverifythatsamplesofreactorcoolantandcontainmentatmospherecanbeobtainedandanalyzedwithinthreehoursfromthetimeadecisionismadetotakeasample.ThePASstationsarepoweredfromanemergencypowersupplyorfromthe250V.D.C.stationbatterysystem,andthereforesamplescanbeobtainedduringlossofoffsitepower.Thesamplesrequiringlaboratoryanalysiscanbeanalyzedonlyafteroffsitepowerisrestored.BasedonthenumberandhighreliabilityofCookPlantoffsitepowersources,thesampleanalysiscanbemadewithinthethreehoursfromthetimeadecisionismadetotakeasample.TableIshowsthesamplingandanalyticalcapabilitiesofthePASsystem.ThesystemhasprovisionsforsamplingthelocationsshowninTableIforeitherunitfollowingaLOCA.(3)
1.Undiluted backupgrabsamplesforin-linemonitoring.
LGSPisdesignedforin-lineanalysisofundilutedsamplesandfordilutionofgrabsamples.In-lineanalysesareprovidedforpHanddissolvedoxygenmeasurements.Dissolvedhydrogenintheireactorcoolantisanalyzedbyanin-linegaschromatograph.Dilutionofliquidgrabsamplesisperformedbyisolatinga10mlsampleofreactorcoolantintheLGSPanddilutingwith10litersofdemineralizedwater.VerificationofthedilutionfactorwasperformedusinglithiumhydroxideandcomparisonofsolubleisotopesI-131,I-133,I-135andNa-24.Acomparisonofallisotopes(suchasCs-134,Te-129andSr-89)wasnotpossiblebecauseofthelowlevelsofradio-activityinthetestdataLGSPdilutedsamples.Themeandilutionfactorwasdeterminedtobe846.TheLGSPandULSShaveeightinchesofleadshielding.TheLGSPhasaventilationsystemtoremoveairborneradiationshouldaleakoccurinthepanel.Thisexhaustisfilteredthroughacharcoaladsorberandahigh-efficiencyparticulatefilterintotheauxiliarybuildingventilationsystem.ThesystemisdesignedtoobtainsamplesunderLOCAconditionswithoutexposinganyindividualtoradiationinexcessof5remtothewholebodyandor75remtotheextremities.TheULSSisdesignedtocollectanundilutedreactorcoolantsamplefromHotLegs1or3within96hoursoftheaccident.Thesampleisremovedbyalead-shieldedsyringein30daystoprovidebackupchlorideanalysis.ThePASsystemincorporatesmeansforadequatepurgingofgasandliquidsamplelines.ThepurgeratesforliquidandgassamplesareSdependentonthepressuredropanddrivingforceofeachsamplepoint.(4)  
2.Heat-tracing containment airsamplelinetopreventplate-out ofiodine.3.Transporting containment atmosphere sampleforhydrogenanalysis.
~.Theminimumpurgetimeforthefurthermostpoint(theUnit2HotLegs1a3)isapproximately5minutesat4gpm.Tominimizesampleleakage@thesamplelinesuptoandfromtheLGSPandULSSarewelded.Demineralizedwaterornitrogenisavailabletobeusedtoflushallpost-accidentsamplelinestominimizeblockage.TheLGSPliquidsampleinletfiltercanbeback-flushedwithdemineralizedwater.SamplepurgeandflushfluidsareroutedtoaPASwastecollectiontank,thenpumpedtothecontainmentoftheunitwheretheaccidenthasoccurred.Thesesamplewastelineshaveremotelyoperatedcontainmentisolationvalvestoshutoffwasteflowifnecessary.AllPASvalvesnotaccessibleafteranaccidenthavebeenmodifiedtobeenvironmentallyqualifiedforconditionsinwhichtheymustoperate.Tooperatethethreeair-operatedsampleisolationvalvesinsidecontainment,proceduresprovideforopeningtheinstrumentaircontainmentisolationvalvesafteracontainmentisolationsignalhasbeeninitiated.Comparisonofanalyticalresultsofsamplesfromthevariouslocationscanbeusedtoevaluatesamplerepresentativenessandadequacyofmixing.Inconjunctionwiththiscomparison,comparisonofphysicalparameters,e.g.,coretemperatureandreactorcoolantsystempressure,isavailabletofurtherensurethatrepresentativesamplesarebeingtaken.Processauxiliarysystemscarryingreactorcoolantorcontainmentatmospheregaseswhichareisolatedpostaccident(i.e.,theletdownsystemorthereactorwatercleanupsystem)arenotrequiredtobeplacedinoperation,butportionsoftheexistingNuclearSamplingSystemmustbeplacedinservicetoobtainpost-accidentsamples.
OurscheduleforclosingoutNUREG-0737, SectionII.B.3(MPA5F-12)isdependent ontheNRC'sresponsetotheaboverequestsforexemption.
APASpreventivemaintenanceprogramhasbeendevelopedandwillbeperformedeverysixmonthsbyanoutsidecontractor,commencingapproximatelyOctober1986.ThisprogramincludesserviceofallPAScomponentsandcomparisontestingtonormalsampledata.ThePAStrainingprogramconsistsofclassroomandon-the-jobtraining.QualificationforthePASSystemoperationisperformedbyclassroomandpaneloperationtesting.Chemistrytechniciansarerequalifiedeverysixmonths.PASANALYTICALCAPABILITIESTableIIdepictstheanalyticalcapabilitiesofthepost-accidentsamplingsystem.Matrixtestingforboron,dissolvedoxygen,chlorideandpHanalysiswereperformedbyNUSCorporation.Adescriptionofeachanalysisfollows.BoronBoronanalysisisperformedusingafluoroborateselectiveionelectrode.Therangeofanalysisis375to2000ppmboronwithanaccuracyof+11.4%.Thisrangeisadequatetoconfirmminimumshutdownmarginduringpost-accidentconditions.ComparisontestingshowedthePASanalysistobewithin11.7%oftheanalysisofanormal(undiluted)sample.Dissolved~sdnoenDissolvedhydrogenanalysisisperformedbyisolating10mlofundilutedreactorcoolantintheLGSP.Thesampleisstrippedand(6) degassedusingnitrogen(revisionsaretobemadetouseargonforthispurpose)andcollectedina150mlpanel-mountedflask.(Adesignchangecurrentlybeingprocessedwillsubstituteargonasthestrippinggas.)ThestrippedgasissweptthroughtheevacuatedsystemintoaBaselineGasChromatograph(GC).Thehydrogencontentisrecordedonastripchart.TheGCiscalibratedovera0-2000cc/kgrange.TheaccuracyoftheGCwasdeterminedtobe+11%for15cc/kgand+5.6%for750cc/kg.ThecomparisontestshowedthePASanalysistobewithin+5cc/kgoftheanalysisofanormalsample(40cc/kg).Dissolved~OxenDissolvedoxygenanalysisisperformedusinganin-lineYellowSpringsInstrumentdissolvedoxygenprobeandremoteanalyzer-recorder.Therangeoftheanalyzeris0-20ppmwithanaccuracyof+10%.APASanalysisshowed2.4ppmand0.05ppmcomparedtotheanalysisofanormalsample(2ppmand0ppm,respectively).pHThepHanalysisisperformedusinganin-lineHorizonanalogpHmeterequippedwithagel-filledcombinationpHsensingelectrode.Thesrangeoftheanalyzeris0-14pHwithaaccuracyof+.15pHunits.Comparisontestingwithnormalsamplinganalyseswaswithin.01to.05pHunits.ChlorideChlorideanalysiscanbeperformedonadilutedreactorcoolantgrabsamplewithin96hoursoftheinitiationoftheLOCA.Thelower limitofdetectabilityisapproximately10ppmusinganIonChromatograph.Additionally,ULSSisusedtoobtainanundilutedbackupgrabsamplefromthereactorcoolantHotLegs1or3forchlorideanalysis.Thissampleiscollectedinanin-line75mlflaskinthesamplestation.(Adesignchangehasbeeninitiatedtoinstallthein-lineflaskwhichisonsite.Presently,samplesarecollectedina50mlbottleinsidealeadpig).Within30days,asamplecanbeobtainedfromtheflaskusingalead-linedsyringeandanalyzedintheIonChromatograph.Theundilutedsample'slowerlimitofdetectabilityis10ppbchlorides.Comparisontestingcouldnotbeperformedduetothelowlevelofchlorideinthereactorcoolant.RadionuclidesRadionuclideanalysisofreactorcoolantisperformedonadilutedgrabsample.Thesampleisremovedusingalead-linedsyringeandtakentothecountingroomforgammaanalysisusingtheSeries85MCAwithpdpll/24computerandGe(Li)/HPGedetector.Thedetectoriscompletelysurroundedbya4-inch-thickleadcavewhichactsasashieldfromexternalradiationfields.Thedetectormustbeshielded,sinceatradiationfieldsgreaterthan10mR/hr,thedetectordoesnotfunctionproperly.Anexternalbackgroundradiation,fieldof50mR/hr,theexpecteddoseratefromunisolatedletdownflowwillbereducedbyafactorof5000toapproximately0.01mR/hr,whichwillnotaffecttheoperationofthedetector.However,intheunlikelyeventofcountingroomventilationfailure,theairborneactivityinthecountingfacilitycouldpotentiallyrisetoadoserateofupto981mR/hr.Therefore,samplescouldnotbeanalyzedasthe(8) doserateinsidethecavewouldexceedthe10mR/hroperationallimitforthedetectorduetoairbornecontamination.Inthatcase,radio-nuclideanalysiswouldhavetobedelayeduntiltheconditionwascorrected.Therangeofthecountingequipmentforradionuclideswillbewithinthe1uCi/gto10Ci/gwithanaccuracyof+10%.DilutionofPASsampleswillreducetheactivitytonormalsamplelevels.Compar-isontodailysurveillancesamplesshowedadeviationrangefrom-7.7%to10.5%.hAnalysisofnoblegasfromthelowercontainmentatmosphereisperformedonadilutedgrabsample.ContainmentatmospheresamplesarecapturedintheLGSPineithera0.5ccor5.0ccisolationchamber.Thesampleisthenpurgedintoanevacuated1literpanel-mountedvesselusingargonfordilution.Samplesarethenremovedfromthevesselusingalead-shieldedsyringeandtransportedtothecountingroomfornoblegasanalysis.Thehydrogenanalysisisperformedonanundilutedcontainmentatmospheresampleusingthein-lineBaselineGasChromatograph.GasdilutionsystemtestingwasperformedbyNUSCorporation.Thedilutionfactorsobtainedfromthetestingdemonstratedadilutionof1:225forthe5.0ccsampleand1:1997forthe0.5ccsamplewithanaccuracyof-0.2%to+11.25%.
Pursuanttotherequirements of10CFR170.12(c),
TABLEIIAMLYSISReaatorCoolantBoronDissolvedHydrogenDissolvedOxygenpHRANGE0.375-2.0ppm0-2000cc/kgO.l-20ppm0-14ACCURACY+11.4%5.6%>50cc/kg+11%,<50cc/kg+0.15pH>5<9+0.15pH<5>9METHODFluoroborateSelectiveIonElectrodeGasChromatographyIn-lineprobeIn-lineprobeChlorideRadionuclidentainmentAtmoshereNobleGasHydrogen'>10ppm(diluted)>10ppb(undiluted)1pCi/g-10Ci/gFactorof21pCi/g-10Ci/gFactorof20-4%IonChromatographyGe(Li)DetectorGe(Li)DetectorGasChromatograph TABLEISAMPLELOCATIONRADIONUCLIDEBBORONCHLORIDED.O.HotLeglor3D,GD,GDorU,GU,IU,IU,IN/APressurizerSteamSpaceRHREorWLowerContainmentSumpLowerContainmentAtmosphereD,GD,GD,GD,GD,GD,GD,GD,GD,GD,GU,IU,IU,IN/AN/AN/AN/AU,IU,IU,IN/AN/AN/A~N/AU,IN/ANotApplicableG-GrabSampleI-In-LineAnalysisD-DilutedU-UndilutedD.O.-DissolvedOxygenD.11.-DissolvedHydrogen
wehaveenclosedanapplication feeof$150.00forreviewofthisexemption request.Thisdocumenthasbeenpreparedfollowing Corporate procedures whichincorporate areasonable setofcontrolstoinsureitsaccuracyandcompleteness priortosignature bytheundersigned.
\reJune24,1986DOCKETNO(S).50-315/316ttr.JohhDohan,ViceePresidentIndianaandMichiganElectricCompanyc/oAmericanElectric,PowerServiceCorporation1RiversidePlazaColumbus,Ohio43216
Verytrulyyours,M.P.AlexichVicePresident
'lgSIcmAttachment cc:JohnE.DolanW.G.Smith,Jr.-BridgmanR.C.CallenG.Bruchmann G.CharnoffNRCResidentInspector
-Bridgman8g07010188 860+2PDRADQCK05000318P ie*A1PEJlJ Attachment toAEP:NRC:0678V 0DEC.COOKPLANTPASPROGRAMAsaresultofNUREG-0578, NUSCorporation wascontracted inMay1980todesignandfabricate apost-accident sampling(PAS)systemfortheDonaldC.CookNuclearPlant.InOctober1980,duringfabrica-tionofthePASpanels,NUREG-0737 wasissued.Newrequirements andclarifications forthePASsystemwereincludedinItemII.B.3.whichhadnotbeenoriginally incorporated inthePASpaneldesign.Theserequirements specifically includedchlorideanalysisofreactorcoolantsamples.Duetosizeconstraints andstipulated installation deadlines, in-linechlorideanalysiscouldnotbeincorporated intothePASsamplingequipment.
Fabrication andtestingoftheequipment werecompleted inAugust1981.Theequipment wasshippedinSeptember 1981.Clarifications toNUREG-0737 ItemII.B.3wereissuedinJune1982addingnewrequire-mentstothePASsystem.Tocomplywiththeserequirements, severalmodifications tothePASsystemwereinitiated.
Aftercompletion ofthesemodifications, NUSwascontracted in1985toprovideverification andcompliance testingofthePASsystem.Thistestworkwascompleted inMay1986.TheresultsofthistestworkandreviewofthePASsystemtomeettheintentofNUREG-0737 haveresultedinarequestforthefollowing exemptions fromNUREG-0737:  
'1)Exemtionfromundiluted backurabsamlesforin-lineIn-linemonitoring forpHanddissolved oxygenandin-linedegassing foidissolved hydrogenarepreferable toandmoreaccuratethangrabsampleanalyses.
Toinsurethefunctional capability ofthesein-lineapparatus, apreventive mainten-anceprogramisperformed semi-annually.
Also,routineuseofthesesystemsisnecessitated bytheplanttrainingprogram.Iffailureshouldoccurduringlong-term post-accident conditions, thecapability existstoflushallsamplelinesandreplacethefailedcomponents.
2)Exemtionfromheat-tracin containment airsamlelinetorevent.late-outofiodine.ThePAScontainment airsamplesareanalyzedforisotopicnoblegasesandhydrogenonly.Isotopiciodinesandnon-volatile fissionproductsareanalyzedinthereactorcoolantandcontainment sumpforassessment ofcoredamage.Therefore, heat-tracing ofthecontainment airsamplelineisnotnecessary andwouldservenopurpose.3)Exemtionfromtransortincontainment atmosheresamleforhdroenanalsis.ThePASsystemhasthecapability toobtainandanalyzeanundiluted containment atmosphere sampleforhydrogenusinganin-linegaschromatograph.
Otherwise, containment atmosphere samplesaredilutedandtransported tothecountingfacility fornoblegasanalysis.
Analysisofthedilutedsampleforhydrogenwouldnotbewithintherangeofthelaboratory gaschromatograph.
PASSYSTEMDESCRIPTION TheD.C.CookPlantPASsystemconsistsofaliquidandgassamplepanel(LGSP),anUndiluted LiquidSampleStation(ULSS),andrelatedcontrolpanels.Thesamplecollection stationsarelocatedonelevation 587'ftheauxiliary building.
Thesampleanalysisfacilities arelocatedonelevation 609'ftheauxiliary buildingapproximately 220'romthePASsamplingpanellocations.
Grabsamplesfromeithersamplingstationareremovedbylead-shielded syringeandtransported inashieldedcontainer totheanalytical facilities.
Timeandmotionstudieshavebeenconducted toverifythatsamplesofreactorcoolantandcontainment atmosphere canbeobtainedandanalyzedwithinthreehoursfromthetimeadecisionismadetotakeasample.ThePASstationsarepoweredfromanemergency powersupplyorfromthe250V.D.C.stationbatterysystem,andtherefore samplescanbeobtainedduringlossofoffsitepower.Thesamplesrequiring laboratory analysiscanbeanalyzedonlyafteroffsitepowerisrestored.
Basedonthenumberandhighreliability ofCookPlantoffsitepowersources,thesampleanalysiscanbemadewithinthethreehoursfromthetimeadecisionismadetotakeasample.TableIshowsthesamplingandanalytical capabilities ofthePASsystem.Thesystemhasprovisions forsamplingthelocations showninTableIforeitherunitfollowing aLOCA.(3)
LGSPisdesignedforin-lineanalysisofundiluted samplesandfordilutionofgrabsamples.In-lineanalysesareprovidedforpHanddissolved oxygenmeasurements.
Dissolved hydrogenintheireactorcoolantisanalyzedbyanin-linegaschromatograph.
Dilutionofliquidgrabsamplesisperformed byisolating a10mlsampleofreactorcoolantintheLGSPanddilutingwith10litersofdemineralized water.Verification ofthedilutionfactorwasperformed usinglithiumhydroxide andcomparison ofsolubleisotopesI-131,I-133,I-135andNa-24.Acomparison ofallisotopes(suchasCs-134,Te-129andSr-89)wasnotpossiblebecauseofthelowlevelsofradio-activityinthetestdataLGSPdilutedsamples.Themeandilutionfactorwasdetermined tobe846.TheLGSPandULSShaveeightinchesofleadshielding.
TheLGSPhasaventilation systemtoremoveairborneradiation shouldaleakoccurinthepanel.Thisexhaustisfilteredthroughacharcoaladsorberandahigh-efficiency particulate filterintotheauxiliary buildingventilation system.ThesystemisdesignedtoobtainsamplesunderLOCAconditions withoutexposinganyindividual toradiation inexcessof5remtothewholebodyandor75remtotheextremities.
TheULSSisdesignedtocollectanundiluted reactorcoolantsamplefromHotLegs1or3within96hoursoftheaccident.
Thesampleisremovedbyalead-shielded syringein30daystoprovidebackupchlorideanalysis.
ThePASsystemincorporates meansforadequatepurgingofgasandliquidsamplelines.ThepurgeratesforliquidandgassamplesareSdependent onthepressuredropanddrivingforceofeachsamplepoint.(4)  
~.Theminimumpurgetimeforthefurthermost point(theUnit2HotLegs1a3)isapproximately 5minutesat4gpm.Tominimizesampleleakage@thesamplelinesuptoandfromtheLGSPandULSSarewelded.Demineralized waterornitrogenisavailable tobeusedtoflushallpost-accident samplelinestominimizeblockage.
TheLGSPliquidsampleinletfiltercanbeback-flushed withdemineralized water.SamplepurgeandflushfluidsareroutedtoaPASwastecollection tank,thenpumpedtothecontainment oftheunitwheretheaccidenthasoccurred.
Thesesamplewastelineshaveremotelyoperatedcontainment isolation valvestoshutoffwasteflowifnecessary.
AllPASvalvesnotaccessible afteranaccidenthavebeenmodifiedtobeenvironmentally qualified forconditions inwhichtheymustoperate.Tooperatethethreeair-operated sampleisolation valvesinsidecontainment, procedures provideforopeningtheinstrument aircontainment isolation valvesafteracontainment isolation signalhasbeeninitiated.
Comparison ofanalytical resultsofsamplesfromthevariouslocations canbeusedtoevaluatesamplerepresentativeness andadequacyofmixing.Inconjunction withthiscomparison, comparison ofphysicalparameters, e.g.,coretemperature andreactorcoolantsystempressure, isavailable tofurtherensurethatrepresentative samplesarebeingtaken.Processauxiliary systemscarryingreactorcoolantorcontainment atmosphere gaseswhichareisolatedpostaccident(i.e.,theletdownsystemorthereactorwatercleanupsystem)arenotrequiredtobeplacedinoperation, butportionsoftheexistingNuclearSamplingSystemmustbeplacedinservicetoobtainpost-accident samples.
APASpreventive maintenance programhasbeendeveloped andwillbeperformed everysixmonthsbyanoutsidecontractor, commencing approximately October1986.ThisprogramincludesserviceofallPAScomponents andcomparison testingtonormalsampledata.ThePAStrainingprogramconsistsofclassroom andon-the-job training.
Qualification forthePASSystemoperation isperformed byclassroom andpaneloperation testing.Chemistry technicians arerequalified everysixmonths.PASANALYTICAL CAPABILITIES TableIIdepictstheanalytical capabilities ofthepost-accident samplingsystem.Matrixtestingforboron,dissolved oxygen,chlorideandpHanalysiswereperformed byNUSCorporation.
Adescription ofeachanalysisfollows.BoronBoronanalysisisperformed usingafluoroborate selective ionelectrode.
Therangeofanalysisis375to2000ppmboronwithanaccuracyof+11.4%.Thisrangeisadequatetoconfirmminimumshutdownmarginduringpost-accident conditions.
Comparison testingshowedthePASanalysistobewithin11.7%oftheanalysisofanormal(undiluted) sample.Dissolved
~sdnoenDissolved hydrogenanalysisisperformed byisolating 10mlofundiluted reactorcoolantintheLGSP.Thesampleisstrippedand(6) degassedusingnitrogen(revisions aretobemadetouseargonforthispurpose)andcollected ina150mlpanel-mounted flask.(Adesignchangecurrently beingprocessed willsubstitute argonasthestripping gas.)Thestrippedgasissweptthroughtheevacuated systemintoaBaselineGasChromatograph (GC).Thehydrogencontentisrecordedonastripchart.TheGCiscalibrated overa0-2000cc/kgrange.TheaccuracyoftheGCwasdetermined tobe+11%for15cc/kgand+5.6%for750cc/kg.Thecomparison testshowedthePASanalysistobewithin+5cc/kgoftheanalysisofanormalsample(40cc/kg).
Dissolved
~OxenDissolved oxygenanalysisisperformed usinganin-lineYellowSpringsInstrument dissolved oxygenprobeandremoteanalyzer-recorder.
Therangeoftheanalyzeris0-20ppmwithanaccuracyof+10%.APASanalysisshowed2.4ppmand0.05ppmcomparedtotheanalysisofanormalsample(2ppmand0ppm,respectively).
pHThepHanalysisisperformed usinganin-lineHorizonanalogpHmeterequippedwithagel-filled combination pHsensingelectrode.
Thesrangeoftheanalyzeris0-14pHwithaaccuracyof+.15pHunits.Comparison testingwithnormalsamplinganalyseswaswithin.01to.05pHunits.ChlorideChlorideanalysiscanbeperformed onadilutedreactorcoolantgrabsamplewithin96hoursoftheinitiation oftheLOCA.Thelower limitofdetectability isapproximately 10ppmusinganIonChromatograph.
Additionally, ULSSisusedtoobtainanundiluted backupgrabsamplefromthereactorcoolantHotLegs1or3forchlorideanalysis.
Thissampleiscollected inanin-line75mlflaskinthesamplestation.(Adesignchangehasbeeninitiated toinstallthein-lineflaskwhichisonsite.Presently, samplesarecollected ina50mlbottleinsidealeadpig).Within30days,asamplecanbeobtainedfromtheflaskusingalead-lined syringeandanalyzedintheIonChromatograph.
Theundiluted sample'slowerlimitofdetectability is10ppbchlorides.
Comparison testingcouldnotbeperformed duetothelowlevelofchlorideinthereactorcoolant.Radionuclides Radionuclide analysisofreactorcoolantisperformed onadilutedgrabsample.Thesampleisremovedusingalead-lined syringeandtakentothecountingroomforgammaanalysisusingtheSeries85MCAwithpdpll/24computerandGe(Li)/HPGe detector.
Thedetectoriscompletely surrounded bya4-inch-thick leadcavewhichactsasashieldfromexternalradiation fields.Thedetectormustbeshielded, sinceatradiation fieldsgreaterthan10mR/hr,thedetectordoesnotfunctionproperly.
Anexternalbackground radiation, fieldof50mR/hr,theexpecteddoseratefromunisolated letdownflowwillbereducedbyafactorof5000toapproximately 0.01mR/hr,whichwillnotaffecttheoperation ofthedetector.
However,intheunlikelyeventofcountingroomventilation failure,theairborneactivityinthecountingfacilitycouldpotentially risetoadoserateofupto981mR/hr.Therefore, samplescouldnotbeanalyzedasthe(8) doserateinsidethecavewouldexceedthe10mR/hroperational limitforthedetectorduetoairbornecontamination.
Inthatcase,radio-nuclideanalysiswouldhavetobedelayeduntilthecondition wascorrected.
Therangeofthecountingequipment forradionuclides willbewithinthe1uCi/gto10Ci/gwithanaccuracyof+10%.DilutionofPASsampleswillreducetheactivitytonormalsamplelevels.Compar-isontodailysurveillance samplesshowedadeviation rangefrom-7.7%to10.5%.hAnalysisofnoblegasfromthelowercontainment atmosphere isperformed onadilutedgrabsample.Containment atmosphere samplesarecapturedintheLGSPineithera0.5ccor5.0ccisolation chamber.Thesampleisthenpurgedintoanevacuated 1literpanel-mounted vesselusingargonfordilution.
Samplesarethenremovedfromthevesselusingalead-shielded syringeandtransported tothecountingroomfornoblegasanalysis.
Thehydrogenanalysisisperformed onanundiluted containment atmosphere sampleusingthein-lineBaselineGasChromatograph.
Gasdilutionsystemtestingwasperformed byNUSCorporation.
Thedilutionfactorsobtainedfromthetestingdemonstrated adilutionof1:225forthe5.0ccsampleand1:1997forthe0.5ccsamplewithanaccuracyof-0.2%to+11.25%.
TABLEIIAMLYSISReaatorCoolantBoronDissolved HydrogenDissolved OxygenpHRANGE0.375-2.0ppm0-2000cc/kgO.l-20ppm0-14ACCURACY+11.4%5.6%>50cc/kg+11%,<50cc/kg+0.15pH>5<9+0.15pH<5>9METHODFluoroborate Selective IonElectrode GasChromatography In-lineprobeIn-lineprobeChlorideRadionuclide ntainment AtmoshereNobleGasHydrogen'>10ppm(diluted)
>10ppb(undiluted) 1pCi/g-10Ci/gFactorof21pCi/g-10Ci/gFactorof20-4%IonChromatography Ge(Li)DetectorGe(Li)DetectorGasChromatograph TABLEISAMPLELOCATIONRADIONUCLIDEB BORONCHLORIDED.O.HotLeglor3D,GD,GDorU,GU,IU,IU,IN/APressurizer SteamSpaceRHREorWLowerContainment SumpLowerContainment Atmosphere D,GD,GD,GD,GD,GD,GD,GD,GD,GD,GU,IU,IU,IN/AN/AN/AN/AU,IU,IU,IN/AN/AN/A~N/AU,IN/ANotApplicable G-GrabSampleI-In-LineAnalysisD-DilutedU-Undiluted D.O.-Dissolved OxygenD.11.-Dissolved Hydrogen
\reJune24,1986DOCKETNO(S).50-315/316 ttr.JohhDohan,ViceePresident IndianaandMichiganElectricCompanyc/oAmericanElectric, PowerServiceCorporation 1Riverside PlazaColumbus, Ohio43216


==SUBJECT:==
==SUBJECT:==
D.C.CookPlant,Units1and2.r/~,~/"/r/er4i/''DISTRIION:w/oenclosure~Docket-F-i.le~PRCSystemNRCPDRLocalPDRPWR84RdgBJYoungbloodRdgt1DuncanDlliggintonOGCACRS(10)JPartlowBGrimesEJordanNThompsonThefollowingdocumentsconcerningourreviewofthesubjectfacilityaretransmittedforyourinformation.DNoticeofReceiptofApplication,datedDDraft/FinalEnvironmentalStatment,datedDNoticeofAvailabilityofDraft/FinalEnvironmentalStatement,datedDSafetyEvaluationReport,orSupplementNo.,datedDNoticeofHearingonApplicationforConstructionPermit,datedDNoticeofConsiderationofIssuanceofFacilityOperatingLicense,datedIIPMonthlyNotice;ApplicationsandAmendmentstoOperatingLicensesInvolvingnoSignificantHazardsConsiderations,datedJul161986.(Seepage25770)DApplicationandSafetyAnalysisReport,VolumeDAmendmentNo.toApplication/SARdatedDConstructionPermitNo.CPPR-DFacilityOperatingLicenseNo.,AmendmentNo.,AmendmentNo.dated,datedDOrderExtendingConstruction'CompletionDate,datedDOther(Specify/
D.C.CookPlant,Units1and2.r/~,~/"/r/er4i/''DISTRIION:w/oenclosure
~Docket-F-i.le~
PRCSystemNRCPDRLocalPDRPWR84RdgBJYoungblood Rdgt1DuncanDlligginton OGCACRS(10)JPartlowBGrimesEJordanNThompson Thefollowing documents concerning ourreviewofthesubjectfacilityaretransmitted foryourinformation.
DNoticeofReceiptofApplication, datedDDraft/Final Environmental
: Statment, datedDNoticeofAvailability ofDraft/Final Environmental Statement, datedDSafetyEvaluation Report,orSupplement No.,datedDNoticeofHearingonApplication forConstruction Permit,datedDNoticeofConsideration ofIssuanceofFacilityOperating License,datedIIPMonthlyNotice;Applications andAmendments toOperating LicensesInvolving noSignificant HazardsConsiderations, datedJul161986.(Seepage25770)DApplication andSafetyAnalysisReport,VolumeDAmendment No.toApplication/SAR datedDConstruction PermitNo.CPPR-DFacilityOperating LicenseNo.,Amendment No.,Amendment No.dated,datedDOrderExtending Construction'Completion Date,datedDOther(Specify/


==Enclosures:==
==Enclosures:==
AsstatedOfficeofNuclearReactorRegulationcc:Seenextpage.PjM4/PN.07/4+86.OrFICe~SURNAME%DATE+aCr~~~~~~~~~~~~~~~NAGFORM318(1/84)NACM0240P.WR/.I'lR.DWigginton..07/.QQBG....
 
AsstatedOfficeofNuclearReactorRegulation cc:Seenextpage.PjM4/PN.07/4+86.
OrFICe~SURNAME%DATE+aCr~~~~~~~~~~~~~~~NAGFORM318(1/84)NACM0240P.WR/.I'lR.DWigginton..
07/.QQBG....
rk~t~~4g~~~E~~.Sra~='r,~r~D}}
rk~t~~4g~~~E~~.Sra~='r,~r~D}}

Revision as of 06:33, 29 June 2018

Forwards Complete & Detailed Description of post-accident Sampling Sys Per Reqirements of NUREG-0737,Section II.B.3. Exemption from Section II.B.3 for Listed Items Requested. Fee Paid
ML17334A975
Person / Time
Site: Cook  
Issue date: 06/27/1986
From: ALEXICH M P
INDIANA MICHIGAN POWER CO. (FORMERLY INDIANA & MICHIG
To: DENTON H R
Office of Nuclear Reactor Regulation
References
RTR-NUREG-0737, RTR-NUREG-737, TASK-2.B.3, TASK-TM AEP:NRC:0678V, AEP:NRC:678V, NUDOCS 8607010188
Download: ML17334A975 (15)


Text

INDIANA8MICHIGANELECTRICCOMPANYP.O.BOX16631COLUMBUS, OHIO43216June27,1986AEP:NRC:0678V DonaldC.CookNuclearPlantUnitNos.1and2DocketNos.50-315and50-316LicenseNos.DPR-58andDPR-74NUREG-0737, SECTIONII.B.3POST-ACCIDENT

SAMPLING, SYSTEMMr.HaroldR.Denton,DirectorOfficeofNuclearReactorRegulation U.S.NuclearRegulatory Commission Washington, D.C.20555

DearMr.Denton:

PerItemIofourletterAEP:NRC:0678S, datedFebruary19,1986,attachedisacompleteanddetaileddescription ofthePost-Accident Sampling(PAS)Systemrelativetotherequirements ofNUREG-0737, SectionII.B.3.Asaresultoftheevaluation completed byNUSCorporation, wearerequesting exemptions fromNUREG-0737, SectionII.BE3forthefollowing:

1.Undiluted backupgrabsamplesforin-linemonitoring.

2.Heat-tracing containment airsamplelinetopreventplate-out ofiodine.3.Transporting containment atmosphere sampleforhydrogenanalysis.

OurscheduleforclosingoutNUREG-0737, SectionII.B.3(MPA5F-12)isdependent ontheNRC'sresponsetotheaboverequestsforexemption.

Pursuanttotherequirements of10CFR170.12(c),

wehaveenclosedanapplication feeof$150.00forreviewofthisexemption request.Thisdocumenthasbeenpreparedfollowing Corporate procedures whichincorporate areasonable setofcontrolstoinsureitsaccuracyandcompleteness priortosignature bytheundersigned.

Verytrulyyours,M.P.AlexichVicePresident

'lgSIcmAttachment cc:JohnE.DolanW.G.Smith,Jr.-BridgmanR.C.CallenG.Bruchmann G.CharnoffNRCResidentInspector

-Bridgman8g07010188 860+2PDRADQCK05000318P ie*A1PEJlJ Attachment toAEP:NRC:0678V 0DEC.COOKPLANTPASPROGRAMAsaresultofNUREG-0578, NUSCorporation wascontracted inMay1980todesignandfabricate apost-accident sampling(PAS)systemfortheDonaldC.CookNuclearPlant.InOctober1980,duringfabrica-tionofthePASpanels,NUREG-0737 wasissued.Newrequirements andclarifications forthePASsystemwereincludedinItemII.B.3.whichhadnotbeenoriginally incorporated inthePASpaneldesign.Theserequirements specifically includedchlorideanalysisofreactorcoolantsamples.Duetosizeconstraints andstipulated installation deadlines, in-linechlorideanalysiscouldnotbeincorporated intothePASsamplingequipment.

Fabrication andtestingoftheequipment werecompleted inAugust1981.Theequipment wasshippedinSeptember 1981.Clarifications toNUREG-0737 ItemII.B.3wereissuedinJune1982addingnewrequire-mentstothePASsystem.Tocomplywiththeserequirements, severalmodifications tothePASsystemwereinitiated.

Aftercompletion ofthesemodifications, NUSwascontracted in1985toprovideverification andcompliance testingofthePASsystem.Thistestworkwascompleted inMay1986.TheresultsofthistestworkandreviewofthePASsystemtomeettheintentofNUREG-0737 haveresultedinarequestforthefollowing exemptions fromNUREG-0737:

'1)Exemtionfromundiluted backurabsamlesforin-lineIn-linemonitoring forpHanddissolved oxygenandin-linedegassing foidissolved hydrogenarepreferable toandmoreaccuratethangrabsampleanalyses.

Toinsurethefunctional capability ofthesein-lineapparatus, apreventive mainten-anceprogramisperformed semi-annually.

Also,routineuseofthesesystemsisnecessitated bytheplanttrainingprogram.Iffailureshouldoccurduringlong-term post-accident conditions, thecapability existstoflushallsamplelinesandreplacethefailedcomponents.

2)Exemtionfromheat-tracin containment airsamlelinetorevent.late-outofiodine.ThePAScontainment airsamplesareanalyzedforisotopicnoblegasesandhydrogenonly.Isotopiciodinesandnon-volatile fissionproductsareanalyzedinthereactorcoolantandcontainment sumpforassessment ofcoredamage.Therefore, heat-tracing ofthecontainment airsamplelineisnotnecessary andwouldservenopurpose.3)Exemtionfromtransortincontainment atmosheresamleforhdroenanalsis.ThePASsystemhasthecapability toobtainandanalyzeanundiluted containment atmosphere sampleforhydrogenusinganin-linegaschromatograph.

Otherwise, containment atmosphere samplesaredilutedandtransported tothecountingfacility fornoblegasanalysis.

Analysisofthedilutedsampleforhydrogenwouldnotbewithintherangeofthelaboratory gaschromatograph.

PASSYSTEMDESCRIPTION TheD.C.CookPlantPASsystemconsistsofaliquidandgassamplepanel(LGSP),anUndiluted LiquidSampleStation(ULSS),andrelatedcontrolpanels.Thesamplecollection stationsarelocatedonelevation 587'ftheauxiliary building.

Thesampleanalysisfacilities arelocatedonelevation 609'ftheauxiliary buildingapproximately 220'romthePASsamplingpanellocations.

Grabsamplesfromeithersamplingstationareremovedbylead-shielded syringeandtransported inashieldedcontainer totheanalytical facilities.

Timeandmotionstudieshavebeenconducted toverifythatsamplesofreactorcoolantandcontainment atmosphere canbeobtainedandanalyzedwithinthreehoursfromthetimeadecisionismadetotakeasample.ThePASstationsarepoweredfromanemergency powersupplyorfromthe250V.D.C.stationbatterysystem,andtherefore samplescanbeobtainedduringlossofoffsitepower.Thesamplesrequiring laboratory analysiscanbeanalyzedonlyafteroffsitepowerisrestored.

Basedonthenumberandhighreliability ofCookPlantoffsitepowersources,thesampleanalysiscanbemadewithinthethreehoursfromthetimeadecisionismadetotakeasample.TableIshowsthesamplingandanalytical capabilities ofthePASsystem.Thesystemhasprovisions forsamplingthelocations showninTableIforeitherunitfollowing aLOCA.(3)

LGSPisdesignedforin-lineanalysisofundiluted samplesandfordilutionofgrabsamples.In-lineanalysesareprovidedforpHanddissolved oxygenmeasurements.

Dissolved hydrogenintheireactorcoolantisanalyzedbyanin-linegaschromatograph.

Dilutionofliquidgrabsamplesisperformed byisolating a10mlsampleofreactorcoolantintheLGSPanddilutingwith10litersofdemineralized water.Verification ofthedilutionfactorwasperformed usinglithiumhydroxide andcomparison ofsolubleisotopesI-131,I-133,I-135andNa-24.Acomparison ofallisotopes(suchasCs-134,Te-129andSr-89)wasnotpossiblebecauseofthelowlevelsofradio-activityinthetestdataLGSPdilutedsamples.Themeandilutionfactorwasdetermined tobe846.TheLGSPandULSShaveeightinchesofleadshielding.

TheLGSPhasaventilation systemtoremoveairborneradiation shouldaleakoccurinthepanel.Thisexhaustisfilteredthroughacharcoaladsorberandahigh-efficiency particulate filterintotheauxiliary buildingventilation system.ThesystemisdesignedtoobtainsamplesunderLOCAconditions withoutexposinganyindividual toradiation inexcessof5remtothewholebodyandor75remtotheextremities.

TheULSSisdesignedtocollectanundiluted reactorcoolantsamplefromHotLegs1or3within96hoursoftheaccident.

Thesampleisremovedbyalead-shielded syringein30daystoprovidebackupchlorideanalysis.

ThePASsystemincorporates meansforadequatepurgingofgasandliquidsamplelines.ThepurgeratesforliquidandgassamplesareSdependent onthepressuredropanddrivingforceofeachsamplepoint.(4)

~.Theminimumpurgetimeforthefurthermost point(theUnit2HotLegs1a3)isapproximately 5minutesat4gpm.Tominimizesampleleakage@thesamplelinesuptoandfromtheLGSPandULSSarewelded.Demineralized waterornitrogenisavailable tobeusedtoflushallpost-accident samplelinestominimizeblockage.

TheLGSPliquidsampleinletfiltercanbeback-flushed withdemineralized water.SamplepurgeandflushfluidsareroutedtoaPASwastecollection tank,thenpumpedtothecontainment oftheunitwheretheaccidenthasoccurred.

Thesesamplewastelineshaveremotelyoperatedcontainment isolation valvestoshutoffwasteflowifnecessary.

AllPASvalvesnotaccessible afteranaccidenthavebeenmodifiedtobeenvironmentally qualified forconditions inwhichtheymustoperate.Tooperatethethreeair-operated sampleisolation valvesinsidecontainment, procedures provideforopeningtheinstrument aircontainment isolation valvesafteracontainment isolation signalhasbeeninitiated.

Comparison ofanalytical resultsofsamplesfromthevariouslocations canbeusedtoevaluatesamplerepresentativeness andadequacyofmixing.Inconjunction withthiscomparison, comparison ofphysicalparameters, e.g.,coretemperature andreactorcoolantsystempressure, isavailable tofurtherensurethatrepresentative samplesarebeingtaken.Processauxiliary systemscarryingreactorcoolantorcontainment atmosphere gaseswhichareisolatedpostaccident(i.e.,theletdownsystemorthereactorwatercleanupsystem)arenotrequiredtobeplacedinoperation, butportionsoftheexistingNuclearSamplingSystemmustbeplacedinservicetoobtainpost-accident samples.

APASpreventive maintenance programhasbeendeveloped andwillbeperformed everysixmonthsbyanoutsidecontractor, commencing approximately October1986.ThisprogramincludesserviceofallPAScomponents andcomparison testingtonormalsampledata.ThePAStrainingprogramconsistsofclassroom andon-the-job training.

Qualification forthePASSystemoperation isperformed byclassroom andpaneloperation testing.Chemistry technicians arerequalified everysixmonths.PASANALYTICAL CAPABILITIES TableIIdepictstheanalytical capabilities ofthepost-accident samplingsystem.Matrixtestingforboron,dissolved oxygen,chlorideandpHanalysiswereperformed byNUSCorporation.

Adescription ofeachanalysisfollows.BoronBoronanalysisisperformed usingafluoroborate selective ionelectrode.

Therangeofanalysisis375to2000ppmboronwithanaccuracyof+11.4%.Thisrangeisadequatetoconfirmminimumshutdownmarginduringpost-accident conditions.

Comparison testingshowedthePASanalysistobewithin11.7%oftheanalysisofanormal(undiluted) sample.Dissolved

~sdnoenDissolved hydrogenanalysisisperformed byisolating 10mlofundiluted reactorcoolantintheLGSP.Thesampleisstrippedand(6) degassedusingnitrogen(revisions aretobemadetouseargonforthispurpose)andcollected ina150mlpanel-mounted flask.(Adesignchangecurrently beingprocessed willsubstitute argonasthestripping gas.)Thestrippedgasissweptthroughtheevacuated systemintoaBaselineGasChromatograph (GC).Thehydrogencontentisrecordedonastripchart.TheGCiscalibrated overa0-2000cc/kgrange.TheaccuracyoftheGCwasdetermined tobe+11%for15cc/kgand+5.6%for750cc/kg.Thecomparison testshowedthePASanalysistobewithin+5cc/kgoftheanalysisofanormalsample(40cc/kg).

Dissolved

~OxenDissolved oxygenanalysisisperformed usinganin-lineYellowSpringsInstrument dissolved oxygenprobeandremoteanalyzer-recorder.

Therangeoftheanalyzeris0-20ppmwithanaccuracyof+10%.APASanalysisshowed2.4ppmand0.05ppmcomparedtotheanalysisofanormalsample(2ppmand0ppm,respectively).

pHThepHanalysisisperformed usinganin-lineHorizonanalogpHmeterequippedwithagel-filled combination pHsensingelectrode.

Thesrangeoftheanalyzeris0-14pHwithaaccuracyof+.15pHunits.Comparison testingwithnormalsamplinganalyseswaswithin.01to.05pHunits.ChlorideChlorideanalysiscanbeperformed onadilutedreactorcoolantgrabsamplewithin96hoursoftheinitiation oftheLOCA.Thelower limitofdetectability isapproximately 10ppmusinganIonChromatograph.

Additionally, ULSSisusedtoobtainanundiluted backupgrabsamplefromthereactorcoolantHotLegs1or3forchlorideanalysis.

Thissampleiscollected inanin-line75mlflaskinthesamplestation.(Adesignchangehasbeeninitiated toinstallthein-lineflaskwhichisonsite.Presently, samplesarecollected ina50mlbottleinsidealeadpig).Within30days,asamplecanbeobtainedfromtheflaskusingalead-lined syringeandanalyzedintheIonChromatograph.

Theundiluted sample'slowerlimitofdetectability is10ppbchlorides.

Comparison testingcouldnotbeperformed duetothelowlevelofchlorideinthereactorcoolant.Radionuclides Radionuclide analysisofreactorcoolantisperformed onadilutedgrabsample.Thesampleisremovedusingalead-lined syringeandtakentothecountingroomforgammaanalysisusingtheSeries85MCAwithpdpll/24computerandGe(Li)/HPGe detector.

Thedetectoriscompletely surrounded bya4-inch-thick leadcavewhichactsasashieldfromexternalradiation fields.Thedetectormustbeshielded, sinceatradiation fieldsgreaterthan10mR/hr,thedetectordoesnotfunctionproperly.

Anexternalbackground radiation, fieldof50mR/hr,theexpecteddoseratefromunisolated letdownflowwillbereducedbyafactorof5000toapproximately 0.01mR/hr,whichwillnotaffecttheoperation ofthedetector.

However,intheunlikelyeventofcountingroomventilation failure,theairborneactivityinthecountingfacilitycouldpotentially risetoadoserateofupto981mR/hr.Therefore, samplescouldnotbeanalyzedasthe(8) doserateinsidethecavewouldexceedthe10mR/hroperational limitforthedetectorduetoairbornecontamination.

Inthatcase,radio-nuclideanalysiswouldhavetobedelayeduntilthecondition wascorrected.

Therangeofthecountingequipment forradionuclides willbewithinthe1uCi/gto10Ci/gwithanaccuracyof+10%.DilutionofPASsampleswillreducetheactivitytonormalsamplelevels.Compar-isontodailysurveillance samplesshowedadeviation rangefrom-7.7%to10.5%.hAnalysisofnoblegasfromthelowercontainment atmosphere isperformed onadilutedgrabsample.Containment atmosphere samplesarecapturedintheLGSPineithera0.5ccor5.0ccisolation chamber.Thesampleisthenpurgedintoanevacuated 1literpanel-mounted vesselusingargonfordilution.

Samplesarethenremovedfromthevesselusingalead-shielded syringeandtransported tothecountingroomfornoblegasanalysis.

Thehydrogenanalysisisperformed onanundiluted containment atmosphere sampleusingthein-lineBaselineGasChromatograph.

Gasdilutionsystemtestingwasperformed byNUSCorporation.

Thedilutionfactorsobtainedfromthetestingdemonstrated adilutionof1:225forthe5.0ccsampleand1:1997forthe0.5ccsamplewithanaccuracyof-0.2%to+11.25%.

TABLEIIAMLYSISReaatorCoolantBoronDissolved HydrogenDissolved OxygenpHRANGE0.375-2.0ppm0-2000cc/kgO.l-20ppm0-14ACCURACY+11.4%5.6%>50cc/kg+11%,<50cc/kg+0.15pH>5<9+0.15pH<5>9METHODFluoroborate Selective IonElectrode GasChromatography In-lineprobeIn-lineprobeChlorideRadionuclide ntainment AtmoshereNobleGasHydrogen'>10ppm(diluted)

>10ppb(undiluted) 1pCi/g-10Ci/gFactorof21pCi/g-10Ci/gFactorof20-4%IonChromatography Ge(Li)DetectorGe(Li)DetectorGasChromatograph TABLEISAMPLELOCATIONRADIONUCLIDEB BORONCHLORIDED.O.HotLeglor3D,GD,GDorU,GU,IU,IU,IN/APressurizer SteamSpaceRHREorWLowerContainment SumpLowerContainment Atmosphere D,GD,GD,GD,GD,GD,GD,GD,GD,GD,GU,IU,IU,IN/AN/AN/AN/AU,IU,IU,IN/AN/AN/A~N/AU,IN/ANotApplicable G-GrabSampleI-In-LineAnalysisD-DilutedU-Undiluted D.O.-Dissolved OxygenD.11.-Dissolved Hydrogen

\reJune24,1986DOCKETNO(S).50-315/316 ttr.JohhDohan,ViceePresident IndianaandMichiganElectricCompanyc/oAmericanElectric, PowerServiceCorporation 1Riverside PlazaColumbus, Ohio43216

SUBJECT:

D.C.CookPlant,Units1and2.r/~,~/"/r/er4i/DISTRIION:w/oenclosure

~Docket-F-i.le~

PRCSystemNRCPDRLocalPDRPWR84RdgBJYoungblood Rdgt1DuncanDlligginton OGCACRS(10)JPartlowBGrimesEJordanNThompson Thefollowing documents concerning ourreviewofthesubjectfacilityaretransmitted foryourinformation.

DNoticeofReceiptofApplication, datedDDraft/Final Environmental

Statment, datedDNoticeofAvailability ofDraft/Final Environmental Statement, datedDSafetyEvaluation Report,orSupplement No.,datedDNoticeofHearingonApplication forConstruction Permit,datedDNoticeofConsideration ofIssuanceofFacilityOperating License,datedIIPMonthlyNotice;Applications andAmendments toOperating LicensesInvolving noSignificant HazardsConsiderations, datedJul161986.(Seepage25770)DApplication andSafetyAnalysisReport,VolumeDAmendment No.toApplication/SAR datedDConstruction PermitNo.CPPR-DFacilityOperating LicenseNo.,Amendment No.,Amendment No.dated,datedDOrderExtending Construction'Completion Date,datedDOther(Specify/

Enclosures:

AsstatedOfficeofNuclearReactorRegulation cc:Seenextpage.PjM4/PN.07/4+86.

OrFICe~SURNAME%DATE+aCr~~~~~~~~~~~~~~~NAGFORM318(1/84)NACM0240P.WR/.I'lR.DWigginton..

07/.QQBG....

rk~t~~4g~~~E~~.Sra~='r,~r~D