Document B8GyYXv7ry92Z6v0ro4K4NBXm
Fluoroc Sample
Cr=ntrrA=nalyticalLaboratories,Inc.
3048 Research Drive
StateCollege,PA 16801
1%
Phone: (814)231-8032 Fax:(814)231-1253 or (814)231-1580
Anawcal Report
FluorochemicalCharacterizatioonf DrinkingWater Samples
Decatur,Alabama (W1979) CentreAnalyticalLaboratoryReport No. 023-007B
TestingLaboratory CentreAnalyticaLlaboratoryI,nc.
3048 Research Drive StateCollege,PA 16801
3M Environmental Laboratory Contact Kent R. Lindstrom Bldg.2-3E-09 P.O. Box 33331
St.Paul,MN 55133-3331 Phone: (651)778-5352
Requester Kds J.Hansen,Ph.D. 3M EnvironmentalTechnology & SafetyServices
Bldg.2-3E-09 P.O. Box 33331 St.Paul,MN 55133-3331
PAGELOFS
Introduction
Resultasrereportfeodrtheanalysoifsa'sedeosfdrinkiwnagtersamplesreceivebdy Centr.9 AnaWcal LaboratorieIsn,c.(Centre)from the3M EnvironmentaLlaboratory.The samples were collectefdrom Decatur,Alabama. The Centrestudynumber assignedtotheprojectis023-007.
Specififcluorochemiicaclharacterizabobny liquicdhromatography/tandem mass spectrometry (LC/MS/MS) was requestedforallsamples. A'totaolf14 sampleswere receivedforanalysis.
The samples were preparedand analyzedby LCIMS/MS forthefollownglisotffluorochemicals:
Table1:TargetAnalysis
ComDound Name PerfluorooctanSeulfonate PerfluorooctanSeulfonviamide Perfluorooctanoate
Acronym PFOS PFOSA POAA
Data generatedin supportof thisstudywas generatedaccordingto USEPA Good Laboratory PraeUces(GLPs).-The analyticamlethod used was validatebdy Centre.The validatiopnrotocol
and resultasreon filweithCentre.Data presentedhereisthehighestqualitdyata availablaetthis time.
2 Sample Receipt
The samples were submittedinindividuapllasticontainersand were not preserved. Fourteen individusaalmple containerwsere received.Samples were receivedon 02/15100.The sample collectiodnateswere notsupplied.Chain-of-custodiynformatonispresentedinAttachmentA-
3. Holding Times.
The analyticamlethod used was validatedagainsta ma)dmum holdingtime of 14 days. The stabiliotfytheanalytesofinteresftorlongerperiodshas notbeen determined.
PAGE 2OF5
4 Methods-Analyticaanld Preparatory
4.1 LCIMS/MS
4.1.1 SamplePreparatifoonrLC/MS/MSAnalysis
Sampleswereinitiatlrleyatewdith200 uL of250 mg/Lsodiumthiosulfsaotleutiotnoremove residucahllodneS.o,lidphase extractio(nSPE) was used to preparethe samplesfor LC/MS/MS anaws. A forty-millilpiotretrionofsample was transferretdo a Cls SPE cartridge. The cartridgweas firsetlutedwith5 mL of 40% methanol inwater solution.The eluatewas discardedand the SPE column was then elutedwith100% methanol. A 5 mi portionof methanol was collectefdoranalysisby LC/MS/MS. This treatmentresultedinan eight-fold concentrationofthe samples priortoanalysis-.
4.1.2 Sample Analysisby LCIMSIMS
In HPLC, an aliquotof extractisinjectedand passed througha liquid@@hascehromatographic column. Based on the affiniotfythe analyteforthestationarpyhase inthe column relativteo theliquimdobile phase,the analyteisretainedfora characteristaimcount oftime. Following HPLC separation,ES/MS providesa rapidand accuratemeans foranawng a wide range of organiccompounds, includingfluorochemicalsE.lectrospraiysgenerallyoperatedatrelatively mildtemperatures;molecules are ionizedf,ragmented,and detected. Ions characteristiocf known fluorochemicalasre observed and quantitatedagainststandards.
A HeWett-Packard HPI 100 HPLC system coupledtoa Micromass Ultma MS/MS was used to analyzethe sample extractsA.nalysiswas performed using selectedreactionmonitoring (SRM). Samples were extractedon 2/18/00and analyzedby MSIMS between 2tiB/00and 2/19100.The HPLC and MS/MS methods used foranalysisand instrumentparameters can be found inattachmentD.
5 Analysis
5.1 Calibration
A 7-p6intcalibratiocnurve was analyzed at the beginningand end of the analyticaslequence forthe compounds of interestT.he calibratiopnointswere preparedat 0, 25, 50, 100, 250, 500, and 1000 ng/L (ppt)The response ofthe quantitatioinonversus the concentrationwas plottedforeach point.Using linearregressionwith1/xweighting,the slope,y-interoepatnd correlatiocnoefficie(nrt)and coefficienotf determination(r-2wjere determined. A calibration curve isacceptableifr> 0.985 (@ > 0.970).
Calibratiosntandardsare prepared usingthe same SPE procedureused forsamples.
Calibratiocnheck standardswere analyzed periodical(leyverythreeto fivesample injectons) throughoutthe analysissequence. Compliance is obtained ff the standard andyte concentrationasre within+/-20% of the actualvalue.
For the resultsreportedhere,calibratiocnriteriwaere met
PAGE30F5
5.2
Blanks
Extractbolnankwsereprepareadndana4eedwitheveryextractbiaotnchofsamplesT.he extractiobnlanksshouldnothave any targetanalytespresentatorabove the concentratioonf thelow-leveclalibratisotnandard.Forthesesamples,theextractonblankswere compliant
Instrumentblanksinthe form of cleanmethanolsolventwere alsoanalyzedaftereveryhigh-leveclalibratisotnandard,and afterknown high-leveslamples. Again,the blanksshould not have any targetanalytespresentat or above the low4evelcalibratisotnandard. For the samples presentedheretheinstrumentblanksare compliant.
5.3 Surrogates
Surrogatespikesare nota component ofthe LCIMS/MS analyticamlethod.
5.4 Matrix Spikes Matrixspikes were prepared for every sample at a concentrationof 100 ng/L using all compounds ofinterestMatrixspikerecoveriesaregiveninAttachmentC.
Fieldspikeswere alsopreparedon severd samples ata concentratioonf 100 ng/L usingall oompounds ofinterestFieldspikerecoveriesarealsogiveninAttachmentC.
5.5 Duplicates Allsamples were analyzedinduplicate.Resultsare givenalongwiththe sample resultsin
AttachmentB.
5.6 Laboratory Control Samples Milliwqaterwas spikedwithallcompound ofinteresatt25 and 250 ng/L.Initianlalysisofthe
25 ngA-LCS showed low recoveryforPFOS. The standardwas reinjecteadnd was foundto have acceptablerecovery(70-130%).Allotherrecoveriefsorallcompounds were between 70130% ineach LCS.
5.7 Sample Related Comments Fieldblank samples consistedof empty containers.Fortymillilitoefrstype I water filtered througha hypercarbcartridgweas added to theempty containerand analyzedinthesame manner as theothersamples.
'6 Data Summary Pleasesee AttachmentB fora detaileldistinogftheanalyticraelsults.
7 DatalSample Retention
Samples are disposedof one month afterthe reportisIssued unlessotherwisespecffied.AJI electronidcata is archivedon retrievablmeedia and hard copy reportsare storedin data foldersmaintainedby Centre.
PAGE4QF5
PM
8 Attachments
8.1 AffadynentA:Chain-of-CustDdy 82 AftachmentB: Resufts. 8.3 AttachmentC: MatrixSpikeRecoveries(Fieladnd LaboratorySpikes) 8.4 AttachmentD: LCIMSIMS Raw AnalyticaDlata
9 Signatures
//'JoJ'ho2nhbn- M. FlahertyM,a naoer-IndustriSaelrvicesGroup KevinJ Uoyd, VicePresident
Z/C?
Date
@ixek-00
Date
Other Lab Members ContributintgoData
Enaksha Wickremesinhe Karen Smith
PAGE5QF5
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Co m ments:
Centrc= Analytical @*Ns6N.4=WwLaboratorieIsn,c,.
3048 ResearchDrive,StateCollegePA 16801 814-231-8032 FAX 814-231-1253
AnalyticRaelsultWs1979DecatuArl,abama
3M Sample Identification
MC-215H MC-217H MC-220H MC-221 H MC-223H MC-226H MC-228H MC-233H
Sample Description
Intake-P/N Intake-P/dNuplicate Intake-FieBlldankEmpty Oufflow-P/N Outflow-P/Nduplicate SiteI P/N SiteI PIN duplicate FieldBlankP/N Empty
PFOS (ng/L)
< 25 < 25 <-25 c@25 < 25 < 25 < 25 < 25
PFOSA (ng/L)
< 25 < 25 <25 <25 <25 <25 < 25 < 25
POAA (ng/L)
< 25 < 25 <25 < 25 < 25 < 25 < 25 < 25
Pleaserefertothe reverseside)orour standardforinsand condhions.