Document LkjRXxZq9w9g0jqm7z3edO7Q

AR226-3357 Application of L G M S /M S Methodology to Determination < Telomer B Alcohols, Perfluorinated Acids, and Fluorosurfactants in Environmental M atrices. Boadan Szostcft. Vladimir CapkA, Keith B. Pricket*. S . M ark Kennedf, Robert C. BucR 1DuPont Haskell Laboratory fo r Health and Environmental Scienc4Q90 Elkton Rd., Newark, DE 19714, U SA 2 DuPont Chemical Solutions Enterprise. Wilmington. DE. U S A - analytical methodology for measurement of perfluoroalkyl subsfee in various biological and environmental matrices continues to be a challenging task despite tremendous progressfhis field in recent years; . - the purpose of this work was the development of analytical radfafor determination of Telomer B Alcohols (TBAs; anl selected perfluorinated acids utilizing LC /M S and L C /M S/M S; ._ . - Telomer B Alcohols are intermediates for manufacturing of a fahrange of anionic, nonionic fluorosurfactants, ana - Telomer B Alcohols based products are brtad! usea in vorieilyaBnsumer products asfluorosurfactants or water/sGil repelling coatings for paper, textiles, and carpets; ......... , - extraction and quantitation by L C /M S /M S of four selected peoftaated acids, potential biodegradation products of 8-2 TBA, were investigated; Telomer B Alcohols by L C /M S and L C / M S / M S Introduction: TTTdine-nBeepllepAfooerormmsdoretmeescoterrhonndeBaBcmbetepeeAAidrocllsocacfamtooUmohahontoocplraellelusscetteudcacadtlataruaenremrtTebiaoloiBomelnew^AcseI(unsocCalanoafrbFionrezlrjeee^mIpdovrt-noCoobpslnyKrtae(aenmnigdt-aeeoCo/lgmzy(H4ais1istin3ioi0s-vau6OebnVr3tyHc)i,l;eoyL,n4faAi6reeca3Sleeg,tcmo3at5rr^te6oenL3rstC)apa^dr/tMi,daonyun5:,c/:Nt;~U 8 - 2 T B^ A b y L C / M S Internal Standard FFFFFF iJJJJJ--.f ~ F ,,I DT -- - D I Chromatographic conditions: j CIP fragmentation) 6-2 TBA, 10 eV Jjj, 8-2 TBA, 10 eV Chromatographie conditions- Calan- Store MSRIS, 1. S* ttsWfe w w : * w w r B Gra.-5.v-: TSo mKm * '7/.1 |(iW0.1;?- M S conditions: I1nnonlfNoc'jvot:'rrt:dGwbtt*i!rr.eMy,rrew;eWoWv*rMn* Cnic*etmvaoiniisiyo:SipVitay: .10tV CPTraw-VsnWxiSiatvcnTnKiEorv,,-:-Ro.'r-vWlrrlIe.i.Snf-7t.0(A5"*AAGO:VC4-J5S?S3<!w2>>CJK}li 50 A. injection 1 tiJrfiL 50- ?BA Mobilptota: A: vaiar B: tnaihenol Gradiant: tlm[raln] KB FlawtmUmln] Sujf .: 1* -C Example calibration curves and chromatograms | .: In 40/60%H20/ACN 3l^ mL s V t B A <U MS,S ] 160ng/mLt l 1 rig/fftL6-ZT8A 10-2 TBA, 10 eV Fragmentation pattern for Telomer 5 Alcohols: - loss of 4 HFs (4 x 20) and CO (2S) i ng/mL 6-2 TBA - m - j - r j it 1 500 ni. Injection 1 rtjsftr.l.1-27BA - 1ni.84T3A 1 fijjftrt. 6-2 TBA Summary: - detection and separation o f Telomer B Alcohols b y L C / M S / M S was demonstrated - linear calibration curves were obtained: fo r three examined T B A s; 0,5-100 ng/mL (50 //l-Injection): and 05-1. rig/mL (5 0 0 ^ injieiettan) fo r samples prepared i n 50 /5 0 %water/methanol; - 5 0 ppt.LQQs a re achievable fo r examined T B A ^ iri aqueous m atrix by L C / M S/ M S with 50 0 fL injection; - further validation o f L C / M S / M S method fo r T M s <n authentic m a trid M i? required; Summary: L C / M S methods f o r analysis o f 8 - 2 T B A weredesigned to monitor signal of deprotonated molecular ion and acetate adduct; aqueous samples of 8 -2 T B A can be qubntitdfiyieiy extracted with acetonitrile (1:2 W4fepiACN);: samples can also be extra cted with M T B E andi M T B E extract iryected a fte r 1;1G dilution with aCetphitrile; ; .. presented method allows: injection o f samples in 100% acetonitrile or 1:10 teffahydrofuran (TfdE)/acet,onitpiie^ ability to analyze:8-2 T B A by L C / M S allows Simpliflaitron o f Sample preparation procedures and makeS: : them compatible with th o se u se d fa r fluorinatedacids analysis; ability to inject e xtra cts originating from d ifferent solvents broadens the applicability o f the method to d iffe ren t sample types (e,g. reduction of matrix e ffe c ts for: samples extracted with M T B E or analysis of polymers: samples: soluble in THF); : finear calibration curves were obtained fo r 8-2: T B A rang/ngfraw 3 ng/mL.tolOiOOQng/mL; sub^ng/mL L O Q f o r 8 -2 TBA: quantitation is achievable using L C / M S system (2.0 j/L injection); Perfluorinated acids by L C /M S /M S