Atmospheric Fate of a New Polyfluoroalkyl Building Block, C 3 F 7 OCHFCF 2 SCH 2 CH 2 OH

Many per- and polyfluoroalkyl substances (PFAS) have been regulated or phased-out of usage due to concerns about persistence, bioaccumulation potential, and toxicity. We investigated the atmospheric fate of a new polyfluorinated alcohol 2-(1,1,2-trifluoro-2-heptafluoropropyloxy-ethylsulfanyl)-ethano...

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Veröffentlicht in:Environmental science & technology 2022-05, Vol.56 (10), p.6027-6035
Hauptverfasser: Joudan, Shira, Orlando, John J, Tyndall, Geoffrey S, Furlani, Teles C, Young, Cora J, Mabury, Scott A
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container_end_page 6035
container_issue 10
container_start_page 6027
container_title Environmental science & technology
container_volume 56
creator Joudan, Shira
Orlando, John J
Tyndall, Geoffrey S
Furlani, Teles C
Young, Cora J
Mabury, Scott A
description Many per- and polyfluoroalkyl substances (PFAS) have been regulated or phased-out of usage due to concerns about persistence, bioaccumulation potential, and toxicity. We investigated the atmospheric fate of a new polyfluorinated alcohol 2-(1,1,2-trifluoro-2-heptafluoropropyloxy-ethylsulfanyl)-ethanol (C F OCHFCF SCH CH OH, abbreviated FESOH) by assessing the kinetics and products of the gas-phase reaction of FESOH with chlorine atoms and hydroxyl radicals. Experiments performed in a stainless-steel chamber interfaced to an FTIR were used to determine reaction kinetics and gas-phase products. We report reaction rate constants of (Cl + FESOH) = (1.5 ± 0.6) × 10 cm molecule s and (OH + FESOH) = (4.2 ± 2.0) × 10 cm molecule s . This leads to a calculated FESOH gas-phase lifetime of 2.8 ± 1.3 days with respect to reaction with OH, assuming [OH] = 10 molecule cm . Gas-phase products of FESOH oxidation included at least two aldehydes, likely C F OCHFCF SCH C(O)H and C F OCHFCF SC(O)H, and secondary products including COF , SO and C F OC(O)F. Additional gas-phase experiments performed in a Teflon chamber were used to assess aqueous products by collecting gaseous samples offline into an aqueous sink prior to analysis with ultrahigh performance liquid chromatography-tandem mass spectrometry, resulting in four acidic products: C F OCHFCF SCH C(O)OH, C F OCHFCF S(O)(O)OH, C F OCHFC(O)OH, and perfluoropropanoic acid (C F C(O)OH).
doi_str_mv 10.1021/acs.est.0c07584
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title Atmospheric Fate of a New Polyfluoroalkyl Building Block, C 3 F 7 OCHFCF 2 SCH 2 CH 2 OH
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