Literature DB >> 25449186

Microbial transformation of 8:2 fluorotelomer acrylate and methacrylate in aerobic soils.

Laurel A Royer1, Linda S Lee2, Mark H Russell3, Loring F Nies4, Ronald F Turco1.   

Abstract

Biotransformation of fluorotelomer (FT) compounds, such as 8:2 FT alcohol (FTOH) is now recognized to be a source of perfluorooctanoic acid (PFOA) as well as other perfluoroalkyl acids. In this study, microbially mediated hydrolysis of FT industrial intermediates 8:2 FT acrylate (8:2 FTAC) and 8:2 FT methacrylate (8:2 FTMAC) was evaluated in aerobic soils for up to 105d. At designated times, triplicate microcosms were sacrificed by sampling the headspace for volatile FTOHs followed by sequential extraction of soil for the parent monomers as well as transient and terminal degradation products. Both FTAC and FTMAC were hydrolyzed at the ester linkage as evidenced by 8:2 FTOH production. 8:2 FTAC and FTMAC degraded rapidly with half-lives ⩽5d and 15d, respectively. Maximum 8:2 FTOH levels were 6-13mol% within 3-6d. Consistent with the known biotransformation pathway of 8:2 FTOH, FT carboxylic acids and perfluoroalkyl carboxylic acids were subsequently generated including up to 10.3mol% of PFOA (105d). A total mass balance (parent plus metabolites) of 50-75mol% was observed on the last sampling day. 7:2 sFTOH, a direct precursor to PFOA, unexpectedly increased throughout the incubation period. The likely, but unconfirmed, concomitant production of acrylic acids was proposed as altering expected degradation patterns. Biotransformation of 8:2 FTAC, 8:2 FTMAC, and previously reported 8:2 FT-stearate for the same soils revealed the effect of the non-fluorinated terminus group linked to the FT chain on the electronic differences that affect microbially-mediated ester cleavage rates.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Biotransformation; Ester cleavage; PFOA; Perfluorinated compounds; Perfluoroalkyl carboxylic acids

Mesh:

Substances:

Year:  2014        PMID: 25449186     DOI: 10.1016/j.chemosphere.2014.09.077

Source DB:  PubMed          Journal:  Chemosphere        ISSN: 0045-6535            Impact factor:   7.086


  4 in total

1.  Development of a PFAS reaction library: identifying plausible transformation pathways in environmental and biological systems.

Authors:  Eric J Weber; Caroline Tebes-Stevens; John W Washington; Rachel Gladstone
Journal:  Environ Sci Process Impacts       Date:  2022-05-25       Impact factor: 5.334

Review 2.  Per- and polyfluoroalkyl substances in the environment.

Authors:  Marina G Evich; Mary J B Davis; James P McCord; Brad Acrey; Jill A Awkerman; Detlef R U Knappe; Andrew B Lindstrom; Thomas F Speth; Caroline Tebes-Stevens; Mark J Strynar; Zhanyun Wang; Eric J Weber; W Matthew Henderson; John W Washington
Journal:  Science       Date:  2022-02-04       Impact factor: 47.728

3.  Sampling and simultaneous determination of volatile per- and polyfluoroalkyl substances in wastewater treatment plant air and water.

Authors:  Ian Ken Dimzon; Joke Westerveld; Christoph Gremmel; Tobias Frömel; Thomas P Knepper; Pim de Voogt
Journal:  Anal Bioanal Chem       Date:  2016-11-25       Impact factor: 4.142

4.  Degradation and Plant Transfer Rates of Seven Fluorotelomer Precursors to Perfluoroalkyl Acids and F-53B in a Soil-Plant System with Maize (Zea mays L.).

Authors:  Hildegard Just; Bernd Göckener; René Lämmer; Lars Wiedemann-Krantz; Thorsten Stahl; Jörn Breuer; Matthias Gassmann; Eva Weidemann; Mark Bücking; Janine Kowalczyk
Journal:  J Agric Food Chem       Date:  2022-07-15       Impact factor: 5.895

  4 in total

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