4.7 Article

Anaerobic biodegradation of 8:2 fluorotelomer alcohol in anaerobic activated sludge: Metabolic products and pathways

Journal

CHEMOSPHERE
Volume 200, Issue -, Pages 124-132

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2018.02.065

Keywords

Anaerobic biodegradation; 8:2 FTOH; Bio-defluorination; Anaerobic activated sludge; Metabolic yields and pathways

Funding

  1. National Natural Science Foundation of China [51108197, 51678255]
  2. National Science and Technology Support Program of China [2015BAL01B01]
  3. Key Projects of International Cooperation in Science and Technology of Fujian Province [201410013]
  4. Guidance Project in Science and Technology of Fujian Province [2015Y0037]
  5. Natural Science Foundation of Fujian Province [2017J01096]
  6. Personnel Training Plan for Distinguished Young Scholar of Fujian Province Colleges [JA14014]

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The anaerobic biodegradability and metabolic pathways of 8:2 fluorotelomer alcohol (8:2 FTOH) were investigated in anaerobic activated sludge. The biodegradation was well described by a double exponential decay model. 8:2 FTOH was biodegraded to poly- and perfluorinated metabolites with the release of fluoride ion. All polyfluorinated metabolites were intermediate metabolic products and could be further transformed to other metabolites, while perfluorinated metabolites were terminal products. 2H-perfluoro-2-decenoic acid (8:2 FTUA) and perfluorooctanoic acid (PFOA) were verified as the most abundant poly- and perfluorinated metabolites, respectively. Two shorter-chain perfluorinated metabolites, perfluoropentanoic acid (PFPeA) and perfluorobutyric acid (PFBA), were first reported in the biodegradation of 8:2 FTOH. However, the total molar recovery of 8:2 FTOH decreased with increasing incubation time, indicating that there might be some unknown metabolites. Thus, the anaerobic biodegradation pathways were proposed as follows: 8:2 FTOH was oxidized to 8:2 FTUA and 2-perfluorooctyl ethanoic acid (8:2 FTCA) via 2-perfluorooctyl acetaldehyde (8:2 FTAL), and then 8:2 FTUA and 8:2 FTCA were further transformed to 1-perfluoroheptyl ethanol (7:2 sFTOH) via 3-perfluoroheptyl propionic acid (7:3 acid) or/and 3-perfluoroheptyl acrylic acid (7:3 Uacid), and eventually 7:2 sFTOH was further biodegraded to PFOA and other perfluorocarboxylates containing less than eight carbons. (C) 2018 Elsevier Ltd. All rights reserved.

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