Spontaneous Perfluorooctanoic Acid Degradation at Gas–Liquid Interfaces

Perfluorooctanoic acid (PFOA), widely used in various industries and released during cooking as a PTFE precursor, poses significant environmental concerns due to its persistence and toxicity. This study investigated the degradation behavior of PFOA at the gas-liquid interface under diverse conditions. The results demonstrate that the coexistence of salts, particularly NaBr, significantly enhances PFOA degradation by promoting electron transfer reactions. Alkaline conditions (pH 9.8) and the presence of oxygen further facilitate its degradation, whereas acidic conditions hinder this process. Mechanistic analysis further confirmed that hydroxyl radicals (•OH) and hydrated electrons (e<sub>aq</sub><sup>-</sup>) play critical roles in the observed degradation. This work provides new insights into the transformation of PFAS under diverse conditions and offers a basis for developing strategies to degrade PFOA into environmentally benign species.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-09-03
DOI
https://doi.org/10.1021/jacs.5c09722
Citations
5
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
4.30

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article

Spontaneous Perfluorooctanoic Acid Degradation at Gas–Liquid Interfaces

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5 citations
Journal of the American Chemical Society
Per- and polyfluoroalkyl substances research
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article

Spontaneous Perfluorooctanoic Acid Degradation at Gas–Liquid Interfaces

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article en
5 citations

Abstract

Perfluorooctanoic acid (PFOA), widely used in various industries and released during cooking as a PTFE precursor, poses significant environmental concerns due to its persistence and toxicity. This study investigated the degradation behavior of PFOA at the gas-liquid interface under diverse conditions. The results demonstrate that the coexistence of salts, particularly NaBr, significantly enhances PFOA degradation by promoting electron transfer reactions. Alkaline conditions (pH 9.8) and the presence of oxygen further facilitate its degradation, whereas acidic conditions hinder this process. Mechanistic analysis further confirmed that hydroxyl radicals (•OH) and hydrated electrons (e<sub>aq</sub><sup>-</sup>) play critical roles in the observed degradation. This work provides new insights into the transformation of PFAS under diverse conditions and offers a basis for developing strategies to degrade PFOA into environmentally benign species.

Journal of the American Chemical SocietyVol. 147(37)
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Fudan University (CN), Institut de Recherches sur la Catalyse et l'Environnement de Lyon (FR)
China Scholarship Council, HORIZON EUROPE European Research Council
Openalex Percentile: Top 6%
Per- and polyfluoroalkyl substances research
4.30
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