Et3N-Enabled Electrochemical PFASDefluorination for Scalable Fluoride Recovery

Abstract Per- and polyfluoroalkyl substances (PFAS) are persistent environmental pollutants, but they also represent a fluorine-rich reservoir, making fluoride recovery from PFAS an attractive and sustainable approach to fluorine reuse. However, methods that enable scalable and high-fluoride recovery from PFAS remain scarce. Here, we report an Et3N-enabled electrochemical strategy for PFAS degradation and fluoride recovery under mild conditions. The introduction of Et3N plays a central role in the system, enabling nearly complete defluorination with high fluoride recovery. In addition, Et3N significantly reduces the sensitivity of the reaction to air and moisture, allowing for simple operation, and it can be readily scaled to the 100 g level. The recovered fluoride can be isolated as LiF, NaF, and KF, and reused in downstream fluorination reactions. These findings establish a practical and scalable electrochemical platform for converting PFAS into synthetically useful fluorine reagents.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-08-03
DOI
https://doi.org/10.1021/jacs.6c06873
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
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article

Et3N-Enabled Electrochemical PFASDefluorination for Scalable Fluoride Recovery

Zhang Pengyuan, Benxiang Zhang, Junwen Wang
Journal of the American Chemical Society
Per- and polyfluoroalkyl substances research
article

Et3N-Enabled Electrochemical PFASDefluorination for Scalable Fluoride Recovery

Zhang Pengyuan, Benxiang Zhang, Junwen Wang
article en

Abstract

Abstract Per- and polyfluoroalkyl substances (PFAS) are persistent environmental pollutants, but they also represent a fluorine-rich reservoir, making fluoride recovery from PFAS an attractive and sustainable approach to fluorine reuse. However, methods that enable scalable and high-fluoride recovery from PFAS remain scarce. Here, we report an Et3N-enabled electrochemical strategy for PFAS degradation and fluoride recovery under mild conditions. The introduction of Et3N plays a central role in the system, enabling nearly complete defluorination with high fluoride recovery. In addition, Et3N significantly reduces the sensitivity of the reaction to air and moisture, allowing for simple operation, and it can be readily scaled to the 100 g level. The recovered fluoride can be isolated as LiF, NaF, and KF, and reused in downstream fluorination reactions. These findings establish a practical and scalable electrochemical platform for converting PFAS into synthetically useful fluorine reagents.

Journal of the American Chemical Society
Jiangxi University of Technology (CN), Chinese Academy of Engineering (CN), University of Chinese Academy of Sciences (CN), Jiangxi University of Science and Technology (CN)
Responsible consumption and production
Openalex Percentile: Top 15%
Per- and polyfluoroalkyl substances research
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