PUBLICATION

Synergistic hydroxyl and chlorine radicals in contact-electro-catalysis for sustainable PFAS remediation

Authors
Zhang, J., Li, W., Ma, J., Cui, J., He, K., Yang, K., Liu, Q., Zhang, M., Lv, S., Cheng, F., Xing, D.
ID
ZDB-PUB-260406-3
Date
2026
Source
Journal of hazardous materials   508: 141988141988 (Journal)
Registered Authors
Keywords
Contact-electro-catalysis, Defluorination, Environmental safety, PFAS, Reactive chlorine species
MeSH Terms
none
PubMed
41936317 Full text @ J. Hazard. Mater.
Abstract
Contact-electro-catalysis (CEC) provides a promising route for per- and polyfluoroalkyl substances (PFAS) remediation, yet the mechanistic role of chloride ions (Cl-) in real water matrices remains unclear. Here, we demonstrate that Cl- markedly enhances removal of perfluorooctanoic acid, perfluorooctanesulfonic acid, hexafluoropropylene oxide dimer acid, perfluorononyloxybenzene sulfonate, and 6:2 fluorotelomer sulfonate, achieving 97.04 -99.99% degradation and 96.90 -99.98% defluorination within 120 min at 200 mM Cl-. These rates were 1.43-2.29-fold higher than Cl--free systems. Mechanistic analyses reveal that hydroxyl radicals (OH) oxidizes Cl- to generate chlorine radicals (Cl), which selectively attack the carboxylate group of PFAS, enabling thermodynamically favorable decarboxylation followed by mineralization. Unlike conventional electrochemical methods, the Cl-mediated pathway avoids oxychlorine and chlorinated byproducts. Zebrafish embryo assays further confirmed negligible toxicity of treated solutions. These results establish a sustainable paradigm that achieves high defluorination efficiency and operational safety, offering strong potential for PFAS remediation in saline and industrial waters.
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