The continuous emission of persistent and bioaccumulative pollutants into aquatic environments has become a critical global issue. Among these, per- and polyfluoroalkyl substances (PFASs) are of particular concern due to their exceptional stability, extensive industrial use, and adverse impacts on ecosystems and human health. Their resistance to conventional physical, chemical, and biological treatments stems from the strength of the carbon-fluorine bond, which prevents efficient degradation under standard conditions. This review provides a concise and updated assessment of emerging advanced oxidation processes (AOPs) for PFAS remediation, with emphasis on heterogeneous photocatalysis and electrochemical oxidation. Photocatalytic systems based on In2O3, Bi-based oxyhalides, and Ga2O3 exhibit high PFAS degradation under UV light, while heterojunctions and MOF-derived catalysts improve defluorination under solar irradiation. Electrochemical oxidation-particularly using Ti4O7 reactive electrochemical membranes and BDD anodes-achieves near-complete mineralization with comparatively low specific energy demand. Energy consumption (EEO) was calculated from literature data for UV- and simulated-solar-driven photocatalytic systems, enabling a direct comparison of their energy performance. Although solar-driven processes offer clear environmental advantages, they generally exhibit higher EEO values, mainly due to lower apparent quantum yields and less efficient utilization of the incident solar photons compared to UV-driven systems. Hybrid systems coupling photocatalysis and electro-oxidation emerge as promising strategies to enhance degradation efficiency and reduce energy requirements. Overall, the review highlights key advances and future research directions toward scalable, energy-efficient, and environmentally sustainable AOP-based technologies for PFAS removal.

Photocatalysis and Electro-Oxidation for PFAS Degradation: Mechanisms, Performance, and Energy Efficiency

Vietri V.;Vaiano V.;Sacco O.;Mancuso A.
2026

Abstract

The continuous emission of persistent and bioaccumulative pollutants into aquatic environments has become a critical global issue. Among these, per- and polyfluoroalkyl substances (PFASs) are of particular concern due to their exceptional stability, extensive industrial use, and adverse impacts on ecosystems and human health. Their resistance to conventional physical, chemical, and biological treatments stems from the strength of the carbon-fluorine bond, which prevents efficient degradation under standard conditions. This review provides a concise and updated assessment of emerging advanced oxidation processes (AOPs) for PFAS remediation, with emphasis on heterogeneous photocatalysis and electrochemical oxidation. Photocatalytic systems based on In2O3, Bi-based oxyhalides, and Ga2O3 exhibit high PFAS degradation under UV light, while heterojunctions and MOF-derived catalysts improve defluorination under solar irradiation. Electrochemical oxidation-particularly using Ti4O7 reactive electrochemical membranes and BDD anodes-achieves near-complete mineralization with comparatively low specific energy demand. Energy consumption (EEO) was calculated from literature data for UV- and simulated-solar-driven photocatalytic systems, enabling a direct comparison of their energy performance. Although solar-driven processes offer clear environmental advantages, they generally exhibit higher EEO values, mainly due to lower apparent quantum yields and less efficient utilization of the incident solar photons compared to UV-driven systems. Hybrid systems coupling photocatalysis and electro-oxidation emerge as promising strategies to enhance degradation efficiency and reduce energy requirements. Overall, the review highlights key advances and future research directions toward scalable, energy-efficient, and environmentally sustainable AOP-based technologies for PFAS removal.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11386/4941876
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