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Innovative hybrid approach for enhanced PFAS degradation and removal: Integrating membrane distillation, cathodic electro-Fenton, and anodic oxidation.

作者信息

Yousefi Afrouz, Omi Farah Rahman, Yang Lingling, Ganiyu Soliu O, Ullah Aman, El-Din Mohamed Gamal, Sadrzadeh Mohtada

机构信息

Department of Mechanical Engineering, 10-241, Donadeo Innovation Center for Engineering, Advanced Water Research Lab (AWRL), University of Alberta, Edmonton, AB, T6G 1H9, Canada; Department of Civil and Environmental Engineering, University of Alberta, Edmonton, Alberta, T6G 1H9, Canada.

Department of Mechanical Engineering, 10-241, Donadeo Innovation Center for Engineering, Advanced Water Research Lab (AWRL), University of Alberta, Edmonton, AB, T6G 1H9, Canada.

出版信息

J Environ Manage. 2025 Apr;379:124818. doi: 10.1016/j.jenvman.2025.124818. Epub 2025 Mar 9.

Abstract

Per- and polyfluoroalkyl substances (PFAS) are persistent environmental contaminants that pose significant toxicity risks to humans and ecosystems. Traditional advanced oxidation processes using boron-doped diamond (BDD) anodes degrade PFAS in wastewater effectively but suffer from slow kinetics and high energy costs, limiting commercial application. This study introduces a hybrid process combining cathodic electro-Fenton (EF), anodic oxidation via a BDD anode, and membrane distillation (MD) to improve perfluorooctanoate (PFOA) degradation efficiency and reduce energy use. Increasing the current density from 50 to 500 A/m significantly raised the concentration of produced HO from 0.25 mM to 2.3 mM, accelerating PFOA degradation and mineralization. At 50 A/m, no mineralization of PFOA occurred in the EF/BDD process, while the EF/BDD-MD process achieved 45% mineralization due to increased PFOA concentration in the electrolytic cell. At 500 A/m, the EF/BDD-MD process achieved 95% PFOA mineralization. Findings reveal that while EF-generated OH radicals assist degradation, the BDD(OH) anode was the primary driver, driving 80% of the reaction. This degradation was initiated by direct electron transfer at the BDD surface, followed by homogeneous and heterogeneous OH radicals enhancing the degradation and mineralization process. The hybrid process also lowered energy consumption, making the treatment feasible for large scales.

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