全氟辛酸
电化学
降级(电信)
阳极
电极
氧化物
结垢
化学
化学工程
材料科学
环境化学
冶金
计算机科学
膜
电信
生物化学
工程类
物理化学
作者
Yunlong Luo,Olalekan Simon Awoyemi,Gopalan Saianand,Annette L. Nolan,Fiona Robinson,Jim Fenstermacher,Lei Xu,Junfeng Niu,Mallavarapu Megharaj,Ravi Naidu,Cheng Fang
标识
DOI:10.1016/j.jclepro.2023.139691
摘要
Advanced electrochemical oxidation methods have demonstrated significant potential in degrading per- and polyfluoroalkyl substances (PFAS). However, the widespread application of these techniques is impeded by the long term performance and limited service life of electrodes. This study introduces a novel approach by investigating the impact of polarity reversal (PR) of the applied current on the electrochemical degradation of perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), 6:2 fluorotelomer sulfonate (6:2 F TS), and aqueous film-forming foam (AFFF) samples. A laboratory-scale electrochemical cell equipped with two titanium sub-oxide (Ti4O7) electrodes is used for the experimental investigation. The results indicate 6-h direct current (DC) operation causes fouling and ageing of the electrode (anode) such as the formation of titanium oxide (TiO2). The application of PR effectively mitigates fouling and aging, leading to enhanced mass transfer and improved long-term defluorination of PFOA, PFOS, 6:2 F TS, and all the AFFF samples. The investigation also suggests that PR can help to reduce the energy consumption by ∼13%. Overall, the application of PR emerges as a promising and practical strategy to augment the electrochemical degradation of PFAS, addressing critical issues related to electrode stability and longevity.
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