阳极
阴极保护
降级(电信)
化学
膜
氧化还原
电极
偶联反应
过滤(数学)
反应机理
电化学
膜电极组件
无机化学
化学工程
催化作用
有机化学
物理化学
计算机科学
生物化学
电信
统计
数学
工程类
作者
Yifan Gao,Shuai Liang,Quanbiao Zhang,Kunpeng Wang,Peng Liang,Xia Huang
出处
期刊:Water Research
[Elsevier BV]
日期:2023-02-14
卷期号:233: 119741-119741
被引量:33
标识
DOI:10.1016/j.watres.2023.119741
摘要
The versatile reaction possibilities arising from the interaction between the anodic and cathodic reactions naturally contained in electrocatalytic membrane filtration (EMF) systems are of great valuable in meeting the current complex water treatment requirements. But currently, most studies only focus on half-cell reactions with a single electrocatalytic membrane, which limits the research progress of the EMF technology. Here we report a coupling strategy that utilizes the interaction between the anodic and cathodic reactions to actuate ultra-efficient degradation performance with regulable reaction mechanisms. An electrocatalytic dual-membrane filtration (EDMF) system was established. Six typical configurations of the EDMF system were set up and systematically investigated by adjusting the electrode distance and filtration sequence. Based on the obtained results of degradation performance and mechanisms, a regulation strategy which enabled flexible tuning of direct nonradical oxidation (e.g., h+) and indirect oxidation (e.g., 1O2, ·OH, HO2·, O2·-, etc.) was proposed. In particular, cathodic reactions were found to adversely affect the anodic reactions at the relatively short electrode distance of 0.9 mm. Anodic reactions could inhibit the generation of 1O2 at short distance of 0.9 mm but promote its generation at long distances of 9 and 17 mm. The A-C_0.9 configuration achieved the highest degradation performance, while the C-A_9 configuration was revealed to be much more conducive to 1O2 production. Overall, our findings demonstrate the versatility and tunability of the reaction mechanism and performance of the EDMF system due to the flexible coupling of the anodic and cathodic reactions, which potentially lays a foundation for future development of ultra-efficient mechanism-adjustable electrocatalysis technologies.
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