Activation of peroxymonosulfate and recycled effluent filtration over cathode membrane CNFs-CoFe2O4/PVDF in a photocatalytic fuel cell for water pollution control

化学 激进的 催化作用 过滤(数学) 降级(电信) 羟基自由基 化学工程 高级氧化法 光催化 阳极 有机化学 电极 工程类 物理化学 统计 电信 生物化学 计算机科学 数学
作者
Yizhen Zhang,Qiyuan Chen,Lifen Liu,Yu Wang,Michael K.H. Leung
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:399: 125731-125731 被引量:47
标识
DOI:10.1016/j.cej.2020.125731
摘要

Few studies integrate catalytic membrane in photocatalytic fuel cell (PFC) with peroxymonosulfate (PMS) activation process. In the present work, a novel PFC-membrane reactor system integrating PMS activation (abbreviated as PMS/PFC-MR) was constructed for wastewater treatment, consisting of CNFs-CoFe2O4/PVDF membrane cathode (CNFs-CoFe2O4/PM) and Ag/ZnO NA/NiF photo-anode. The PMS/PFC-MR with enlarged volume exhibited favorable performance, increased berbine degradation by 65.9% and electricity production by 0.33 V, comparing with PFC-MR after 1 h operation. Relative to CNFs/PM (0.89 h−1) and PM (0.53 h−1), the PMS/PFC-MR with CNFs-CoFe2O4/PM had greatly enhanced rate constant (4.32 h−1). The results also indicate that recycled filtration over membrane accelerates catalytic degradation of organic pollutant in PMS/PFC-MR. Revealed by the radical quenching and EPR tests, hydroxyl radicals (OH), singlet oxygen (1O2), superoxide radical (O2−) and sulfate radicals (SO4−) were all confirmed present and responsible for pollutant degradation in PMS/PFC-MR. Consequently, the system expands the radical reactions to enhance degradation and electricity generation, due to the synergy of accelerated Co(II)/PMS oxidation with membrane filtration and photo-electro catalysis. This system provides a new efficient strategy towards wastewater treatment with energy recovery.
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