激进的
化学
催化作用
间苯二酚
环境修复
光化学
甲醛
降级(电信)
铁
羟基自由基
吸附
无机化学
有机化学
污染
生态学
电信
计算机科学
生物
作者
Qiang Li,Biao Xue,Zhengjie Wang,Huaze Zhu,Hao Zhou,Hao Deng,Jia‐Le Song,Xin Ma,Hao Du,Qi Wang,Si Chen,Huayue Zhu
标识
DOI:10.1016/j.seppur.2024.126450
摘要
Efficient generation and rapid activation of H2O2 are essential for a self-sufficient photo-Fenton-like system. Herein, ferric-ellagate complex (EA-Fe), the atomically distributed Fe active catalyst, was first employed to activate the H2O2 photo-generated by resorcinol–formaldehyde (RF) resins. During the photo-Fenton-like reactions, the photoinduced holes (h+), hydroxyl radicals (•OH) and superoxide radicals (•O2–) work together for organics degradation and bacteria inactivation. The degradation intermediates were identified by HPLC-EIS-MS and the possible degradation pathways of TC were proposed. Meanwhile, the QSAR prediction revealed that the catalytic processes could significantly eliminate ecotoxicity. Moreover, the RF/EA-Fe could effectively inactivate both E. coli and S. aureus. Theoretical calculations indicated that the H2O2 molecule was adsorbed on the Fe atom through a single Fe-O coordination, followed by conversion to *OH (Fe-OH) via directly breaking the peroxy bond. This activation pathway effectively maximizes the utilization of H2O2. This study can provide a new platform for rationally designing a self-cycled photo-Fenton-like system with outstanding degradation and antibacterial properties.
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