催化作用
化学
降级(电信)
草酸
四环素
吸附
激进的
无机化学
核化学
化学工程
有机化学
计算机科学
生物化学
电信
工程类
抗生素
作者
Weichen Zhu,Wei Zuo,Pu Wang,Wei Zhan,Jun Zhang,LI Li-pin,Yu Tian,Hong Qi,Rui Huang
标识
DOI:10.1016/j.cclet.2023.109341
摘要
Fe-N-C materials have received increasing attention, due to its distinctive catalytic activity. However, the Fe-N coordination number dependence of catalytic ability and mechanism for H2O2 activation remain elusive. Herein, a series of Fe-N-C heterogeneous Fenton-like catalysts with different Fe-N coordination number were prepared for tetracycline degradation. The results demonstrated that samples with Fe-N4 structure exhibited high activity. The excellent performance was mainly ascribed to the high adsorption capacity and the formation of superoxide radicals (•O2−) catalyzed by Fe linked to pyridinic nitrogen. The intermediates and degradation pathways of tetracycline degradation by Fe-N-C/H2O2 system were analyzed by Liquid Chromatography Coupled to Tandem Mass Spectrometry (LC-MS/MS). Furthermore, we applied our Fe-N-C catalysts to treat simulated pharmaceutical wastewater with high tetracycline degradation capacity despite high concentrations of organic matter such as oxalic acid and various ionic interferences. Our work reveals the dependence of the activation H2O2 on the Fe-N coordination environment and the degradation mechanism of these catalysts. It provides insights into the prospects for tuning the catalyst in practical applications.
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