电子顺磁共振
化学
催化作用
腐植酸
金属
核化学
降级(电信)
激进的
反应速率常数
羟基自由基
热液循环
橙色(颜色)
无机化学
氧化物
污染物
猝灭(荧光)
环境修复
化学工程
动力学
污染
荧光
有机化学
肥料
工程类
物理
生物
电信
量子力学
核磁共振
计算机科学
食品科学
生态学
作者
Yusong Yang,Ying Zhao,Yuan Zong,Ruiqi Wu,Mingyi Zhang,Jing Feng,Tong Wei,Yueming Ren,Jun Ma
标识
DOI:10.1016/j.envres.2022.112919
摘要
Developing high-efficiency catalysts for peroxymonosulfate (PMS)-based advanced oxidation processes is important for eliminating pollutants in water. Herein, α-MnO2 with major exposed {110} and {100} facets prepared via a hydrothermal method were used as catalysts to activate PMS for the degradation of Orange Ⅰ (OⅠ). α-MnO2-100, with more abundant surface hydroxyl groups and greater reductive ability, performed remarkably better than α-MnO2-110 for degrading OⅠ. OⅠ removal of 86.20% was obtained in the α-MnO2-100/PMS system. The apparent rate constant of OⅠ removal over α-MnO2-100 was 2.11 times higher than that of α-MnO2-110. The effects of PMS concentration, catalyst dosage, OⅠ concentration, initial pH, anions and humic acid (HA) on OⅠ degradation in the α-MnO2-100/PMS system were systematically investigated. Quenching experiments and electron paramagnetic resonance (EPR) demonstrated that SO4•-, •OH, O2•- and 1O2 were the reactive oxygen species (ROS) in the α-MnO2-100/PMS system. Moreover, the possible degradation pathway of OⅠ in the α-MnO2-100/PMS system was proposed. This work provides an ideal metal oxide catalyst for sewage remediation.
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