甲苯
化学
矿化(土壤科学)
催化作用
分解
活性炭
激进的
电子顺磁共振
降级(电信)
光化学
吸附
无机化学
有机化学
氮气
物理
电信
核磁共振
计算机科学
作者
Ruijie Xie,Jian Ji,Haibao Huang,Dongxue Lei,Ruimei Fang,Yajie Shu,Yujie Zhan,Kaiheng Guo,Dennis Y.C. Leung
标识
DOI:10.1016/j.cej.2018.02.045
摘要
Abstract Gas-phase VOCs decomposition generally produces intermediates and causes secondary air pollution. To avoid this issue, we proposed a novel method for a typical gaseous VOC (toluene) degradation via catalytic activation of peroxymonosulfate (PMS) in the liquid phase. Herein, activated carbon supported monodispersed Co3O4 nanoparticles (Co3O4/AC) were prepared via a facile deposition method. It is highly efficient in PMS activation for toluene degradation due to the presence of Co-OH+ species and well dispersed Co3O4 on Co3O4/AC. A toluene removal efficiency of nearly 90% was maintained during the reaction, and few gaseous intermediates were discharged. Sulfate radical (SO4 −) and hydroxyl radical (HO ) derived from PMS activation played different roles during toluene oxidation and mineralization. Electron spin resonance (EPR) suggested that the generation of plentiful SO4 − resulted in the superior toluene degradation, and the presence of HO can improve carbon mineralization. Radical quenching tests further confirmed that SO4 − played a dominant role for toluene degradation, whereas the absence of HO inhibited the carbon mineralization. The toluene degradation pathway in the Co3O4/AC-PMS system was proposed based on the intermediates identified by GC–MS.
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