Comparative investigation on catalytic ozonation of VOCs in different types over supported MnO catalysts

催化作用 化学 氯苯 甲酸 臭氧 二氯甲烷 空间速度 吸附 核化学 有机化学 选择性 溶剂
作者
Guanyi Chen,Zhi Wang,Fawei Lin,Zhiman Zhang,Hongdi Yu,Beibei Yan,Zhihua Wang
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:391: 122218-122218 被引量:114
标识
DOI:10.1016/j.jhazmat.2020.122218
摘要

This paper conducted catalytic ozonation of CB (chlorobenzene) over a series of MnOx based catalysts with different supports (Al2O3, TiO2, SiO2, CeO2, and ZrO2) at 120 °C. Mn/Al2O3 exhibited highest CB conversion efficiency, ca. 82.92 %, due to its excellent textual properties, O2 desorption, redox ability, and desirable surface adsorbed oxygen species and acidity. O3 conversion all approached nearly 100.0%, with residual <10 ppm. Mn/Al2O3 was further employed to investigate effect of temperature, O3/CB, and space velocity on CB conversion. Hereafter, catalytic ozonation of single and binary VOCs in different types was performed, i.e., CB, DCE (dichloroethane), DCM (dichloromethane), and PhH (Benzene). Conversion results demonstrated aromatics degraded easier than alkanes and more carbon atoms decreased difficulty, as CB∼PhH > DCE∼DCM, and DCE > DCM; but chlorinated substitution increased difficulty, as PhH > CB. Catalytic co-ozonation of CB/DCE indicated that DCE significantly improved CB conversion to reach totally degradation at low O3 input, but inhibited DCE conversion, especially at higher ratio of DCE/CB. Co-ozonation improved ozone utilization efficiency, and maintained the original property of catalyst. By contrast, CB/PhH co-ozonation displayed very mild effects. Finally, critical intermediates during catalytic CB ozonation, i.e., DCM, carboxyl and formic acid, were detected from mass spectrum results.
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