Degradation of chlorobenzene by non-thermal plasma with Mn based catalyst

被引:0
作者
Shi X. [1 ]
Liang W. [1 ]
Yin G. [1 ]
Wang J. [1 ]
机构
[1] Beijing Key Laboratory of Regional Air Pollution Control, Beijing University of Technology, Beijing
来源
Huagong Xuebao/CIESC Journal | 2022年 / 73卷 / 10期
关键词
chlorobenzene; Mn based catalyst; non-thermal plasma; ozone; precursor;
D O I
10.11949/0438-1157.20220696
中图分类号
学科分类号
摘要
Chlorobenzene (CB), a typical representative of chlorinated volatile organic compounds (CVOCs), was selected as the research object. Mn based catalysts were prepared by impregnation method with manganese nitrate (MN) and manganese acetate (MA) as precursors, respectively. The effects of non-thermal plasma cooperating with Mn based catalysts on the degradation of CB and the inhibition of ozone generation, a by-product of the reaction, were investigated. It is found that increasing the discharge voltage can improve the degradation efficiency of CB for different reaction systems. The introduction of catalyst can greatly improve the degradation performance of CB. Compared with MnOx(MN)/γ-Al2O3, the introduction of MnOx(MA)/γ-Al2O3 has better degradation effect and higher inhibition performance on ozone generation. The catalysts before and after the reaction were characterized by N2 adsorption-desorption, scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). It was found that the discharge had no effect on the pore size and crystal structure of the catalyst. The variation of Cl elements during the degradation of CB were analyzed by Cl selectivity and tail GC-MS. Compared with MnOx(MN)/γ-Al2O3 catalyst, the specific surface area of the MnOx(MA)/γ-Al2O3 catalyst is relatively large, and the active components have higher and more uniform dispersion, resulting in more ozone of the reaction system being decomposed into active oxygen atoms on the catalyst surface, which improves the degradation performance of CB and inhibits the formation of ozone in the reaction system. © 2022 Chemical Industry Press. All rights reserved.
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页码:4472 / 4483
页数:11
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