Plasma-catalytic removal of toluene over CeO2-MnOx catalysts in an atmosphere dielectric barrier discharge

介质阻挡放电 催化作用 甲苯 选择性 吸附 氧气 化学工程 X射线光电子能谱 钙钛矿(结构) 氧化还原 化学 氮氧化物 无机化学 电极 有机化学 物理化学 燃烧 工程类
作者
Baowei Wang,Chunmei Chi,Meng Xu,Chao Wang,Meng Dajun
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:322: 679-692 被引量:280
标识
DOI:10.1016/j.cej.2017.03.153
摘要

The destruction of toluene in dielectric barrier discharge (DBD) reactor coupled with a series of CeO2-MnOx catalysts was investigated in this work. All catalysts prepared by sol-gel method were characterized in detail using N2 adsorption, XRD, TEM, H2-TPR, Raman, O2-TPD and XPS analysis technology. The effect of input power, molar ratio of Ce/Mn, gas flow rate and initial concentration of toluene on the removal efficiency of toluene and CO2 selectivity has been investigated. The plasma-catalytic system improves the removal efficiency and CO2 selectivity significantly compared with the plasma alone system. The catalytic performance of CeO2-MnOx catalysts are higher than pure CeO2 and MnOx, which might be contributed to the synergistic effect between CeO2 and MnOx (such as Mn3+/Mn2+ and Ce4+/Ce3+ redox couples) in the CeO2-MnOx catalysts. The highest removal efficiency of toluene (95.94%) and CO2 selectivity (90.73%) are acquired with Ce1Mn1 catalyst. The reason may be that: (1) the increased BET specific surface area and the decreased grain size can be obtained from CeO2-MnOx catalyst. (2) The formation of CeO2-MnOx solid solution resulted from the incorporation of Mn cations into the CeO2 lattice could generate more oxygen vacancies and improve the mobility of oxygen. On the basis of the analytic results of GC/MS, the pathways of toluene destruction in the plasma-catalysis system are discussed.
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