Alumina-supported nickel oxide for ozone decomposition and catalytic ozonation of CO and VOCs

催化作用 臭氧 化学 氧化剂 分解 无机化学 一氧化碳 吸附 氧气 催化氧化 氧化物 X射线光电子能谱 化学工程 有机化学 工程类
作者
M. Stoyanova,P. Konova,P. Nikolov,A. Naydenov,St. Christoskova,D. Mehandjiev
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:122 (1-2): 41-46 被引量:94
标识
DOI:10.1016/j.cej.2006.05.018
摘要

An alumina-supported nickel oxide system with overstoichiometric oxygen (NiOx/Al2O3) was investigated with respect to heterogeneous catalytic decomposition of ozone, complete oxidation of volatile organic compounds (VOCs) and oxidation of CO. The catalyst was prepared by a deposition oxidation–precipitation method and was characterized by chemical analysis, XPS, XRD, IR techniques, magnetic and adsorption measurements. The experiments were performed in the temperature range of −50 to 250 °C in an isothermal plug-flow reactor. A very high activity of the catalyst towards ozone decomposition was observed even at temperatures below −45 °C and at the same time the catalyst remained active for a long time. The activity of the catalyst with respect to complete oxidation of VOCs and oxidation of carbon monoxide was studied in presence of different oxidizing agents (ozone or oxygen). A significant increase in catalytic activity and decrease in reaction temperature were observed using ozone as an oxidant. Two main reasons for this behaviour were found: (i) the high content of active and mobile oxygen obtained during the synthesis on the catalyst surface, and (ii) the catalytically active complex of Ni4+O(OH)2, formed during the reaction of ozone decomposition and able to oxidize VOCs at room temperature.
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