简介概要

Valence State of Active Copper in CuOx/CeO2 Catalysts for CO Oxidation

来源期刊:JOURNAL OF RARE EARTHS2006年第2期

论文作者:Zeng Shanghong Liu Yuan Wang Xiaoyan Yu Wenguo Bai Xue

Key words:active center; carbon monoxide; ceria; copper; preferential oxidation; hydrogen production; rare earths;

Abstract: CuOx/CeO2 catalysts were prepared by adsorption-impregnation method.CO conversion was tested over the catalysts pretreated under different conditions for preferential CO oxidation in H2, and the catalysts were characterized with X-ray photoelectron spectroscopy and temperature programmed reduction.Experimental results show that there are two kinds of copper, which are Cu+ and Cu2+ in calcined CuOx/CeO2.Among them, the Cu+ is the key active component for CO oxidation.The main reason is as follows: CO is activated by copper for CO oxidation over CuOx/CeO2, while CO can not be activated by Cu2+.Only when Cu2+ is reduced to Cu+ or Cu0, the copper may be active for CO oxidation, moreover, the experimental results show that the reduction of Cu2+ does not lead to an increase of catalytic activity.So the active species is Cu+ in CuOx/CeO2 catalysts.

详情信息展示

Valence State of Active Copper in CuOx/CeO2 Catalysts for CO Oxidation

Zeng Shanghong1,Liu Yuan1,Wang Xiaoyan2,Yu Wenguo2,Bai Xue2

(1.Department of Catalysis Sciences and Technology, College of Chemical Engineering, Tianjin University, Tianjin 300072, China;
2.School of Chemical Engineering, Inner Mongolia University of Technology, Huhhot 010062, China)

Abstract:CuOx/CeO2 catalysts were prepared by adsorption-impregnation method.CO conversion was tested over the catalysts pretreated under different conditions for preferential CO oxidation in H2, and the catalysts were characterized with X-ray photoelectron spectroscopy and temperature programmed reduction.Experimental results show that there are two kinds of copper, which are Cu+ and Cu2+ in calcined CuOx/CeO2.Among them, the Cu+ is the key active component for CO oxidation.The main reason is as follows: CO is activated by copper for CO oxidation over CuOx/CeO2, while CO can not be activated by Cu2+.Only when Cu2+ is reduced to Cu+ or Cu0, the copper may be active for CO oxidation, moreover, the experimental results show that the reduction of Cu2+ does not lead to an increase of catalytic activity.So the active species is Cu+ in CuOx/CeO2 catalysts.

Key words:active center; carbon monoxide; ceria; copper; preferential oxidation; hydrogen production; rare earths;

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