Low temperature CO oxidation on Ni-promoted CuO-CeO2 catalysts

被引:40
作者
Chen Guoxing [1 ]
Li Qiaoling [1 ]
Wei Yucai [1 ]
Fang Weiping [1 ,2 ,3 ]
Yang Yiquan [1 ,2 ,3 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem & Biochem Engn, Xiamen 361005, Fujian, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Fujian, Peoples R China
[3] Xiamen Univ, Natl Engn Lab Green Chem Prod Alcohols Ethers & E, Xiamen 361005, Fujian, Peoples R China
关键词
Copper; Cerium; Carbon monoxide; Oxidation; Nickel; Solid solution; CARBON-MONOXIDE OXIDATION; PREFERENTIAL OXIDATION; SELECTIVE OXIDATION; REDOX PROPERTIES; SOLID-SOLUTIONS; OXIDE CATALYST; X-RAY; CU; TRANSITION; XPS;
D O I
10.1016/S1872-2067(11)60468-3
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of Ce20Cu5NiyOx catalysts for CO oxidation at low temperature were prepared and characterized by N-2 adsorption, X-ray diffraction, temperature-program reduction by H-2, X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Ce20Cu5Ni0.4Ox exhibited the highest catalytic activity. The addition of NiO increased the amount of copper ions doped into the CeO2 matrix and gave more oxygen vacancies in ceria by the formation of a Ni-O-Ce solid solution. XPS results showed that large quantities of Cu+, Ce3+, and lattice oxygen existed in the fresh Ce20Cu5Ni0.4Ox catalyst. Cu+ ions in the catalyst can easily migrate to the ceria lattice to form a Cu-O-Ce solid solution, which enhanced the release of the lattice oxygen of the oxides under a reducing atmosphere. The high catalytic activity of Ce20Cu5Ni0.4Ox is due to the promoter giving increased amounts of Cu+ in the catalyst and the formation of solid solutions of both Cu-O-Ce and Ni-O-Ce. (C) 2013, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:322 / 329
页数:8
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