Inverse CeO2/CuO Catalyst As an Alternative to Classical Direct Configurations for Preferential Oxidation of CO in Hydrogen-Rich Stream

被引:271
作者
Hornes, A. [1 ]
Hungria, A. B. [2 ]
Bera, P. [1 ]
Lopez Camara, A. [1 ]
Fernandez-Garcia, M. [1 ]
Martinez-Arias, A. [1 ]
Barrio, L. [3 ]
Estrella, M. [3 ]
Zhou, G. [3 ]
Fonseca, J. J. [3 ]
Hanson, J. C. [3 ]
Rodriguez, J. A. [3 ]
机构
[1] CSIC, Inst Catalisis & Petroleoquim, Madrid 28049, Spain
[2] Univ Cadiz, Fac Ciencias, Dept Ciencia Mat Ingn Met & Quim Inorgan, Cadiz 11510, Spain
[3] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
关键词
CUO-CEO2; CATALYSTS; CARBON-MONOXIDE; REDUCTION; SUBOXIDES; CUO/CEO2; OXIDES; OXYGEN; CU2O; GAS; CUO;
D O I
10.1021/ja9089846
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel inverse CeO2/CuO catalyst for preferential oxidation of CO in H-2-rich stream (CO-PROX) has been developed on the basis of a hypothesis extracted from previous work of the group (JACS 2007, 129, 12064). Possible separation of the two competing oxidation reactions involved in the process (of CO and H-2, respectively) is the key to modulation of overall CO-PROX activity and is based on involvement of different sites as most active ones for each of the two reactions. Achievement of large size CuO particles and adequate CeO2-CuO interfacial configurations in the inverse catalyst apparently allows appreciable enhancement of the catalytic properties of this kind of system for CO-PROX, constituting an interesting alternative to classic direct configurations so far explored for this process. Reasons for such behavior are analyzed on the basis of operando-XRD, -XAFS, and -DRIFTS studies.
引用
收藏
页码:34 / +
页数:4
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