Preferential oxidation of CO in rich H2 over CuO/CeO2: Operando-DRIFTS analysis of deactivating effect of CO2 and H2O

被引:255
作者
Gamarra, Daniel [1 ]
Martinez-Arias, Arturo [1 ]
机构
[1] CSIC, Inst Catalisis & Petroleoquim, Madrid 28049, Spain
关键词
CuO-CeO2; catalysts; CO-PROX; Operando-DRIFTS; CO2; H2O; Deactivation; TRANSFORM INFRARED-SPECTROSCOPY; CARBON-MONOXIDE OXIDATION; AREA CUO-CEO2 CATALYSTS; SELECTIVE OXIDATION; REDOX PROPERTIES; HYDROGEN PROX; EXCESS H-2; COPPER; CERIA; CEO2;
D O I
10.1016/j.jcat.2009.02.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A catalyst of copper oxide supported on nanoStructured ceria has been examined with the aim of exploring deactivating effects produced by CO2 or H2O presence on its activity for preferential oxidation of CO in a H-2-rich stream. For this purpose, the catalyst is explored by means of operando-DRIFTS experiments. The results allow determining most relevant deactivating effects induced by CO2 and H2O. These are mainly related to modifications of interfacial sites upon formation of specific carbonates and a blocking effect induced by the presence of adsorbed molecular water, respectively, which limit redox/catalytic activity of the interfacial zone of the catalyst active for CO oxidation. Such modifications are directly evidenced by the difficulties of ceria to promote the generation of partially reduced states at interfacial sites of the dispersed copper oxide particles or to propagate the reduction over such particles, which affects to the hydrogen oxidation activity of the catalyst, leading on the whole to a general decrease of the CO-PROX performance of the system. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:189 / 195
页数:7
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