Preferential oxidation of carbon monoxide on Co/CeO2 nanoparticles

被引:119
|
作者
Woods, Matthew P. [1 ]
Gawade, Preshit [1 ]
Tan, Bing [1 ]
Ozkan, Umit S. [1 ]
机构
[1] Ohio State Univ, Dept Chem & Biomol Engn, Columbus, OH 43210 USA
关键词
PROX; CO oxidation; H-2; combustion; Cobalt; Ceria; CeO2; Cobalt oxide; Co/CeO2; Co3O4; REPORTING PHYSISORPTION DATA; GAS SOLID SYSTEMS; CO OXIDATION; SELECTIVE OXIDATION; SURFACE-AREA; HYDROGEN; CATALYSTS; REMOVAL; OXIDE; KINETICS;
D O I
10.1016/j.apcatb.2010.03.015
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 highly active CoO/CeO2 nanoparticle catalyst with high surface area (78 m(2)/g) has been prepared and tested in the preferential oxidation of carbon monoxide (PROX) in the presence of hydrogen Three distinct temperature regions of catalyst activity are observed corresponding to CO oxidation, H-2 oxidation and methanation. The catalyst achieves near 100% CO conversion under a wide range of reaction conditions demonstrating peak activity near 175 degrees C The catalyst is stable with time-on-stream at the temperature of highest CO conversion The presence of H-2 decreases the CO oxidation rate, possibly clue to competitive adsorption between H-2 and CO CO oxidation and H-2 oxidation activation energies were 52 and 74 kj/mol, respectively Raman spectroscopy and X-ray diffraction experiments have demonstrated that the cobalt takes the form of Co3O4 and no CoO was detected under any experimental conditions (C) 2010 Elsevier B V All rights reserved
引用
收藏
页码:28 / 35
页数:8
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