Selective CO methanation catalysts for fuel processing applications

被引:146
作者
Dagle, Robert A.
Wang, Yong
Xia, Guan-Guang
Strohm, James J.
Holladay, Jamelyn
Palo, Daniel R.
机构
[1] Pacific NW Natl Lab, Richland, WA 99352 USA
[2] Microprod Breakthrough Inst, Corvallis, OR 97339 USA
关键词
methanation; CO removal; Ru/Al2O3; catalysts; fuel processing; microreactor; HYDROGEN;
D O I
10.1016/j.apcata.2007.04.015
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
Selective CO methanation as a strategy for CO removal in fuel processing applications was investigated over Ru-based catalysts. Ru metal loading and crystallite size were shown to affect catalyst activity and selectivity. Even operating at a gas-hourly-space-velocity as high as 13,500 h(-1), a 3% Ru/Al2O3 catalyst with a 34.2 nm crystallite was shown to be capable of reducing CO in a reformate to less than 100 ppm over a wide temperature range front 240 to 280 degrees C, while keeping hydrogen consumption below 10%. We present the effects of metal loading, preparation method, and crystallite size on performance for Ru-based catalysts in the selective methanation of CO in the presence of H-2 and CO2. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:213 / 218
页数:6
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