CO2 reforming of CH4 over ceria-supported metal catalysts

被引:55
作者
Asami, K
Li, XH
Fujimoto, K
Koyama, Y
Sakurama, A
Kometani, N
Yonezawa, Y
机构
[1] Univ Kitakyushu, Fac Environm Engn, Dept Chem Proc & Environm, Kitakyushu, Fukuoka 8080135, Japan
[2] Osaka City Univ, Grad Sch Engn, Dept Appl Chem, Sumiyoshi Ku, Osaka 5588585, Japan
关键词
ceria-supported; activity; catalyst;
D O I
10.1016/S0920-5861(03)00297-9
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
CO2 reforming of CH4 was studied over Fe, Co and Ni catalysts supported on cerium oxide at atmospheric pressure. Ni catalyst gave the highest activity; equilibrium conversion of methane was attained under the conditions of 1123 K, 1 g h/mol, and CO2/CH4 = 1, and the composition of syngas formed was almost H-2/CO = 1. Carbon deposition was not observed, and the catalytic activity and the syngas selectivity were stable for 24h over the catalyst. It was found that the high temperature treatment of the catalyst at 1123 K is important for such an excellent catalytic performance. Co catalyst exhibited an activity nearly equal to that of Ni catalyst when reduced sufficiently, whereas Fe catalyst showed a poor activity. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 31
页数:5
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