Production of hydrogen from methanol over Cu/ZnO and Cu/ZnO/Al2O3 catalysts prepared by homogeneous precipitation:: Steam reforming and oxidative steam reforming

被引:105
|
作者
Shishido, Tetsuya
Yamamoto, Yoshihiro
Morioka, Hiroyuki
Takehira, Katsuomi
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishigyo Ku, Kyoto 6158510, Japan
[2] Hiroshima Univ, Grad Sch Engn, Dept Chem & Chem Engn, Higashihiroshima 7398527, Japan
[3] Hiroshima Prefectural Inst Ind Sci & Technol, Higashihiroshima 7398527, Japan
关键词
hydrogen production; steam reforming; methanol; Cu/ZnO/Al2O3; catalyst; homogeneous precipitation;
D O I
10.1016/j.molcata.2006.12.018
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
Two series of Cu/ZnO and Cu/ZnO/Al2O3 catalysts with varying Cu/Zn ratio have been prepared by the homogeneous precipitation (hp) method using urea hydrolysis. Steam reforming and oxidative steam reforming of methanol were degrees performed using the hp-Cu/Zn-based catalysts for catalytic production of hydrogen. The hp-Cu/ZnO/Al2O3 catalyst showed a higher activity than the hp-Cu/ZnO catalysts. In both cases, the catalytic activity was well correlated with the surface area of Cu metal, and the maximum activity was obtained on the hp-Cu/ZnO/Al2O3 catalyst with the Cu/Zn ratio of 1/1. Although a large amount of Cu+ was detected on the surface of the Cu/Zn-based catalysts after the reduction at 260 C, no obvious correlation was observed between the activity and the surface amount of Cu+. The hp-Cu/ZnO/Al2O3 catalyst showed a high and stable activity not only for steam reforming but also for oxidative steam reforming of methanol, and the latter reaction effectively produced H-2 with a low CO selectivity at a low temperature around 200 degrees C. It was confirmed by the temperature-programmed desorption experiments that CH3OH was first dehydrogenated to HCHO, which then underwent a nucleophilic attack of H2O to form HCOOH, followed by the decomposition to H-2 and CO2 on the hp-Cu/Zn-based catalysts. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:185 / 194
页数:10
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