Production of hydrogen from methanol over Cu/ZnO and Cu/ZnO/Al2O3 catalysts prepared by homogeneous precipitation:: Steam reforming and oxidative steam reforming
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作者:
Shishido, Tetsuya
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机构:Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishigyo Ku, Kyoto 6158510, Japan
Shishido, Tetsuya
Yamamoto, Yoshihiro
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机构:Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishigyo Ku, Kyoto 6158510, Japan
Yamamoto, Yoshihiro
Morioka, Hiroyuki
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机构:Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishigyo Ku, Kyoto 6158510, Japan
Morioka, Hiroyuki
Takehira, Katsuomi
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机构:Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishigyo Ku, Kyoto 6158510, Japan
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
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.
机构:
Ajou Univ, Dept Chem Engn, Suwon 443749, South Korea
Ajou Univ, Dept Energy Syst Res, Suwon 443749, South KoreaAjou Univ, Dept Chem Engn, Suwon 443749, South Korea
Park, Jung Eun
Yim, Sun-Dae
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Korea Inst Energy Res, Taejon 305343, South KoreaAjou Univ, Dept Chem Engn, Suwon 443749, South Korea
Yim, Sun-Dae
Kim, Chang Soo
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Korea Inst Energy Res, Taejon 305343, South KoreaAjou Univ, Dept Chem Engn, Suwon 443749, South Korea
Kim, Chang Soo
Park, Eun Duck
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Ajou Univ, Dept Chem Engn, Suwon 443749, South Korea
Ajou Univ, Dept Energy Syst Res, Suwon 443749, South KoreaAjou Univ, Dept Chem Engn, Suwon 443749, South Korea