Steam reforming of ethanol over nickel molybdenum carbides for hydrogen production
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作者:
Miyamoto, Yukihiro
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Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, JapanTokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, Japan
Miyamoto, Yukihiro
[1
]
Akiyama, Masato
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Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, JapanTokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, Japan
Akiyama, Masato
[1
]
Nagai, Masatoshi
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Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, JapanTokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, Japan
Nagai, Masatoshi
[1
]
机构:
[1] Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, Japan
The steam reforming of ethanol over carburized NiMo catalysts was studied to determine the effects of the Ni content, carburization temperature in 20% CH4/H-2, GHSV, potassium addition and a comparison of the reduced catalyst. The catalysts were characterized by CO adsorption, XRD, X-ray electron spectroscopy (XPS) and temperature-programmed surface reaction after ethanol adsorption. The 798 K-carburized NiMo catalyst gradually increased below 500 min and it exhibited a higher activity than the reduced NiMo catalyst. The addition of potassium promoted more hydrogen selectivity than the nonpotassium-added catalysts. The 798 K-carburized catalyst exhibited the high intensity peaks of MoO2 and small peaks Of beta-Mo2C and Ni metal (or NiMo) were present, while the 823 K-carburized catalyst showed broad and small peaks. The 873 and 848 K-carburized catalysts contained a strong intensity of beta-Mo2C and clear Ni metal (or NiMo). The XPS measurements revealed that the hydrogen production was proportional to Ni-0 of the carburized NiMo catalyst. The addition of potassium significantly increases the Ni-0 ratio, which was stabilized instead of increasing the Mo oxidation during the reaction. (C) 2009 Elsevier B.V. All rights reserved.