Hydrogen production by auto-thermal reforming of ethanol over nickel catalyst supported on metal oxide-stabilized zirconia

被引:29
|
作者
Youn, Min Hye [1 ]
Sea, Jeong Gil [1 ]
Song, In Kyu [1 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc, Seoul 151744, South Korea
关键词
Metal oxide-stabilized mesoporous zirconia; Nickel catalyst; Ethanol; Auto-thermal reforming; Hydrogen production; BIO-ETHANOL; STEAM; ZRO2; ENERGY; COPPER; OXIDATION; BEHAVIOR; LNG; CAO; YSZ;
D O I
10.1016/j.ijhydene.2010.01.121
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
Metal oxide-stabilized mesoporous zirconia supports (M-ZrO2) with different metal oxide stabilizer (M = Zr, Y, La, Ca, and Mg) were prepared by a templating sol-gel method. 20 wt% Ni catalysts supported on M-ZrO2 (M = Zr, Y, La, Ca, and Mg) were then prepared by an incipient wetness impregnation method for use in hydrogen production by auto-thermal reforming of ethanol. The effect of metal oxide stabilizer (M = Zr, Y, La, Ca, and Mg) on the catalytic performance of supported nickel catalysts was investigated. Ni/M-ZrO2 (M = Y, La, Ca, and Mg) catalysts exhibited a higher catalytic performance than Ni/Zr-ZrO2, because surface oxygen vacancy of M-ZrO2 (M = Y, La, Ca, and Mg) and reducibility of Nil M-ZrO2 (M = Y, La, Ca, and Mg) were enhanced by the addition of lower valent metal cation. Hydrogen yield over Ni/M-ZrO2 (M = Zr, Y, La, Ca, and Mg) catalyst was monotonically increased with increasing both surface oxygen vacancy of M-ZrO2 support and reducibility of Ni/M-ZrO2 catalyst. Among the catalysts tested, Ni catalyst supported on yttria-stabilized mesoporous zirconia (Ni/Y-ZrO2) showed the best catalytic performance. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3490 / 3498
页数:9
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