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Carbon dioxide methanation over Ni catalysts supported on various metal oxides
被引:299
作者:

Muroyama, Hiroki
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan

Tsuda, Yuji
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan

Asakoshi, Toshiki
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan

Masitah, Hasan
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan

Okanishi, Takeou
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan

Matsui, Toshiaki
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan

Eguchi, Koichi
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
机构:
[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
关键词:
Carbon dioxide methanation;
Nickel catalyst;
Basic property;
In situ infrared spectroscopy;
CO2;
METHANATION;
TEMPERATURE;
D O I:
10.1016/j.jcat.2016.07.018
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:
Carbon dioxide methanation is well known to offer some advantages and be catalyzed by Ru, Rh, Pd, and Ni. In this study, Ni catalysts supported on various metal oxides were fabricated and their catalytic activity for CO2 methanation was evaluated. The CO2 conversion for most of catalysts drastically increased at 225-250 degrees C and reached a maximal value at 300-350 degrees C. The order of CH4 yield at 250 degrees C was as follows: Ni/Y2O3 > Ni/Sm2O3 > Ni/ZrO2 > Ni/CeO2 > Ni/Al2O3 > Ni/La2O3. The catalytic activity could be partly explained by the basic property of the catalysts. Moreover, the chemical species formed on the catalyst surface during CO2 methanation were examined by in situ infrared spectroscopy. From the obtained results, the difference in the activity depending on the support material of Ni catalysts was discussed. (C) 2016 Elsevier Inc. All rights reserved.
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页码:178 / 184
页数:7
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