Catalytic performance of mesoporous silica-covered nickel core-shell particles for selective CO methanation

被引:10
|
作者
Hayashi, Katsuhiko [1 ,2 ]
Miyao, Toshihiro [1 ]
Higashiyama, Kazutoshi [1 ]
Deki, Shigehito [1 ]
Tabira, Yasunori [2 ]
Watanabe, Masahiro [1 ]
机构
[1] Univ Yamanashi, Fuel Cell Nanomat Ctr, Kofu, Yamanashi 4000021, Japan
[2] Mitsui Min & Smelting Co Ltd, MITSUI KINZOKU, Ageo, Saitama 3620021, Japan
关键词
Selective CO methanation; Core-shell structure; CO2; methanation; Reverse water-gas shift reaction; Selectivity controlling additives; STRUCTURE SENSITIVITY; NI/TIO2; CATALYST; CARBON-MONOXIDE; METAL-CATALYSTS; GAS; CHLORINE; REMOVAL; STREAM;
D O I
10.1016/j.apcata.2015.09.003
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
A novel catalyst with a core-shell structure composed of vanadium oxide and Ni particles covered by mesoporous silica for the selective CO methanation in reformate gas was investigated. In order to improve the catalytic activity in the low temperature region, an unsupported metallic Ni catalyst with a significantly large surface area was developed, which can replace previous preferential oxidation catalysts. The core-shell structure of the catalysts actualized high activity, selectivity and durability for selective CO methanation. Inhibition of Ni sintering by the surface vanadium oxide and the mesoporous silica may be responsible for the remarkable improvement of the catalytic activity. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 150
页数:8
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