Promotion of Alumina Supported Cobalt Catalysts by Iron

被引:19
|
作者
Das, Taraknath [1 ]
Deo, Goutam [1 ]
机构
[1] Indian Inst Technol, Dept Chem Engn, Kanpur 208016, Uttar Pradesh, India
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2012年 / 116卷 / 39期
关键词
FISCHER-TROPSCH SYNTHESIS; METHANE DECOMPOSITION; BIMETALLIC CATALYSTS; MODERATE TEMPERATURES; REDUCTION BEHAVIOR; CARBON NANOTUBES; OXIDE CATALYSTS; FE-CO; HYDROGENATION; SYNGAS;
D O I
10.1021/jp3007206
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
Several alumina supported cobalt (Co), iron (Fe) mono metallic, and Co-Fe bimetallic catalysts were synthesized, characterized, and studied for the carbon dioxide (CO2) hydrogenation reaction. The catalysts were synthesized by coimpregnation and double-impregnation methods, and characterized by X-ray diffraction (XRD), ultraviolet-visible-near infrared (UV-vis-NIR), and diffuse reflectance infrared fourier transform (DRIFT) spectroscopy. The surface areas of the catalysts were also determined. Appropriate amounts of Fe promote the catalytic reactivity of alumina supported cobalt catalysts for the CO2 hydrogenation reaction. Furthermore, it was beneficial that this catalyst was synthesized by the double-impregnation method, where Fe was initially deposited, and then, Co was deposited on the alumina support. The hydrogenation of CO2 revealed the presence of formate species on the catalyst during reaction. It appears that iron promotes the supported cobalt catalyst by (i) protecting cobalt from strongly interacting with the alumina support and (ii) forming a Co-Fe alloy.
引用
收藏
页码:20812 / 20819
页数:8
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