Highly anti-sintering and anti-coking ordered mesoporous silica carbide supported nickel catalyst for high temperature CO methanation

被引:21
作者
Han, Yahong [1 ]
Quan, Yanhong [1 ]
Hao, Panpan [1 ]
Zhao, Jinxian [1 ]
Ren, Jun [1 ]
机构
[1] Taiyuan Univ Technol, Minist Educ & Shanxi Prov, Key Lab Coal Sci & Technol, 79 Yingze West St, Taiyuan 030024, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon-monoxide methanation; Anti-sintering; Anti-coking; Ordered mesoporous silica carbide; Spatial confinement effect; SYNTHETIC NATURAL-GAS; ONE-POT SYNTHESIS; HYDROGEN-PRODUCTION; ENHANCED ACTIVITY; DOPED GRAPHENE; NI CATALYSTS; AL CATALYSTS; CARBON; STABILITY; SURFACE;
D O I
10.1016/j.fuel.2019.116006
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The inhibition of sintering and coking of supported nickel catalysts remains a great challenge in high-temperature carbon-monoxide (CO) methanation. Ordered mesoporous silica carbide (OM-SiC) was fabricated via a nanocasting technique as a nickel catalyst support for CO methanation. Compared with either SiC or SBA-15 supported nickel catalysts, the Ni/OM-SiC exhibited the best activity for CO methanation from 240 to 600 degrees C, originated from the highest dispersion of Ni. Below 800 degrees C, 1.0 MPa, and a gas hourly space velocity (GHSV) of 15,000 mL g(-1) h(-1), a superior activity is close to the theoretical values. In addition, the Ni/OM-SiC catalyst shows far superior anti-coking and anti-sintering properties than the other two kinds of catalysts. The improved catalytic performance can be attributed to a unique pore structure that offers a spatial confinement effect for the nickel particles, and the high thermal conductivity that avoids the formation of hot-spots during reaction. These findings are helpful to develop an efficient nickel-based methanation catalyst to produce synthetic natural gas.
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页数:11
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