Ni nanocatalysts supported on mesoporous Al2O3-CeO2 for CO2 methanation at low temperature

被引:22
|
作者
Wu, Yushan [1 ]
Lin, Jianghui [1 ]
Ma, Guangyuan [1 ]
Xu, Yanfei [1 ]
Zhang, Jianli [2 ]
Samart, Chanatip [3 ]
Ding, Mingyue [1 ,2 ,4 ]
机构
[1] Wuhan Univ, Sch Power & Mech Engn, Hubei Int Sci & Technol Cooperat Base Sustainable, Hubei Prov Key Lab Accoutrement Tech Fluid Machin, Wuhan 430072, Peoples R China
[2] Ningxia Univ, State Key Lab Highefficiency Utilizat Coal & Gree, Yinchuan 750021, Peoples R China
[3] Thammasat Univ, Fac Sci & Technol, Dept Chem, Rangsit Campus, Klongluang 12120, Pathumtani, Thailand
[4] Wuhan Univ, Shenzhen Res Inst, Shenzhen 518108, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROTALCITE-DERIVED CATALYSTS; CARBON-DIOXIDE; NI/AL2O3; CATALYSTS; CEO2; ADDITION; SYNGAS; HYDROGENATION; GASIFICATION; STATE;
D O I
10.1039/c9ra08967e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The selectivity and activity of a nickel catalyst for the hydrogenation of carbon dioxide to form methane at low temperatures could be enhanced by mesoporous Al2O3-CeO2 synthesized through a one-pot sol-gel method. The performances of the as-prepared Ni/Al2O3-CeO2 catalysts exceeded those of their single Al2O3 counterpart giving a conversion of 78% carbon dioxide with 100% selectivity for methane during 100 h testing, without any deactivation, at the low temperature of 320 degrees C. The influence of CeO2 doping on the structure of the catalysts, the interactions between the mesoporous support and nickel species, and the reduction behaviors of Ni2+ ions were investigated in detail. In this work, the addition of CeO2 to the composites increased the oxygen vacancies and active metallic nickel sites, and also decreased the size of the nickel particles, thus improving the low temperature catalytic activity and selectivity significantly.
引用
收藏
页码:2067 / 2072
页数:6
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