Facile synthesis of ordered mesoporous Ni-Zr-Al catalysts with high hydrothermal stability for CO methanation

被引:14
|
作者
Liu, Qing [1 ]
Gu, Fangna [1 ]
Wang, Xiaoyan [1 ]
Jin, Guojing [1 ]
Li, Huifang [1 ]
Gao, Feng [2 ]
Zhong, Ziyi [2 ]
Xu, Guangwen [1 ]
Su, Fabing [1 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[2] ASTAR, Inst Chem Engn & Sci, Jurong Isl 627833, Singapore
来源
RSC ADVANCES | 2015年 / 5卷 / 102期
基金
中国国家自然科学基金;
关键词
ZIRCONIA; PERFORMANCE; CLUSTERS; ALUMINA;
D O I
10.1039/c5ra17255a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For supported nickel catalysts used for catalytic reactions with presence of water vapor, it is a great challenge to let them have high resistance to sintering, coking as well as water vapor simultaneously. To address this problem, we synthesized a series of ternary ordered mesoporous Ni-Zr-Al metal oxide composites via an evaporation-induced self-assembly (EISA) and applied them to the CO methanation reaction. Compared to the ordered mesoporous Ni-Al catalyst, the ordered mesoporous Ni-Zr-Al catalyst showed much improved hydrothermal stability, because the incorporated Zr species could act as the supporter for the OMA framework, effectively preventing it from sintering-caused structural collapse and phase transition during the hydrothermal treatment; also, in a 120 h-lifetime test, the ordered mesoporous Ni-Zr-Al catalyst showed high anti-coking and anti-sintering properties, mainly because of the confinement effect of the mesopore channels as well as the incorporation of the zirconia promoter.
引用
收藏
页码:84186 / 84194
页数:9
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