Effects of the surface adsorbed oxygen species tuned by rare-earth metal doping on dry reforming of methane over Ni/ZrO2 catalyst

被引:148
|
作者
Zhang, Meng [1 ,2 ]
Zhang, Junfeng [1 ]
Zhou, Zeling [1 ,2 ]
Chen, Shuyao [1 ,2 ]
Zhang, Tao [1 ]
Song, Faen [1 ]
Zhang, Qingde [1 ]
Tsubaki, Noritatsu [3 ]
Tan, Yisheng [1 ]
Han, Yizhuo [1 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Univ Toyama, Grad Sch Engn, Dept Appl Chem, Gofuku 3190, Toyama 9308555, Japan
基金
中国国家自然科学基金;
关键词
Dry reforming; Ni/ZrO2; Oxygen species; Metal doping; Carbon deposition; CARBON-DIOXIDE; CO2; HYDROGENATION; ELECTRIC-FIELD; NI CATALYSTS; ZIRCONIA; CEO2; NANOPARTICLES; PERFORMANCE; PEROVSKITE; INSIGHT;
D O I
10.1016/j.apcatb.2019.118522
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
During dry reforming of methane, oxygen species over the catalyst surface play an important role in CH4/CO2 reactivity, catalytic performance and carbon deposition. Herein, the effects of the surface adsorbed oxygen species tuned by doping with different rare-metal metals (such as Ce, La, Sm and Y) on the catalytic behavior were elaborated systematically. It was found that Y-doped catalyst exhibited the most amount of surface adsorbed oxygen species, followed by Sm, La, Ce and non-doped catalysts. The results confirmed that the surface adsorbed oxygen species were remarkably beneficial to enhance both CO2 activation and CH4 dissociation. Nevertheless, carbon formation and removal did not keep pace at low temperature due to more promotional effects of the surface adsorbed oxygen species on CH4 dissociation than CO2 activation. The gap between carbon deposition and removal was potential to be ameliorated through the accelerated activation to CO2 at high temperature.
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页数:12
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