CO2 methanation on Co/TiO2 catalyst: Effects of Y on the support

被引:44
|
作者
Qin, Zuzeng [1 ]
Wang, Xiaodi [1 ]
Dong, Lihui [1 ]
Su, Tongming [1 ]
Li, Bin [1 ]
Zhou, Yuwen [1 ]
Jiang, Yuexiu [1 ]
Luo, Xuan [1 ]
Ji, Hongbing [1 ,2 ]
机构
[1] Guangxi Univ, Sch Chem & Chem Engn, Guangxi Key Lab Petrochem Resource Proc & Proc In, Nanning 530004, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; hydrogenation; Methanation; Co3O4; catalyst; Y doped TiO2 support; Oxygen vacancy; CARBON-DIOXIDE; PHOTOCATALYTIC REDUCTION; TIO2; PHOTOCATALYST; LOW-TEMPERATURE; PARTICLE-SIZE; PERFORMANCE; NANOPARTICLES; PHASE; LA; NI;
D O I
10.1016/j.ces.2019.115245
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The Y was used for improving the structural performance of TiO2 support. The results showed that the BET surface area was increased by doping Y, and more oxygen vacancies were generated in the TiO2 support, which would promote the activation of CO2. The reduction temperature of the Co3O4 was decreased and more Co3O4 can be reduced into Co for the Y doped Co/TiO2 samples compared to that of the Co/TiO2. Furthermore, the doped Y enhanced the basicity of the catalysts and the adsorption capacity of the CO2 was greatly increased, which was beneficial to the activation of the CO2 and the CO2 methanation reaction. The activity test indicated that the CO2 conversion and CH4 selectivity was highest when using the 20% Co/2%Y-TiO2 catalyst. The 20% Co/2%Y-TiO2 catalyst exhibited the highest CO2 conversion of 85.9%, and CH4 selectivity of 99.5% at 350 degrees C, and kept stable in 40 h. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页数:10
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