Cobalt-doped Ni-based catalysts for low-temperature CO2 methanation

被引:4
|
作者
Guo, Lei [1 ,3 ]
Zhang, Tong [2 ]
Qiu, Juan [4 ]
Bai, Jing [2 ]
Li, Zhongrui [1 ]
Wang, Hanying [2 ]
Cai, Xiaolong [2 ]
Yang, Yonglin [2 ]
Xu, Yunhua [1 ,2 ]
机构
[1] Xian Univ Technol, Sch Mat Sci & Engn, Xian 710048, Peoples R China
[2] Yulin Univ, Sch Chem & Chem Engn, Yulin 719000, Peoples R China
[3] Shenmu Vocat & Tech Coll, Sch Sch Mech & Elect Engn, Shenmu 719300, Peoples R China
[4] Yulin City Special Equipment Inspect & Testing Ins, Yulin 719000, Peoples R China
关键词
Co-doped; Ni-based catalysts; Low temperature; CO2; methanation; Electron density; FISCHER-TROPSCH SYNTHESIS; NICKEL-CATALYSTS; HYDROGENATION; SELECTIVITY; REDUCTION; FE; CE;
D O I
10.1016/j.renene.2024.121512
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The study of the process and mechanism of CO(2 )activation and the development of low-temperature, high-activity and selective catalysts for CO(2 )methanation are current research hotspots. In this paper, a series of Ni/ Al2O3 catalysts with different Co contents were prepared by using layered double hydroxides (LDHs) as precursors for low-temperature CO2 methanation, and the incorporation of Co promoted the electron transfer from Ni to Co, which facilitated the adsorption and activation of CO2 and H-2. The spent catalyst still maintained the layered structure with no significant change in the metal particle size, indicating that the addition of Co significantly improved the long-term stability of the catalysts. The CO2 conversion was 55.5 % and STYCH4 was 148.0 mmol & sdot;gcat (- 1) h(- 1) at 200 degrees C, 2.0 MPa and 1000 h(- 1). The in situ DRIFTS experiments showed that the addition of Co accelerated the conversion of the reaction intermediates and promoted the generation of methane.
引用
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页数:10
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