Cooperation Between Active Metal and Basic Support in Ni-Based Catalyst for Low-Temperature CO2 Methanation

被引:76
作者
Ma, Yuan [1 ]
Liu, Jiao [2 ]
Chu, Mo [1 ]
Yue, Junrong [2 ]
Cui, Yanbin [2 ]
Xu, Guangwen [3 ]
机构
[1] China Univ Min Sr Technol Beijing, Sch Chem & Environm Engn, Beijing 100083, Peoples R China
[2] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[3] Shenyang Univ Chem Technol, Inst Ind Chem & Energy Technol, Shenyang 110142, Liaoning, Peoples R China
关键词
CO2; methanation; Ni/CeO2; Catalyst; Support; Basic site; TPD; CARBON-DIOXIDE METHANATION; STRUCTURE SENSITIVITY; PARTICLE-SIZE; HYDROGENATION; NANOPARTICLES; PERFORMANCE; BEHAVIORS; PROMOTER; ALUMINA; NICKEL;
D O I
10.1007/s10562-019-03033-w
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
The key challenge for CO2 methanation, an eight-electron process under kinetic limitation, relies on the design of non-noble metal catalysts so as to achieve high activity at low reaction temperatures. In this work, four Ni-based catalysts with different supports were prepared and tested for CO2 methanation at 250-550 degrees C in a fixed bed quartz reactor and further characterized to reveal the structure-function relationship. The Ni-based catalysts followed an activity order of Ni/CeO2 > Ni/Al2O3 > Ni/TiO2 > Ni/ZrO2, especially at temperatures lower than 350 degrees C. H-2-TPR and TPD results indicated that the interaction between nickel and support was strong and the metallic nickel was well dispersed in the Ni/Al2O3 catalyst, while more amount of CO2 was adsorbed on the weak basic sites in the Ni/CeO2 catalyst. By establishing the correlation between the catalytic performance and the catalyst structure, it was found that the Ni nanoparticles and basic support serve as H-2 and CO2 active centers respectively and cooperatively catalyze CO2 methanation, resulting in high low-temperature reaction activity. [GRAPHICS] .
引用
收藏
页码:1418 / 1426
页数:9
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