Catalysis mechanisms of CO2 and CO methanation

被引:386
作者
Miao, Bin [1 ]
Ma, Su Su Khine [1 ]
Wang, Xin [2 ]
Su, Haibin [3 ,4 ]
Chan, Siew Hwa [1 ,5 ]
机构
[1] Nanyang Technol Univ, Energy Res Inst NTU ERI N, 50 Nanyang Ave, Singapore 639798, Singapore
[2] Nanyang Technol Univ, Sch Chem & Biomed Engn, 50 Nanyang Ave, Singapore 639798, Singapore
[3] Nanyang Technol Univ, Div Mat Sci, 50 Nanyang Ave, Singapore 639798, Singapore
[4] Energy Res Inst, Tianneng Grp, Huaxi Ind Funct Zone, Hangzhou 313100, Zhejiang, Peoples R China
[5] Nanyang Technol Univ, Sch Mech & Aerosp Engn, 50 Nanyang Ave, Singapore 639798, Singapore
关键词
SINGLE-CRYSTAL NICKEL; CARBON-MONOXIDE; SELECTIVE METHANATION; SULFUR; HYDROGENATION; SURFACE; NI; DEACTIVATION; DISSOCIATION; RUTHENIUM;
D O I
10.1039/c6cy00478d
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
Understanding the reaction mechanisms of CO2 and CO methanation processes is critical towards the successful development of heterogeneous catalysts with better activity, selectivity, and stability. This review provides detailed mechanisms of methanation processes and undesired catalyst deactivation. We characterize the methanation processes into two categories: (1) associative scheme, in which hydrogen atoms are involved in the C-O bond breaking process, and (2) dissociative scheme, where C-O bond breaking takes place before hydrogenation. For the catalyst deactivation mechanisms, we highlight three important factors, i.e. sulfur poisoning, carbon deposition and metal sintering.
引用
收藏
页码:4048 / 4058
页数:11
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