Insight into CO2 methanation mechanism over NiUSY zeolites: An operando IR study

被引:245
作者
Westermann, A. [1 ]
Azambre, B. [2 ]
Bacariza, M. C. [1 ]
Graca, I. [1 ]
Ribeiro, M. F. [1 ]
Lopes, J. M. [1 ]
Henriques, C. [1 ]
机构
[1] Univ Tecn Lisboa, CQE, Inst Super Tecn, P-1049001 Lisbon, Portugal
[2] Univ Lorraine, Inst Jean Barriol, Lab Chim & Phys Approche Multiechelle Milieux Com, EA 4632, F-57500 St Avold, France
关键词
Infrared operando spectroscopy; Ni-based zeolite; Mechanism; Formates; Carbonyls; CARBON-DIOXIDE; FORMIC-ACID; ADSORPTION; HYDROGENATION; CATALYST; DECOMPOSITION; CONVERSION; FORMATE; ENERGY; H-2;
D O I
10.1016/j.apcatb.2015.02.026
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
Ni-impregnated USY zeolites with increasing Ni content (5, 10, 14%(wt).) were investigated by operando IR spectroscopy for both CO2 adsorption and CO2 methanation conditions reaction. In-situ FTIR and TPD experiments highlighted a rather weak CO2 adsorption, which occurs namely as carbonates or CO2 linear complexes over cations (e.g., Na+). Under methanation conditions, dissociated hydrogen reacts with carbonates and/or physisorbed CO2, leading to monodentate formates, then carbonyls (both adsorbed onto Ni-0 particles), and finally to methane. A detailed mechanism of the pathways involved in CO2 methanation over NiUSY catalysts is then discussed in accordance with infrared spectroscopic data. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 125
页数:6
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