Highly Active Ce- and Mg-Promoted Ni Catalysts Supported on Cellulose-Derived Carbon for Low-Temperature CO2 Methanation

被引:18
|
作者
Tarifa, Pilar [1 ]
Megias-Sayago, Cristina [1 ]
Cazana, Fernando [1 ]
Gonzalez-Martin, Miguel [1 ]
Latorre, Nieves [1 ]
Romeo, Eva [1 ]
Jose Delgado, Juan [2 ]
Monzon, Antonio [1 ]
机构
[1] Univ Zaragoza, Dept Chem & Environm Engn, Inst Nanociencia & Mat Aragon INMA, CSIC, E-50018 Zaragoza, Spain
[2] Univ Cadiz, Dept Mat Sci Met Engn & Inorgan Chem, E-11510 Puerto Real, Spain
关键词
NANOPARTICLES; HYDROGENATION; BIOMASS; NICKEL; GAS; PD; HYDROCARBONS; NANOFIBERS;
D O I
10.1021/acs.energyfuels.1c01682
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The CO2 methanation performance of Mg- and/or Ce-promoted Ni catalysts supported on cellulose-derived carbon (CDC) was investigated. The samples, prepared by biomorphic mineralization techniques, exhibit pore distributions correlated to the particle sizes, revealing a direct effect of the metal content in the textural properties of the samples. The catalytic performance, evaluated as CO2 conversion and CH4 selectivity, reveals that Ce is a better promoter than Mg, reaching higher conversion values in all of the studied temperature range (150-500 degrees C). In the interval of 350-400 degrees C, Ni-Mg-Ce/CDC attains the maximum yield to methane, 80%, reaching near 100% CH4 selectivity. Ce-promoted catalysts were highly active at low temperatures (175 degrees C), achieving 54% CO2 conversion with near 100% CH4 selectivity. Furthermore, the large potential stability of the Ni-Mg-Ce/CDC catalyst during consecutive cycles of reaction opens a promising route for the optimization of the Sabatier process using this type of catalyst.
引用
收藏
页码:17212 / 17224
页数:13
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