A study of the methanation of carbon dioxide on Ni/Al2O3 catalysts at atmospheric pressure

被引:244
作者
Garbarino, Gabriella [1 ]
Riani, Paola [2 ]
Magistri, Loredana [3 ]
Busca, Guido [1 ]
机构
[1] Univ Genoa, Chim Ambientale DICCA, Dipartimento Ingn Civile, I-16129 Genoa, Italy
[2] Univ Genoa, Dept Chim, Chim Ind DCCI, I-16146 Genoa, Italy
[3] Univ Genoa, Dipartirnento Ingn Meccan Energet Gestionale Tras, I-16145 Genoa, Italy
关键词
Hydrogen; Carbon dioxide; Methanation; Nickel on alumina; CO2 capture and storage; WATER-GAS SHIFT; CO DISSOCIATION; NICKEL; NI; HYDROGEN; NANOPARTICLES; MECHANISMS; CONVERSION; INTERFACE; KINETICS;
D O I
10.1016/j.ijhydene.2014.05.111
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 hydrogenation of carbon dioxide producing methane and CO has been investigated over Ni/Al2O3 catalysts. The as prepared catalysts have been characterized by XRD and Temperature Programmed Reduction. Spent catalysts have been characterized by XRD and Field Emission SEM. Catalytic activity needs the presence of Ni metal particles which may form in situ if the Ni loading is higher than that needed to cover the alumina surface with a complete monolayer. If Ni content is lower, pre-reduction is needed. Catalysts containing very small Ni particles obtained by reducing moderate loading materials are very selective to methane without CO formation. The larger the Ni particles, due to higher Ni loadings, the higher the CO production. Cubic Ni metal particles are found in the spent catalysts mostly without carbon whiskers. The data suggest that fast methanation occurs at the expense of CO intermediate on the corners of nanoparticles interacting with alumina, likely with a "via oxygenate" mechanism. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11557 / 11565
页数:9
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