The role of Gadolinia Doped Ceria support on the promotion of CO2 methanation over Ni and Ni-Fe catalysts

被引:40
作者
Frontera, P. [1 ,4 ]
Macario, A. [2 ]
Monforte, G. [3 ]
Bonura, G. [3 ]
Ferraro, M. [3 ]
Dispenza, G. [3 ]
Antonucci, V. [3 ]
Arico, A. S. [3 ]
Antonucci, P. L. [1 ,4 ]
机构
[1] Mediterranean Univ Reggio Calabria, Dept Civil Energy Environm & Mat Engn, I-89124 Reggio Di Calabria, Italy
[2] Univ Calabria, Dept Mech Energy & Management Engn, Via P Bucci 87036, Cosenza, Italy
[3] CNR, Inst Adv Technol Energy Nicola Giordano ITAE, Salita S Lucia Contesse 5, I-98126 Messina, Italy
[4] Consorzio Interuniv Nazl Sci & Tecnol Mat, INSTM, Via G Giusti 9, I-50121 Florence, Italy
关键词
Methanation; Gadolinia doped ceria; Nickel/iron catalyst; Basicity; RICE HUSK ASH; CARBON-DIOXIDE; NICKEL-CATALYSTS; TETRAGONAL ZRO2; HYDROGENATION; SURFACE; OXIDES; ALUMINA; DECOMPOSITION; TRANSIENT;
D O I
10.1016/j.ijhydene.2017.09.025
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
In the present work, CO2 methanation was investigated over Ni, Fe, Ni3Fe1, Ni1Fe1 and Ni1Fe3 catalysts supported on Gadolinia Doped Ceria (GDC) in the temperature range 200-400 degrees C. Both CO2 and H-2 conversion decreased in the order Ni/GDC > Ni3Fe1/GDC > Ni1Fe1/GDC > Ni1Fe3/GDC. No catalytic activity was displayed by Fe/GDC. Maximum CO2 conversion (>90%) was observed at 400 degrees C, with almost 100% selectivity to CH4. The catalysts were characterized by X Ray Diffraction (XRD), N-2 adsorption/desorption, H-2 Temperature Programmed Reduction (H-2-TPR), Transmission Electron Microscopy (TEM), X-ray Photoelectron Spectroscopy (XPS) and CO2 Temperature Programmed Desorption (CO2-TPD). The superior activity of monometallic Ni/GDC with respect to bimetallic Ni Fe/GDC catalysts was ascribed to the presence of surface oxygen vacancies induced by the GDC support, an enhanced basicity of the Ni-rich samples, as well as to the ability of the Ni-GDC to interact with CO2, as suggested by XPS data. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26828 / 26842
页数:15
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