CO2 methanation of Ni catalysts supported on tetragonal ZrO2 doped with Ca2+ and Ni2+ ions

被引:81
作者
Takano, H. [1 ,2 ]
Shinomiya, H. [1 ]
Izumiya, K. [1 ]
Kumagai, N. [1 ]
Habazaki, H. [3 ]
Hashimoto, K. [4 ]
机构
[1] Hitachi Zosen Corp, Kashiwa, Chiba 2778515, Japan
[2] Hokkaido Univ, Grad Sch Chem Sci & Engn, Sapporo, Hokkaido 0608628, Japan
[3] Hokkaido Univ, Fac Engn, Div Mat Chem & Frontier Chem Ctr, Sapporo, Hokkaido 0608628, Japan
[4] Tohoku Inst Technol, Sendai, Miyagi 9828577, Japan
关键词
CO2; Hydrogenation; Ni catalyst; Tetragonal ZrO2; Oxygen vacancies; CARBON-DIOXIDE; NI/ZRO2; CATALYST; NICKEL; ADSORPTION; RH/CEO2; SURFACE; ENERGY;
D O I
10.1016/j.ijhydene.2015.04.128
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
This paper reports highly active CO2 methanation catalysts of Ni supported on tetragonal ZrO2 for supply of renewable energy in the form of CH4 via electrolytic H-2 generation. The Ni/tetragonal ZrO2 catalysts with the nominal cationic compositions of 50 at.% Ni-(Zr + Ca) (Ca/(Zr + Ca) molar ratios of 0.125-0.333), were prepared by calcination of a ZrO2 sol mixed with nickel and calcium nitrates at 650 and 800 degrees C and subsequent H-2 reduction of NiO. All the catalysts prepared exhibited almost 100% CH4 selectivity, and the activity increased with the calcium content up to a Ca/(Zr + Ca) molar ratio between 0.167 and 0.200, above which the activity tended to decrease. At the optimized calcium content, a tetragonal ZrO2 phase with cation vacancies introduced by Ca2+ and Ni2+ doping was predominant, in addition to fcc Ni. A monoclinic ZrO2 phase was also present below the optimized calcium content, while a Ca-rich amorphous or CaZrO3 phase was formed with tetragonal ZrO2 above the optimized calcium content. The high catalytic activity of the catalyst with the optimized composition could be correlated with the presence of tetragonal ZrO2 with oxygen vacancies. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8347 / 8355
页数:9
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