Enhanced low-temperature activity for CO2 methanation over Ru doped the Ni/CexZr(1-⁢x⁢)O2 catalysts prepared by one-pot hydrolysis method

被引:50
作者
Shang, Xingfu [1 ]
Deng, Digu [1 ]
Wang, Xueguang [1 ]
Xuan, Weidong [1 ]
Zou, Xiujing [1 ]
Ding, Weizhong [1 ]
Lu, Xionggang [1 ]
机构
[1] Shanghai Univ, Sch Mat Sci & Engn, State Key Lab Adv Special Steel, Shanghai Key Lab Adv Ferromet, Shanghai 200072, Peoples R China
关键词
CO2; methanation; Nickel catalyst; Ceria-zirconia; Low-temperature activity; One-pot hydrolysis method; CARBON-DIOXIDE; RU-NI/TIO2; CATALYSTS; CERIA-ZIRCONIA; PLASMA; NANOPARTICLES; SURFACE; OXIDES; CE; HYDROGENATION; PERFORMANCE;
D O I
10.1016/j.ijhydene.2018.02.059
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
A series of 30 wt%Ni/CexZr1-xO2 catalysts doped with Ru ranging from 0 to 5 wt% were prepared by one-pot hydrolysis of metal nitrates with ammonium carbonate for carbon dioxide methanation at low temperature range of 150-310 degrees C. The influences of Ce/Zr molar ratios and Ru contents on the physicochemical properties and catalytic activities of prepared catalysts were systematically investigated. The addition Ru can improve the Ni dispersion and the basicity of the yRu-30Ni/Ce0.9Zr0.1O2 catalysts surface. As a result, their low-temperature catalytic activity had been enhanced over these doped Ru promoted catalysts. The optimal catalyst was 3Ru-30Ni/Ce0.9Zr0.1O2 on which the CO2 conversion reached theoretical equilibrium value as high as 98.2% with the methane selectivity of 100% at a reaction temperature as low as 230 degrees C. Moreover, there was almost no deactivation for the 3Ru-30Ni/Ce0.9Zr0.1O2 catalyst during 300 h at 230 degrees C indicating excellent catalytic stability and coke resistence ability. It was also found that the low-temperature activity of 3Ru-30Ni/Ce0.9Zr0.1O2 catalyst prepared by one-pot hydrolysis method was much higher than the one prepared by impregnation method. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7179 / 7189
页数:11
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