甲烷化
催化作用
阿累尼乌斯方程
镍
铈
活化能
选择性
无机化学
化学
烧结
色散(光学)
材料科学
核化学
物理化学
有机化学
物理
光学
作者
Zhanggui Hou,Yiming Chen,Xin Ma,Ling Zhou,Wen Wang,Jiesan Qiu,Yi Zhang
摘要
Abstract Ce‐promoted Ni catalysts were developed and applied in a CO methanation reaction. The 10%Ni/SiO 2 catalyst exhibits poor initial CO conversion (32.8%) and rapid deactivation with the highest methane selectivity during CO the methanation reaction. In contrast, the 4%Ce–10%Ni/SiO 2 catalyst shows dramatically increased initial CO conversion, which is up to 90.7%. Additionally, the apparent activation energy, Ea value, of 4%Ce–10%Ni/SiO 2 was calculated to be 102.2 kJ/mol according to the Arrhenius equation, which is much lower than that of the 10%Ni/SiO 2 catalyst, which was 139.1 kJ/mol. Based on various characterization results, it is found that the added Ce significantly improves the dispersion of the supported nickel, suppresses the sintering of nickel particles, and forms more adsorbed CO species of three‐fold carbonyl species, resulting in higher CO conversion and good stability during the CO methanation reaction.
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