钴
甲烷化
催化作用
镍
水滑石
氢
无机化学
微晶
烧结
化学工程
材料科学
化学
冶金
有机化学
工程类
作者
Paulina Summa,Katarzyna Świrk,Ye Wang,Bogdan Samojeden,Magnus Rønning,Changwei Hu,Monika Motak,Patrick Da Costa
标识
DOI:10.1016/j.apmt.2021.101211
摘要
A series of cobalt-promoted Ni-Mg-Al hydrotalcite-derived catalysts were tested towards CO2 methanation reaction. The best among examined catalysts was the one with 1 wt% of cobalt in fresh hydrotalcite, obtaining 77% of CO2 conversion and 99% of CH4 selectivity at 300 °C. Above that temperature, the catalyst was working with-near-equilibrium parameters. It was also stable for up to 24 h on stream. Other cobalt-containing samples were likewise very active and selective during the time on stream. Due to the use of a low amount of cobalt (0.5–4 wt%) the Co-Ni alloy was not the subject of research – both materials formed probably solid solution of cobalt in the nickel matrix. Although the behavior of cobalt as a textural and electronic promoter was confirmed. Co was found to improve reducibility of nickel species, hydrogen uptake, and the acidic/basic properties by increasing the number of medium strength and strong basic sites. Tendency to sintering of nickel crystallites on cobalt-promoted catalysts was not confirmed in this study, however, with increased content of Co, bigger metal crystallites were formed under the reduction conditions.
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