甲烷化
催化作用
碱度
镍
化学
无机化学
金属
碳酸氢盐
格式化
碳酸盐
有机化学
作者
Chuanfei Liang,Zhiran Gao,Huqiang Lian,Xianglin Li,Shu Zhang,Qing Liu,Dehua Dong,Xun Hu
标识
DOI:10.1016/j.ijhydene.2020.04.070
摘要
Both metal sites and alkaline sites are essential parameters for a catalyst used in methanation of CO2. This study investigated the impacts of the relative abundance of metal sites and alkaline sites on the catalytic performances of nickel-based catalyst with attapulgite, a natural mineral, as the support. The results showed that the increase of nickel loading to attapulgite significantly decreased the abundance of alkaline sites, remarkably enhanced the catalytic activity, and suppressed the formation of CO. The in situ DRIFTS characterization of the CO2 methanation indicated that the alkaline sites favored formation of the oxygen-containing reaction intermediates such as CO∗, –OH, ∗CO2, formate, carbonate and bicarbonate species. In comparison, metallic nickel species promoted their further hydrogenation to form CH4. Besides the absorption/activation of ∗CO2 was more preferable on surface of metallic nickel, but not on the alkaline sites. The availability of the alkaline sites was not as important as the metallic nickel species for preparation of an efficient catalyst for CO2 methanation.
科研通智能强力驱动
Strongly Powered by AbleSci AI