甲烷化
催化作用
镍
离解(化学)
格式化
化学工程
材料科学
金属
替代天然气
复合数
无机化学
化学
合成气
冶金
物理化学
有机化学
复合材料
工程类
作者
Hao Fu,Shaohui Sun,Honglei Lian
标识
DOI:10.1016/j.jcou.2023.102415
摘要
It is desirable but challenging to obtain high CO2 conversion in low-temperature CO2 methanation and elucidate the reaction mechanism on nickel-based catalysts. In this work, we incorporated Al into Ni/ZrO2 to form nickel-based catalysts supported by ZrO2-Al2O3 composite support. The addition of the appropriate amount of Al increased the dispersion of metal Ni on the catalyst surface, promoted the activation and dissociation of H2, and thus significantly improved the activity of CO2 methanation at low-temperature (< 300 °C). The CO2 methanation on nickel-based catalysts supported on ZrO2-Al2O3 composite supports all follow the formate reaction pathway. Since adding Al removes the ability of ZrO2 to activate H2, the active sites of the catalyst change from the surrounding support to the support-Ni interface, which improves the efficiency of the hydrogenation reaction of the active intermediate.
科研通智能强力驱动
Strongly Powered by AbleSci AI