甲烷化
双金属片
双金属
催化作用
过渡金属
介孔材料
材料科学
无机化学
金属
化学工程
化学
冶金
有机化学
工程类
作者
Leilei Xu,Yan Cui,Mindong Chen,Xueying Wen,Chufei Lv,Xianyun Wu,Caie Wu,Zhichao Miao,Xun Hu
标识
DOI:10.1021/acs.iecr.1c00656
摘要
The Ni monometallic catalyst usually exhibits poor CO 2 methanation activity, although its low cost is beneficial for conducting large-scale application in industries. Herein, the transition metal (Mn, Fe, Co, and Cu)-doped Ni-based bimetallic catalysts loaded on mesoporous Ce 0.8 Zr 0.2 O 2 solid solution were prepared to address this challenge in CO 2 methanation. We found that the Co-doped catalysts exhibited much higher activity than the corresponding counterparts. Therefore, the relationship between the Co/Ni ratio and activity was further investigated to acquire the optimum ratio. The obtained catalysts were characterized by various measurements. The results demonstrated that doping the second transition metals could promote Ni dispersion and strengthen metal–support interaction. Resultantly, serious agglomeration of the metallic active sites was successfully inhibited. Besides, we also carried out the in situ diffuse reflectance infrared spectroscopy and online temperature-programmed surface reaction of CO 2 methanation to study the possible reaction intermediates and pathways over the Ni–Co bimetallic catalysts. A dynamic study was also conducted to further study the effect of the doped transition metals on the apparent activation energies. Besides, the present research also revealed that the Ni–Co synergistic effect significantly improved the low-temperature activity by regulating the reaction intermediates. As a result, the Ni–Co bimetallic catalysts supported by mesoporous Ce 0.8 Zr 0.2 O 2 solid solution were considered as a series of promising and efficient low-temperature CO 2 methanation catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI