甲烷化
催化作用
非阻塞I/O
材料科学
X射线光电子能谱
镍
化学工程
碳纳米管
纳米颗粒
替代天然气
碳纤维
打赌理论
纳米技术
化学
合成气
冶金
复合材料
复合数
有机化学
工程类
作者
Manuel Romero‐Sáez,Ana Belén Dongil,Noelia Benito,Rodrigo Espinoza-González,N. Escalona,F. Gracia
标识
DOI:10.1016/j.apcatb.2018.06.045
摘要
Ni-ZrO2 catalysts supported on CNT synthesized by sequential and co-impregnation were tested in the CO2 methanation reaction. The catalysts were characterized using different physico-chemical techniques including BET surface area analysis, TGA, H2-TPR analysis, CO2-TPD analysis, XRD analysis, TEM-EDS analysis and XPS. Both samples were found to be active in the CO2 methanation; however, the catalyst prepared by co-impregnation was notably less active and selective to CH4 than the catalyst synthesized by sequential impregnation method. The characterization results gave significant insight on the disposition of active phases in CNT surface. The catalyst prepared by co-impregnation showed NiO nanoparticles surrounded by ZrO2 in core-shell structures that growth over the CNT, reducing reactant access to Ni and Ni – ZrO2 interface. Additionally, TEM analysis of this catalyst prepared by sequential impregnation showed NiO nanoparticles available and deposited either on the surface or next to the ZrO2 nanoparticles, increasing the extent of the Ni – ZrO2 interface thus improving the catalytic performance.
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