甲烷化
催化作用
X射线光电子能谱
格式化
离解(化学)
镍
纳米棒
无机化学
化学
价(化学)
氧气
化学工程
材料科学
物理化学
纳米技术
有机化学
工程类
作者
Zhoufeng Bian,Yi Meng Chan,Yang Yu,Sibudjing Kawi
标识
DOI:10.1016/j.cattod.2018.04.067
摘要
Ceria has been used for catalyst support for long time due to its unique structural properties resulting from oxygen vacancies and reversible valence change (Ce4+ and Ce3+). In this report, ceria nanorods (NR) and nanocubs (NC) were prepared with hydrothermal method and 5 wt% nickel was loaded on it. The effect of morphology of ceria supports for CO2 methanation reaction was studied. Characterization including TPR, TEM, XRD and XPS shows that Ni/CeO2-NR had a higher number of Ce3+ proportion compared with Ni/CeO2-NC. Both catalysts showed high conversion and selectivity for methane at low temperature range at200–250 °C and interestingly Ni/CeO2-NR exhibited a higher activity than Ni/CeO2–NC. A kinetic study and DRIFTs investigation were carried out to formulate the mechanism. It turned out that CO2 methanation on Ni/CeO2 goes through a formate route instead of CO2 dissociation and the oxygen vacant sites are supposed to be the active sites for the formate formation in this mechanism.
科研通智能强力驱动
Strongly Powered by AbleSci AI