甲烷化
催化作用
空间速度
尖晶石
烧结
化学吸附
化学计量学
焦炭
材料科学
煅烧
X射线光电子能谱
物理吸附
无机化学
非阻塞I/O
化学工程
化学
冶金
物理化学
有机化学
选择性
工程类
作者
Cristina Italiano,Jordi Llorca,L. Pino,Marco Ferraro,V. Antonucci,Antonio Vita
标识
DOI:10.1016/j.apcatb.2019.118494
摘要
Methanation of carbon oxides (CO and CO2) was studied over Ni-based catalysts supported on CeO2, Al2O3, and Y2O3 oxides. Catalysts were synthesized by solution combustion synthesis and characterized by N2-physisorption, XRD, H2-TPR, TEM, CO-chemisorption, UV–vis DRS, XPS, and CO2-TPD. The effect of reaction temperature (250−500 °C) was investigated under atmospheric pressure, space velocity (GHSV) of 10,000 h−1, and stoichiometric reactants ratio of (H2-CO2)/(CO + CO2) = 3. It can be concluded that the nature of Ni-support interactions played a crucial role in enhancing CO and CO2 hydrogenation at low reaction temperature. Ni/CeO2 catalyst deactivated rapidly due to coke deposition, while the formation of NiAl2O4 spinel explained the lower activity of the Al2O3-supported system. Activity data for Ni/Y2O3 catalysts were closely related to the degree of Ni dispersion as well as to the medium-strength basicity. Good anti-coking and anti-sintering ability were observed after 200 h of lifetime test.
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