选择性
催化作用
乙醇
化学吸附
合成气
解吸
钴
吸附
无机化学
化学
X射线吸收精细结构
金属
X射线光电子能谱
纳米颗粒
化学工程
核化学
有机化学
材料科学
纳米技术
光谱学
工程类
物理
量子力学
作者
Kang An,Siran Zhang,Jiaming Wang,Qiang Liu,Ziyang Zhang,Yuan Liu
标识
DOI:10.1016/j.jechem.2020.08.045
摘要
A new catalyst of Co/La4Ga2O9 for CO2 hydrogenation to produce ethanol was prepared by reducing LaCo0.5Ga0.5O3, which showed excellent selectivity to ethanol (≈35C-mol%) at mild reaction conditions (270 °C, 3.5 MPa, 3000 mL g−1 h−1). The catalysts were characterized by N2 adsorption/desorption, XRD, XAFS, CO and CO2-TPD, H2 chemisorption, XPS and TEM techniques. The interaction between Co nanoparticles (NPs) and La4Ga2O9 oxide resulted in Co0-Co2+ on the surface of Co NPs. It was proposed that La4Ga2O9 could catalyze reverse water gas shift reaction (r-WGS), which converted CO2 to CO. Then, the CO migrated to Co0-Co2+ on Co NPs, where it was hydrogenated to form ethanol like higher alcohols synthesis from syngas. The results suggest that by controlling the oxidation state of cobalt, and combined with a kind of active site for activating CO2 to form CO, a catalyst with excellent selectivity to ethanol could be obtained for CO2 hydrogenation, which means that the complex reaction may be proceed with high selectivity using only one active metal component.
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