催化作用
铜
甲醇
乙二醇
材料科学
纳米颗粒
无机化学
碳酸乙烯酯
碳酸二甲酯
乙烯
金属
氢
化学工程
核化学
冶金
化学
纳米技术
有机化学
物理化学
工程类
电解质
电极
作者
Huabo Li,Yuanyuan Cui,Yixin Liu,Songlin Wang,Wei‐Lin Dai
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2022-07-19
卷期号:33 (43): 435703-435703
被引量:4
标识
DOI:10.1088/1361-6528/ac8233
摘要
The hydrogenation of CO2-derived carbonates to methanol is an alternative route for the indirect utilization of abundant C1 sources. Various Cu/SiO2catalysts with different copper loading content prepared by using an ammonia evaporation hydrothermal method are implemented to evaluate the catalytic performance of ethylene carbonate (EC) hydrogenation to methanol and ethylene glycol (EG). The Cu loading content was identified to significantly affect the Cu nanoparticles (NPs) size and metal-support interaction. Highly dispersed Cu NPs restricted and embedded in copper phyllosilicate presented a smaller average particle size than the impregnated Cu/SiO2-IM catalyst. ThexCu/SiO2catalyst with ultrafine Cu NPs showed abundant Cu-O-Si interfaces, acidic sites, and coherent Cu0and Cu+species. The 5Cu/SiO2catalyst achieved methanol yield of 76% and EG yield of 98% at EC conversion of 99%, and no obvious deactivation was observed after long-term operation. The superior catalytic performance of the 5Cu/SiO2catalyst is attributed to the synergetic effect between the appropriate Cu0surface area which provides sufficient active hydrogen, and the atomic ratio of Cu+for the polarization and activation of carbon-oxygen bonds.
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