Production of glycerol carbonate by coupling glycerol and CO2 over various metal oxide catalyst

被引:9
作者
Ke, Yi-Hu [1 ,2 ]
Xu, Huanhuan [1 ,2 ]
Wang, Xue [1 ,2 ]
Liu, Hai [1 ,2 ]
Yuan, Hong [1 ,2 ]
机构
[1] North Minzu Univ, Key Lab Chem Engn & Technol, State Ethn Affairs Commiss, Yinchuan 750021, Peoples R China
[2] North Minzu Univ Yinchuan, Ningxia Key Lab Solar Chem Convers Technol, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
Glycerol; Carbon dioxide; Glycerol carbonate; Coupling; Metal oxide; SELECTIVE HYDROGENOLYSIS; DIMETHYL CARBONATE; CARBONYLATION; SURFACE; CEO2; UREA; TRANSESTERIFICATION; CARBOXYLATION; ACETYLATION; PERFORMANCE;
D O I
10.1016/j.jcou.2024.102813
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of metal oxides, i.e., CuO,NiO,Co3O4,ZrO2,Al2O3, catalysts were prepared by hydrothermal method and evaluated in the production of glycerol carbonate by coupling of glycerol and CO2 under lower temperature. The results show that CuO showed the best catalytic performance (glycerol conversion and the glycerol carbonate selectivity were 89.0 % and 69.4 %, respectively) at 120 degree celsius under 3.0 MPa of CO2 for 5 h. This is the highest yield of glycerol carbonate using same mothed reported in the literature so far. The structures, morphologies and surface properties of the catalysts were characterized by X-ray powder diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), N2 adsorption-desorption, Temperature programmed reduction (H2-TPR), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), Temperature programmed desorption (TPD). It is speculated that the high catalytic activity of CuO mainly depends on its unique structure and acid-base physicochemical properties. In addition, the CuO catalyst was used 7 times without obvious deactivation, which suggesting this catalysis has excellent reusability.
引用
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页数:10
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