Direct synthesis of dimethyl carbonate from CO2 and methanol in dual supercritical phases over YxFe1−xO catalysts

超临界流体 碳酸二甲酯 催化作用 甲醇 产量(工程) 材料科学 高压灭菌器 化学工程 钙钛矿(结构) 核化学 化学 无机化学 有机化学 复合材料 工程类
作者
Wen Sun,Lan Zheng,Yuqi Wang,Weihua Jia,Wenzhao Guo,Zhiru Liu,Xin Ding,Le Wu,Tao Fang
出处
期刊:Journal of CO2 utilization [Elsevier BV]
卷期号:58: 101912-101912 被引量:17
标识
DOI:10.1016/j.jcou.2022.101912
摘要

In this study, the dual supercritical phases were proposed and employed to facilitate the synthesis of dimethyl carbonate (DMC) from CO2 and methanol, which may improve the diffusion rate and contact opportunities of reactant molecules. Under the novel reaction conditions, the synthesis temperature was higher than the supercritical temperatures of each reactant (>239 °C), and the partial pressure for each reactant constituent was larger than its partial supercritical pressure (pCO2 > 7.4 MPa & pmethanol > 8.1 MPa), respectively. A series of YxFe1−xOδ-T catalysts with perovskite-structure were applied in the dual supercritical phases, whose surface properties, crystal phase, microstructure, acidic−basic amounts, and the concentration of oxygen vacancies were detected by BET, XRD, SEM, NH3/CO2-TPD, XPS and EPR, respectively. It was evident from the characterization results that the Y0.5Fe0.5Oδ-850 catalyst possessed the largest acidic−basic amounts, which enabled its highest catalytic activity. The experimental results revealed that higher DMC yield could be achieved under the novel dual supercritical phases (240 °C, 16 MPa), and the increased DMC yield without stirring in the autoclave can be obtained in an impressive shorter reaction time of 3 h, surpassing it acquired at the regular synthesis time of 9 h with stirring during the reaction.
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