TY - JOUR
T1 - Direct synthesis of dimethyl carbonate from CO2 and methanol in dual supercritical phases over YxFe1−xOδ catalysts
AU - Sun, Wen
AU - Zheng, Lan
AU - Wang, Yuqi
AU - Jia, Weihua
AU - Guo, Wenzhao
AU - Liu, Zhiru
AU - Ding, Xin
AU - Wu, Le
AU - Fang, Tao
N1 - Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/4
Y1 - 2022/4
N2 - 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.
AB - 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.
KW - CO activation
KW - Dual supercritical phases
KW - Lewis acid
KW - Oxygen vacancy
KW - Perovskite-structure
UR - https://www.scopus.com/pages/publications/85123851018
U2 - 10.1016/j.jcou.2022.101912
DO - 10.1016/j.jcou.2022.101912
M3 - 文章
AN - SCOPUS:85123851018
SN - 2212-9820
VL - 58
JO - Journal of CO2 Utilization
JF - Journal of CO2 Utilization
M1 - 101912
ER -