Acid-base bifunctional ZnNbCl/eg-C3N4 materials towards catalytic synthesis of dimethyl carbonate via transesterification of ethylene carbonate

被引:7
作者
Yu, Lin-Zhi [1 ]
Sun, Xiao-Hua [1 ]
Wang, Fei [1 ]
Xue, Bing [1 ]
Xu, Jie [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Gehu Middle Rd 21, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphitic carbon nitride (g-C 3 N 4 ); Base catalyst; Transesterification; Dimethyl carbonate; METAL-FREE CATALYST; EFFICIENT SYNTHESIS; HETEROGENEOUS CATALYST; PROPYLENE CARBONATE; NITRIDE; OXIDE; METHANOL; PERFORMANCE; CONVERSION; NANOSHEETS;
D O I
10.1016/j.apcata.2023.119432
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The catalytic transesterification reaction between ethylene carbonate (EC) with methanol is a sustainable approach for the production of dimethyl carbonate (DMC). In this work, exfoliated carbon nitride (eg-C3N4) was supported with ZnCl2 and NbCl5. The synthesized materials (ZnNbCl/eg-C3N4) were analyzed by XRD, N2 adsorption-desorption, FT-IR, XPS, SEM, TG, CO2-TPD, and NH3-TPD. The eg-C3N4 could disperse well Zn2+ and Nb5+ species via nitrogen-containing groups. The combined Zn2+ and Nb5+ components enhanced the alkaline strength of eg-C3N4 and introduced acidic sites, enabling ZnNbCl/eg-C3N4 as solid-base bifunctional catalysts. As heterogeneous catalysts, ZnNbCl/eg-C3N4 exhibited superior activity to ZnCl2/eg-C3N4 or NbCl5/eg-C3N4 in the transesterification of EC. At 140 degrees C of reaction temperature, EC conversion and DMC selectivity reached 80.1% and 100%, respectively. The catalysts showed good recycling performance and were also compared with other recently reported heterogeneous catalysts.
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页数:10
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