Transesterification of dimethyl oxalate with phenol over a MoO3/SiO2 catalyst prepared by thermal spreading

被引:6
作者
Zhang, Fubao [1 ,3 ]
Yu, Xiaopeng [2 ]
Ma, Fei [1 ,4 ]
Yang, Xiangui [1 ,4 ]
Hu, Jing [1 ,4 ]
Deng, Zhiyong [1 ,4 ]
Wang, Gongying [1 ,4 ]
机构
[1] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ Sci & Engn, Dept Mat & Chem Engn, Zigong 643000, Sichuan, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Chengdu Organ Chem Co Ltd, Chengdu 610041, Sichuan, Peoples R China
关键词
Thermal spreading method; MoO3/SiO2; catalyst; Methyl phenyl oxalate; Diphenyl oxalate; Transesterification; MOLYBDENUM OXIDE CATALYSTS; SLURRY IMPREGNATION METHOD; DIPHENYL CARBONATE; METATHESIS CATALYSTS; SURFACE-PROPERTIES; DIETHYL OXALATE; REACTIVITY; PHOSGENE; SUPPORTS; MOO3;
D O I
10.1016/S1872-2067(14)60042-5
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
MoO3/SiO2 catalysts for the transesterification of dimethyl oxalate (DMO) with phenol were prepared by both the thermal spreading (TS) and incipient wetness impregnation methods. The results showed that the 10%MoO3/SiO2 catalyst prepared by TS (10%MoO3/SiO2-TS) exhibited higher catalytic performance compared with the 10%MoO3/SiO2 catalyst prepared by incipient wetness impregnation (10%MoO3/SiO2-C). The catalysts were characterized by X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, pyridine-IR spectroscopy, and NH3 temperature-programmed desorption. These analyses indicated that weak Lewis acid sites were formed on the catalyst surfaces and that the Mo species were present as monomeric MoO3 rather than as isolated molybdenum oxide or polymolybdate species on both catalysts, although the 10%MoO3/SiO2-TS exhibited better dispersion of MoO3 and a higher surface Mo content than the 10%MoO3/SiO2-C. Under the optimal transesterification reaction conditions (1.2 g 10%MoO3/SiO2-TS, T = 180 degrees C, n(DMO)/n(phenol) = 2, t = 4 h), the conversion of phenol was 70.9%, and the yields of methyl phenyl oxalate and diphenyl oxalate were 63.1% and 7.7%, respectively. (C) 2013, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1043 / 1053
页数:11
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