Ordered mesoporous BaCO3/C-catalyzed synthesis of glycerol carbonate from glycerol and dimethyl carbonate

被引:23
|
作者
Wang, Yin [1 ]
Liu, Chunling [1 ]
Sun, Jihong [2 ]
Yang, Rongzhen [1 ]
Dong, Wensheng [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Appl Surface & Colloid Chem SNNU, Minist Educ, Xian 710062, Peoples R China
[2] Beijing Univ Technol, Coll Energy Environm & Engn, Beijing 100022, Peoples R China
关键词
nanocomposites; mesoporous; carbon; barium carbonate; glycerol carbonate; CATALYZED SYNTHESIS; OXIDATIVE CARBONYLATION; SELECTIVE OXIDATION; BASE CATALYSTS; TRANSESTERIFICATION; EFFICIENT; HYDROGENOLYSIS; NANOCOMPOSITES; NANOPARTICLES; COMPOSITES;
D O I
10.1007/s11426-014-5173-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
BaCO3/C composites were synthesized by a multi-component co-assembly method combined with a carbonization process using phenolic resol as carbon source, barium nitrate as barium precursor, and triblock copolymer Pluronic F127 as template. The synthesized materials were characterized by X-ray diffraction, transmission electron microscopy, N-2 physical adsorption, thermogravimetric analysis, and temperature-programmed desorption of CO2. When BaCO3 contents were increased from 9.1 wt% to 44.7 wt%, pore size increased from 3.1 to 4.3 nm and the BET (Brunauer-Emmett-Teller) surface area initially increased to a maximum value of 390 m(2) g(-1) (at a BaCO3 content of 18.5 wt%) before subsequently decreasing. BaCO3 was well dispersed in the amorphous carbon framework, and no phase separation was observed. The mesoporous Ba-CO3/C composites exhibited high catalytic activities toward the transesterification of glycerol and dimethyl carbonate into glycerol carbonate. A glycerol conversion of 97.8% and a glycerol carbonate selectivity of 98.5% were obtained under the optimized reaction conditions.
引用
收藏
页码:708 / 715
页数:8
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