Synthesis of glycerol carbonate from glycerol and dimethyl carbonate by transesterification: Catalyst screening and reaction optimization

被引:316
作者
Ochoa-Gomez, Jose R. [1 ]
Gomez-Jimenez-Aberasturi, Olga [2 ]
Maestro-Madurga, Belen [2 ]
Pesquera-Rodriguez, Amaia [2 ]
Ramirez-Lopez, Camilo [2 ]
Lorenzo-Ibarreta, Leire [2 ]
Torrecilla-Soria, Jesus [2 ]
Villaran-Velasco, Maria C. [2 ]
机构
[1] Univ Alfonso X Sabio, Dept Ind Technol, Villanueva De La Canada 28696, Spain
[2] Fdn LEIA, Ctr Technol, Dept Sustainable Chem, Minano 01510, Spain
关键词
Glycerol carbonate; Base-catalyzed transesterification; Glycerol; Calcium oxide; SOLID BASE CATALYST; CALCIUM-OXIDE; SOYBEAN OIL; DIOXIDE; SEPARATION;
D O I
10.1016/j.apcata.2009.07.020
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 synthesis of glycerol carbonate from glycerol and dimethyl carbonate by transesterification is reported. Firstly, a catalyst screening has been performed by studying the influence of different basic and acid homogeneous and heterogeneous catalysts on reaction results. Catalytic activity is extremely low for acidic catalysts indicating that reaction rate is very slow. On the contrary, high conversions and yields are obtained for basic catalysts. Catalytic activity increases with catalyst basic strength. The best heterogeneous catalyst is CaO. Calcination of CaO increases dramatically its activity due to calcium hydroxide removal from its surface. A reaction optimization study has been carried out with CaO as catalyst by using a factorial design of experiments leading to operation conditions for achieving a 100% conversion and a >95% yield at 1.5 h reaction time: 95 degrees C, catalyst/glycerol molar ratio = 0.06 and dimethyl carbonate/glycerol molar ratio = 3.5. Carbonate glycerol can be easily isolated by filtering the catalyst out and evaporating the filtrate at vacuum. Leaching of catalyst in reaction medium was lower than 0.34%. Catalyst recycling leads to a quick decrease in both conversions and yields probably due to a combination of catalyst deactivation by CaO exposure to air between catalytic runs, and a decrease in the catalyst surface area available for reaction due to particle agglomeration. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:315 / 324
页数:10
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