RETRACTED: One-pot synthesis of glycidol from glycerol and dimethyl carbonate over a highly efficient and easily available solid catalyst NaAlO2 (Retracted article. See vol. 18, pg. 6144, 2016)

被引:42
作者
Bai, Rongxian [1 ]
Zhang, Hongkun [1 ]
Mei, Fuming [1 ]
Wang, Shu [1 ]
Li, Tao [1 ]
Gu, Yanlong [1 ,2 ]
Li, Guangxing [1 ]
机构
[1] Huazhong Univ Sci & Technol, Hubei Key Lab Mat Chem & Serv Failure, Key Lab Large Format Battery Mat & Syst, Minist Educ,Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
SODIUM ALUMINATE; BASE CATALYST; TRANSESTERIFICATION; BIODIESEL; BIOMASS; OXIDE; UREA;
D O I
10.1039/c3gc40855h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The one-pot synthesis of glycidol from glycerol and dimethyl carbonate (DMC) was developed by using a solid base catalyst. A series of solid base catalysts have been investigated in this reaction. It was found that NaAlO2, a cheap and easily available raw material, was a highly efficient heterogeneous catalyst for the one-pot synthesis of glycidol, and it can be easily recovered and reused. Under the reaction conditions of a DMC glycerol molar ratio of 2, catalyst glycerol weight ratio of 3%, reaction time of 90 min, and temperature of 80-92 degrees C, the conversion of glycerol and the selectivity to glycidol reached 94.7% and 80.7%, respectively. Activity tests of the catalyst after exposure to the air showed that, to a certain extent, the NaAlO2 catalyst is tolerant to water and carbon dioxide, which makes the present system a practically interesting process for glycidol synthesis.
引用
收藏
页码:2929 / 2934
页数:6
相关论文
共 32 条
[1]   Synthesis of glycerol carbonate from glycerol and dimethyl carbonate catalyzed by NaOH/γ-Al2O3 [J].
Bai, Rongxian ;
Wang, Yi ;
Wang, Shu ;
Mei, Fuming ;
Li, Tao ;
Li, Guangxing .
FUEL PROCESSING TECHNOLOGY, 2013, 106 :209-214
[2]   Glycerol transesterification with methyl stearate over solid basic catalysts I. Relationship between activity and basicity [J].
Bancquart, S ;
Vanhove, C ;
Pouilloux, Y ;
Barrault, J .
APPLIED CATALYSIS A-GENERAL, 2001, 218 (1-2) :1-11
[3]   Improved utilisation of renewable resources: New important derivatives of glycerol [J].
Behr, Arno ;
Eilting, Jens ;
Irawadi, Ken ;
Leschinski, Julia ;
Lindner, Falk .
GREEN CHEMISTRY, 2008, 10 (01) :13-30
[4]   New concepts for process intensification in the conversion of glycerol carbonate to glycidol [J].
Bolivar-Diaz, C. L. ;
Calvino-Casilda, V. ;
Rubio-Marcos, F. ;
Fernandez, J. F. ;
Banares, M. A. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2013, 129 :575-579
[5]   THEORETICAL AND CALORIMETRIC EVALUATION OF THERMAL-STABILITY OF GLYCIDOL [J].
CARDILLO, P ;
NEBULONI, M .
JOURNAL OF LOSS PREVENTION IN THE PROCESS INDUSTRIES, 1991, 4 (04) :242-245
[6]   Liquid-phase catalytic processing of biomass-derived oxygenated hydrocarbons to fuels and chemicals [J].
Chheda, Juben N. ;
Huber, George W. ;
Dumesic, James A. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (38) :7164-7183
[7]  
Claude S., 2000, U.S. Patent, Patent No. [6025504, 6,025,504]
[8]   Chemicals from biomass: Synthesis of glycerol carbonate by transesterification and carbonylation with urea with hydrotalcite catalysts. The role of acid-base pairs [J].
Climent, Maria J. ;
Corma, Avelino ;
De Frutos, Pilar ;
Iborra, Sara ;
Noy, Maria ;
Velty, Alexandra ;
Concepcion, Patricia .
JOURNAL OF CATALYSIS, 2010, 269 (01) :140-149
[9]  
Contreras C., 2006, AZOJOMO, V8, P122, DOI [10.2240/azojomo0220, DOI 10.2240/AZ0J0M00220]
[10]   Chemical routes for the transformation of biomass into chemicals [J].
Corma, Avelino ;
Iborra, Sara ;
Velty, Alexandra .
CHEMICAL REVIEWS, 2007, 107 (06) :2411-2502