1-n-Butyl-3-methylimidazolium tetrachloro-indate (BMI•InCl4) as a media for the synthesis of biodiesel from vegetable oils

被引:117
作者
Neto, Brenno A. DaSilveira [1 ]
Alves, Melquizedeque B.
Lapis, Alexandre A. M.
Nachtigall, Fabiane M.
Eberlin, Marcos N.
Dupont, Jairton
Suarez, Paulo A. Z.
机构
[1] Pontificia Univ Catolica Rio Grande do Sul, Ctr Pesquisas Biol Mol & Funcional Tecnopuc, BR-70919970 Porto Alegre, RS, Brazil
[2] IQ UnB, BR-91501970 Porto Alegre, RS, Brazil
[3] IQ UFRGS, BR-13084862 Porto Alegre, RS, Brazil
[4] Univ Estadual Campinas, INst Chem, ThoMSon Mass Spectrometry Lab, Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
biodiesel; biofuels; ionic liquids; transesterification; tin catalyst; vegetable oils; electrospray ionization mass spectrometry;
D O I
10.1016/j.jcat.2007.04.015
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 complex [Sn(3-hydroxy-2-methyl-4-pyrone)(2)(H2O)(2)] immobilized in 1-n-butyl-3-methylimidazolium tetrachloro-indate (BMI.InCl4) ionic liquid forms an effective biphasic catalytic system for the production of biodiesel from the alcoholysis of soybean oil. ESI-MS experiments during the transesterification reaction indicate that the reaction may proceed through the formation of a cationic species formed through the substitution of one pyrone ligand by one alcohol molecule, followed by coordination of the carboxylate compound to tin. The adduct thus formed undergoes transesterification with liberation of the catalytic active species. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:154 / 161
页数:8
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