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Base/acid-catalyzed FAEE production from hydroxylated vegetable oils
Authors:Marcelo G Montes D’Oca  Paula L Haertel  Danielle C de Moraes  Franciéli JP Callegaro  Márcia HS Kurz  Ednei G Primel  Rosilene M Clementin  Joaquín A Morón-Villarreyes
Affiliation:Laboratório Kolbe de Síntese Orgânica, Escola de Química e Alimentos, Universidade Federal do Rio Grande-FURG, Av. Itália Km 08, 96201-900 Rio Grande, RS, Brazil
Abstract:In this study was developed a new methodology to produce fatty acid ethyl esters from castor oil. The base-catalyzed transesterification step was followed by on pot addition of sulfuric acid. That addition implicated the successful separation of FAEEs/glycerin phases due to soap breaking. The study was carried out through an experimental design where the variables studied in the first step were the molar ratio alcohol:oil and the catalyst amount in the transesterification process. As expected, the on pot addition of concentrated sulfuric acid yields FFAs that increase the acid value in the FAEEs phase. A second step esterification of these free fatty acids from FAEE raw mixture was investigated. The esterification of FFA was carried out in 60:1 and 80:1 M ratios (alcohol:free fatty acids) and concentrated sulfuric acid 5% and 10% w/w (based on free fatty acids). Consequently, these two steps yielded more fatty ethyl esters and assure that the following important requirements in the FAEEs production process from castor oil are satisfied: complete reaction, best separation of FAEEs/glycerin phases, removal of catalyst, limpid glycerin, and absence of free fatty acids.
Keywords:Ethylic biodiesel  Two-step process  Transesterification  Castor oil  Ricinoleic acid
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