Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/5464
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Campo DCValorIdioma
dc.contributor.authorFerrão-Gonzales, Astria Dias-
dc.contributor.authorVéras, Ilvania Costa-
dc.contributor.authorSilva, Frederico Augusto Lima-
dc.contributor.authorAlvarez, Heiddy Márquez-
dc.contributor.authorMoreau, Vitor Hugo-
dc.creatorFerrão-Gonzales, Astria Dias-
dc.creatorVéras, Ilvania Costa-
dc.creatorSilva, Frederico Augusto Lima-
dc.creatorAlvarez, Heiddy Márquez-
dc.creatorMoreau, Vitor Hugo-
dc.date.accessioned2012-02-27T11:10:50Z-
dc.date.issued2011-
dc.identifier.issn0378-3820-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/5464-
dc.descriptionAcesso restrito: Texto completo. p. 1007-1011.pt_BR
dc.description.abstractBiodiesel is a biofuel expected to become a substitute for petroleum diesel. One of the most promising technologies for production of biodiesel is enzymatic catalysis. However, low catalytic performance of most of the enzymes employed makes such processes expensive and time-consuming. This work describes a kinetic study of the enzymatic production of biodiesel at different temperatures using either methanolysis or ethanolysis, using immobilized lipase from Candida antarctica (Novozym 435) as catalyst. Reactions kinetics were followed by GC, and data were used to perform thermodynamic analysis of the transition state using Arrhenius equation. We found that methanolysis is faster than ethanolysis at temperatures above 13 °C. Thermodynamic analysis of the kinetics of reactions showed that methanol is favored as acyl acceptor due to the positive activation entropy change of reaction. These data may be useful in the development of new enzymes and new processes for enzymatic production of biodiesel.pt_BR
dc.language.isoenpt_BR
dc.sourceDOI: 10.1016/j.fuproc.2010.12.023pt_BR
dc.subjectBiodieselpt_BR
dc.subjectBiocatalysispt_BR
dc.subjectLipasept_BR
dc.subjectActivation entropypt_BR
dc.subjectKineticspt_BR
dc.titleThermodynamic analysis of the kinetics reactions of the production of FAME and FAEE using Novozyme 435 as catalystpt_BR
dc.title.alternativeFuel Processing Technologypt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 92, n. 5.pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (ICS)

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