Cargando…

Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study

A new method for the preparation of anhydrous ethyl ester of lactic acid was studied. The selected method is based on catalytic transesterification of lactic acid oligomers, which were prepared for this purpose by autocatalytic oligomerization of lactic acid. In this work, a kinetic model for the ca...

Descripción completa

Detalles Bibliográficos
Autores principales: Figalla, Silvestr, Petrůj, Jaroslav, Švestková, Tereza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222406/
https://www.ncbi.nlm.nih.gov/pubmed/30111729
http://dx.doi.org/10.3390/molecules23082044
_version_ 1783369199758868480
author Figalla, Silvestr
Petrůj, Jaroslav
Švestková, Tereza
author_facet Figalla, Silvestr
Petrůj, Jaroslav
Švestková, Tereza
author_sort Figalla, Silvestr
collection PubMed
description A new method for the preparation of anhydrous ethyl ester of lactic acid was studied. The selected method is based on catalytic transesterification of lactic acid oligomers, which were prepared for this purpose by autocatalytic oligomerization of lactic acid. In this work, a kinetic model for the case of catalytic alcoholysis of oligoesters was derived assuming a first-order reaction and equimolar content of reactants in the reaction mixture. The model makes it possible to obtain the values of the reaction rate and equilibrium constants and the equilibrium alcohol concentration by regression analysis at one time. The model was verified by measuring the rate of consumption of ethanol over the time at various reaction temperatures with anhydrous FeCl(3) as the catalyst. The reaction was studied at overpressure under autogenous conditions in the temperature range of 100–180 °C. For the catalyst concentration of 1 mol %, the activation energy value was 64.35 kJ·mol(−1). The dependence of equilibrium composition and rate constant on the temperature was obtained. The derived model is generally applicable to all first-order equilibrium reactions. The presumption is that the forward and reverse reactions are of the same order and have the same stoichiometry and equivalent amounts of reactants at the beginning of the reaction.
format Online
Article
Text
id pubmed-6222406
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62224062018-11-13 Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study Figalla, Silvestr Petrůj, Jaroslav Švestková, Tereza Molecules Article A new method for the preparation of anhydrous ethyl ester of lactic acid was studied. The selected method is based on catalytic transesterification of lactic acid oligomers, which were prepared for this purpose by autocatalytic oligomerization of lactic acid. In this work, a kinetic model for the case of catalytic alcoholysis of oligoesters was derived assuming a first-order reaction and equimolar content of reactants in the reaction mixture. The model makes it possible to obtain the values of the reaction rate and equilibrium constants and the equilibrium alcohol concentration by regression analysis at one time. The model was verified by measuring the rate of consumption of ethanol over the time at various reaction temperatures with anhydrous FeCl(3) as the catalyst. The reaction was studied at overpressure under autogenous conditions in the temperature range of 100–180 °C. For the catalyst concentration of 1 mol %, the activation energy value was 64.35 kJ·mol(−1). The dependence of equilibrium composition and rate constant on the temperature was obtained. The derived model is generally applicable to all first-order equilibrium reactions. The presumption is that the forward and reverse reactions are of the same order and have the same stoichiometry and equivalent amounts of reactants at the beginning of the reaction. MDPI 2018-08-15 /pmc/articles/PMC6222406/ /pubmed/30111729 http://dx.doi.org/10.3390/molecules23082044 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Figalla, Silvestr
Petrůj, Jaroslav
Švestková, Tereza
Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study
title Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study
title_full Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study
title_fullStr Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study
title_full_unstemmed Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study
title_short Transesterification of Lactic Acid Oligomers with Ethanol, a Way to Anhydrous Ethyl Lactate: A Kinetic Study
title_sort transesterification of lactic acid oligomers with ethanol, a way to anhydrous ethyl lactate: a kinetic study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222406/
https://www.ncbi.nlm.nih.gov/pubmed/30111729
http://dx.doi.org/10.3390/molecules23082044
work_keys_str_mv AT figallasilvestr transesterificationoflacticacidoligomerswithethanolawaytoanhydrousethyllactateakineticstudy
AT petrujjaroslav transesterificationoflacticacidoligomerswithethanolawaytoanhydrousethyllactateakineticstudy
AT svestkovatereza transesterificationoflacticacidoligomerswithethanolawaytoanhydrousethyllactateakineticstudy