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Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties

The state of the art on the glycerol carbonate (GC) synthesis has been updated since the last published reviews in 2012, 2013, and 2016. Three types of reactions continue to be studied: glycerolysis of urea, transcarbonation of DMC, DEC, or cyclic carbonates with glycerol and reaction using CO(2). A...

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Autores principales: de Caro, Pascale, Bandres, Matthieu, Urrutigoïty, Martine, Cecutti, Christine, Thiebaud-Roux, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543549/
https://www.ncbi.nlm.nih.gov/pubmed/31179264
http://dx.doi.org/10.3389/fchem.2019.00308
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author de Caro, Pascale
Bandres, Matthieu
Urrutigoïty, Martine
Cecutti, Christine
Thiebaud-Roux, Sophie
author_facet de Caro, Pascale
Bandres, Matthieu
Urrutigoïty, Martine
Cecutti, Christine
Thiebaud-Roux, Sophie
author_sort de Caro, Pascale
collection PubMed
description The state of the art on the glycerol carbonate (GC) synthesis has been updated since the last published reviews in 2012, 2013, and 2016. Three types of reactions continue to be studied: glycerolysis of urea, transcarbonation of DMC, DEC, or cyclic carbonates with glycerol and reaction using CO(2). Among these different routes, DMC and glycerol were selected as the raw materials for the GC synthesis in this work since the transcarbonation from these green reagents leads to high yields and selectivities, using mild conditions including a less energy consuming GC separation process. Catalytic conditions using Na(2)CO(3) seem to be a good compromise to achieve a high yield of GC, leading to an easier purification step without GC distillation. Mild temperatures for the reaction (73–78°C) as well as a low waste amount confirmed by the E-factor calculation, are in favor of controlled costs. Plasticizing properties of synthesized GC were compared to the behaviors of a commercial plasticizer and natural dialkyl carbonates, for a colorless nail polish formulation. The resulting films subjected to mechanical and thermal stresses (DMA and Persoz pendulum) showed the high plasticizing effect of GC toward nitrocellulose based films, probably due to hydrogen bond interactions between GC and nitrocellulose. The GC efficiency gives the possibility to decrease the content of the plasticizer in the formulation. Glycerol carbonate can be thus considered as a biobased ingredient abiding by the green chemistry concepts, and safe enough to be used in an ecodesigned nail polish formulation.
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spelling pubmed-65435492019-06-07 Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties de Caro, Pascale Bandres, Matthieu Urrutigoïty, Martine Cecutti, Christine Thiebaud-Roux, Sophie Front Chem Chemistry The state of the art on the glycerol carbonate (GC) synthesis has been updated since the last published reviews in 2012, 2013, and 2016. Three types of reactions continue to be studied: glycerolysis of urea, transcarbonation of DMC, DEC, or cyclic carbonates with glycerol and reaction using CO(2). Among these different routes, DMC and glycerol were selected as the raw materials for the GC synthesis in this work since the transcarbonation from these green reagents leads to high yields and selectivities, using mild conditions including a less energy consuming GC separation process. Catalytic conditions using Na(2)CO(3) seem to be a good compromise to achieve a high yield of GC, leading to an easier purification step without GC distillation. Mild temperatures for the reaction (73–78°C) as well as a low waste amount confirmed by the E-factor calculation, are in favor of controlled costs. Plasticizing properties of synthesized GC were compared to the behaviors of a commercial plasticizer and natural dialkyl carbonates, for a colorless nail polish formulation. The resulting films subjected to mechanical and thermal stresses (DMA and Persoz pendulum) showed the high plasticizing effect of GC toward nitrocellulose based films, probably due to hydrogen bond interactions between GC and nitrocellulose. The GC efficiency gives the possibility to decrease the content of the plasticizer in the formulation. Glycerol carbonate can be thus considered as a biobased ingredient abiding by the green chemistry concepts, and safe enough to be used in an ecodesigned nail polish formulation. Frontiers Media S.A. 2019-05-24 /pmc/articles/PMC6543549/ /pubmed/31179264 http://dx.doi.org/10.3389/fchem.2019.00308 Text en Copyright © 2019 de Caro, Bandres, Urrutigoïty, Cecutti and Thiebaud-Roux. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
de Caro, Pascale
Bandres, Matthieu
Urrutigoïty, Martine
Cecutti, Christine
Thiebaud-Roux, Sophie
Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties
title Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties
title_full Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties
title_fullStr Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties
title_full_unstemmed Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties
title_short Recent Progress in Synthesis of Glycerol Carbonate and Evaluation of Its Plasticizing Properties
title_sort recent progress in synthesis of glycerol carbonate and evaluation of its plasticizing properties
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543549/
https://www.ncbi.nlm.nih.gov/pubmed/31179264
http://dx.doi.org/10.3389/fchem.2019.00308
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