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Bio-Based Aromatic Epoxy Monomers for Thermoset Materials

The synthesis of polymers from renewable resources is a burning issue that is actively investigated. Polyepoxide networks constitute a major class of thermosetting polymers and are extensively used as coatings, electronic materials, adhesives. Owing to their outstanding mechanical and electrical pro...

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Autores principales: Ng, Feifei, Couture, Guillaume, Philippe, Coralie, Boutevin, Bernard, Caillol, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155700/
https://www.ncbi.nlm.nih.gov/pubmed/28106795
http://dx.doi.org/10.3390/molecules22010149
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author Ng, Feifei
Couture, Guillaume
Philippe, Coralie
Boutevin, Bernard
Caillol, Sylvain
author_facet Ng, Feifei
Couture, Guillaume
Philippe, Coralie
Boutevin, Bernard
Caillol, Sylvain
author_sort Ng, Feifei
collection PubMed
description The synthesis of polymers from renewable resources is a burning issue that is actively investigated. Polyepoxide networks constitute a major class of thermosetting polymers and are extensively used as coatings, electronic materials, adhesives. Owing to their outstanding mechanical and electrical properties, chemical resistance, adhesion, and minimal shrinkage after curing, they are used in structural applications as well. Most of these thermosets are industrially manufactured from bisphenol A (BPA), a substance that was initially synthesized as a chemical estrogen. The awareness on BPA toxicity combined with the limited availability and volatile cost of fossil resources and the non-recyclability of thermosets implies necessary changes in the field of epoxy networks. Thus, substitution of BPA has witnessed an increasing number of studies both from the academic and industrial sides. This review proposes to give an overview of the reported aromatic multifunctional epoxide building blocks synthesized from biomass or from molecules that could be obtained from transformed biomass. After a reminder of the main glycidylation routes and mechanisms and the recent knowledge on BPA toxicity and legal issues, this review will provide a brief description of the main natural sources of aromatic molecules. The different epoxy prepolymers will then be organized from simple, mono-aromatic di-epoxy, to mono-aromatic poly-epoxy, to di-aromatic di-epoxy compounds, and finally to derivatives possessing numerous aromatic rings and epoxy groups.
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spelling pubmed-61557002018-11-13 Bio-Based Aromatic Epoxy Monomers for Thermoset Materials Ng, Feifei Couture, Guillaume Philippe, Coralie Boutevin, Bernard Caillol, Sylvain Molecules Review The synthesis of polymers from renewable resources is a burning issue that is actively investigated. Polyepoxide networks constitute a major class of thermosetting polymers and are extensively used as coatings, electronic materials, adhesives. Owing to their outstanding mechanical and electrical properties, chemical resistance, adhesion, and minimal shrinkage after curing, they are used in structural applications as well. Most of these thermosets are industrially manufactured from bisphenol A (BPA), a substance that was initially synthesized as a chemical estrogen. The awareness on BPA toxicity combined with the limited availability and volatile cost of fossil resources and the non-recyclability of thermosets implies necessary changes in the field of epoxy networks. Thus, substitution of BPA has witnessed an increasing number of studies both from the academic and industrial sides. This review proposes to give an overview of the reported aromatic multifunctional epoxide building blocks synthesized from biomass or from molecules that could be obtained from transformed biomass. After a reminder of the main glycidylation routes and mechanisms and the recent knowledge on BPA toxicity and legal issues, this review will provide a brief description of the main natural sources of aromatic molecules. The different epoxy prepolymers will then be organized from simple, mono-aromatic di-epoxy, to mono-aromatic poly-epoxy, to di-aromatic di-epoxy compounds, and finally to derivatives possessing numerous aromatic rings and epoxy groups. MDPI 2017-01-17 /pmc/articles/PMC6155700/ /pubmed/28106795 http://dx.doi.org/10.3390/molecules22010149 Text en © 2017 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 Review
Ng, Feifei
Couture, Guillaume
Philippe, Coralie
Boutevin, Bernard
Caillol, Sylvain
Bio-Based Aromatic Epoxy Monomers for Thermoset Materials
title Bio-Based Aromatic Epoxy Monomers for Thermoset Materials
title_full Bio-Based Aromatic Epoxy Monomers for Thermoset Materials
title_fullStr Bio-Based Aromatic Epoxy Monomers for Thermoset Materials
title_full_unstemmed Bio-Based Aromatic Epoxy Monomers for Thermoset Materials
title_short Bio-Based Aromatic Epoxy Monomers for Thermoset Materials
title_sort bio-based aromatic epoxy monomers for thermoset materials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155700/
https://www.ncbi.nlm.nih.gov/pubmed/28106795
http://dx.doi.org/10.3390/molecules22010149
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