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Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components

One-hundred percent renewable triphenol—GTF—(glycerol trihydroferulate) and novel bisphenols—GDF(x)–(glycerol dihydroferulate) were prepared from lignocellulose-derived ferulic acid and vegetal oil components (fatty acids and glycerol) using highly selective lipase-catalyzed transesterifications. Es...

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Autores principales: Hollande, Louis, Do Marcolino, Izia, Balaguer, Patrick, Domenek, Sandra, Gross, Richard A., Allais, Florent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445855/
https://www.ncbi.nlm.nih.gov/pubmed/30972325
http://dx.doi.org/10.3389/fchem.2019.00159
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author Hollande, Louis
Do Marcolino, Izia
Balaguer, Patrick
Domenek, Sandra
Gross, Richard A.
Allais, Florent
author_facet Hollande, Louis
Do Marcolino, Izia
Balaguer, Patrick
Domenek, Sandra
Gross, Richard A.
Allais, Florent
author_sort Hollande, Louis
collection PubMed
description One-hundred percent renewable triphenol—GTF—(glycerol trihydroferulate) and novel bisphenols—GDF(x)–(glycerol dihydroferulate) were prepared from lignocellulose-derived ferulic acid and vegetal oil components (fatty acids and glycerol) using highly selective lipase-catalyzed transesterifications. Estrogenic activity tests revealed no endocrine disruption for GDF(x) bisphenols. Triethyl-benzyl-ammonium chloride (TEBAC) mediated glycidylation of all bis/triphenols, afforded innocuous bio-based epoxy precursors GDF(x)EPO and GTF-EPO. GDF(x)EPO were then cured with conventional and renewable diamines, and some of them in presence of GTF-EPO. Thermo-mechanical analyses (TGA, DSC, and DMA) and degradation studies in acidic aqueous solutions of the resulting epoxy-amine resins showed excellent thermal stabilities (T(d)5% = 282–310°C), glass transition temperatures (T(g)) ranging from 3 to 62°C, tunable tan α, and tunable degradability, respectively. It has been shown that the thermo-mechanical properties, wettability, and degradability of these epoxy-amine resins, can be finely tailored by judiciously selecting the diamine nature, the GTF-EPO content, and the fatty acid chain length.
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spelling pubmed-64458552019-04-10 Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components Hollande, Louis Do Marcolino, Izia Balaguer, Patrick Domenek, Sandra Gross, Richard A. Allais, Florent Front Chem Chemistry One-hundred percent renewable triphenol—GTF—(glycerol trihydroferulate) and novel bisphenols—GDF(x)–(glycerol dihydroferulate) were prepared from lignocellulose-derived ferulic acid and vegetal oil components (fatty acids and glycerol) using highly selective lipase-catalyzed transesterifications. Estrogenic activity tests revealed no endocrine disruption for GDF(x) bisphenols. Triethyl-benzyl-ammonium chloride (TEBAC) mediated glycidylation of all bis/triphenols, afforded innocuous bio-based epoxy precursors GDF(x)EPO and GTF-EPO. GDF(x)EPO were then cured with conventional and renewable diamines, and some of them in presence of GTF-EPO. Thermo-mechanical analyses (TGA, DSC, and DMA) and degradation studies in acidic aqueous solutions of the resulting epoxy-amine resins showed excellent thermal stabilities (T(d)5% = 282–310°C), glass transition temperatures (T(g)) ranging from 3 to 62°C, tunable tan α, and tunable degradability, respectively. It has been shown that the thermo-mechanical properties, wettability, and degradability of these epoxy-amine resins, can be finely tailored by judiciously selecting the diamine nature, the GTF-EPO content, and the fatty acid chain length. Frontiers Media S.A. 2019-03-27 /pmc/articles/PMC6445855/ /pubmed/30972325 http://dx.doi.org/10.3389/fchem.2019.00159 Text en Copyright © 2019 Hollande, Do Marcolino, Balaguer, Domenek, Gross and Allais. 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
Hollande, Louis
Do Marcolino, Izia
Balaguer, Patrick
Domenek, Sandra
Gross, Richard A.
Allais, Florent
Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components
title Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components
title_full Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components
title_fullStr Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components
title_full_unstemmed Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components
title_short Preparation of Renewable Epoxy-Amine Resins With Tunable Thermo-Mechanical Properties, Wettability and Degradation Abilities From Lignocellulose- and Plant Oils-Derived Components
title_sort preparation of renewable epoxy-amine resins with tunable thermo-mechanical properties, wettability and degradation abilities from lignocellulose- and plant oils-derived components
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445855/
https://www.ncbi.nlm.nih.gov/pubmed/30972325
http://dx.doi.org/10.3389/fchem.2019.00159
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