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Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition

In this study, previously developed acetoacetates of two tall-oil-based and two commercial polyols were used to obtain polymers by the Michael reaction. The development of polymer formulations with varying cross-link density was enabled by different bio-based monomers in combination with different a...

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Autores principales: Pomilovskis, Ralfs, Mierina, Inese, Fridrihsone, Anda, Kirpluks, Mikelis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571392/
https://www.ncbi.nlm.nih.gov/pubmed/36236017
http://dx.doi.org/10.3390/polym14194068
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author Pomilovskis, Ralfs
Mierina, Inese
Fridrihsone, Anda
Kirpluks, Mikelis
author_facet Pomilovskis, Ralfs
Mierina, Inese
Fridrihsone, Anda
Kirpluks, Mikelis
author_sort Pomilovskis, Ralfs
collection PubMed
description In this study, previously developed acetoacetates of two tall-oil-based and two commercial polyols were used to obtain polymers by the Michael reaction. The development of polymer formulations with varying cross-link density was enabled by different bio-based monomers in combination with different acrylates—bisphenol A ethoxylate diacrylate, trimethylolpropane triacrylate, and pentaerythritol tetraacrylate. New polymer materials are based on the same polyols that are suitable for polyurethanes. The new polymers have qualities comparable to polyurethanes and are obtained without the drawbacks that come with polyurethane extractions, such as the use of hazardous isocyanates or reactions under harsh conditions in the case of non-isocyanate polyurethanes. Dynamic mechanical analysis, differential scanning calorimetry, thermal gravimetric analysis, and universal strength testing equipment were used to investigate the physical and thermal characteristics of the created polymers. Polymers with a wide range of thermal and mechanical properties were obtained (glass transition temperature from 21 to 63 °C; tensile modulus (Young’s) from 8 MPa to 2710 MPa and tensile strength from 4 to 52 MPa). The synthesized polymers are thermally stable up to 300 °C. The suggested method may be used to make two-component polymer foams, coatings, resins, and composite matrices.
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spelling pubmed-95713922022-10-17 Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition Pomilovskis, Ralfs Mierina, Inese Fridrihsone, Anda Kirpluks, Mikelis Polymers (Basel) Article In this study, previously developed acetoacetates of two tall-oil-based and two commercial polyols were used to obtain polymers by the Michael reaction. The development of polymer formulations with varying cross-link density was enabled by different bio-based monomers in combination with different acrylates—bisphenol A ethoxylate diacrylate, trimethylolpropane triacrylate, and pentaerythritol tetraacrylate. New polymer materials are based on the same polyols that are suitable for polyurethanes. The new polymers have qualities comparable to polyurethanes and are obtained without the drawbacks that come with polyurethane extractions, such as the use of hazardous isocyanates or reactions under harsh conditions in the case of non-isocyanate polyurethanes. Dynamic mechanical analysis, differential scanning calorimetry, thermal gravimetric analysis, and universal strength testing equipment were used to investigate the physical and thermal characteristics of the created polymers. Polymers with a wide range of thermal and mechanical properties were obtained (glass transition temperature from 21 to 63 °C; tensile modulus (Young’s) from 8 MPa to 2710 MPa and tensile strength from 4 to 52 MPa). The synthesized polymers are thermally stable up to 300 °C. The suggested method may be used to make two-component polymer foams, coatings, resins, and composite matrices. MDPI 2022-09-28 /pmc/articles/PMC9571392/ /pubmed/36236017 http://dx.doi.org/10.3390/polym14194068 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pomilovskis, Ralfs
Mierina, Inese
Fridrihsone, Anda
Kirpluks, Mikelis
Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition
title Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition
title_full Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition
title_fullStr Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition
title_full_unstemmed Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition
title_short Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition
title_sort bio-based polymer developments from tall oil fatty acids by exploiting michael addition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571392/
https://www.ncbi.nlm.nih.gov/pubmed/36236017
http://dx.doi.org/10.3390/polym14194068
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