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Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties
Cardanol is a renewable resource based on cashew nut shell liquid (CNSL), which consists of a phenol ring with a C15 long aliphatic side chain in the meta position with varying degrees of unsaturation. Cardanol glycidyl ether was chemically modified to form side-chain epoxidized cardanol glycidyl et...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563135/ https://www.ncbi.nlm.nih.gov/pubmed/32872398 http://dx.doi.org/10.3390/polym12091956 |
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author | Kinaci, Emre Can, Erde Scala, John J. La Palmese, Giuseppe R. |
author_facet | Kinaci, Emre Can, Erde Scala, John J. La Palmese, Giuseppe R. |
author_sort | Kinaci, Emre |
collection | PubMed |
description | Cardanol is a renewable resource based on cashew nut shell liquid (CNSL), which consists of a phenol ring with a C15 long aliphatic side chain in the meta position with varying degrees of unsaturation. Cardanol glycidyl ether was chemically modified to form side-chain epoxidized cardanol glycidyl ether (SCECGE) with an average epoxy functionality of 2.45 per molecule and was cured with petroleum-based epoxy hardeners, 4-4′-methylenebis(cyclohexanamine) and diethylenetriamine, and a cardanol-based amine hardener. For comparison, cardanol-based diphenol diepoxy resin, NC514 (Cardolite), and a petroleum-based epoxy resin, diglycidyl ether of bisphenol-A (DGEBA) were also evaluated. Chemical and thermomechanical analyses showed that for SCECGE resins, incomplete cure of the secondary epoxides led to reduced cross-link density, reduced thermal stability, and reduced elongation at break when compared with difunctional resins containing only primary epoxides. However, because of functionality greater than two, amine-cured SCECGE produced a T(g) very similar to that of NC514 and thus could be useful in formulating epoxy with renewable cardanol content. |
format | Online Article Text |
id | pubmed-7563135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75631352020-10-27 Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties Kinaci, Emre Can, Erde Scala, John J. La Palmese, Giuseppe R. Polymers (Basel) Article Cardanol is a renewable resource based on cashew nut shell liquid (CNSL), which consists of a phenol ring with a C15 long aliphatic side chain in the meta position with varying degrees of unsaturation. Cardanol glycidyl ether was chemically modified to form side-chain epoxidized cardanol glycidyl ether (SCECGE) with an average epoxy functionality of 2.45 per molecule and was cured with petroleum-based epoxy hardeners, 4-4′-methylenebis(cyclohexanamine) and diethylenetriamine, and a cardanol-based amine hardener. For comparison, cardanol-based diphenol diepoxy resin, NC514 (Cardolite), and a petroleum-based epoxy resin, diglycidyl ether of bisphenol-A (DGEBA) were also evaluated. Chemical and thermomechanical analyses showed that for SCECGE resins, incomplete cure of the secondary epoxides led to reduced cross-link density, reduced thermal stability, and reduced elongation at break when compared with difunctional resins containing only primary epoxides. However, because of functionality greater than two, amine-cured SCECGE produced a T(g) very similar to that of NC514 and thus could be useful in formulating epoxy with renewable cardanol content. MDPI 2020-08-29 /pmc/articles/PMC7563135/ /pubmed/32872398 http://dx.doi.org/10.3390/polym12091956 Text en © 2020 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 Kinaci, Emre Can, Erde Scala, John J. La Palmese, Giuseppe R. Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties |
title | Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties |
title_full | Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties |
title_fullStr | Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties |
title_full_unstemmed | Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties |
title_short | Influence of Epoxidized Cardanol Functionality and Reactivity on Network Formation and Properties |
title_sort | influence of epoxidized cardanol functionality and reactivity on network formation and properties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563135/ https://www.ncbi.nlm.nih.gov/pubmed/32872398 http://dx.doi.org/10.3390/polym12091956 |
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