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Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer
Functional liquid fluoroelastomers are in high demand in new energy fields. And these materials have potential applications in high-performance sealing materials and as electrode materials. In this study, a novel high-performance hydroxyl-terminated liquid fluoroelastomer (t-HTLF) with a high fluori...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10255101/ https://www.ncbi.nlm.nih.gov/pubmed/37299372 http://dx.doi.org/10.3390/polym15112574 |
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author | Li, Donghan Yang, Chen Li, Ping Yu, Lu Zhao, Shufa Li, Long Kang, Hailan Yang, Feng Fang, Qinghong |
author_facet | Li, Donghan Yang, Chen Li, Ping Yu, Lu Zhao, Shufa Li, Long Kang, Hailan Yang, Feng Fang, Qinghong |
author_sort | Li, Donghan |
collection | PubMed |
description | Functional liquid fluoroelastomers are in high demand in new energy fields. And these materials have potential applications in high-performance sealing materials and as electrode materials. In this study, a novel high-performance hydroxyl-terminated liquid fluoroelastomer (t-HTLF) with a high fluorine content, temperature resistance, and curing efficiency was synthesised from a terpolymer of vinylidene fluoride (VDF), tetrafluoroethylene (TFE), and hexafluoropylene (HFP). A carboxyl-terminated liquid fluoroelastomer (t-CTLF) with controllable molar mass and end-group content was first prepared from a poly(VDF-ter-TFE-ter-HFP) terpolymer using a unique oxidative degradation method. Subsequently, an efficient “one-step” reduction of the carboxyl groups (COOH) in t-CTLF into hydroxyl groups (OH) was achieved via the functional-group conversion method using lithium aluminium hydride (LiAlH(4)) as the reductant. Thus, t-HTLF with a controllable molar mass and end-group content and highly active end groups was synthesised. Owing to the efficient curing reaction between OH and isocyanate groups (NCO), the cured t-HTLF exhibits good surface properties, thermal properties, and chemical stability. The thermal decomposition temperature (T(d)) of the cured t-HTLF reaches 334 °C, and it exhibits hydrophobicity. The oxidative degradation, reduction, and curing reaction mechanisms were also determined. The effects of solvent dosage, reaction temperature, reaction time, and ratio of the reductant to the COOH content on the carboxyl conversion were also systematically investigated. An efficient reduction system comprising LiAlH(4) can not only achieve an efficient conversion of the COOH groups in t-CTLF to OH groups but also the in situ hydrogenation and addition reactions of residual double bonds (C=C) groups in the chain, such that the thermal stability and terminal activity of the product are improved while maintaining a high fluorine content. |
format | Online Article Text |
id | pubmed-10255101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102551012023-06-10 Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer Li, Donghan Yang, Chen Li, Ping Yu, Lu Zhao, Shufa Li, Long Kang, Hailan Yang, Feng Fang, Qinghong Polymers (Basel) Article Functional liquid fluoroelastomers are in high demand in new energy fields. And these materials have potential applications in high-performance sealing materials and as electrode materials. In this study, a novel high-performance hydroxyl-terminated liquid fluoroelastomer (t-HTLF) with a high fluorine content, temperature resistance, and curing efficiency was synthesised from a terpolymer of vinylidene fluoride (VDF), tetrafluoroethylene (TFE), and hexafluoropylene (HFP). A carboxyl-terminated liquid fluoroelastomer (t-CTLF) with controllable molar mass and end-group content was first prepared from a poly(VDF-ter-TFE-ter-HFP) terpolymer using a unique oxidative degradation method. Subsequently, an efficient “one-step” reduction of the carboxyl groups (COOH) in t-CTLF into hydroxyl groups (OH) was achieved via the functional-group conversion method using lithium aluminium hydride (LiAlH(4)) as the reductant. Thus, t-HTLF with a controllable molar mass and end-group content and highly active end groups was synthesised. Owing to the efficient curing reaction between OH and isocyanate groups (NCO), the cured t-HTLF exhibits good surface properties, thermal properties, and chemical stability. The thermal decomposition temperature (T(d)) of the cured t-HTLF reaches 334 °C, and it exhibits hydrophobicity. The oxidative degradation, reduction, and curing reaction mechanisms were also determined. The effects of solvent dosage, reaction temperature, reaction time, and ratio of the reductant to the COOH content on the carboxyl conversion were also systematically investigated. An efficient reduction system comprising LiAlH(4) can not only achieve an efficient conversion of the COOH groups in t-CTLF to OH groups but also the in situ hydrogenation and addition reactions of residual double bonds (C=C) groups in the chain, such that the thermal stability and terminal activity of the product are improved while maintaining a high fluorine content. MDPI 2023-06-04 /pmc/articles/PMC10255101/ /pubmed/37299372 http://dx.doi.org/10.3390/polym15112574 Text en © 2023 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 Li, Donghan Yang, Chen Li, Ping Yu, Lu Zhao, Shufa Li, Long Kang, Hailan Yang, Feng Fang, Qinghong Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer |
title | Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer |
title_full | Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer |
title_fullStr | Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer |
title_full_unstemmed | Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer |
title_short | Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer |
title_sort | synthesis and properties of the novel high-performance hydroxyl-terminated liquid fluoroelastomer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10255101/ https://www.ncbi.nlm.nih.gov/pubmed/37299372 http://dx.doi.org/10.3390/polym15112574 |
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