基于环氧-硫醇点击反应的室温固化方法的合理设计,用于具有超高强度和附着力的紫外线固化硬质涂层

IF 3.9 3区 化学 Q2 POLYMER SCIENCE Journal of Polymer Science Pub Date : 2024-09-17 DOI:10.1002/pol.20240661
Yuya Tanaka, Nanae Tanaka, Daisuke Aoki, Koji Arimitsu
{"title":"基于环氧-硫醇点击反应的室温固化方法的合理设计,用于具有超高强度和附着力的紫外线固化硬质涂层","authors":"Yuya Tanaka, Nanae Tanaka, Daisuke Aoki, Koji Arimitsu","doi":"10.1002/pol.20240661","DOIUrl":null,"url":null,"abstract":"In recent years, there has been a growing demand for UV‐curable hard coatings because they offer several advantages, for example, lower energy consumption and the absence of volatile organic compound emissions. Anionic UV curing with photobase generators (PBGs), such as epoxy–thiol cross‐linking, enables curing under ambient conditions. However, designing a room‐temperature photoanionic curing system for epoxy–thiols remains challenging due to the complex effects of resin combinations on the cured products, thus making it difficult to prepare films with high hardness. Herein, we present a controlled reaction design for an anionic UV‐curing system by combining the chemical structures of epoxy resins and multifunctional thiols. The anionic UV‐curing system using PBGs that generate organic superbases demonstrated UV‐delayed curability, as evidenced by FT‐IR and photorheological analyses. To achieve high hardness, it was necessary to create the thiols with ultrarigid structures; epoxy resins with a bisphenol F structure were optimal for reacting with thiols for ultrarigid structures. This combination afforded an indentation hardness of 262 MPa with an epoxy conversion rate of 77% even at room temperature.","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"212 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rational design of a room‐temperature curing method, based on the epoxy–thiol click reaction, for UV‐curable hard coatings with ultrahigh strength and adhesion\",\"authors\":\"Yuya Tanaka, Nanae Tanaka, Daisuke Aoki, Koji Arimitsu\",\"doi\":\"10.1002/pol.20240661\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In recent years, there has been a growing demand for UV‐curable hard coatings because they offer several advantages, for example, lower energy consumption and the absence of volatile organic compound emissions. Anionic UV curing with photobase generators (PBGs), such as epoxy–thiol cross‐linking, enables curing under ambient conditions. However, designing a room‐temperature photoanionic curing system for epoxy–thiols remains challenging due to the complex effects of resin combinations on the cured products, thus making it difficult to prepare films with high hardness. Herein, we present a controlled reaction design for an anionic UV‐curing system by combining the chemical structures of epoxy resins and multifunctional thiols. The anionic UV‐curing system using PBGs that generate organic superbases demonstrated UV‐delayed curability, as evidenced by FT‐IR and photorheological analyses. To achieve high hardness, it was necessary to create the thiols with ultrarigid structures; epoxy resins with a bisphenol F structure were optimal for reacting with thiols for ultrarigid structures. This combination afforded an indentation hardness of 262 MPa with an epoxy conversion rate of 77% even at room temperature.\",\"PeriodicalId\":16888,\"journal\":{\"name\":\"Journal of Polymer Science\",\"volume\":\"212 1\",\"pages\":\"\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-09-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Polymer Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/pol.20240661\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/pol.20240661","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

摘要

近年来,人们对紫外线固化硬质涂料的需求越来越大,因为这种涂料具有多种优点,例如能耗低、无挥发性有机化合物排放等。使用光碱发生器(PBG)(如环氧硫醇交联)的阴离子紫外线固化可在环境条件下固化。然而,由于树脂组合对固化产物的复杂影响,设计环氧硫醇的室温光阴离子固化系统仍然具有挑战性,因此很难制备出具有高硬度的薄膜。在此,我们结合环氧树脂和多功能硫醇的化学结构,提出了一种阴离子紫外线固化体系的受控反应设计。通过傅立叶变换红外光谱(FT-IR)和光流变学分析,使用生成有机超碱的 PBGs 的阴离子紫外线固化体系表现出紫外线延迟固化性。为了获得高硬度,有必要制造出具有超硬结构的硫醇;具有双酚 F 结构的环氧树脂最适合与硫醇反应制造超硬结构。这种组合即使在室温下也能产生 262 兆帕的压痕硬度和 77% 的环氧树脂转化率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Rational design of a room‐temperature curing method, based on the epoxy–thiol click reaction, for UV‐curable hard coatings with ultrahigh strength and adhesion
In recent years, there has been a growing demand for UV‐curable hard coatings because they offer several advantages, for example, lower energy consumption and the absence of volatile organic compound emissions. Anionic UV curing with photobase generators (PBGs), such as epoxy–thiol cross‐linking, enables curing under ambient conditions. However, designing a room‐temperature photoanionic curing system for epoxy–thiols remains challenging due to the complex effects of resin combinations on the cured products, thus making it difficult to prepare films with high hardness. Herein, we present a controlled reaction design for an anionic UV‐curing system by combining the chemical structures of epoxy resins and multifunctional thiols. The anionic UV‐curing system using PBGs that generate organic superbases demonstrated UV‐delayed curability, as evidenced by FT‐IR and photorheological analyses. To achieve high hardness, it was necessary to create the thiols with ultrarigid structures; epoxy resins with a bisphenol F structure were optimal for reacting with thiols for ultrarigid structures. This combination afforded an indentation hardness of 262 MPa with an epoxy conversion rate of 77% even at room temperature.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Polymer Science
Journal of Polymer Science POLYMER SCIENCE-
CiteScore
6.30
自引率
5.90%
发文量
264
期刊介绍: Journal of Polymer Research provides a forum for the prompt publication of articles concerning the fundamental and applied research of polymers. Its great feature lies in the diversity of content which it encompasses, drawing together results from all aspects of polymer science and technology. As polymer research is rapidly growing around the globe, the aim of this journal is to establish itself as a significant information tool not only for the international polymer researchers in academia but also for those working in industry. The scope of the journal covers a wide range of the highly interdisciplinary field of polymer science and technology.
期刊最新文献
Insight Into the Role of Fiber Diameter on Electrospun Polysulfone Mats Issue Information - Cover Description Agglomerating Agent Emulsions Synergistically Stabilized by Surfactants and SiO2 Nanoparticles: Stability, Mechanism, and Applications for PBL Agglomeration Issue Information - Cover Description Cover Image, Volume 62, Issue 21
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1