聚合诱导热响应胶束的自组装及其润滑适应性

IF 2.7 4区 化学 Q3 POLYMER SCIENCE
Linjie Yang, Hanfeng Liu, Pengrui Cao, Junhui Gong, Xinrui Zhang, Tingmei Wang, Liming Tao, Xianqiang Pei, Qihua Wang, Jianqiang Zhang, Yaoming Zhang
{"title":"聚合诱导热响应胶束的自组装及其润滑适应性","authors":"Linjie Yang, Hanfeng Liu, Pengrui Cao, Junhui Gong, Xinrui Zhang, Tingmei Wang, Liming Tao, Xianqiang Pei, Qihua Wang, Jianqiang Zhang, Yaoming Zhang","doi":"10.1038/s41428-025-01057-1","DOIUrl":null,"url":null,"abstract":"Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. Poly(N-isopropylacrylamide) (PNIPAM) is widely used to form micelles, particularly for drug delivery, because its lower critical solution temperature (LCST) is close to body temperature. However, the preparation of micelles based on PNIPAM block copolymers often involves complex processes, which limit their broader application. Here, we employed polymerization-induced self-assembly (PISA) combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B (PGMAx-b-PNIPAMy-B), which are spherical micelles with a thermoresponsive core of PNIPAM and a crosslinked shell of PGMA formed by sodium tetraborate decahydrate. The micelles exhibited rapid and reversible self-assembly and collapsed at 31 °C, enabling temperature regulation through light transmittance, which makes them suitable for smart window applications. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties at various temperatures (25–36 °C) and under various loads (20–70 N), indicating their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field. Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. We employed polymerization-induced self-assembly combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B, which exhibited rapid and reversible self-assembly. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties showcasing their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field.","PeriodicalId":20302,"journal":{"name":"Polymer Journal","volume":"57 10","pages":"1115-1125"},"PeriodicalIF":2.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polymerization-induced self-assembly of thermoresponsive micelles and their lubrication adaptivity\",\"authors\":\"Linjie Yang, Hanfeng Liu, Pengrui Cao, Junhui Gong, Xinrui Zhang, Tingmei Wang, Liming Tao, Xianqiang Pei, Qihua Wang, Jianqiang Zhang, Yaoming Zhang\",\"doi\":\"10.1038/s41428-025-01057-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. Poly(N-isopropylacrylamide) (PNIPAM) is widely used to form micelles, particularly for drug delivery, because its lower critical solution temperature (LCST) is close to body temperature. However, the preparation of micelles based on PNIPAM block copolymers often involves complex processes, which limit their broader application. Here, we employed polymerization-induced self-assembly (PISA) combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B (PGMAx-b-PNIPAMy-B), which are spherical micelles with a thermoresponsive core of PNIPAM and a crosslinked shell of PGMA formed by sodium tetraborate decahydrate. The micelles exhibited rapid and reversible self-assembly and collapsed at 31 °C, enabling temperature regulation through light transmittance, which makes them suitable for smart window applications. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties at various temperatures (25–36 °C) and under various loads (20–70 N), indicating their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field. Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. We employed polymerization-induced self-assembly combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B, which exhibited rapid and reversible self-assembly. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties showcasing their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field.\",\"PeriodicalId\":20302,\"journal\":{\"name\":\"Polymer Journal\",\"volume\":\"57 10\",\"pages\":\"1115-1125\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.nature.com/articles/s41428-025-01057-1\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Journal","FirstCategoryId":"92","ListUrlMain":"https://www.nature.com/articles/s41428-025-01057-1","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

摘要

响应性材料具有重要的应用价值,因为它们具有响应外部刺激主动调整其结构或性能的能力。聚n -异丙基丙烯酰胺(PNIPAM)被广泛用于形成胶束,特别是用于药物输送,因为它的较低临界溶液温度(LCST)接近体温。然而,基于PNIPAM嵌段共聚物的胶束制备通常涉及复杂的工艺,这限制了其更广泛的应用。在这里,我们采用聚合诱导自组装(PISA)结合原位交联来合成稳定的热响应胶束,如聚(甲基丙烯酸甘油)-B -聚(n-异丙基丙烯酰胺)-B (PGMAx-b-PNIPAMy-B),这是一种球形胶束,具有PNIPAM的热响应核和由十水四硼酸钠形成的PGMA的交联壳。胶束表现出快速和可逆的自组装,并在31°C下崩溃,通过透光率实现温度调节,这使得它们适合智能窗口应用。此外,这些胶束在不同温度(25-36°C)和不同载荷(20-70 N)下表现出优异的减摩和耐磨性能,表明它们作为添加剂具有自适应润滑作用。本工作展示了热响应胶束的简易制备,扩展了PISA技术在摩擦学领域的应用。响应性材料具有重要的应用价值,因为它们具有响应外部刺激主动调整其结构或性能的能力。我们采用聚合诱导自组装与原位交联相结合的方法合成了稳定的热响应胶束,如聚(甲基丙烯酸甘油)-B -聚(n-异丙基丙烯酰胺)-B,它具有快速可逆的自组装特性。此外,这些胶束表现出优异的减摩和耐磨性能,展示了它们作为添加剂的自适应润滑性能。本工作展示了热响应胶束的简易制备,扩展了PISA技术在摩擦学领域的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polymerization-induced self-assembly of thermoresponsive micelles and their lubrication adaptivity

Polymerization-induced self-assembly of thermoresponsive micelles and their lubrication adaptivity
Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. Poly(N-isopropylacrylamide) (PNIPAM) is widely used to form micelles, particularly for drug delivery, because its lower critical solution temperature (LCST) is close to body temperature. However, the preparation of micelles based on PNIPAM block copolymers often involves complex processes, which limit their broader application. Here, we employed polymerization-induced self-assembly (PISA) combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B (PGMAx-b-PNIPAMy-B), which are spherical micelles with a thermoresponsive core of PNIPAM and a crosslinked shell of PGMA formed by sodium tetraborate decahydrate. The micelles exhibited rapid and reversible self-assembly and collapsed at 31 °C, enabling temperature regulation through light transmittance, which makes them suitable for smart window applications. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties at various temperatures (25–36 °C) and under various loads (20–70 N), indicating their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field. Responsive materials have significant application value because of their ability to actively adjust their structure or properties in response to external stimuli. We employed polymerization-induced self-assembly combined with in situ crosslinking to synthesize stabilized thermoresponsive micelles, such as poly(glycerol methacrylate)-b-poly(N-isopropylacrylamide)-B, which exhibited rapid and reversible self-assembly. Furthermore, these micelles demonstrated excellent friction-reducing and wear-resistant properties showcasing their adaptive lubrication as additives. This work presents the facile fabrication of thermoresponsive micelles and expands the application of PISA technology in the tribological field.
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
Polymer Journal
Polymer Journal 化学-高分子科学
CiteScore
5.60
自引率
7.10%
发文量
131
审稿时长
2.5 months
期刊介绍: Polymer Journal promotes research from all aspects of polymer science from anywhere in the world and aims to provide an integrated platform for scientific communication that assists the advancement of polymer science and related fields. The journal publishes Original Articles, Notes, Short Communications and Reviews. Subject areas and topics of particular interest within the journal''s scope include, but are not limited to, those listed below: Polymer synthesis and reactions Polymer structures Physical properties of polymers Polymer surface and interfaces Functional polymers Supramolecular polymers Self-assembled materials Biopolymers and bio-related polymer materials Polymer engineering.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信