Scalable Routes to Acrylate and Methacrylate Block Copolymers via Copper-Mediated Reversible Deactivation Radical Polymerization

IF 3.8 3区 工程技术 Q2 ENGINEERING, CHEMICAL Industrial & Engineering Chemistry Research Pub Date : 2024-06-24 DOI:10.1021/acs.iecr.4c01811
Hayden M. Deacon,  and , Robin A. Hutchinson*, 
{"title":"Scalable Routes to Acrylate and Methacrylate Block Copolymers via Copper-Mediated Reversible Deactivation Radical Polymerization","authors":"Hayden M. Deacon,&nbsp; and ,&nbsp;Robin A. Hutchinson*,&nbsp;","doi":"10.1021/acs.iecr.4c01811","DOIUrl":null,"url":null,"abstract":"<p >Cu-mediated reversible deactivation radical polymerization (RDRP) is investigated as a method to produce (meth)acrylic polymers of high chain-end functionality and well-defined structure, enabling the production of uniform block copolymer materials. The use of inexpensive reagents with scale-appropriate reactor configurations is a key feature in overcoming the hurdles to commercialization. Using methyl acrylate (MA) as a model system, reaction conditions and feeding strategies were optimized in a semibatch system to reach &gt;95% monomer conversion and 70 wt % polymer in solution in 1.5 h with excellent control (<i>Đ</i> = 1.10). It was concurrently demonstrated that prepolymerization in the copper tube reactor could be eliminated while still providing a chain-extendible species, a result that simplifies reactor operation, offers greater flexibility in initiator choice, and improves compositional control of the final product. The conditions developed for the homopolymerization system were applied to produce acrylate-acrylate and acrylate-methacrylate block copolymers, also exploring the influence of block order. Achieving high conversions for each monomer fed, reactions were completed in 4 h or less with no intermediate purification or additional catalyst, thus yielding a scalable method of producing block copolymer materials at Cu levels &lt;100 ppm.</p>","PeriodicalId":39,"journal":{"name":"Industrial & Engineering Chemistry Research","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Research","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.iecr.4c01811","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Cu-mediated reversible deactivation radical polymerization (RDRP) is investigated as a method to produce (meth)acrylic polymers of high chain-end functionality and well-defined structure, enabling the production of uniform block copolymer materials. The use of inexpensive reagents with scale-appropriate reactor configurations is a key feature in overcoming the hurdles to commercialization. Using methyl acrylate (MA) as a model system, reaction conditions and feeding strategies were optimized in a semibatch system to reach >95% monomer conversion and 70 wt % polymer in solution in 1.5 h with excellent control (Đ = 1.10). It was concurrently demonstrated that prepolymerization in the copper tube reactor could be eliminated while still providing a chain-extendible species, a result that simplifies reactor operation, offers greater flexibility in initiator choice, and improves compositional control of the final product. The conditions developed for the homopolymerization system were applied to produce acrylate-acrylate and acrylate-methacrylate block copolymers, also exploring the influence of block order. Achieving high conversions for each monomer fed, reactions were completed in 4 h or less with no intermediate purification or additional catalyst, thus yielding a scalable method of producing block copolymer materials at Cu levels <100 ppm.

Abstract Image

Abstract Image

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
通过铜介导的可逆失活自由基聚合制备丙烯酸酯和甲基丙烯酸酯嵌段共聚物的可扩展途径
研究人员将铜介导的可逆去活化自由基聚合(RDRP)作为一种生产具有高链端功能性和明确结构的(甲基)丙烯酸聚合物的方法,从而能够生产出均匀的嵌段共聚物材料。使用价格低廉的试剂和适合规模的反应器配置是克服商业化障碍的关键特征。以丙烯酸甲酯(MA)为模型系统,在半间歇系统中对反应条件和进料策略进行了优化,在 1.5 小时内达到 95% 的单体转化率和 70 wt % 的溶液聚合物,且控制良好(Đ = 1.10)。同时还证明,铜管反应器中的预聚合可以取消,但仍能提供一种可延长链的物质,这一结果简化了反应器的操作,为引发剂的选择提供了更大的灵活性,并改善了最终产品的成分控制。为均聚体系开发的条件被用于生产丙烯酸酯-丙烯酸酯和丙烯酸酯-甲基丙烯酸酯嵌段共聚物,同时还探索了嵌段顺序的影响。每种单体进料的转化率都很高,反应在 4 小时或更短时间内完成,无需中间纯化或额外催化剂,因此产生了一种可扩展的方法,可在 Cu 含量为 100 ppm 的条件下生产嵌段共聚物材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Industrial & Engineering Chemistry Research
Industrial & Engineering Chemistry Research 工程技术-工程:化工
CiteScore
7.40
自引率
7.10%
发文量
1467
审稿时长
2.8 months
期刊介绍: ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.
期刊最新文献
Illumination Invariant Automated Drop Size Estimation Catalytic CO2 Capture Performance of a MEA-EAE-DEEA Trisolvent in a Hot Silicon Oil-Based Pilot Plant CCU-Llama: A Knowledge Extraction LLM for Carbon Capture and Utilization by Mining Scientific Literature Data One-Pot Coating of Ceramic Powders by Exfoliated Boron Nitride Layers with a Dense CO2 Medium and Ultrasound-Aided Mixing Ammonium Chloride Powder Feeding for the Simultaneous Reduction of NOx and Oxidation of Hg0 in the SCR Process
×
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