In-Situ Grafted Ethylene Propylene Diene Monomer (EPDM) Rubber Multiblock Copolymers as Compatibilizers for Polyethylene (PE) and Isotactic Polypropylene (iPP) Blends

IF 4.1 2区 化学 Q2 POLYMER SCIENCE Polymer Pub Date : 2024-12-16 DOI:10.1016/j.polymer.2024.127959
Feng Yu, Chuanjiang Long, Sitong Feng, Zhen Dong, Xiaoqing Liu, Yuanzhi Li, Zhong-Ren Chen
{"title":"In-Situ Grafted Ethylene Propylene Diene Monomer (EPDM) Rubber Multiblock Copolymers as Compatibilizers for Polyethylene (PE) and Isotactic Polypropylene (iPP) Blends","authors":"Feng Yu, Chuanjiang Long, Sitong Feng, Zhen Dong, Xiaoqing Liu, Yuanzhi Li, Zhong-Ren Chen","doi":"10.1016/j.polymer.2024.127959","DOIUrl":null,"url":null,"abstract":"Addressing the mounting issue of plastic waste, particularly the recycling of polyethylene (PE) and isotactic polypropylene (iPP), requires inventive and economically viable solutions. Employing compatibilizers for physical recycling is one of the most promising ways. This study utilizes reversible free radical reaction to facilitate the grafting reaction of ethylene propylene diene monomer (EPDM) between PE (or iPP) at the interface. Only 1wt.%-3wt.% EPDM is required for reactive blending, resulting in the formation of a graft multi-block copolymer that significantly improves the compatibility between PE and PP. This improvement notably enhances the mechanical properties, especially the elongation at break, which can reach up to 700%. Even after three processing cycles, the elongation at break of samples can still reach approximately 400%. The mechanism for reactive compatibilization has been supported by various characterization techniques, including tensile, rheology, peeling, and transmission electron microscope (TEM) tests. The mechanical properties of the samples were diminished when EPDM was replaced by the synthesized copolymer of ethylene and ethylidene norbornene (CEENB) and vinyl-terminated polyethylene (VPE). This observation confirms that EPDM located at the PE/iPP interface significantly contributes to the formation of grafted multi-block copolymers. Notably, the grafting reaction causes a negligible shift in the molecular weight peak, indicating minimal degradation and cross-linking of the polymers. The reversible free radical reaction involving sulfur and tetramethyl thiuramyl monosulfide (TMTM) reagents plays an important role in reducing side reactions.","PeriodicalId":405,"journal":{"name":"Polymer","volume":"30 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.polymer.2024.127959","RegionNum":2,"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

Abstract

Addressing the mounting issue of plastic waste, particularly the recycling of polyethylene (PE) and isotactic polypropylene (iPP), requires inventive and economically viable solutions. Employing compatibilizers for physical recycling is one of the most promising ways. This study utilizes reversible free radical reaction to facilitate the grafting reaction of ethylene propylene diene monomer (EPDM) between PE (or iPP) at the interface. Only 1wt.%-3wt.% EPDM is required for reactive blending, resulting in the formation of a graft multi-block copolymer that significantly improves the compatibility between PE and PP. This improvement notably enhances the mechanical properties, especially the elongation at break, which can reach up to 700%. Even after three processing cycles, the elongation at break of samples can still reach approximately 400%. The mechanism for reactive compatibilization has been supported by various characterization techniques, including tensile, rheology, peeling, and transmission electron microscope (TEM) tests. The mechanical properties of the samples were diminished when EPDM was replaced by the synthesized copolymer of ethylene and ethylidene norbornene (CEENB) and vinyl-terminated polyethylene (VPE). This observation confirms that EPDM located at the PE/iPP interface significantly contributes to the formation of grafted multi-block copolymers. Notably, the grafting reaction causes a negligible shift in the molecular weight peak, indicating minimal degradation and cross-linking of the polymers. The reversible free radical reaction involving sulfur and tetramethyl thiuramyl monosulfide (TMTM) reagents plays an important role in reducing side reactions.

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
原位接枝三元乙丙橡胶(EPDM)多嵌段共聚物作为聚乙烯(PE)和同方聚丙烯(iPP)混合物的相容剂
要解决日益严重的塑料废弃物问题,尤其是聚乙烯(PE)和异方性聚丙烯(iPP)的回收利用问题,就必须采用创新且经济可行的解决方案。使用相容剂进行物理回收是最有前途的方法之一。本研究利用可逆自由基反应促进乙丙橡胶(EPDM)在聚乙烯(或 iPP)界面之间的接枝反应。反应共混只需 1 重量百分比-3 重量百分比的三元乙丙橡胶,从而形成接枝多嵌段共聚物,显著改善聚乙烯和聚丙烯之间的相容性。这种改善显著提高了机械性能,尤其是断裂伸长率,最高可达 700%。即使经过三个加工周期,样品的断裂伸长率仍可达到约 400%。各种表征技术,包括拉伸、流变、剥离和透射电子显微镜(TEM)测试,都支持了反应性相容的机理。当 EPDM 被合成的乙烯和亚乙基降冰片烯共聚物(CEENB)和乙烯基封端聚乙烯(VPE)取代时,样品的机械性能降低。这一观察结果证实,位于 PE/iPP 界面的三元乙丙橡胶对接枝多嵌段共聚物的形成有重要作用。值得注意的是,接枝反应导致的分子量峰值移动微乎其微,这表明聚合物的降解和交联程度极低。涉及硫和四甲基秋氨酰单硫化物(TMTM)试剂的可逆自由基反应在减少副反应方面发挥了重要作用。
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
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
期刊最新文献
Molecular Orientation and Solvent Affinity in Electrospun Fibers of Miscible Blends Eco-friendly fabrication and luminescent properties of flexible Ag-In-Zn-S/ZnS QD-WPU composite film Superparamagnetic Iron Oxide Nanoparticle – Vitrimer Nanocomposites: Reprocessable and Multi-Responsive Materials Self-healing, high mechanical strength and adhesive supramolecular hydrogel based on triblock copolymer for flexible electronics Emulsion-templated macroporous polycaprolactone: Synthesis, degradation, additive manufacturing, and cell-growth
×
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