聚合物的离子增容

IF 4.7 Q1 POLYMER SCIENCE ACS polymers Au Pub Date : 2022-07-22 DOI:10.1021/acspolymersau.2c00026
Glenn H. Fredrickson*, Shuyi Xie, Jerrick Edmund, My Linh Le, Dan Sun, Douglas J. Grzetic, Daniel L. Vigil, Kris T. Delaney, Michael L. Chabinyc and Rachel A. Segalman, 
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引用次数: 12

摘要

高分子量聚合物混合的小比熵意味着大多数不同聚合物的共混物是不相混的,物理性质很差。历史上,人们一直在追求各种各样的增容策略,包括添加共聚物或乳化剂,或安装互补反应基团,以促进共混过程中嵌段共聚物或接枝共聚物的原位形成。通常,这种反应性共混利用可逆或不可逆的共价键或氢键来生产所需的共聚物,但也有其他选择。在这里,我们认为离子键和静电相关性代表了一种未被充分利用的工具,用于聚合物相容和裁剪材料,应用范围从可持续聚合物合金到有机电子和固体聚合物电解质。对离子相容的理论基础进行了调查,并将其置于现有实验文献和新兴功能高分子材料的背景下。我们总结了静电相互作用如何在塑料废物升级回收中被利用的观点。
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Ionic Compatibilization of Polymers

The small specific entropy of mixing of high molecular weight polymers implies that most blends of dissimilar polymers are immiscible with poor physical properties. Historically, a wide range of compatibilization strategies have been pursued, including the addition of copolymers or emulsifiers or installing complementary reactive groups that can promote the in situ formation of block or graft copolymers during blending operations. Typically, such reactive blending exploits reversible or irreversible covalent or hydrogen bonds to produce the desired copolymer, but there are other options. Here, we argue that ionic bonds and electrostatic correlations represent an underutilized tool for polymer compatibilization and in tailoring materials for applications ranging from sustainable polymer alloys to organic electronics and solid polymer electrolytes. The theoretical basis for ionic compatibilization is surveyed and placed in the context of existing experimental literature and emerging classes of functional polymer materials. We conclude with a perspective on how electrostatic interactions might be exploited in plastic waste upcycling.

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