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Ionic Compatibilization of Polymers
[Image: see text] 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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576261/ https://www.ncbi.nlm.nih.gov/pubmed/36267546 http://dx.doi.org/10.1021/acspolymersau.2c00026 |
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author | Fredrickson, Glenn H. Xie, Shuyi Edmund, Jerrick Le, My Linh Sun, Dan Grzetic, Douglas J. Vigil, Daniel L. Delaney, Kris T. Chabinyc, Michael L. Segalman, Rachel A. |
author_facet | Fredrickson, Glenn H. Xie, Shuyi Edmund, Jerrick Le, My Linh Sun, Dan Grzetic, Douglas J. Vigil, Daniel L. Delaney, Kris T. Chabinyc, Michael L. Segalman, Rachel A. |
author_sort | Fredrickson, Glenn H. |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-9576261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95762612022-10-18 Ionic Compatibilization of Polymers Fredrickson, Glenn H. Xie, Shuyi Edmund, Jerrick Le, My Linh Sun, Dan Grzetic, Douglas J. Vigil, Daniel L. Delaney, Kris T. Chabinyc, Michael L. Segalman, Rachel A. ACS Polym Au [Image: see text] 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. American Chemical Society 2022-07-22 /pmc/articles/PMC9576261/ /pubmed/36267546 http://dx.doi.org/10.1021/acspolymersau.2c00026 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Fredrickson, Glenn H. Xie, Shuyi Edmund, Jerrick Le, My Linh Sun, Dan Grzetic, Douglas J. Vigil, Daniel L. Delaney, Kris T. Chabinyc, Michael L. Segalman, Rachel A. Ionic Compatibilization of Polymers |
title | Ionic Compatibilization
of Polymers |
title_full | Ionic Compatibilization
of Polymers |
title_fullStr | Ionic Compatibilization
of Polymers |
title_full_unstemmed | Ionic Compatibilization
of Polymers |
title_short | Ionic Compatibilization
of Polymers |
title_sort | ionic compatibilization
of polymers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576261/ https://www.ncbi.nlm.nih.gov/pubmed/36267546 http://dx.doi.org/10.1021/acspolymersau.2c00026 |
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