Development of the modern theory of polymeric complex coacervation
Oppositely charged polymers can undergo the process of complex coacervation, which refers to a liquid–liquid phase separation driven by electrostatic attraction. These materials have demonstrated considerable promise as the basis for complex, self-assembled materials. In this review, we provide a br...
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| Published in | Advances in colloid and interface science Vol. 239; pp. 2 - 16 |
|---|---|
| Main Author | |
| Format | Journal Article |
| Language | English |
| Published |
Netherlands
Elsevier B.V
01.01.2017
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| Subjects | |
| Online Access | Get full text |
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| Abstract | Oppositely charged polymers can undergo the process of complex coacervation, which refers to a liquid–liquid phase separation driven by electrostatic attraction. These materials have demonstrated considerable promise as the basis for complex, self-assembled materials. In this review, we provide a broad overview of the theoretical tools used to understand the physical properties of polymeric coacervates. In particular, we discuss historic theories (Voorn–Overbeek, Random Phase Approximation), and then describe recent developments in the field (Field Theoretic, Counterion Release, Molecular Simulation, and Polymer Reference Interaction Site Model methods). We provide context for these methods, and map out the patchwork of theoretical models that are used to describe a diverse array of coacervate systems. We use this review of the literature to clarify a number of important theoretical challenges remaining in our physical understanding of complex coacervation.
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•Polymeric complex coacervates are an important class of electrostatically-driven polymer materials.•Historic theories are often invoked to describe polymer coacervates, however do not capture important physical behaviors•A broad palette of new theoretical methods capture many relevant physical effects in coacervates, albeit with limitations•New methods are needed to describe or predict all the physical effects in emerging coacervate-driven self-assembly |
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| AbstractList | Oppositely charged polymers can undergo the process of complex coacervation, which refers to a liquid–liquid phase separation driven by electrostatic attraction. These materials have demonstrated considerable promise as the basis for complex, self-assembled materials. In this review, we provide a broad overview of the theoretical tools used to understand the physical properties of polymeric coacervates. In particular, we discuss historic theories (Voorn–Overbeek, Random Phase Approximation), and then describe recent developments in the field (Field Theoretic, Counterion Release, Molecular Simulation, and Polymer Reference Interaction Site Model methods). We provide context for these methods, and map out the patchwork of theoretical models that are used to describe a diverse array of coacervate systems. We use this review of the literature to clarify a number of important theoretical challenges remaining in our physical understanding of complex coacervation.
[Display omitted]
•Polymeric complex coacervates are an important class of electrostatically-driven polymer materials.•Historic theories are often invoked to describe polymer coacervates, however do not capture important physical behaviors•A broad palette of new theoretical methods capture many relevant physical effects in coacervates, albeit with limitations•New methods are needed to describe or predict all the physical effects in emerging coacervate-driven self-assembly Oppositely charged polymers can undergo the process of complex coacervation, which refers to a liquid-liquid phase separation driven by electrostatic attraction. These materials have demonstrated considerable promise as the basis for complex, self-assembled materials. In this review, we provide a broad overview of the theoretical tools used to understand the physical properties of polymeric coacervates. In particular, we discuss historic theories (Voorn-Overbeek, Random Phase Approximation), and then describe recent developments in the field (Field Theoretic, Counterion Release, Molecular Simulation, and Polymer Reference Interaction Site Model methods). We provide context for these methods, and map out the patchwork of theoretical models that are used to describe a diverse array of coacervate systems. We use this review of the literature to clarify a number of important theoretical challenges remaining in our physical understanding of complex coacervation. |
| Author | Sing, Charles E. |
| Author_xml | – sequence: 1 givenname: Charles E. surname: Sing fullname: Sing, Charles E. email: cesing@illinois.edu organization: Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 600 S. Mathews Ave. Urbana IL, 61801, United States |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27161661$$D View this record in MEDLINE/PubMed |
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| Keywords | Polyelectrolytes Complexation Coacervation Electrostatics Polymer physics |
| Language | English |
| License | Copyright © 2016 Elsevier B.V. All rights reserved. |
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| PublicationTitle | Advances in colloid and interface science |
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| Snippet | Oppositely charged polymers can undergo the process of complex coacervation, which refers to a liquid–liquid phase separation driven by electrostatic... Oppositely charged polymers can undergo the process of complex coacervation, which refers to a liquid-liquid phase separation driven by electrostatic... |
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| SubjectTerms | Coacervation Complexation Electrostatics Polyelectrolytes Polymer physics |
| Title | Development of the modern theory of polymeric complex coacervation |
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