凝聚
聚电解质
粘弹性
氢键
分子间力
相(物质)
聚合物
化学工程
离子强度
微观结构
壳聚糖
高分子化学
静电学
化学
材料科学
离子键合
化学物理
复合材料
有机化学
色谱法
物理化学
分子
水溶液
离子
工程类
作者
Julien Es Sayed,Clément Caïto,Abinaya Arunachalam,Armin Amirsadeghi,Larissa van Westerveld,D. Maret,Roshan Akdar Mohamed Yunus,Eleonora Calicchia,Olivia Dittberner,Giuseppe Portale,Daniele Parisi,Marleen Kamperman
出处
期刊:Macromolecules
[American Chemical Society]
日期:2023-07-18
卷期号:56 (15): 5891-5904
被引量:17
标识
DOI:10.1021/acs.macromol.3c00269
摘要
Complex coacervates make up a class of versatile materials formed as a result of the electrostatic associations between oppositely charged polyelectrolytes. It is well-known that the viscoelastic properties of these materials can be easily altered with the ionic strength of the medium, resulting in a range of materials from free-flowing liquids to gel-like solids. However, in addition to electrostatics, several other noncovalent interactions could influence the formation of the coacervate phase depending on the chemical nature of the polymers involved. Here, the importance of intermolecular hydrogen bonds on the phase behavior, microstructure, and viscoelasticity of hyaluronic acid (HA)-chitosan (CHI) complex coacervates is revealed. The density of intermolecular hydrogen bonds between CHI units increases with increasing pH of coacervation, which results in dynamically arrested regions within the complex coacervate, leading to elastic gel-like behavior. This pH-dependent behavior may be very relevant for the controlled solidification of complex coacervates and thus for polyelectrolyte material design.
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