聚电解质
化学
离子
化学物理
静电学
水溶液
分子动力学
计算化学
聚合物
物理化学
有机化学
作者
Alec Glisman,Sriteja Mantha,Decai Yu,Eric P. Wasserman,Scott A. Backer,Zhen‐Gang Wang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2024-02-19
卷期号:57 (5): 1941-1949
被引量:4
标识
DOI:10.1021/acs.macromol.3c02437
摘要
Polyelectrolytes are commonly used to chelate multivalent ions in aqueous solutions, playing a critical role in water softening and the prevention of mineralization. At sufficient ionic strength, ion-mediated polyelectrolyte–polyelectrolyte interactions can precipitate polyelectrolyte–ion complexes, a phenomenon known as "like-charge attraction". While the significant influence of small ions on polyelectrolyte solution phase behavior is recognized, the precise molecular mechanisms driving the counterintuitive phenomenon remain largely elusive. In this study, we employ all-atom molecular dynamics simulations to investigate the molecular mechanism of like-charge attraction between two poly(acrylic acid) (PAA) chains in solution. We find that moderate quantities of Ca2+ ions induce attraction between PAA chains, facilitated by the formation of PAA–Ca2+–PAA bridges and a significant increase in the coordination of Ca2+ ions by the PAA chains. At high Ca2+ number densities, ion bridges are disfavored due to electrostatic screening, yet the chains are still attracted to each other due to solvent-mediated interactions between the chains and their chelated ions. The insights gleaned from this study not only enrich our understanding of the intricate mechanism of like-charge attraction between polyanions in solution but also illuminate the influence of multivalent ions on polyelectrolyte interactions.
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