Cho Junhan
Department of Polymer Science & Engineering, Dankook University, 152 Jukjeon-ro, Suji-gu, Yongin 16890, Gyeonggi-do, Republic of Korea.
Polymers (Basel). 2024 Aug 8;16(16):2255. doi: 10.3390/polym16162255.
To understand the phase behaviors of polyelectrolyte solutions, we provide two analytical methods to formulate a molecular equation of state for a system of fully charged polyanions (PAs) and polycations (PCs) in a monomeric neutral component, based on integral equation theories. The mixture is treated in a primitive and restricted manner. The first method utilizes Blum's approach to charged hard spheres, incorporating the chain connectivity contribution by charged spheres via Stell's cavity function method. The second method employs Wertheim's multi-density Ornstein-Zernike treatment of charged hard spheres with Baxter's adhesive potential. The pressures derived from these methods are compared to available molecular dynamics simulations data for a solution of PAs and monomeric counterions as a limiting case. Two-phase equilibrium for the system is calculated using both methods to evaluate the relative strength of phase segregation that leads to complex coacervation. Additionally, the scaling exponents for a selected solution near its critical point are examined.
为了理解聚电解质溶液的相行为,我们基于积分方程理论提供了两种分析方法,用于推导由完全带电的聚阴离子(PAs)和聚阳离子(PCs)以及单体中性组分组成的体系的分子状态方程。该混合物被采用原始且受限的方式处理。第一种方法利用布卢姆处理带电硬球的方法,通过斯泰尔的腔函数法将带电球体的链连接贡献纳入其中。第二种方法采用韦特海姆对带电硬球的多密度奥恩斯坦 - 泽尔尼克处理方法以及巴克斯特的粘附势。将这些方法得出的压力与作为极限情况的聚阴离子和单体抗衡离子溶液的现有分子动力学模拟数据进行比较。使用这两种方法计算体系的两相平衡,以评估导致复合凝聚的相分离相对强度。此外,还研究了选定溶液在其临界点附近的标度指数。