Two Methods Based on Integral Equation Approaches in Analyzing Polyelectrolyte Solutions: Macrophase Separation

被引:0
|
作者
Cho, Junhan [1 ]
机构
[1] Dankook Univ, Dept Polymer Sci & Engn, 152 Jukjeon ro,Gyeonggi do, Yongin 16890, South Korea
关键词
polyelectrolyte solutions; molecular equation of state; charged hard spheres; connectivity; volumetric properties; complex coacervation; critical behavior; DIRECTIONAL ATTRACTIVE FORCES; THERMODYNAMIC PERTURBATION-THEORY; WEAKLY CHARGED POLYELECTROLYTES; MEAN SPHERICAL APPROXIMATION; RESTRICTED PRIMITIVE MODEL; RANDOM-PHASE-APPROXIMATION; CHEMICAL ASSOCIATION; IONIC FLUIDS; OF-STATE; MICROPHASE SEPARATION;
D O I
10.3390/polym16162255
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
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.
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页数:26
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