Phase Separation in Symmetric Mixtures of Oppositely Charged Rodlike Polyelectrolytes

被引:20
|
作者
Kumar, Rajeev [1 ]
Audus, Debra [1 ]
Fredrickson, Glenn H. [1 ]
机构
[1] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2010年 / 114卷 / 31期
关键词
DEBYE-HUCKEL THEORY; COMPLEX COACERVATION; THERMODYNAMIC CALCULATIONS; ELECTROSTATIC INTERACTION; LIMITING LAWS; TRANSITIONS; CONDENSATION; MODEL; SALT;
D O I
10.1021/jp101413a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Phase separation in salt-free symmetric mixtures of oppositely charged rodlike polyelectrolytes is studied using quasi-analytical calculations Stability analyses for the isotropic-isotropic and the isotropic-nematic phase transitions in the mixtures are carried out and demonstrate that electrostatic interactions favor nematic ordering Coexistence curves for the symmetric mixtures are also constructed and are used to examine the effects of linear charge density and electrostatic interaction strength on rodlike polyelectrolyte complexation It is found that the counterions are uniformly distributed in the coexisting phases for low electrostatic interaction strengths dictated by the linear charge density of the polyelectrolytes and Bjerrum's length. However, the counterions also partition along with the rodlike polyelectrolytes with an increase in the electrostatic interaction strength. It is shown that the number density of the counterions is higher in the concentrated (or "coacervate") phase than in the dilute (or supernatant) phase In contrast to such rodlike mixtures, flexible polyelectrolyte mixtures can undergo only isotropic isotropic phase separation A comparison of the coexistence curves for weakly charged rodlike mixtures with those of analogous flexible polyelectrolyte mixtures reveals that the electrostatic driving force for the isotropic isotropic phase separation is stronger in the flexible mixtures.
引用
收藏
页码:9956 / 9976
页数:21
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