Adv Colloid Interface Sci. 2010 Apr 22;156(1-2):70-82. doi: 10.1016/j.cis.2010.02.009. Epub 2010 Feb 25.
The stability of mixed micelles in general has been extensively studied by the molecular thermodynamic approaches as well as by the phenomenological or thermodynamic approaches. In this article, phenomenological approaches in the thermodynamics of charged mixed micelles, mostly on ionic/nonionic mixed micelles, are reviewed. The electrostatic interaction constitutes a main contribution to the excess free energy per monomer (in kT unit) g(ex) in the case of ionic/nonionic mixed micelles and the corresponding contribution is generally negative, known as the electric synergism. The origin of the electric synergism is shown to reside in positive curvatures of g(ex,el) (the electric part of g(ex)) when plotted against the mole fraction of the ionic species x. Two types of the micellar Gibbs-Duhem (MGD) relations with (type 1) or without (type 2) the contribution from counterions are discussed to clarify various confusions found in the literature. Effects of varying ionic strengths with the micelle composition in the case of charged mixed micelles without any supporting electrolyte are discussed and a relevant way to correct for the effects is proposed. For ionic/nonionic mixed micelles, the regular solution model (RSM) and some two-parameter models to overcome the limitations inherent to the RSM are discussed. For mixed micelles subject to type 2 MGD relation, hydrogen ion titrations could provide g(el) experimentally just as in the case of linear polyelectrolytes and for those micelles subject to RSM, the titration curve becomes a straight line. Useful information is presented originating from the thermodynamic analysis on the difference of the intrinsic proton dissociation constants between the micelle and the monomer. An analytical expression of the dependence of the degree of counterion binding on x is discussed in comparison with the molecular thermodynamic results. The Corrin-Harkins relation is compared with the degree of counterion binding for ionic/nonionic mixed micelles. Mixed micelles in the concentration range higher than the critical micelle concentration (cmc) are discussed for three cases, the general method of Funasaki-Hada, the ideal mixing case, and the RSM.
混合胶束的稳定性已被分子热力学方法以及唯象学或热力学方法广泛研究。本文综述了带电混合胶束热力学中的唯象学方法,主要是离子/非离子混合胶束。在离子/非离子混合胶束的情况下,静电相互作用构成了每个单体过剩自由能(以 kT 为单位)g(ex)的主要贡献,并且该贡献通常为负,称为电协同作用。电协同作用的起源表明,当以离子物种的摩尔分数 x 为横坐标绘制 g(ex,el)(g(ex)的电部分)时,它具有正曲率。讨论了两种类型的胶束吉布斯-杜恒(MGD)关系,一种带有(类型 1)或不带有(类型 2)抗衡离子的贡献,以澄清文献中发现的各种混淆。在没有任何支持电解质的带电混合胶束中,讨论了随着胶束组成变化的离子强度的影响,并提出了一种校正这种影响的相关方法。对于离子/非离子混合胶束,讨论了正则溶液模型(RSM)和一些克服 RSM 固有局限性的双参数模型。对于受类型 2 MGD 关系支配的混合胶束,氢离子滴定可以像在线性聚电解质的情况下一样从实验上提供 g(el),并且对于那些受 RSM 支配的胶束,滴定曲线成为直线。从热力学分析中呈现出与胶束和单体之间的固有质子离解常数差异有关的有用信息。讨论了与分子热力学结果相比,依赖于 x 的抗衡离子结合度的解析表达式。将 Corrin-Harkins 关系与离子/非离子混合胶束的抗衡离子结合度进行了比较。讨论了高于临界胶束浓度(cmc)的三个浓度范围内的混合胶束,分别为 Funasaki-Hada 的通用方法、理想混合情况和 RSM。