Stranski Laboratorium für Physikalische Chemie und Theoretische Chemie, Institut für Chemie, Technische Universität Berlin, Strasse des 17. Juni 124, Sekr. TC7, D-10623 Berlin, Germany.
Soft Matter. 2017 Jul 26;13(29):4988-4996. doi: 10.1039/c7sm00747g.
The formation of water insoluble polyelectrolyte/surfactant complexes (PESCs) upon mixing two homogeneous polycation/anionic surfactant and polycation/nonionic surfactant solutions is reported here. This phase separation is unexpected and differs markedly from the commonly observed enhanced solubility of colloidal systems in mixed surfactant systems. The study was performed on mixtures of the cationic biopolysaccharide chitosan (poly d-glucosamine) and mixed micelles composed of an ethoxylated fatty alcohol and its carboxylic acid terminated equivalent. The thermodynamics of mixing was probed via isothermal titration calorimetry (ITC), while the structural characterisation was conducted by means of light and neutron scattering (SANS). The results show that the substitution of a weakly anionic surfactant with its nonionic equivalent has profound effects on the interactions at very different length scales. The dilution of the ionic headgroups allows for a more efficient interaction between micelles and polymer chains, and results in an elongation of the mixed micelles which reduces the bending cost of the semi-rigid chitosan and introduces an additional attractive potential of entropic origin. In this work, as a result of a comprehensive thermodynamic and structural analysis, we demonstrate how the subtle interplay of different forces leads to such an unexpected behaviour, where the addition of a nonionic surfactant causes the phase separation of electrostatic complexes.
本文报道了在混合两种均相聚阳离子/阴离子表面活性剂和聚阳离子/非离子表面活性剂溶液时,水不溶性聚电解质/表面活性剂复合物(PESCs)的形成。这种相分离是出乎意料的,与通常观察到的胶体系统在混合表面活性剂系统中增强的溶解度明显不同。该研究是在阳离子多糖壳聚糖(聚葡萄糖胺)与由乙氧基化脂肪醇及其羧酸端等效物组成的混合胶束的混合物上进行的。通过等温滴定微量热法(ITC)探测混合的热力学,通过光和中子散射(SANS)进行结构表征。结果表明,用其非离子等价物取代弱阴离子表面活性剂对非常不同长度尺度上的相互作用具有深远的影响。离子头基的稀释允许胶束和聚合物链之间更有效地相互作用,导致混合胶束的伸长,从而降低半刚性壳聚糖的弯曲成本,并引入额外的熵起源的吸引力势能。在这项工作中,由于全面的热力学和结构分析,我们展示了不同力的微妙相互作用如何导致这种出乎意料的行为,其中非离子表面活性剂的添加导致静电复合物的相分离。