York Structural Biology Laboratory, Department of Chemistry, University of York, Heslington, York YO10 5DD, UK.
Phys Chem Chem Phys. 2021 Apr 14;23(14):8705-8716. doi: 10.1039/d0cp06479c. Epub 2021 Mar 30.
Sudden onset of solubilization is observed widely around or below the critical micelle concentration (CMC) of surfactants. It has also been reported that micellization is induced by the solutes even below CMC and the solubilized solute increases the aggregation number of the surfactant. These observations suggest enhanced cooperativity in micellization upon solubilization. Recently, we have developed a rigorous statistical thermodynamic theory of cooperative solubilization. Its application to hydrotropy revealed the mechanism of cooperative hydrotropy: hydrotrope self-association enhanced by solutes. Here we generalize our previous cooperative solubilization theory to surfactants. We have shown that the well-known experimental observations, such as the reduction of CMC in the presence of the solutes and the increase of aggregation number, are the manifestations of cooperative solubilization. Thus, the surfactant self-association enhanced by a solute is the driving force of cooperativity and a part of a universal cooperative solubilization mechanism common to hydrotropes and surfactants at low concentrations.
表面活性剂在临界胶束浓度(CMC)附近或以下会广泛观察到突然溶解。也有报道称,即使在 CMC 以下,溶质也会诱导胶束化,并且增溶的溶质会增加表面活性剂的聚集数。这些观察结果表明,增溶会增强胶束化的协同性。最近,我们开发了一种严格的协同增溶统计热力学理论。其在助溶作用中的应用揭示了协同助溶的机制:溶质增强了助溶剂的自组装。在这里,我们将之前的协同增溶理论推广到表面活性剂中。我们已经表明,一些常见的实验观察结果,如存在溶质时 CMC 的降低和聚集数的增加,都是协同增溶的表现。因此,溶质增强的表面活性剂自组装是协同性的驱动力,也是低浓度下水增溶和表面活性剂共有的普遍协同增溶机制的一部分。