Micellar Solutions of Ionic Surfactants and Their Mixtures with Nonionic Surfactants: Theoretical Modeling vs. Experiment1

Here, we review two recent theoretical models in the field of ionic surfactant micelles and discuss the comparison of their predictions with experimental data. The first approach is based on the analysis of the stepwise thinning (stratification) of liquid films formed from micellar solutions. From the experimental step wise dependence of the film thickness on time, it is possible to determine the micelle aggregation number and charge. The second approach is based on a complete system of equations (a generalized phase separation model), which describes the chemical and mechanical equilibrium of ionic micelles, including the effects of electrostatic and non electrostatic interactions, and counterion binding. The parameters of this model can be determined by fitting a given set of experimental data, for example, the dependence of the critical micel lization concentration on the salt concentration. The model is generalized to mixed solutions of ionic and nonionic surfactants. It quantitatively describes the dependencies of the critical micellization concentration on the composition of the surfactant mixture and on the electrolyte concentration, and predicts the concen trations of the monomers that are in equilibrium with the micelles, as well as the solution’s electrolytic con ductivity; the micelle composition, aggregation number, ionization degree and surface electric potential. These predictions are in very good agreement with experimental data, including data from stratifying films. The model can find applications for the analysis and quantitative interpretation of the properties of various micellar solutions of ionic surfactants and mixed solutions of ionic and nonionic surfactants. DOI: 10.1134/S1061933X14030065