Effect of Divalent and Monovalent Salts on Interfacial Dilational Rheology of Sodium Dodecylbenzene Sulfonate Solutions

This study presents the equilibrium surface tension (ST), critical micelle concentration (CMC) and the dilational viscoelasticity of sodium dodecylbenzene sulfonate (SDBS)-adsorbed layers in the presence of NaCl, KCl, LiCl, CaCl2 and MgCl2 at 0.001-0.1 M salt concentration. The ST and surface dilational viscoelasticity were determined using bubble-shape analysis technique. To capture the complete profile of dilational viscoelastic properties of SDBS-adsorbed layers, experiments were conducted within a wide range of SDBS concentrations at a fixed oscillating frequency of 0.01 Hz. Salts were found to lower the ST and induce micellar formation at all concentrations. However, the addition of salts increased dilational viscoelastic modulus only at a certain range of SDBS concentration (below 0.01-0.02 mM SDBS). Above this concentration range, salts decreased dilational viscoelasticity due to the domination of the induced molecular exchange dampening the ST gradient. The dilational viscoelasticity of the salts of interest were in the order CaCl2 > MgCl2 > KCl > NaCl > LiCl. The charge density of ions was found as the corresponding factor for the higher impact of divalent ions compared to monovalent ions, while the impact of monovalent ions was assigned to the degree of matching in water affinities, and thereby the tendency for ion-pairing between SDBS head groups and monovalent ions.

Automated summary

This study investigates the equilibrium surface tension, critical micelle concentration, and dilational viscoelasticity of SDBS-adsorbed layers in the presence of different types of salts. The results show that salts decrease the surface tension and induce micelle formation, and their impact on dilational viscoelasticity depends on the SDBS concentration. The order of dilational viscoelasticity is influenced by the type of salt. The charge density of ions and the matching degree of water affinities are factors affecting the ion effects.