Experimental Studies on the Adsorption of Two Surfactants on Solid−Aqueous Interfaces: Adsorption Isotherms and Kinetics

Abstract

A quartz crystal microbalance with dissipation (QCM-D) was used to measure the adsorption from aqueous solutions of CTAB (cationic) and C(12)E(6) (nonionic) surfactants on gold and silica surfaces. QCM-D allows for the determination of adsorption isotherms and also the monitoring of the dynamics of adsorption in real time. By considering the atomic-scale roughness of the solid surfaces and the surface area per head group at the air/water interface, our experiments indicate that at bulk concentrations above the critical micelle concentration adsorbed C(12)E(6) forms a monolayer-like structure on both surfaces and CTAB yields a bilayer-like structure. Although our measurements do not allow us to discriminate between the morphology of the aggregates (i.e., between flat monolayers, hemicylinders, or hemispheres in the case of C(12)E(6) and between flat bilayers, cylinders, or spheres in the case of CTAB), these results are particularly significant when compared to recent QCM-D data reported by Macakova et al. (Macakova, L.; Blomberg, E.; Claesson, P. M. Langmuir 2007, 23, 12436). These authors reported that QCM-D overestimates the amount of CTAB adsorbed on silica by as much as 30-40% as a result of entrapped water. Our analysis suggests that the effect of entrapped solvent is not as important as previously assumed and, in fact, QCM-D may not overestimate the amount of CTAB adsorbed when roughness is considered. Results for the kinetics of adsorption suggest that the aggregate structure as well as whether micelles are present may influence the adsorption mechanism. We discuss our results in the perspective of molecular theories for both the equilibrium and kinetics of surfactant adsorption.