Abstract
Adsolubilization, solubilization of organic compounds into adsorbed surfactant aggregates, has attracted much attention in the past few years. It is being explored for a variety of new commercial applications including the formation of engineered surfaces, pharmaceutical applications, and nanotechnology. Adsolubilization is strongly influenced by the amount of adsorbed surfactant, which in turn depends upon pH, ionic strength, and surfactant type and concentration. In this study, the adsorption of a cationic surfactant, cetyltrimethylammonium bromide (CTAB) on precipitated silica and the adsolubilization of organic solutes (toluene and acetophenone) into the adsorbed surfactant aggregates were examined as a function of surfactant adsorption at two pH values (5 and 8). Three levels of surfactant adsorption, corresponding to equilibrium concentration low in region II, high in region II, and low in region III of the adsorption isotherm, and the adsolubilization of toluene and acetophenone were investigated both in single- and mixed-solute systems. The results showed that the adsorption of CTAB depended strongly on pH and for each pH the adsolubilization increased with increasing surface adsorption. However, the adsolubilization behaviors of the adsorbed CTAB aggregates in different adsorption regions were quite distinct, suggesting that the structural arrangement of the surfactant aggregates may play an important part in addition to the amount of adsorbed surfactant. This phenomenon was more noticeable at low surfactant adsorption than at higher surface adsorption. In mixed-solute systems, the presence of acetophenone had little effect on the toluene adsolubilization. In contrast, a synergetic effect was observed in the adsolubilization of acetophenone in the presence of toluene.
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