Investigation of Surfactant AOT Mediated Charging of PS Particles Dispersed in Aqueous Solutions

Abstract

Nano/submicron particles can be activated by surfactants and aggregate at the air-water interface to generate and stabilize foams. Such systems have been applied extensively in the food, medicine, and cosmetic industries. Studying particle charging behavior in a particle/surfactant/water system is a fundamental way to understand the activation of the particle surface. This paper presents an investigation of the charging behavior of polystyrene (PS) particles dispersed in aqueous solutions of the surfactant sodium di-2-ethylhexylsulfosuccinate (AOT). The results showed that zeta potential of PS was related to the AOT concentration with two different concentration regions. Below the critical micelle concentration (CMC), the charging of PS particles was effected by AOT ions; while above the CMC, it came from both AOT ions and AOT micelles. This behavior was different from that observed for PS in aqueous salt solutions. Additionally, the particle concentration and size were found to affect the zeta potential differently in the two AOT concentration regions. By analyzing these results, the charging mechanism of the PS/AOT/water system was revealed to be preferential adsorption. In summary, the study disclosed the internal connection between the PS charging in aqueous AOT solution and the activation of PS particles, as well as their influence to foam formation and stability.