Charging of Oxide Nanoparticles in Media of Intermediate Dielectric Constant.

The use of surfactants to charge colloidal particles in solvents of intermediate dielectric constants (5 < ε < 40) is investigated. While particle charging mechanisms in aqueous (ε = 80) and apolar (ε < 5) media are well understood, the interplay of these different charging mechanisms, which can all occur in solvents of intermediate dielectric constants (sometimes referred to as "leaky dielectrics"), remains to be fully explored. Conductometric titrations determining the critical micelle concentration (CMC) of the surfactant (aerosol-OT) confirm the existence of reverse micelles in intermediate dielectrics and show that as the solvent dielectric constant decreases, the CMC decreases as well. Electrophoretic mobility measurements of three oxide particles (SiO2, TiO2, and MgO) highlight various charging mechanisms that arise from particle-solvent, particle-surfactant, and solvent-surfactant interactions in a solvent series of alcohols and ketones. The results show that a combination of donor-acceptor particle-solvent interactions, surfactant ion adsorption, and reverse micelle-mediated acid-base interactions can all charge oxide particles in intermediate dielectrics. Furthermore, the results show that the dielectric constant of the solvent affects the relative magnitudes of each charging mechanism.

Effects of Reverse Micellar Structure on the Particle Charging Capabilities of the Span Surfactant Series.

This paper investigates the effects of reverse micellar core size on the particle charging behavior of a series of acidic surfactants in apolar media. A series of Span surfactants was dissolved in deuterated decane at concentrations above the critical micelle concentration. The structures of the reverse micelles were measured using small-angle neutron scattering. It was determined that as the tail length of the surfactant increased, the size of the polar reverse micellar core decreased. Tritailed surfactants formed reverse micelles with the smallest polar cores, with radii of ∼4 Å. The sizes of the polar cores were correlated with the particle charging behavior of the Span surfactant series, as measured in a previous study. It was found that reverse micelles with intermediate core sizes imparted the largest electrophoretic mobilities to the particles. Reverse micelles with very small cores did not offer a large enough polar environment to favor charge stabilization, while very large polar cores favored disproportionation reactions in the bulk, resulting in increased electrostatic screening.