Quantifying the Influence of Electrolytes on the Kinetics of Spontaneous Emulsification

Abstract

This study quantifies the influence of electrolytes on the kinetics of the spontaneous emulsification phenomenon (SEP) of heavy hydrocarbons in a nonionic surfactant solution. The rate of emulsifying hexadecane in Triton X-100, with the presence of sodium chloride and potassium chloride, has been measured using a technique of monitoring single oil droplet photography. The emulsion droplet size produced in the process was measured under the same conditions by using dynamic light scattering. The data obtained from the two experiments were employed to investigate the mass transfer coefficient of the surfactant molecules through the intermediate layer formed between hexadecane and the surfactant solution. It was found that the electrolytes in an aqueous solution increase the surfactant diffusion rate through the intermediate layer and reduce the emulsion droplet size. As a result, both electrolytes reduce the rate of spontaneous emulsification, with potassium chloride having a more substantial reduction. A model was developed to quantify the influence of electrolytes on the kinetics of the SEP. The data and modeling results verify the influence of ions on the kinetics of spontaneous emulsification. The results provide a significant foundation for predicting the solubilization of heavy hydrocarbons in an electrolyte solution.