Adsorption of Binary Mixture of Highly Positively Charged PTMA5M and Partially Negatively Charged PAA onto PSL Particles Studied by Means of Brownian Motion Particle Tracking and Electrophoresis

Abstract

Effects of ionic strength on the adsorption of highly charged polycationic ((2-dimethylamino)ethyl methacrylate) methyl chloride quaternary salt (PTMA5M) individually as well as in a binary mixture with polyanionic acrylic acid (PAA) onto polystyrene sulfate latex (PSL) particles with negative charges were investigated by means of Brownian movement particle tracking and measurement of electrophoretic mobility. In addition, the adsorption mechanism was confirmed by Fourier transform infrared (FT-IR) and energy-dispersive X-ray (EDX) spectroscopic methods. The hydrodynamic thickness of the adsorbed polyelectrolyte layer (δH) and electrophoretic mobility (EPM) of particles as a function of concentration ratios of the two polyelectrolytes were measured to clarify the effect of negatively charged molecules on the structure of the positively charged adsorbed layer at various ionic strengths. Extremely thick δH was confirmed for the case of excess dosage of polycations. The δH decreased more significantly with the addition of PAA than increasing ionic strength. Interestingly, in the presence of PAA, the adsorbed layer thickness increased more at lower ionic strength than at higher ionic strength. In addition, the initial δH decreases remarkably after a time lapse of 1 h. Contrary to the decrease of the δH, almost all EPM either remained unchanged or increased over time depending on the concentration ratio of the two polyelectrolytes. Constant charge density, desorption of polyanions, and then reconformation of the adsorbed polycationic layer are proposed model components.