Abstract: A silver particle suspension obtained by a chemical reduction was used in this work. Monolayers of these particles (average size 28 nm) on mica modified by poly(allylamine hydrochloride) were produced under diffusion-controlled transport. Monolayer coverages, quantitatively determined by atomic force microscopy (AFM) and SEM, was regulated by adjusting the nanoparticle deposition time and the suspension concentration. The zeta potential of the monolayers was determined by streaming potential measurements carried out under in situ (wet) conditions. These measurements performed for various ionic strengths and pH were interpreted in terms of the three-dimensional (3D) electrokinetic model. The stability of silver monolayers was also investigated using streaming potential and the AFM methods. The decrease in the surface coverage of particles as a function of time and ionic strength varied between 10-1 and 10-4 M was investigated. This allowed one to determine the equilibrium adsorption constant Ka and the binding energy of silver particles (energy minima depth). Energy minima depth were calculated that varied between -18 kT for I = 10-1 M and -19 kT for I = 10-4 for pH 5.5 and T = 298 K. Our investigations suggest that the interactions between surface and nanoparticles are controlled by the electrostatic interactions among ion pairs. It was also shown that the in situ electrokinetic measurements are in accordance with those obtained by more tedious ex situ AFM measurements. This confirmed the utility of the streaming potential method for direct kinetic studies of nanoparticle deposition/release processes.
Keywords: Deposition of silver particles; Monolayers of silver particles; Release kinetics of silver nanoparticles; Streaming potential of silver particle monolayers.