Polyelectrolyte-particle complex formation. Polyelectrolyte linear charge density and ionic concentration effects. Monte Carlo simulations

Abstract

The influence of the linear charge density (LCD) of a polyelectrolyte on its adsorption on an oppositely charged colloidal particle is investigated by Monte Carlo simulations. Adsorption characteristics are studied at different linear charge densities and ionic concentrations and for a given polyelectrolyte/particle size ratio so that particle curvature has full effect. The isolated polyelectrolyte goes through a smooth transition from a collapsed structure to an extended rod-like conformation with increasing the linear charge density in the low ionic concentration regime. In the high ionic concentration regime, the polyelectrolyte is less sensitive to the increase in the linear charge density and adopts a coil conformation. We found that complex formation is promoted by decreasing the ionic concentration and increasing the linear charge density and that large changes in the polymer dimensions are observed at the adsorption–desorption limit. By adjusting the linear charge density and ionic strength, we demonstrate that the adsorption–desorption limit corresponds to a sharp transition from non-adsorbed to adsorbed conformations and that the mean adsorption energy per monomer has to be less than –0.4 kT to achieve adsorption. We calculated that the linear charge density at the adsorption–desorption limit is related to the Debye-Huckel length according to LCDcrit ~κ 2. At small values of the linear charge density and low ionic strength (no adsorption is observed at high ionic strength), a large amount of monomers are present in loops and tails. By increasing LCD, the amount of monomers in trains reaches a maximum value and the polyelectrolyte adopt flat conformation at the surface of the particle.