Phase Behavior of Polyelectrolyte-Surfactant Complexes at Planar Surfaces

TL;DR

This study theoretically explores the phase diagram of charged surfactant monolayers interacting with polyelectrolyte solutions, revealing how electrostatic and chemical interactions influence surface phase behavior and critical temperature shifts.

Contribution

It introduces a comprehensive theoretical model analyzing the combined effects of electrostatic and short-range interactions on surfactant-polyelectrolyte systems, including salt effects.

Findings

Polyelectrolyte depletion occurs with short-range repulsion.

Electrostatic attraction shifts the surfactant critical temperature upward.

Salt increases critical temperature for attractive surfaces.

Abstract

We investigate theoretically the phase diagram of an insoluble charged surfactant monolayer in contact with a semi-dilute polyelectrolyte solution (of opposite charge). The polyelectrolytes are assumed to have long-range and attractive (electrostatic) interaction with the surfactant molecules. In addition, we introduce a short-range (chemical) interaction which is either attractive or repulsive. The surfactant monolayer can have a lateral phase separation between dilute and condensed phases. Three different regimes of the coupled system are investigated depending on system parameters. A regime where the polyelectrolyte is depleted due to short range repulsion from the surface, and two adsorption regimes, one being dominated by electrostatics, whereas the other by short range chemical attraction (similar to neutral polymers). When the polyelectrolyte is more attracted (or at least less repelled) by the surfactant molecules as compared with the bare water/air interface, it will shift upwards the surfactant critical temperature. For repulsive short-range interactions the effect is opposite. Finally, the addition of salt to the solution is found to increase the critical temperature for attractive surfaces, but does not show any significant effect for repulsive surfaces.