Evaporation of sessile droplets of aqueous solutions in pure vapor environment

We develop a lubrication-type model of an axisymmetric evaporating sessile liquid droplet in contact with pure vapor. The liquid is a symmetric electrolyte, a two-component expression for disjoining pressure accounts for both unbalanced London–van der Waals interactions and repulsion of electrical double layers formed near liquid–solid and liquid–vapor interfaces. We consider nonequilibirum effects during evaporation from the liquid surface and an increase of solute concentration as a result of solvent evaporation. The presence of solute leads to reduction of the evaporation rates at initial stages of evolution but the trend is reversed at the later stages, resulting in lower lifetimes of evaporating droplets. The apparent contact angle, defined by the maximum interfacial slope, tends to be lower when the electrostatic effects are more significant. Evaporative cooling is also considered in the framework that accounts for heat conduction in the substrate and shown to increase the droplet lifetime. Extensions of the model describing the more general case of evaporating sessile droplets of complex fluids are discussed.