Evaporation of droplets of surfactant solutions.

The simultaneous spreading and evaporation of droplets of aqueous trisiloxane (superspreader) solutions onto a hydrophobic substrate has been studied both experimentally, using a video-microscopy technique, and theoretically. The experiments have been carried out over a wide range of surfactant concentration, temperature, and relative humidity. Similar to pure liquids, four different stages have been observed: the initial one corresponds to spreading until the contact angle, θ, reaches the value of the static advancing contact angle, θad. Duration of this stage is rather short, and the evaporation during this stage can be neglected. The evaporation is essential during the next three stages. The next stage after the spreading, which is referred to herein as the first stage, takes place at constant perimeter and ends when θ reaches the static receding contact angle, θr. During the next, second stage, the perimeter decreases at constant contact angle θ = θr for surfactant concentration above the critical wetting concentration (CWC). The static receding contact angle decreases during the second stage for concentrations below CWC because the concentration increases due to the evaporation. During the final stage both the perimeter and the contact angle decrease. In what follows, we consider only the longest stages I and II. The developed theory predicts universal curves for the contact angle dependency on time during the first stage, and for the droplet perimeter on time during the second stage. A very good agreement between theory and experimental data has been found for the first stage of evaporation, and for the second stage for concentrations above CWC; however, some deviations were found for concentrations below CWC.

Evaporation kinetics of sessile droplets of aqueous suspensions of inorganic nanoparticles.

Evaporation kinetics of sessile droplets of aqueous suspension of inorganic nanoparticles on solid substrates of various wettabilities is investigated from both experimental and theoretical points of view. Experimental results on evaporation of various kinds of inorganic nanosuspensions on solid surfaces of different hydrophobicities/hydrophilicities are compared with our theoretical predictions of diffusion limited evaporation of sessile droplets in the presence of contact angle hysteresis. The theory describes two main stages of evaporation process: (I) evaporation with a constant radius of the droplet base when the contact angle decreases from static advancing contact angle down to static receding contact angle and (II) evaporation with constant contact angle equal to the static receding contact angle when the radius of the droplet base decreases. Theoretically predicted universal dependences for both evaporation stages are compared with experimental data, and a very good agreement is found.