In this paper, we experimentally studied the evaporative behavior of the nanofluid droplets (fluid containing metal nanoparticles) on nanoporous superhydrophobic surfaces. Uniformly dispersed in water, gold chloride (AuCl3) nanoparticles of varying sizes (10–250 nm) and concentrations (0.001–0.1% wt) were tested as nanofluids. Porous anodized aluminum oxide (AAO) with a pore size of 250 nm was tested as a nanoporous superhydrophobic surface, coated by a self assembled monolayer (SAM). During the evaporation in a room temperature and pressure, the evaporation kinetics (e.g., contact angle, contact diameter, and volume) of the nanofluid droplets was measured over time by using a goniometer. In the beginning, the initial droplet contact angles were significantly affected by the nanoparticle sizes and concentrations such that as the concentration increased, the initial contact angle decreased, which was more pronounced at larger particle sizes. During evaporation, despite the different particle sizes and concentrations, there were two distinct stages shown, especially for the change of contact angles, i.e., gradual decrease in the beginning, followed by rapid decrease in the end. No remarkable wetting transition from de-wetting (Cassie) to wetting (Wenzel) state was shown during the evaporation. Evaporation rate was influenced by nanoparticles such that it was significantly mitigated with the nanofluid droplet of the highest concentration (0.1% wt). The scanning electron microscope (SEM) images show that the ring-like dry-out pattern forms after the evaporation of nanofluids with lower concentrations (0.001%, 0.01% wt), whereas the one with higher concentrations (0.1%wt) forms a uniformly distributed pattern. These results demonstrate that nanoparticle sizes and concentrations make significant effects on interfacial phenomena in droplet evaporation on nanostructured surfaces, which will impact many engineering applications and system designs based on droplets such as microfluidics and heat transfer.

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