Effects of surface wettability on contact line motion in liquid-liquid displacement

Abstract

The behaviors of oil-water-solid interfaces are of basic and applied importance for many fields, such as energy, geochemistry, and biomedical sciences, yet molecular mechanisms are still poorly known. In particular, the traditional adsorption-desorption mechanism based on a single compound does not work to describe the contact line for liquid-liquid-solid systems where the two liquids have similar interactions with the solid surface. Here, we present a series of experiments of water spreading in alkanes, i.e., n-decane, n-dodecane, and n-hexadecane, under various surface wettabilities. The contact line motion is captured by the high-speed camera, allowing us to analyze the friction coefficient, displacement distance and frequency, and activation free energy during the contact line motion via the molecular kinetic theory. We further develop a friction model of contact line motion in liquid-liquid-solid systems by establishing the activation free energy of liquid-liquid-solid systems as a function of the activation free energies of separate one-liquid systems. Results show that the contact line friction coefficients increase with the increasing hydrophobicity (e.g., for n-decane, the coefficient changes from 0.3072 to 2.1967 Pa·s), explained by the increase in the displacement distance and sharp decrease in the displacement frequency of the molecules. Additionally, we find a non-monotonic dependence of the contribution of the surface part to the activation free energy on the wettability, with a maximum percentage of 70%-80% at the intermediate wettability, where the reduced collisions of liquid molecules weaken the molecular adsorption/desorption process. Finally, we find that the correlation coefficient n in our model is affected by the surface wettability, with a maximum at the intermediate wettability, showing a good prediction of the results in the literature. The reason can be attributed to the non-monotonic effects of wettability on the surface part of the activation free energy in two-liquid systems.