Molecular explanation for why talc surfaces can be both hydrophilic and hydrophobic

Benjamin Rotenberg (1) , Amish J. Patel (2) , David Chandler (3)

1 PECSA - Physicochimie des Electrolytes, Colloïdes et Sciences Analytiques
2 RPI - Rensselaer Polytechnic Institute
3 LBNL - Lawrence Berkeley National Laboratory [Berkeley]

While individual water molecules adsorb strongly on a talc surface (hydrophilic behavior), a droplet of water beads up on the same surface (hydrophobic behavior). To rationalize this dichotomy, we investigate the influence of the microscopic structure of the surface and the strength of adhesive (surface-water) interactions on surface hydrophobicity. We show that at low relative humidity, the competition between adhesion and the favorable entropy of being in the vapor phase determines the surface coverage. However, at saturation, it is the competition between adhesion and cohesion (water-water interactions) that determines surface hydrophobicity. The adhesive interactions in talc are strong enough to overcome the unfavorable entropy, and water adsorbs strongly on talc surfaces. However, they are too weak to overcome the cohesive interactions, and water thus beads up on talc surfaces. Surprisingly, even (talc-like) surfaces that are highly adhesive, do not fully wet at saturation. Instead, a water droplet forms on top of a strongly adsorbed monolayer of water. Our results imply that the interior of hydrophobic zeolites suspended in water may contain adsorbed water molecules at pressures much smaller than the intrusion pressure.

Domaines: Chimie-Physique [physics.chem-ph]

Benjamin Rotenberg, Amish J. Patel, David Chandler. Molecular explanation for why talc surfaces can be both hydrophilic and hydrophobic. 2018. ⟨hal-01897604⟩