Hydrophobic interactions between polymer surfaces: using polystyrene as a model system

Abstract

The hydrophobic interaction plays a critical role in a wide range of molecular phenomena in numerous biological and engineering systems. Using a Surface Forces Apparatus (SFA) coupled with a top-view optical microscope, we have directly measured and visualized the interactions between two polystyrene surfaces in different electrolyte solutions (i.e., NaCl, CaCl₂, HCl and CH₃COOH). It is evident that the long-range hydrophobic interaction measured is due to bridging of microscopic and sub-microscopic bubbles on polystyrene surfaces. The range of the hydrophobic interaction decreases with increasing the electrolyte concentration for NaCl and CaCl₂, but shows no significant change for HCl and CH₃COOH, which is related to the formation and stability of bubbles on hydrophobic surfaces due to the ion specificity. The range of the hydrophobic interactions was reduced to about 10–20 nm by degassing the aqueous solutions, but gradually recovered when re-exposing the degassed solution to air. Our results indicate that dissolved gasses in solutions play a crucial role in the hydrophobic interactions of polymer surfaces, and support a three-regime hydrophobic interaction model proposed. More interesting, spontaneous cavitation of water between two interacting polystyrene surfaces was directly observed in degassed aqueous solution at a separation of ≤20 nm. The interfacial energy of polystyrene in various aqueous solutions was determined to be γ = 42 ± 5 mJ m⁻², close to the values measured in air. Interesting fracture patterns were also observed associated with the separation of two hydrophobic polymer surfaces in aqueous solutions, but not in air, indicating that hydrophobic force plays an important role in adhesion-induced fracture of polymer surfaces and thin films. Our study provides new insight into the basic hydrophobic interaction mechanism of polymers and biomacromolecules.