Boundary Slip of Superoleophilic, Oleophobic, and Superoleophobic Surfaces Immersed in Deionized Water, Hexadecane, and Ethylene Glycol

Abstract

The boundary slip condition is an important property, and its existence can reduce fluid drag in micro/nanofluidic systems. The boundary slip on various surfaces immersed in water and various electrolytes has been widely studied. For the surfaces immersed in oil, the boundary slip on superoleophilic and oleophilic surfaces has been studied, but there is no data on oleophobic and superoleophobic surfaces. In this paper, experiments are carried out to study electrostatic force and boundary slip on superoleophilic, oleophobic, and superoleophobic surfaces immersed in deionized (DI) water, hexadecane, and ethylene glycol. In addition, the surface charge density of the samples immersed in DI water is quantified. Results show that the electrostatic force and the absolute value of the surface charge density of an octadecyltrichlorosilane surface are larger than that of a polystyrene surface, and the electrostatic force and the absolute value of surface charge density of a superoleophilic surface are larger than that of oleophobic and superoleophobic surfaces. For the same liquid, the larger contact angle leads to a larger slip length at the solid-liquid interface. For the same surface, the larger liquid viscosity leads to a larger slip length. The relevant mechanisms are discussed in this paper.