Experiments of water wicking in 1D silicon-dioxide nanochannels of heights 59 nm, 87 nm, 124 nm and 1015 nm are used to estimate the disjoining pressure of water which was found to be as high as ~1.5 MPa while exponentially decreasing with increasing channel height. Such a relation resulting from curve fitting of experimentally-derived data was implemented and validated in computational fluid dynamics. This methodology integrates experimental nanoscale physics into continuum simulations thus enabling the numerical study of various phenomena where disjoining pressure plays an important role.
Main TextA nanoscale thin liquid film on a surface can have significantly different properties than its bulk form [1]. At such short distances, intermolecular interactions with surface atoms can dominate and define new equilibrium positions/velocities of liquid atoms; as these fundamental parameters are statistically averaged to estimate thermodynamic properties [2], substantial changes in density, pressure, surface tension, viscosity, etc. can occur. Distances at which a surface can affect liquid properties depends on the atomic composition: if either atom is non-polar, the presence of only weak and short-range van der Waal's force limits such changes to <5 nm [3,4]; however, if both atoms are polar, strong and long-range electrostatic forces can alter properties up to tens to hundreds of nanometers from the surface [5][6][7]. The latter scenario often occurs in practical situations involving water on various surfaces.