We study boundary lubrication characteristics of a liquid crystal (LC) monolayer sheared between two crystalline surfaces by nonequilibrium molecular dynamics simulations, using a simplified rigid bead-necklace model of the LC molecules. We consider LC monolayers confined by surfaces with three different atomic structures, subject to different shearing velocities, thus approximating a wide variety of materials and driving conditions. The time dependence of the friction force is studied and correlated with that of the orientational order exhibited by the LC molecules, arising from the competition between the effect of the structure of the confining surfaces and that of the imposed sliding direction. We show that the observed stick-slip events for low shear rates involve order-disorder transitions, and that the LC monolayer no longer has enough time to reorder at high shear rates, resulting in a smooth sliding regime. An irregular stick-slip phase between the regular stick-slip and smooth sliding is observed for intermediate shear rates regardless of the surface structure.

I analyze the fluid-fluid phase separation of nonadditive hard sphere fluid mixture absorbed in random porous media. An equation of state is derived by using the perturbation theory to this complex system with quenched disorders. The results of this theory are in good agreement with those obtained from semi-grand canonical ensemble Monte Carlo simulations. The contact value of the fluid-fluid radial distribution functions of the reference which is the key point of the perturbation process is derived as well, the comparison against Monte Carlo simulations shows that it has an excellent accuracy.