Flow-induced surface crystallization of granular particles in cylindrical confinement

An interesting phenomenon that a layer of crystallized shell formed at the container wall during an orifice flow in a cylinder is observed experimentally and is investigated in DEM simulation. Different from shear or vibration driven granular crystallization, our simulation shows during the flow the shell layer is formed spontaneously from stagnant zone at the base and grows at a constant rate to the top with no external drive. Roughness of the shell surface is defined as a standard deviation of the surface height and its development is found to disobey existed growth models. The growth rate of the shell is found linearly proportional to the flow rate. This shell is static and served as a rough wall in an orifice flow with frictionless sidewall, which changes the flow profiles and its stress properties, and in turn guarantees a constant flow rate.

Entropy-Driven Heterogeneous Crystallization of Hard-Sphere Chains under Unidimensional Confinement

We investigate, through Monte Carlo simulations, the heterogeneous crystallization of linear chains of tangent hard spheres under confinement in one dimension. Confinement is realized through flat, impenetrable, and parallel walls. A wide range of systems is studied with respect to their average chain lengths (N = 12 to 100) and packing densities (ϕ = 0.50 to 0.61). The local structure is quantified through the Characteristic Crystallographic Element (CCE) norm descriptor. Here, we split the phenomenon into the bulk crystallization, far from the walls, and the projected surface crystallization in layers adjacent to the confining surfaces. Once a critical volume fraction is met, the chains show a phase transition, starting from regions near the hard walls. The established crystal morphologies consist of alternating hexagonal close-packed or face-centered cubic layers with a stacking direction perpendicular to the confining walls. Crystal layer perfection is observed with an increasing concentration. As in the case of the unconstrained phase transition of athermal polymers at high densities, crystal nucleation and growth compete with the formation of sites of a fivefold local symmetry. While surface crystallites show perfection with a predominantly triangular character, the morphologies of square crystals or of a mixed type are also formed. The simulation results show that the rate of perfection of the surface crystallization is not significantly faster than that of the bulk crystallization.