ABSTRACT
The breakup and coalescence of drops are elementary topological transitions in interfacial flows. The breakup of a drop changes dramatically when polymers are added to the fluid. With the strong elongation of the polymers during the process, long threads connecting the two droplets appear prior to their eventual pinch-off. Here, we demonstrate how elasticity affects drop coalescence, the complement of the much studied drop pinch-off. We reveal the emergence of an elastic singularity, characterized by a diverging interface curvature at the point of coalescence. Intriguingly, while the polymers dictate the spatial features of coalescence, they hardly affect the temporal evolution of the bridge. These results are explained using a novel viscoelastic similarity analysis and are relevant for drops created in biofluids, coating sprays, and inkjet printing.
ABSTRACT
A basic feature of liquid drops is that they can merge upon contact to form a larger drop. In spite of its importance to various applications, drop coalescence on prewetted substrates has received little attention. Here, we experimentally and theoretically reveal the dynamics of drop coalescence on a thick layer of a low viscosity liquid. It is shown that these so-called "liquid lenses" merge by the self-similar vertical growth of a bridge connecting the two lenses. Using a slender analysis, we derive similarity solutions corresponding to the viscous and inertial limits. Excellent agreement is found with the experiments without any adjustable parameters, capturing both the spatial and temporal structures of the flow during coalescence. Finally, we consider the crossover between the two regimes and show that all data of different lens viscosities collapse on a single curve capturing the full range of the coalescence dynamics.
ABSTRACT
Ensembles of interacting drops that slide down an inclined plate show a dramatically different coarsening behavior as compared to drops on a horizontal plate: As drops of different size slide at different velocities, frequent collisions result in fast coalescence. However, above a certain size individual sliding drops are unstable and break up into smaller drops. Therefore, the long-time dynamics of a large drop ensemble is governed by a balance of merging and splitting. We employ a long-wave film height evolution equation and determine the dynamics of the drop size distribution towards a stationary state from direct numerical simulations on large domains. The main features of the distribution are then related to the bifurcation diagram of individual drops obtained by numerical path continuation. The gained knowledge allows us to develop a Smoluchowski-type statistical model for the ensemble dynamics that well compares to full direct simulations.
ABSTRACT
The wetting behavior of a liquid on solid substrates is governed by the nature of the effective interaction between the liquid-gas and the solid-liquid interfaces, which is described by the binding or wetting potential g(h) which is an excess free energy per unit area that depends on the liquid film height h. Given a microscopic theory for the liquid, to determine g(h), one must calculate the free energy for liquid films of any given value of h, i.e., one needs to create and analyze out-of-equilibrium states, since at equilibrium there is a unique value of h, specified by the temperature and chemical potential of the surrounding gas. Here we introduce a Nudged Elastic Band (NEB) approach to calculate g(h) and illustrate the method by applying it in conjunction with a microscopic lattice density functional theory for the liquid. We also show that the NEB results are identical to those obtained with an established method based on using a fictitious additional potential to stabilize the non-equilibrium states. The advantages of the NEB approach are discussed.
