Impact of surface viscosity on the stability of a droplet translating through a stagnant fluid

This study examines the impact of interfacial viscosity on the stability of an initially deformed droplet translating through an unbounded quiescent fluid. The boundary-integral formulation is employed to investigate the time evolution of a droplet in the Stokes flow limit. The droplet interface is modelled using the Boussinesq–Scriven constitutive relationship having surface shear viscosity $\eta _\mu$ and surface dilatational viscosity $\eta _\kappa$ . We observe that, below a critical value of the capillary number, $Ca_C$ , the initially perturbed droplet reverts to its spherical shape. Above $Ca_C$ , the translating droplet deforms continuously, growing a tail at the rear end for initial prolate perturbations and a cavity for initial oblate perturbations. We find that surface shear viscosity inhibits the tail/cavity growth at the droplet's rear end and increases the $Ca_C$ compared with a clean droplet. In contrast, surface dilatational viscosity increases tail/cavity growth and lowers $Ca_C$ compared with a clean droplet. Surprisingly, both shear and dilatational surface viscosity appear to delay the time at which pinch off occurs, and hence satellite droplets form. Lastly, we explore the combined influence of surface viscosity and surfactant transport on droplet stability by assuming a linear dependence of surface tension on surfactant concentration and exponential dependence of interfacial viscosities on the surface pressure. We find that pressure-thinning/thickening effects significantly affect the droplet dynamics for surface shear viscosity but play a small role for surface dilatational viscosity. We lastly provide phase diagrams for the critical capillary number for different values of the droplet's viscosity ratio and initial Taylor deformation parameter.

Simulated microgravity in the ring-sheared drop

The ring-sheared drop is a module for the International Space Station to study sheared fluid interfaces and their influence on amyloid fibril formation. A 2.54-cm diameter drop is constrained by a stationary sharp-edged ring at some latitude and sheared by the rotation of another ring in the other hemisphere. Shearing motion is conveyed primarily by the action of surface shear viscosity. Here, we simulate microgravity in the laboratory using a density-matched liquid surrounding the drop. Upon shearing, the drop’s deformation away from spherical is found to be a result of viscous and inertial forces balanced against the capillary force. We also present evidence that the deformation increases with increasing surface shear viscosity.

Modelling steady shear flows of Newtonian liquids with non-Newtonian interfaces

In countless biological and technological processes, the flow of Newtonian liquids with a non-Newtonian interface is a common occurrence, such as in monomolecular films in ‘solid’ phases atop of aqueous bulk fluid. There is a lack of models that can predict the flow under conditions different from those used to measure the rheological response of the interface. Here, we present a model which describes interfacial hydrodynamics, including two-way coupling to a bulk Newtonian fluid described by the Navier–Stokes equations, that allows for shear-thinning response of the interface. The model includes a constitutive equation for the interface under steady shear that takes the Newtonian functional form but where the surface shear viscosity is generalized to be a function of the local shear rate. In the limit of a highly viscous interface, the interfacial hydrodynamics is decoupled from the bulk flow and the model can be solved analytically. This provides not only insight into the flow but also a means to validate the numerical technique for solving the two-way coupled problem. The numerical results of the coupled problem shed new light on existing experimental results on steadily sheared monolayers of dipalmitoylphosphatidylcholine (DPPC), the primary constituent of lung surfactant and the bilayers of mammalian cell walls. For low packing density DPPC monolayers, a Newtonian shear-independent surface shear viscosity model can reproduce the interfacial flows, but at high packing density, the shear-thinning properties of the new model presented here are needed.