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The interface between two immiscible fluids can become unstable under the effect of an imposed tangential electric field along with a stagnation point flow. This canonical situation, which arises in a wide range of electrohydrodynamic systems including at the equator of electrified droplets, can result in unstable interface deflections where the perturbed interface gets drawn along the extensional axis of the flow while experiencing strong charge build-up. Here, we present analytical and numerical analyses of the stability of a planar interface separating two immiscible fluid layers subject to a tangential electric field and a stagnation point flow. The interfacial charge dynamics is captured by a conservation equation accounting for Ohmic conduction, advection by the flow and finite charge relaxation. Using this model, we perform a local linear stability analysis in the vicinity of the stagnation point to study the behaviour of the system in terms of the relevant dimensionless groups of the problem. The local theory is complemented with a numerical normal-mode linear stability analysis based on the full system of equations and boundary conditions using the boundary element method. Our analysis demonstrates the subtle interplay of charge convection and conduction in the dynamics of the system, which oppose one another in the dominant unstable eigenmode. Finally, numerical simulations of the full nonlinear problem demonstrate how the coupling of flow and interfacial charge dynamics can give rise to nonlinear phenomena such as tip formation and the growth of charge density shocks. 

Membrane bending is an extensively studied problem from both modeling and experimental perspectives because of the wide implications of curvature generation in cell biology. Many of the curvature generating aspects in membranes can be attributed to interactions between proteins and membranes. These interactions include protein diffusion and formation of aggregates due to protein–protein interactions in the plane of the membrane. Recently, we developed a model that couples the in-plane flow of lipids and diffusion of proteins with the out-of-plane bending of the membrane. Building on this work, here, we focus on the role of explicit aggregation of proteins on the surface of the membrane in the presence of membrane bending and diffusion. We develop a comprehensive framework that includes lipid flow, membrane bending, the entropy of protein distribution, along with an explicit aggregation potential and derive the governing equations for the coupled system. We compare this framework to the Cahn–Hillard formalism to predict the regimes in which the proteins form patterns on the membrane. We demonstrate the utility of this model using numerical simulations to predict how aggregation and diffusion, when coupled with curvature generation, can alter the landscape of membrane–protein interactions. 

Electrohydrodynamics of drops is a classic fluid mechanical problem where deformations and microscale flows are generated by application of an external electric field. In weak fields, electric stresses acting on the drop surface drive quadrupolar flows inside and outside and cause the drop to adopt a steady axisymmetric shape. This phenomenon is best explained by the leaky-dielectric model under the premise that a net surface charge is present at the interface while the bulk fluids are electroneutral. In the case of dielectric drops, increasing the electric field beyond a critical value can cause the drop to start rotating spontaneously and assume a steady tilted shape. This symmetry-breaking phenomenon, called Quincke rotation, arises due to the action of the interfacial electric torque countering the viscous torque on the drop, giving rise to steady rotation in sufficiently strong fields. Here, we present a small-deformation theory for the electrohydrodynamics of dielectric drops for the complete Melcher–Taylor leaky-dielectric model in three dimensions. Our theory is valid in the limits of strong capillary forces and highly viscous drops and is able to capture the transition to Quincke rotation. A coupled set of nonlinear ordinary differential equations for the induced dipole moments and shape functions are derived whose solution matches well with experimental results in the appropriate small-deformation regime. Retention of both the straining and rotational components of the flow in the governing equation for charge transport enables us to perform a linear stability analysis and derive a criterion for the applied electric field strength that must be overcome for the onset of Quincke rotation of a viscous drop. 

Cellular membranes are elastic lipid bilayers that contain a variety of proteins, including ion channels, receptors and scaffolding proteins. These proteins are known to diffuse in the plane of the membrane and to influence the bending of the membrane. Experiments have shown that lipid flow in the plane of the membrane is closely coupled with the diffusion of proteins. Thus, there is a need for a comprehensive framework that accounts for the interplay between these processes. Here, we present a theory for the coupled in-plane viscous flow of lipids, diffusion of transmembrane proteins and elastic deformation of lipid bilayers. The proteins in the membrane are modelled such that they influence membrane bending by inducing a spontaneous curvature. We formulate the free energy of the membrane with a Helfrich-like curvature elastic energy density function modified to account for the chemical potential energy of proteins. We derive the conservation laws and equations of motion for this system. Finally, we present results from dimensional analysis and numerical simulations and demonstrate the effect of coupled transport processes in governing the dynamics of membrane bending and protein diffusion.