This study deals with the motion and deformation of a compound drop system, subject to arbitrary but Stokesian far-field flow conditions, in the presence of bulk-insoluble surfactants. We derive solutions for fluid velocities and the resulting surfactant concentrations, assuming the capillary number and surface Péclet number to be small, as compared with unity. We first focus on a concentric drop configuration and apply Lamb’s general solution, assuming the far-field flow to be arbitrary in nature. As representative case studies, we consider two cases: (i) flow dynamics in linear flows and (ii) flow dynamics in a Poiseuille flow, although for the latter case, the concentric configuration does not remain valid in general. We further look into the effective viscosity of a dilute suspension of compound drops, subject to linear ambient flow, and compare our predictions with previously reported experiments. Subsequently, the eccentric drop configuration is addressed by using a bipolar coordinate system where the far-field flow is assumed to be axisymmetric but otherwise arbitrary in nature. As a specific example for eccentric drop dynamics, we focus on Poiseuille flow and study the drop migration velocities. Our analysis shows that the presence of surfactant generally opposes the imposed flows, thereby acting like an effective augmented viscosity. Our analysis reveals that maximizing the effects of surfactant makes the drops behave like solid particles suspended in a medium. However, in uniaxial extensional flow, the presence of surfactants on the inner drop, in conjunction with the drop radius ratio, leads to a host of interesting and non-monotonic behaviours for the interface deformation. For eccentric drops, the effect of eccentricity only becomes noticeable after it surpasses a certain critical value, and becomes most prominent when the two interfaces approach each other. We further depict that surfactant and eccentricity generally tend to suppress each other’s effects on the droplet migration velocities.
In the present study, we attempt to analyse the electro-osmotic flow of two superimposed fluids through narrow confinements in the presence of axially modulated surface charges. We attempt to solve for the flow structure as well as the interface deformation by both analytical and numerical techniques. Approximate analytical solutions are obtained through asymptotic analysis for low deformations, whereas numerical solutions are obtained by applying the phase field formalism; the numerical solutions are obtained for small as well as large interfacial deformations. The analytical solutions are derived only for the transient deformation of the interface, neglecting the transience in the flow, i.e. the flow is assumed to be quasisteady. The numerical solutions, however, are derived including the effects of inertia and transients in the flow. We attempt to compare our analytical and numerical results and explore the effects of several physico-chemical parameters on the deformation of the interface as well as the nature of the flow. Our analysis reveals that parameters such as the modulation wavelength, surface tension (described through the capillary number), viscosity ratio, permittivity ratio and extent of asymmetry in the potential on the two walls are the major contributors to the deformation and the resulting flow features.
We investigate the contact-line dynamics of two immiscible fluids in a narrow fluidic confinement comprising wettability-gradient surfaces, where the bulk fluid motion is actuated by an externally applied electric field. We assume that the channel walls bear spatially uniform surface potential. Our analysis, based on the diffuse interface formalism, reveals that the contact line undergoes stick-slip motion over the chemical patches and its velocity is a strong function of the interfacial electrokinetics. We also show that the tendency of the contact line of getting pinned to the selected patches can decrease or increase with its progression along the channel, depending on the ratio of the permittivities of the two fluids. Finally, we establish the functional dependency of the time taken by the contact line to move across the patches (capillary filling time) on the combined consequences of interfacial electrochemistry and wettability patterning.
We consider the filling of a capillary by a viscoelastic fluid described by the Phan-Thien-Tanner (PTT) constitutive behavior. By considering both vertical capillary filling and horizontal capillary filling, we demarcate the role played by gravity and fluid rheology towards long-time oscillations in the capillary penetration depth. We also consider the isothermal filling of the capillary for a closed channel and thus bring out the fundamental differences in the nature of capillary filling for PTT and Newtonian fluids for closed channels in comparison to open channels. Through a scaling analysis, we highlight a distinct viscoelastic regime in the horizontal capillary filling which is in contrast to the Washburn scaling seen in the case of Newtonian fluids. Such an analysis with a very general constitutive behavior is therefore expected to shed light on many areas of microfluidics which focus on biofluids that are often well described by the PTT constitutive behavior.
We consider electrically driven dynamics of an incompressible binary fluid, with contrasting densities and viscosities of the two phases, flowing through narrow fluidic channel with walls with predefined surface wettabilities. Through phase field formalism, we describe the interfacial kinetics in the presence of electro-hydrodynamic coupling and address the contact line dynamics of the two-fluid system. We unveil the interplay of the substrate wettability and the contrast in the fluid properties culminating in the forms of two distinct regimes—interface breakup regime and a stable interface regime. Through a parametric study, we demarcate the effect of the density and viscosity contrasts along with the electrokinetic parameters such as the surface charge and ionic concentration on the underlying contact-line-dynamics over interfacial scales.
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