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Alexandra J. Hardy

Publications and source records attributed to Alexandra J. Hardy.

3 recordsLinked to original sources

Surfactant reorientation under shear: dynamic surface tension and droplet deformation

Surfactants are amphiphilic molecules that are generally anisotropic rather than spherical. Their orientation is therefore governed by the interplay between shear-induced reorientation, thermal rotational diffusion, and energetic alignment with the interface. The relative importance of these processes is characterized by the rotational Peclet number, $Pe_r$. We show that this microscopic coupling between flow and surfactant orientation can give rise to new macroscopic interfacial phenomena, including a shear-dependent effective surface tension and non-trivial droplet deformation. To investigate this mechanism, we develop a phase-field model that incorporates both the surfactant concentration and its local average orientation (polarization field). Using perturbation theory, we derive an analytical expression for the effective surface tension, which depends not only on the surfactant concentration but also on the local shear rate. We then employ a hybrid numerical method to study the deformation of a surfactant-covered droplet under imposed shear flow. For small $Pe_r$, droplet deformation can be accurately captured by a modified Taylor and Maffettone-Minale theories. For large $Pe_r$, shear-induced reorientation strongly distorts the surfactant polarization, and the droplet deformation progressively approaches that of a pure (surfactant-free) droplet.

cond-mat.soft

Kinetic theory of coupled binary-fluid-surfactant systems

We derive a self-consistent hydrodynamic theory of coupled binary-fluid-surfactant systems from the underlying microscopic physics using Rayleigh's variational principle. At the microscopic level, surfactant molecules are modelled as dumbbells that exert forces and torques on the fluid and interface while undergoing Brownian motion. We obtain the overdamped stochastic dynamics of these particles from a Rayleighian dissipation functional, which we then coarse-grain to derive a set of continuum equations governing the surfactant concentration, orientation, and the fluid density and velocity. This approach introduces a polarization field, representing the average orientation of surfactants, and yields a mesoscopic free energy functional from which all governing equations are consistently derived. The resulting model accurately captures key surfactant phenomena, including surface tension reduction and droplet stabilization, as confirmed by both perturbation theory and numerical simulations.

cond-mat.soft

Hybrid particle-phase field model and renormalized surface tension in dilute suspensions of nanoparticles

We present a two-phase field model and a hybrid particle-phase field model to simulate dilute colloidal sedimentation and flotation near a liquid-gas interface (or fluid-fluid interface in general). Both models are coupled to the incompressible Stokes equation, which is solved numerically using a combination of sine and regular Fourier transforms to account for the no-slip boundary conditions at the boundaries. The continuum two-phase field model allows us to analytically solve the equilibrium interfacial profile using a perturbative approach, demonstrating excellent agreement with numerical simulations. Notably, we show that strong coupling to particle dynamics can significantly alter the liquid-gas interface, thereby modifying the liquid-gas interfacial tension. In particular, we show that the renormalized surface tension is monotonically decreasing with increasing colloidal particle concentration and decreasing buoyant mass.

cond-mat.soft