Kinetic theory of binary fluid–surfactant systems: A variational framework

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, fluid density and velocity. This approach introduces a polarisation field p(r,t) , representing the average orientation of surfactants, which plays a central role in suppressing droplet coalescence. The remaining hydrodynamic equations are consistently obtained from a mesoscopic free energy functional. The resulting model accurately captures key surfactant phenomena, including surface tension reduction and droplet stabilisation, as confirmed by both perturbation theory and numerical simulations, and is thermodynamically consistent with both the Gibbs adsorption isotherm and Henry’s law for adsorbed surfactant concentration.