Abstract

Drainage in microscopic circular foam films depends significantly on the radial (tangential) mobility of the film surfaces and is accelerated as compared to the limiting case of tangentially immobile surfaces, where velocity of thinning is described by the classical Reynolds’ equation (outflow of viscous fluid from a cylindrical gap between two solid plates). The structure and composition of the adsorption layer and the interfacial mass transfer determine the tangential mobility of the film surfaces and, hence, the measured velocity of film thinning. Experiments with soluble surfactants below the critical micelle concentrations (CMC) have exhibited the effect of dynamic interfacial elasticity. At relatively low bulk concentrations, the interfacial mass transfer is governed by surface diffusion; close to CMC (saturated adsorption layer), the limiting case of tangentially immobile surfaces can be reached and at concentrations above the CMC the film thinning is accelerated again. Here, we report freshly established data on the kinetic behavior of foam films from micellar solutions of soluble nonionic surfactants (decyl-octaoxyethylene alcohol and dodecyl-octaoxyethylene alcohol) in a wide range of concentrations above the CMC aiming to investigate the effect of partially disintegrated micelles acting as sources of surfactant molecules at the surface.

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