Foam film stratification, viscosity, and small-angle X-ray scattering of micellar SDS solutions over an extended concentration range (1< c/CMC < 75).

Ultrathin foam films (thickness, h < 100 nm) containing micelles undergo drainage via stratification manifested as coexisting thick-thin flat regions, nanoscopic non-flat topography, and the stepwise decrease in film thickness that yields a characteristic step-size. Most studies characterize the variation in step size and stratification kinetics in micellar foam films in a limited concentration range, c/CMC < 12.5 (c < 100 mM). Likewise, most scattering studies characterize micelle dimensions, intermicellar distance, and volume fraction in bulk aqueous SDS solutions in this limited concentration range. In this contribution, we show drainage via stratification can be observed for concentrations up to c/CMC < 75 (c < 600 mM). Understanding the stratification behavior of freely draining micellar films with sodium dodecyl sulfate (SDS) concentration varying in the range 10 mM ≤ cSDS ≤ 600 mM is essential for molecular engineering, consumer product formulations, and controlling foaming in industrial processes. Here, we visualize and analyze nanoscopic thickness variations and transitions in stratifying foam films using Interferometry Digital Imaging Optical Microscopy (IDIOM) protocols. We compare step size obtained from foam stratification to micelle dimension, micelle volume fraction, and intermicellar distance obtained from small angle X-ray scattering studies. Even though the volume fraction increases and approaches 25% at c = 600 mM, the solution viscosity only increases by a factor of four compared to the solvent, consistent with the findings from both stratification and scattering studies. These comparisons allow us to explore the effect of micelle size, morphology, and intermicellar interactions on supramolecular oscillatory structural disjoining pressure, which influences the stratification behavior of draining foam films containing micelles under confinement.

Salt Weakens Intermicellar Interactions and Structuring in Bulk Solutions and Foam Films.

Drainage via stratification in micellar foam films formulated with ionic surfactants shows dramatic changes on salt addition: both the step size and the number of steps in their stepwise thinning diminish. As the stratification process is governed by supramolecular oscillatory structural forces that arise due to confinement-induced structuring of micelles, it is apparent that salt addition reduces the magnitude, periodicity, and decay length of the oscillatory forces. In this contribution, we characterize the changes in micellar size, shape, and interactions on salt addition in bulk solutions using small-angle X-ray scattering (SAXS) to understand and elucidate the influence of salt on stratification in micellar foam films and, more broadly, on the oscillatory structural forces. Adding salt leads to a significant reduction in long-range correlations between micelles and smaller intermicellar distances. These effects manifest as a weakening of the primary peak of the structure factor, ascertained from SAXS spectra, accompanied by its shift to higher wave vectors. Weakened long-range correlations diminish the magnitude and periodicity of the oscillatory disjoining pressure leading to smaller step sizes, fewer steps, and a rich nanoscopic topography, due to the influence of disjoining pressure on the deformable interfaces. The step sizes in stratifying thin films and intermicellar distances in bulk solutions present incongruous values, implying an imperfect analogy with studies on charged nanoparticles with matched and salt concentration-independent values of measured interparticle distances that equal the periodicity of force-distance curves. We anticipate that our findings are significant for multicomponent soft and biological matter containing self-assembled supramolecular structures wherein screened Coulomb interactions govern the self-assembly, interfacial adsorption, interactions, dynamics, and stability.

Drainage via stratification and nanoscopic thickness transitions of aqueous sodium naphthenate foam films.

Sodium naphthenates (NaNs), found in crude oils and oil sands process-affected water (OSPW), can act as surfactants and stabilize undesirable foams and emulsions. Despite the critical impact of soap-like NaNs on the formation, properties, and stability of petroleum and OSPW foams, there is a significant lack of studies that characterize foam film drainage, motivating this study. Here, we contrast the drainage of aqueous foam films formulated with NaN with foams containing sodium dodecyl sulfate (SDS), a well-studied surfactant system, in the relatively low concentration regime (c/CMC < 12.5). The foam films exhibit drainage via stratification, displaying step-wise thinning and coexisting thick-thin regions manifested as distinct shades of gray in reflected light microscopy due to thickness-dependent interference intensity. Using IDIOM (interferometry digital imaging optical microscopy) protocols that we developed, we analyze pixel-wise intensity to obtain thickness maps with high spatiotemporal resolution (thickness <1 nm, lateral ∼500 nm, time ∼10 ms). The analysis of interference intensity variations over time reveals that the aqueous foam films of both SDS and NaN possess an evolving, dynamic, and rich nanoscopic topography. The nanoscopic thickness transitions for stratifying SDS foam films are attributed to the role played by damped supramolecular oscillatory structural disjoining pressure contributed by the confinement-induced layering of spherical micelles. In comparison with SDS, we find smaller concentration-dependent step size and terminal film thickness values for NaN, implying weaker intermicellar interactions and oscillatory structural disjoining pressure with shorter decay length and periodicity.

Foam film stratification studies probe intermicellar interactions.

Ultrathin foam films containing supramolecular structures like micelles in bulk and adsorbed surfactant at the liquid-air interface undergo drainage via stratification. At a fixed surfactant concentration, the stepwise decrease in the average film thickness of a stratifying micellar film yields a characteristic step size that also describes the quantized thickness difference between coexisting thick-thin flat regions. Even though many published studies claim that step size equals intermicellar distance obtained using scattering from bulk solutions, we found no reports of a direct comparison between the two length scales. It is well established that step size is inversely proportional to the cubic root of surfactant concentration but cannot be estimated by adding micelle size to Debye length, as the latter is inversely proportional to the square root of surfactant concentration. In this contribution, we contrast the step size obtained from analysis of nanoscopic thickness variations and transitions in stratifying foam films using Interferometry Digital Imaging Optical Microscopy (IDIOM) protocols, that we developed, with the intermicellar distance obtained using small-angle X-ray scattering. We find that stratification driven by the confinement-induced layering of micelles within the liquid-air interfaces of a foam film provides a sensitive probe of non-DLVO (Derjaguin-Landau-Verwey-Overbeek) supramolecular oscillatory structural forces and micellar interactions.