Spatiotemporal mapping of nanotopography and thickness transitions of ultrathin foam films.

Freshly formed soap films, soap bubbles, or foam films display iridescent colors due to thin film interference that changes as squeeze flow drives drainage and a progressive decrease in film thickness. Ultrathin (thickness <100 nm) freestanding films of soft matter containing micelles, particles, polyelectrolyte-surfactant complexes, or other supramolecular structures or liquid crystalline phases display drainage via stratification. A fascinating array of thickness variations and transitions, including stepwise thinning and coexistence of thick-thin flat regions, arise in micellar foam films that undergo drainage via stratification. In this tutorial, we describe the IDIOM (interferometry digital imaging optical microscopy) protocols that combine the conventional interferometry principle with digital filtration and image analysis to obtain nanometer accuracy for thickness determination while having high spatial and temporal resolution. We provide fully executable image analysis codes and algorithms for the analysis of nanotopography and summarize some of the unique insights obtained for stratified micellar foam films.

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.

Polymer-Surfactant Complexes Impact the Stratification and Nanotopography of Micellar Foam Films.

Freestanding films of soft matter drain via stratification due to confinement-induced structuring and layering of supramolecular structures such as micelles. Neutral polymers, added as rheology modifiers to cosmetics, foods, pharmaceuticals, and petrochemical formulations, often interact with monomers and micelles of surfactants, forming polymer-surfactant complexes. Despite many studies that explore interfacial and bulk rheological properties, the corresponding influence of polymer-surfactant complexes on foam drainage and lifetime is not well understood and motivates this study. Here, we report the discovery and evidence of drainage via stratification in foam films formed with polymer-surfactant (PEO-SDS) complexes. We show that the stratification trifecta of coexisting thick-thin regions, stepwise thinning, and nanoscopic topological features such as nanoridges and mesas can be observed using IDIOM (interferometry, digital imaging, and optical microscopy) protocols we developed for nanoscopic thickness mapping. We determine that for polymer concentrations below overlap concentration and surfactant concentrations beyond the excess micelle point, polymer-surfactant complexation impact the nanoscopic topography but not the step size, implying the amplitude of disjoining pressure changes, but periodicity remains unchanged.

Ultrathin Micellar Foam Films of Sodium Caseinate Protein Solutions.

Sodium caseinates (NaCas), derived from milk proteins called caseins, are often added to food formulations as emulsifiers, foaming agents, and ingredients for producing dairy products. In this contribution, we contrast the drainage behavior of single foam films made with micellar NaCas solutions with well-established features of stratification observed for the micellar sodium dodecyl sulfate (SDS) foam films. In reflected light microscopy, the stratified SDS foam films display regions with distinct gray colors due to differences in interference intensity from coexisting thick-thin regions. Using IDIOM (interferometry digital imaging optical microscopy) protocols we pioneered for mapping nanotopography of foam films, we showed that drainage via stratification in SDS films proceeds by the expansion of flat domains that are thinner than surrounding by a concentration-dependent step-size, and nonflat features (nanoridges and mesas) form at the moving front. Furthermore, stratifying SDS foam films show stepwise thinning, such that the step-size and terminal film thickness decrease with concentration. Here we visualize the nanotopography in protein films with high spatiotemporal resolution using IDIOM protocols to address two long-standing questions. Do protein foam films formulated with NaCas undergo drainage via stratification? Are thickness transitions and variations in protein foam films determined by intermicellar interactions and supramolecular oscillatory disjoining pressure? In contrast with foam films containing micellar SDS, we find that micellar NaCas foam films display just one step, nonflat and noncircular domains that expand without forming nanoridges and a terminal thickness that increases with NaCas concentration. We infer that the differences in adsorbing and self-assembling unimers triumph over any similarities in the structure and interactions of their micelles.

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.

The rheologically-complex fluid beauty of nail lacquer formulations.

Nail lacquer formulations are multi-ingredient complex fluids with additives that affect color, smell, texture, evaporation rate, viscosity, stability, leveling behavior, consumer's sensory experience, and dried coating's decorative and wear performance. Optimizing and characterizing the formulation rheology is critical for achieving longer shelf-life, better control over the nail painting process and adhesion, continuous manufacturing of large product volumes, and increasing overall consumer satisfaction. Dispensing, bottle filling, brush application, and dripping, as well as perceived tackiness of nail polishes, all involve capillarity-driven pinching flows associated with strong extensional deformation fields. However, a significant lack of characterization of pinching dynamics and extensional rheology response of multicomponent formulations, especially particle suspensions in viscoelastic solutions, motivates this study. Here, we characterize the shear rheology response of twelve commercial nail lacquer formulations using torsional rheometry and characterize pinching dynamics and extensional rheology response using dripping-onto-substrate (DoS) rheometry protocols we developed. We visualize and analyze brush loading, nail coating, dripping from brush, sagging, and lacquer application on a nail to outline the challenges posed by free-surface flows and non-Newtonian rheology. We find that the radius evolution over time obtained using DoS rheometry displays power law exponents distinct from those exhibited in shear thinning. Both shear and extensional viscosity decrease with deformation rate. However, the extensional viscosity appears to be rate-independent at the highest rates and displays nearly an order of magnitude larger values than the high shear rate viscosity. We envision that the findings and protocols described here will help and motivate industrial scientists to design better multicomponent formulations through a better characterization and understanding of the influence of ingredients like particles and polymers on rheology, processing, and applications.