Search arXivSearch

arXiv · 2209.03468

Thickness profiles of giant soap films

Abstract

Production, drainage and stability of foams films, i.e. films in contact with their menisci, are fascinating problems that remain still unsolved. In this article, we propose to explore the regime of large velocities and large film sizes. This one is not accessible in experiments classically conducted in the literature, and allows us to study the regime of large extension and large extension rates. With our setup, we make soap films up to two meters high by pulling a horizontal fishing line driven by belts out of a soapy solution at velocities ranging from 20~cm/s to 250~cm/s. We characterize the thickness profile of the central part of the film that behaves like a rubber band under tension. We show that its thickness profile is well described by a static model in which a homogeneous elastic film is stretched by its own weight. This leads to an exponential thickness profile with a characteristic length given by a competition between gravity and surface elasticity. The prefactor is fixed by the shape and area of the film, governed by the fishing line motion but also by a continuous extraction of foam film from the lateral menisci, thicker than the central part, and that progressively invades the film from its lateral boundaries. The model we propose captures the subtle interplay between gravity, film elasticity and film extraction and leads to predictions in good agreement with our experimental data.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Marina Pasquet, Frédéric Restagno, Isabelle Cantat, Emmanuelle Rio. 2023-04-21. Thickness profiles of giant soap films. https://arxiv.org/abs/2209.03468

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Transient Elasticity -- A Unifying Framework for Thixotropy, Polymers, and Granular Media

Thixotropic yield stress fluids, such as paint or ketchup, are traditionally viewed as elastic structures that, under shear rates, break into viscous liquids with lumps, and reconnect at rest. An alternative framework is presented here: Upon shear, structural destruction is incomplete, leaving sufficient connections. As a result, elasticity fundamentally underlies their non-Newtonian behavior, though they do appear purely viscous under a steady shear, displaying little direct evidence of elastic rebound---same as granular media and polymers. Consequently, all three are described by the same set of evolution equations, differing only in their parameters. These equations are set up by starting from solid dynamics and allowing the elastic strain $\varepsilon^e$ to relax, which in effect interpolates between solid and fluid behavior, appropriate for systems that display both types of behavior. Incorporating in addition a two-temperature framework, tracking how energy is dissipated in two consecutive stages, yields the nonlinear model of Transient Elasticity (TE). It describes an elasticity that is transient in time yet persistent under shear. Previously validated for polymers and granular media, TE is here applied to thixotropic yield-stress fluids. As shown, it successfully accounts for a wide range of characteristic phenomena, including over- and undershoot, viscosity bifurcation, shear banding, and oscillatory rheography. Given its appropriateness across structurally diverse systems, TE offers a unified, surprisingly general account of non-Newtonian phenomena.

cond-mat.soft

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft