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Many ionic surfactants, such as sodium dodecyl sulfate (SDS) crystallize out of solution if the temperature falls below the crystallization boundary. The crystallization temperature is impacted by solution properties and can be decreased with the addition of salt. We studied SDS crystallization at liquid/vapor interfaces from solutions at high ionic strength (sodium chloride). We show that the surfactant crystals at the surface grow from adsorbed SDS molecules, as evidenced by the preferential orientation of the crystals identified by using grazing incidence X-ray diffraction. We find a unique time scale for the crystal growth from the evolution of structure, surface tension, and visual inspection, which can be controlled through varying the SDS or NaCl concentrations.
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We consider the lifetime of rectangular vertical soap films and we explore the influence of relative humidity and both dimensions on the stability of large soap films, reaching heights of up to 1.2 m. Using an automated rupture detection system, we achieve a robust statistical measurement of their lifetimes and we also measure the film thinning dynamics. We demonstrate that drainage has a negligible impact on the film stability as opposed to evaporation. To do so, we compare the measured lifetimes with predictions from the Boulogne & Dollet model, originally designed to describe the convective evaporation of hydrogels. Interestingly, we show that this model can predict a maximum film lifetime for all sizes.
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Various parameters affect foam stability: surface and bulk rheology of the solution, gravitational drainage, mechanical vibrations, bubble gas composition, and also evaporation. Evaporation is often considered through the prism of liquid loss but also induces a cooling effect due to the enthalpy of vaporization. In this study, we combine a theoretical and experimental approach to explore the temperature field in a foam column evaporating from the top. We show that a measurable temperature profile exists in this geometry, with temperatures at the interface lower than the environmental temperature by a few degrees. We demonstrate that the temperature profile is the result of a balance between the enthalpy of vaporization and heat fluxes originating from the thermal conduction of foam and air and thermal radiation. For small foam thicknesses compared to the radius, we found that the temperature gradient is established over the foam thickness, while for large aspect ratios, the gradient spans over a length scale comparable to the tube radius.
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When an open tube of small diameter touches a bubble of a larger diameter, the bubble spontaneously shrinks and pushes a soap film into the tube. We characterize the dynamics for different bubble sizes and number of soap films in the tube. We rationalize this observation from a mechanical force balance involving the Laplace pressure of the bubble and the viscous force from the advancing soap lamellae in the tube. We propose a numerical resolution of this model, and an analytical solution in an asymptotic regime. These predictions are then compared to the experiments. The emptying duration is primarily affected by the initial bubble to tube diameter ratio and by the number of soap films in the tube.
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Recent advances have demonstrated that evaporation can play a significant role on soap film stability, which is a key concern in many industrial areas but also for children playing with bubbles. Thus, evaporation leads to a film thinning but also to a film cooling, which has been overlooked for soapy objects. Here, we study the temperature variation of an evaporating soap film for different values of relative humidity and glycerol concentrations. We evidence that the temperature of soap films can decrease after their creation up to 8 °C. We propose a model describing the temperature drop of soap films after their formation that is in quantitative agreement with our experiments. We emphasize that this cooling effect is significant and must be carefully considered in future studies on the dynamics of soap films.
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In this paper, we investigate the thinning dynamics of evaporating surfactant-stabilised surface bubbles by considering the role of physical-chemistry of solutions used in a liquid bath. We study the impact of the surfactant concentration below and above the cmc (critical micelle concentration) and the role of ambient humidity. First, in a humidity-saturated atmosphere, we show that if the initial thickness depends on the surfactant concentration and is limited by the surface elasticity, the drainage dynamics are very well described from the capillary and gravity contributions. These dynamics are independent of the surfactant concentration. Second, our study reveals that the physical-chemistry impacts the thinning dynamics through evaporation. We include in the model the additional contribution due to evaporation, which shows a good description of the experimental data below the cmc. Above the cmc, although this model is unsatisfactory at short times, the dynamics at long times is correctly rendered and we establish that the increase of the surfactant concentration decreases the impact of evaporation. Finally, the addition of a hygroscopic compound, glycerol, can be also rationalized by our model. We demonstrate that glycerol decreases the bubble thinning rate at ambient humidity, thus increasing their stability.
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Complex liquids flow is known to be drastically affected by the roughness condition at the interfaces. We combined stresses measurements and observations of the flow during the motion of different rough surfaces in dry liquid foams. We visually show that three distinct friction regimes exist: slippage, stick-slip motion, and anchored soap films. Our stress measurements are validated for slippage and anchored regimes based on existing models, and we propose a leverage rule to describe the stresses during the stick-slip regime. We find that the occurrence of the stick-slip or anchored regimes is controlled by the roughness factor, defined as the ratio between the size of the surface asperities and the radius of curvature of the Plateau borders.
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The control of environmental conditions is crucial in many experimental work across scientific domains. In this technical note, we present how to realize a cheap humidity regulator based on a PID controller driven by an Arduino microcontroller. We argue our choices on the components and we show that the presented designs can serve as a basis to the reader for the realization of humidity regulators with specific requirements and experimental constraints.
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This corrects the article DOI: 10.1103/PhysRevLett.119.154502.
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Although soap films are prone to evaporate due to their large surface to volume ratio, the effect of evaporation on macroscopic film features has often been disregarded in the literature. In this work, we experimentally investigate the influence of environmental humidity on soap film stability. An original experiment allows to measure both the maximum length of a film pulled at constant velocity and its thinning dynamics in a controlled atmosphere for various values of the relative humidity [Formula: see text]. At first order, the environmental humidity seems to have almost no impact on most of the film thinning dynamics. However, we find that the film length at rupture increases continuously with [Formula: see text]. To rationalize our observations, we propose that film bursting occurs when the thinning due to evaporation becomes comparable to the thinning due to liquid drainage. This rupture criterion turns out to be in reasonable agreement with an estimation of the evaporation rate in our experiment.
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Motivated by the evaporation of soap films, which has a significant effect on their lifetime, we performed an experimental study on the evaporation of vertical surfaces with model systems based on hydrogels. From the analogy between heat and mass transfer, we adopt a model describing the natural convection in the gas phase due to a density contrast between dry and saturated air. Our measurements show a good agreement with this model, both in terms of scaling law with the Grashof number and in terms of order of magnitude. We discuss the corrections to take into account, notably the contribution of edge effects, which have a small but visible contribution when lateral and bottom surface areas are not negligible compared to the main evaporating surface area.
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Inks of permanent markers and waterproof cosmetics create elastic thin films upon application on a surface. Such adhesive materials are deliberately designed to exhibit water-repellent behavior. Therefore, patterns made up of these inks become resistant to moisture and cannot be cleaned by water after drying. However, we show that sufficiently slow dipping of such elastic films, which are adhered to a substrate, into a bath of pure water allows for complete removal of the hydrophobic coatings. Upon dipping, the air-water interface in the bath forms a contact line on the substrate, which exerts a capillary-induced peeling force at the edge of the hydrophobic thin film. We highlight that this capillary peeling process is more effective at lower velocities of the air-liquid interface and lower viscosities. Capillary peeling not only removes such thin films from the substrate but also transfers them flawlessly onto the air-water interface.
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We report an experimental study on the manipulation of colloidal particles in a drop sitting on a hydrogel. The manipulation is achieved by diffusiophoresis, which describes a directed motion of particles induced by solute gradients. By letting the solute concentrations for the drop and the hydrogel be different, we control the motion of particles in a stable suspension, which is otherwise difficult to achieve. We show that diffusiophoresis can cause the particles to move either toward or away from the liquid-air interface depending on the direction of the solute gradient and the surface charge of the particles. We measure the particle adsorption experimentally and rationalize the results with a one-dimensional numerical model. We show that diffusiophoretic motion is significant at the lengthscale of a drop deposited on a hydrogel, which suggests a simple method for the deposition of particles on hydrogels.
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This work aims to identify common challenges in the preparation of the blister test devices designed for the measurement of the energy release rate for brittle thin films and to propose easy-to-implement solutions accordingly. To this end, we provide a step-by-step guide for fabricating a blister test device comprised of thin polystyrene films adhered to glass substrates. Thin films are first transferred from donor substrates to an air-water interface, which is then used as a platform to locate them on a receiver substrate. We embed a microchannel at the back of the device to evacuate the air trapped in the opening, through which the pressure is applied. We quantify the height and the radius of the blister to estimate the adhesion energy using the available expressions correlating the normal force and the moment with the shape of the blister. The present blister test provided an adhesion energy per unit area of G = 18±2 mJ/m^2 for polystyrene on glass, which is in good agreement with the measurement of G = 14±2 mJ/m^2 found in our independent cleavage test.
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Surface coatings and patterning technologies are essential for various physicochemical applications. In this Letter, we describe key parameters to achieve uniform particle coatings from binary solutions. First, multiple sequential Marangoni flows, set by solute and surfactant simultaneously, prevent nonuniform particle distributions and continuously mix suspended materials during droplet evaporation. Second, we show the importance of particle-surface interactions that can be established by surface-adsorbed macromolecules. To achieve a uniform deposit in a binary mixture, a small concentration of surfactant and surface-adsorbed polymer (0.05 wt% each) is sufficient, which offers a new physicochemical avenue for control of coatings.
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We study the stress developed during the drying of a colloidal drop of silica nanoparticles. In particular, we use the wrinkling instability of a thin floating sheet to measure the net stress applied by the deposit on the substrate and we focus on the effect of the particle polydispersity. In the case of a bidisperse suspension, we show that a small number of large particles substantially decreases the expected stress, which we interpret as the formation of lower hydrodynamic resistance paths in the porous material. As colloidal suspensions are usually polydisperse, we show for different average particle sizes that the stress is effectively dominated by the larger particles of the distribution and not by the average particle size.
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Control of the swelling, chemical functionalization, and adhesivity of hydrogels are finding new applications in a wide range of material systems. We investigate experimentally the effect of adsorbed particles on hydrogels on the depinning of contact lines. In our experiments, a water drop containing polystyrene microspheres is deposited on a swelling hydrogel, which leads to the drop absorption and particle deposition. Two regimes are observed: a decreasing drop height with a pinned contact line followed by a receding contact line. We show that increasing the particles concentration increases the duration of the first regime and significantly decreases the total absorption time. The adsorbed particles increase the pinning force at the contact line. Finally, we develop a method to measure the receding contact angle with the consideration of the hydrogel swelling.
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When droplets impact fibrous media, the liquid can be captured by the fibers or contact then break away. Previous studies have shown that the efficiency of drop capture by a rigid fiber depends on the impact velocity and a threshold velocity was defined below which the drop is captured. However, it is necessary to consider the coupling of elastic and capillary effects to achieve an improved understanding of the capture process for soft substrates. Here, we study experimentally the dynamics of a single drop impacting on a thin flexible fiber. Our results demonstrate that the threshold capture velocity depends on the flexibility of fibers in a non-monotonic way. We conclude that tuning the mechanical properties of fibers can optimize the efficiency of droplet capture.
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Various materials are made of long thin fibers that are randomly oriented to form a complex network in which drops of wetting liquid tend to accumulate at the nodes. The capillary force exerted by the liquid can bend flexible fibers, which in turn influences the morphology adopted by the liquid. In this paper, we investigate through a model situation the role of the fiber flexibility on the shape of a small volume of liquid on a pair of crossed flexible fibers. We characterize the liquid morphologies as we vary the volume of liquid, the angle between the fibers, and the length of the fibers. The drop morphologies previously reported for rigid crossed fibers, i.e., a drop, a column and a mixed morphology, are also observed on flexible crossed fibers with modified domains of existence. In addition, at small tilt angles between the fibers, a new behavior is observed: the fibers bend and collapse. Depending on the volume of liquid, a thin column with or without a drop is reported on the collapsed fibers. Our study suggests that the fiber flexibility adds a rich variety of behaviors that may be important for some applications.
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Soft solids differ from stiff solids in an important way: their surface stresses can drive large deformations. Based on a topical workshop held in the Lorentz Center in Leiden, this Opinion highlights some recent advances in the growing field of solid capillarity and poses key questions for its advancement.