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Thin liquid films are a potential game changer in the quest for efficient gas separation strategies. Such fluid membranes, which are complementary to their solid counterparts involving porous materials, can achieve complex separation by combining permeability and adsorption mechanisms in their liquid core and at their surface. In addition, unlike porous solid membranes that must be regenerated between separation steps to recover a gas-free porosity, thus preventing continuous operation, liquid membranes can be regenerated using continuous liquid flow through the fluid film. Here, building on the self-sustained mobile film technique, we propose a simple experimental setup allowing direct quantitative assessment of the gas permeability of soap films stabilized by different surfactant types. Using a simple prototypical example involving O2/N2 mixtures, the measurement principle is first presented to establish a proof of concept. As the gas solubilities and diffusivities are known, the results of such experiments can be compared with microscopic models to disentangle the liquid core and surface permeabilities from a direct macroscopic transport response of the film subjected to a gas concentration difference. The same dynamical experiments performed for air enriched in CO2 indicate that the permeability of the soap film varies with the molar fraction in the gas compartment, a feature not observed for O2/N2. These experimental findings pave the way for the design of novel separation technologies in fields and situations where porous solid membranes are of limited efficiency.
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The evolution of a foam driven by the transfer of two gases of different solubilities across the soap films is studied. A bamboo foam, or a train of films, is used as a model system; it is made of a poorly soluble gas and put into contact with a reservoir of a soluble gas at an initial time. The measurement of the time evolution of the volume of each bubble shows that the foam swells as it progressively incorporates the soluble gas. The dynamics is modeled from the gas fluxes across each film. The continuous limit of this model at a large number of bubbles is studied in detail: it gives an effective nonlinear diffusion equation, which fits the data very well. The corresponding diffusion constant, given by the product of the permeability of the soluble gas and the initial size of the bubbles, is shown to be the key parameter governing the coarsening dynamics of the foam.
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We probe the complex rheological behaviour of liquid foams flowing through a conical constriction. With fast X-ray tomographic microscopy we measure in situ the displacement and deformation of up to fifty thousand bubbles at any single time instance while varying systematically the foam liquid fraction, the bubble size and the flow direction - convergent vs. divergent. The large statistics and high spatio-temporal resolution allows to observe and quantify the deviations from a purely viscous flow. We indeed reveal an asymmetry between the convergent and divergent flows associated to the emergence of elastic stresses in the latter case, and enhanced as the liquid fraction is reduced. Such effect is related to the reorientation of the deformed bubbles flowing out of the constriction, from a prolate to an oblate shape in average, while they pass through the hopper waist.
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Liquid foams are multi-scale structures whose structural characterization requires the combination of very different techniques. This inherently complex task is made more difficult by the fact that foams are also intrinsically unstable systems and that their properties are highly dependent on the production protocol and sample container. To tackle these issues, a new device has been developed that enables the simultaneous time-resolved investigation of foams by small-angle neutron scattering (SANS), electrical conductivity, and bubbles imaging. This device allows the characterization of the foam and its aging from nanometer up to centimeter scale in a single experiment. A specific SANS model was developed to quantitatively adjust the scattering intensity from the dry foam. Structural features such as the liquid fraction, specific surface area of the Plateau borders and inter-bubble films, and thin film thickness were deduced from this analysis, and some of these values were compared with values extracted from the other applied techniques. This approach has been applied to a surfactant-stabilized liquid foam under free drainage and the underlying foam destabilization mechanisms were discussed with unprecedented detail. For example, the information extracted from the image analysis and SANS data allows for the first time to determine the disjoining pressure vs. thickness isotherm in a real, draining foam.
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Underwater bubbles are extremely good acoustic resonators, but are freely evolving and dissolving. Recently it was found that bubbles can be stabilized in frames, but the influence of the frame shape is still undocumented. Here we first explore the vibration of polyhedral bubbles with a low number of faces, shaped as the five Platonic solids. Their resonance frequency is well approximated by the formula for spherical bubbles with the same volume. Then we extend these results to shapes with a larger number of faces using fullerenes, paving the way to obtain arbitrary large resonant bubbles.
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The formation of dense protein interfacial layers at a free air-water interface is known to result from both diffusion and advection. Furthermore, protein interactions in concentrated phases are strongly dependent on their overall positive or negative net charge, which is controlled by the solution pH. As a consequence, an interesting question is whether the presence of an advection flow of water toward the interface during protein adsorption produces different kinetics and interfacial structure of the adsorbed layer, depending on the net charge of the involved proteins and, possibly, on the sign of this charge. Here we test a combination of the following parameters using ovalbumin and lysozyme as model proteins: positive or negative net charge and the presence or absence of advection flow. The formation and the organization of the interfacial layers are studied by neutron reflectivity and null-ellipsometry measurements. We show that the combined effect of a positive charge of lysozyme and ovalbumin and the presence of advection flow does induce the formation of interfacial multilayers. Conversely, negatively charged ovalbumin forms monolayers, whether advection flow is present or not. We show that an advection/diffusion model cannot correctly describe the adsorption kinetics of multilayers, even in the hypothesis of a concentration-dependent diffusion coefficient as in colloidal filtration, for instance. Still, it is clear that advection is a necessary condition for making multilayers through a mechanism that remains to be determined, which paves the way for future research.
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Aire , Agua , Adsorción , Cinética , Transporte de Proteínas , Propiedades de SuperficieRESUMEN
We introduce a model that describes spherical oscillations of encapsulated microbubbles in an unbounded surrounding fluid. A Rayleigh-Plesset-like equation is derived by coupling the Navier-Stokes equation that describes fluid dynamics with the Navier equation that describes solid dynamics via the internal/external boundary conditions. While previous models were restricted to incompressible isotropic shells, the solid shell is modeled here as a compressible viscoelastic isotropic material and then generalized to an anisotropic material. The exact value of the resonance frequency is calculated analytically, and the damping constant is computed in the approximation of weak damping. A correction of the widely used Church model for incompressible shells is evidenced, and the effects of shell compressibility and anisotropy are discussed.
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To clarify the role of wetting properties on the damping of liquid oscillations, we studied the decay of oscillations of liquid columns in a U-shaped tube with controlled surface conditions. In the presence of sliding triple lines, oscillations are strongly and nonlinearly damped, with a finite-time arrest and a dependence on initial amplitude. We reveal that contact angle hysteresis explains and quantifies this solidlike friction.
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A foam film, free to move and stabilized with tetradecyltrimethylammonium bromide or sodium dodecylsulfate surfactants, is deposited inside of a cylindrical tube. It separates the tube into two distinct gaseous compartments. The first compartment is filled with air, while the second one contains a mixture of air and perfluorohexane vapor (C6F14), which is a barely water-soluble fluorinated compound. This foam film thus acts as a liquid semipermeable membrane for gases equivalent to the solid semipermeable membranes conventionally used in fluid separation processes. To infer the rate of air transfer through the membrane, we measure the displacement of the mobile foam film. From this, we deduce the instantaneous permeability of the membrane. In contrast to the permeability of solid membranes, which inexorably decreases over time because they become clogged, an anticlogging effect is observed with a permeability that systematically increases over time. Because the thickness of the film is constant over time, we attribute this to the possibility of adsorbing or desorbing fluorinated gas molecules on the liquid membrane. Indeed, because the partial pressure of the fluorinated gas is high at the beginning of the experiment, the density of the adsorbed molecules is also high, which leads to a low permeability to air transfer. On the contrary, at the end of the experiment, the partial pressure in fluorinated gas and thus the density of the adsorbed molecules are low. This leads to a higher permeability and a less clogged membrane.
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We quantify the spatiotemporal transformation of a monodisperse and well-ordered monolayer of bubbles, as they undergo Ostwald ripening, by tracking the size polydispersity of the bubbles and local ordering of the foam. After nuclei of disorder appear at random locations, the transition takes place through two successive phases: first, the disordered regions grow while the value of polydispersity increases slowly, then the polydispersity grows rapidly once the disordered zones begin to merge together. The transition is captured by a modified logistic model.
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While coalescence is ultimately the most drastic destabilization process in foams, its underlying processes are still unclear. To better understand them, we track individual coalescence events in two-dimensional foams at controlled capillary pressure. We obtain statistical information revealing the influence of the different parameters which have been previously proposed to explain coalescence. Our main conclusion is that coalescence probability is simply proportional to the area of the thin film separating two bubbles, suggesting that coalescence is mostly stochastic.
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We report an experimental study concerning the capillary relaxation of a confined liquid droplet in a microscopic channel with a rectangular cross section. The confinement leads to a droplet that is extended along the direction normal to the cross section. These droplets, found in numerous microfluidic applications, are pinched into a peanutlike shape thanks to a localized, reversible deformation of the channel. Once the channel deformation is released, the droplet relaxes back to a pluglike shape. During this relaxation, the liquid contained in the central pocket drains towards the extremities of the droplet. Modeling such viscocapillary droplet relaxation requires considering the problem as 3D due to confinement. This 3D consideration yields a scaling model incorporating dominant dissipation within the droplet menisci. As such, the self-similar droplet dynamics is fully captured.
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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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We flow a 2D foam through a model 2D porous medium and study experimentally and numerically how the bubble size distribution evolves along the medium. The dominant mechanism of bubble creation is a fragmentation process occurring when bubbles pinched against obstacles are split in two smaller bubbles. We infer the statistics of these individual and local fragmentation events from the experimental data and propose a fragmentation equation to relate that statistics to the evolution of the global size distribution. The predicted evolution shows very good agreement with direct experimental measurements of the bubble size distribution.
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Pinning of the contact line and gas oversaturation explain the stability of single surface nanobubbles. In this article, we theoretically show that the pinning also suppresses the Ostwald ripening process between neighboring surface nanobubbles, thus explaining why in a population of neighboring surface nanobubbles different radii of curvature of the nanobubbles can be observed.
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Liquid foams are excellent systems to mitigate pressure waves such as acoustic or blast waves. The understanding of the underlying dissipation mechanisms however still remains an active matter of debate. In this paper, we investigate the attenuation of a weak blast wave by a liquid foam. The wave is produced with a shock tube and impacts a foam, with a cylindrical geometry. We measure the wave attenuation and velocity in the foam as a function of bubble size, liquid fraction, and the nature of the gas. We show that the attenuation depends on the nature of the gas and we experimentally evidence a maximum of dissipation for a given bubble size. All features are qualitatively captured by a model based on thermal dissipation in the gas.
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We study experimentally the flow of a foam confined as a bubble monolayer between two plates through a convergent channel. We quantify the velocity, the distribution and orientation of plastic events, and the elastic stress, using image analysis. We use two different soap solutions: a sodium dodecyl sulfate (SDS) solution, with a negligible wall friction between the bubbles and the confining plates, and a mixture containing a fatty acid, giving a large wall friction. We show that for SDS solutions, the velocity profile obeys a self-similar form which results from the superposition of plastic events, and the elastic deformation is uniform. For the other solution, the velocity field differs and the elastic deformation increases towards the exit of the channel. We discuss and quantify the role of wall friction on the velocity profile, the elastic deformation, and the rate of plastic events.
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We measured the dispersion relation for acoustic longitudinal waves in liquid foams, over a broad frequency range (60-600 kHz). Strong dispersion was found, with two nondispersive behaviors, separated by a negative density regime. A new model, based on the coupled displacements of films, liquid channels, and gas in the foam, rationalizes all the experimental findings.
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Modelos Químicos , Sustancias Viscoelásticas/química , Acústica , Dodecil Sulfato de Sodio/química , Xantenos/químicaRESUMEN
Drought poses a significant threat to forest survival worldwide by potentially generating air bubbles that obstruct sap transport within plants' hydraulic systems. However, the detailed mechanism of air entry and propagation at the scale of the veins remains elusive. Building upon a biomimetic model of leaf which we developed, we propose a direct comparison of the air embolism propagation in Adiantum (maidenhair fern) leaves, presented in Brodribb et al. (Brodribb TJ, Bienaimé D, Marmottant P. 2016 Revealing catastrophic failure of leaf networks under stress. Proc. Natl Acad. Sci. USA 113, 4865-4869 (doi:10.1073/pnas.1522569113)) and in our biomimetic leaves. In particular, we evidence that the jerky dynamics of the embolism propagation observed in Adiantum leaves can be recovered through the introduction of micrometric constrictions in the section of our biomimetic veins, mimicking the nanopores present in the bordered pit membranes in real leaves. We show that the intermittency in the propagation can be retrieved by a simple model coupling the variations of pressure induced by the constrictions and the variations of the volume of the compliant microchannels. Our study marks a step with the design of a biomimetic leaf that reproduces particular aspects of embolism propagation in real leaves, using a minimal set of controllable and readily tunable components. This biomimetic leaf constitutes a promising physical analogue and sets the stage for future enhancements to fully embody the unique physical features of embolizing real leaves.
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Modelos Biológicos , Hojas de la Planta , Biomimética , Materiales Biomiméticos/químicaRESUMEN
Liquid foams are widely used in industry for their high effective viscosity, whose local origin is still unclear. This Letter presents new results on the extension of a suspended soap film, in a configuration mimicking the elementary deformation occurring during foam shearing. We evidence a surprising two-step evolution: the film first extends homogeneously, then its extension stops, and a new thicker film is extracted from the meniscus. The second step is independent of the nature of the surfactant solution, whereas the initial extension is only observed for surfactant solutions with negligible dilatational moduli. We predict this complex behavior using a model based on Frankel's theory and on interface rigidification induced by confinement.