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The debonding criterion of fibrils of soft adhesive materials is a key element regarding the quantitative modelisation of pressure sensitive adhesive tapes' peeling energy. We present in this article an experimental study of the detachment of a commercial acrylic adhesive tape from the top surface of a single micrometric pillar of PDMS elastomer. During an experiment, the pillar and the adhesive, after being put in contact, are separated at a constant displacement rate, resulting in the formation, the elongation and the final detachment of a fibril of adhesive material. A systematic study allows us to uncover power laws for the maximum force and the critical elongation of the fibril at debonding as a function of the diameter of the cylindrical pillar which controls the diameter of the fibril. The scaling law evidenced for the critical elongation appears as a first step toward the understanding of the debonding criterion of fibrils of soft adhesive materials. In addition, viscoelastic digitation at the triple debonding line is observed during detachment for large pillar diameters. The wavelength and penetration length of the fingers that we report appear to be consistent with existing models based on pure elastic mechanical response.
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We measured the thickness of MDCK epithelia grown on substrates with a sinusoidal profile. We show that while at long wavelength the profile of the epithelium follows that of the substrate, at short wavelengths cells are thicker in valleys than on ridges. This is reminiscent of the so-called «healing length in the case of a thin liquid film wetting a rough solid substrate. We explore the ability of continuum mechanics models to account for these observations. Modeling the epithelium as a thin liquid film, with surface tension, does not fully account for the measurements. Neither does modeling the epithelium as a thin incompressible elastic film. On the contrary, the addition of an apical active stress gives satisfactory agreement with measurements, with one fitting parameter, the ratio between the active stress and the elastic modulus.
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Epitelio , Módulo de Elasticidad , Tensión SuperficialRESUMEN
It is nearly impossible to separate two interleaved phonebooks by pulling their spines. The very slight force exerted by the outer sheets of the assembly is amplified as the exponential of the square of the number of sheets, meaning that even a small number of sheets can create a highly resistant system. We present a systematic and detailed study of the influences of the normal external force and the geometrical parameters of the booklets on the assembly strength. We conclude that the paper-paper adhesion force between the two outer sheets, on the order of a few [Formula: see text], is the one amplified by the interleaved-book system. The two-phonebook experiment-which has attracted the attention of students and the non-scientific public all around the world as an outstanding demonstration of the strength of friction-appears to also be a spectacular macroscopic manifestation of the microscopic coupling of friction and adhesion.
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This corrects the article DOI: 10.1103/PhysRevLett.119.154502.
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Our understanding of the structural features of foams and emulsions has advanced significantly over the last 20 years. However, with a search for "super-stable" liquid dispersions, foam and emulsion science employs increasingly complex formulations which create solid-like visco-elastic layers at the bubble/drop surfaces. These lead to elastic, adhesive and frictional forces between bubbles/drops, impacting strongly how they pack and deform against each other, asking for an adaptation of the currently available structural description. The possibility to modify systematically the interfacial properties makes these dispersions ideal systems for the exploration of soft granular materials with complex interactions. We present here a first systematic analysis of the structural features of such a system using a model silicone emulsion containing millimetre-sized polyethylene glycol drops (PEG). Solid-like drop surfaces are obtained by polymeric cross-linking reactions at the PEG-silicone interface. Using a novel droplet-micromanipulator, we highlight the presence of elastic, adhesive and frictional interactions between two drops. We then provide for the first time a full tomographic analysis of the structural features of these emulsions. An in-depth analysis of the angle of repose, local volume fraction distributions, pair correlation functions and the drop deformations for different skin formulations allow us to put in evidence the striking difference with "ordinary" emulsions having fluid-like drop surfaces. While strong analogies with frictional hard-sphere systems can be drawn, these systems display a set of unique features due to the high deformability of the drops which await systematic exploration.
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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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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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It is nearly impossible to separate two interleaved phone books when held by their spines. A full understanding of this astonishing demonstration of solid friction in complex assemblies remains elusive. In this Letter, we report on experiments with controlled booklets and show that the force required increases sharply with the number of sheets. A model captures the effect of the number of sheets, their thickness, and the overlapping distance. Furthermore, the data collapse onto a self-similar master curve with one dimensionless amplification parameter. In addition to solving a long-standing familiar enigma, this model system provides a framework with which one can accurately measure friction forces and coefficients at low loads, and that has relevance to complex assemblies from the macro- to the nanoscale.
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Macrocellular silicone polymers are obtained after solidification of the continuous phase of a poly(dimethylsiloxane) emulsion, which contains poly(ethylene glycol) drops of sub-millimetric dimensions. Coalescence of the liquid template emulsion is prohibited by a reactive blending approach. The relationship is investigated in detail between the interfacial properties and the emulsion stability, and micro- and millifluidic techniques are used to generate macrocellular polymers with controlled structural properties over a wider range of cell sizes (0.2-2 mm) and volume fractions of the continuous phase (0.1%-40%). This approach could easily be transferred to a wide range of polymeric systems.
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Dimetilpolisiloxanos/síntesis química , Siliconas/química , Dimetilpolisiloxanos/química , Emulsiones/síntesis química , Emulsiones/química , Tamaño de la Partícula , Propiedades de SuperficieRESUMEN
Wrinkled morphology is a distinctive phenotype observed in mature biofilms produced by a great number of bacteria. Here we study the formation of macroscopic structures (wrinkles and folds) observed during the maturation of Bacillus subtilis pellicles in relation to their mechanical response. We show how the mechanical buckling instability can explain their formation. By performing simple tests, we highlight the role of confining geometry and growth in determining the symmetry of wrinkles. We also experimentally demonstrate that the pellicles are soft elastic materials for small deformations induced by a tensile device. The wrinkled structures are then described by using the equations of elastic plates, which include the growth process as a simple parameter representing biomass production. This growth controls buckling instability, which triggers the formation of wrinkles. We also describe how the structure of ripples is modified when capillary effects are dominant. Finally, the experiments performed on a mutant strain indicate that the presence of an extracellular matrix is required to maintain a connective and elastic pellicle.
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Bacillus subtilis/fisiología , Biopelículas/crecimiento & desarrollo , Bacillus subtilis/citología , Bacillus subtilis/crecimiento & desarrollo , Fenómenos Biomecánicos , Elasticidad , Conceptos Matemáticos , Modelos Biológicos , FenotipoRESUMEN
Dispersions of immiscible liquids, such as emulsions and polymer blends, are at the core of many industrial applications which makes the understanding of their properties (morphology, stability, etc.) of great interest. A wide range of these properties depend on interfacial phenomena, whose understanding is therefore of particular importance. The behaviour of interfacial tension in emulsions and polymer blends is well-understood - both theoretically and experimentally - in the case of non-reactive stabilization processes using pre-made surfactants. However, this description of the interfacial tension behaviour in reactive systems, where the stabilizing agents are created in-situ (and which is more efficient as a stabilization route for many systems), does not yet find a consensus among the community. In this review, we compare the different theories which have been developed for non-reactive and for reactive systems, and we discuss their ability to capture the behaviour found experimentally. Finally, we address the consequences of the reactive stabilization process both on the global emulsions or polymer blend morphologies and at the interfacial scale.
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In this paper, we present an experimental study of the friction between a smooth elastomer lens and an elastomer substrate micropatterned with hexagonal arrays of cylindrical pillars. Depending on the normal load, the surfaces can be in top or mixed contact. The friction force can be interpreted in terms of friction stresses in the full contact and top contact zones. The latter is higher than that on smooth surfaces evidencing the role of the elastic deformations of the surfaces in the dissipation processes.
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A new experimental technique is proposed to easily measure both advancing and receding contact angles of a liquid on a solid surface, with unprecedented accuracy. The technique is based on the analysis of the evolution of a capillary bridge formed between a liquid bath and a solid surface (which needs to be spherical) when the distance between the surface and the liquid bath is slowly varied. The feasibility of the technique is demonstrated using a low-energy perfluorinated surface with two different test liquids (water and hexadecane). A detailed description of both experimental procedures and computational modeling are given, allowing one to determine contact angle values. It is shown that the origin of the high accuracy of this technique relies on the fact that the contact angles are automatically averaged over the whole periphery of the contact. This method appears to be particularly adapted to the characterization of surfaces with very low contact angle hysteresis.
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Wrinkling patterns at the metallized surface of thin polymer films are shown to be sensitive to the sticky or slippery character of the polymer-substrate interface. Existing theoretical models were expanded to specific boundary conditions (adhesive versus slippery) in order to rationalize these observations. Based on this concept, we were able to propose a new and simple method to orient the wrinkles by chemically patterning the substrate with regions of high and low adhesion.