Role of uncrosslinked chains in droplets dynamics on silicone elastomers

We report an unexpected behavior in wetting dynamics on soft silicone substrates: the dynamics of aqueous droplets deposited on vertical plates of such elastomers exhibits two successive speed regimes. This macroscopic observation is found to be closely related to microscopic phenomena occurring at the scale of the polymer network: we show that uncrosslinked chains found in most widely used commercial silicone elastomers are responsible for this surprising behavior. A direct visualization of the uncrosslinked oligomers collected by water droplets is performed, evidencing that a capillarity-induced phase separation occurs: uncrosslinked oligomers are extracted from the silicone elastomer network by the water-glycerol mixture droplet. The sharp speed change is shown to coincide with an abrupt transition in surface tension of the droplets, when a critical surface concentration in uncrosslinked oligomer chains is reached. We infer that a droplet shifts to a second regime with a faster speed when it is completely covered with a homogeneous oil film

Une goutte, deux vitesses : la dynamique surprenante d’une goutte d’eau sur un élastomère silicone

Une goutte d’eau dévale généralement un plan incliné à vitesse constante. Néanmoins, nous avons observé que deux allures successives peuvent exister lorsque la goutte dévale sur certains élastomères silicones. Ces matériaux, très utilisés dans l’industrie et la recherche, sont un outil essentiel en microfluidique par exemple. La plupart des élastomères silicones commerciaux sont constitués d’un réseau de chaînes de polymères réticulées, c’est-à-dire interconnectées, mais contiennent également une petite proportion de chaînes libres, non réticulées. Notre enquête pour comprendre l’origine de la dynamique étonnante d’une goutte sur un tel matériau va nous mener sur leurs traces

Extraction of Silicone Uncrosslinked Chains at Air–Water–Polydimethylsiloxane Triple Lines

International audienceSilicone elastomers such as polydimethylsiloxane (PDMS) are convenient materials routinely used in laboratories that combine ease of preparation, flexibility, transparency, and gas permeability. However, these elastomers are known to contain a small fraction of uncrosslinked low-molecular-weight oligomers, the effects of which are not completely understood, particularly when used in contact with liquids. Here, we show that triple lines involving air, water, and PDMS elastomers are responsible for the contamination of water–air interfaces by uncrosslinked silicone oligomers through a capillarity-induced extraction mechanism. We investigate both the case of static and moving contact lines and study various geometries ranging from partially immersed PDMS plates to water droplets or air bubbles deposited on PDMS plates, all involving air–water–elastomer triple lines. We demonstrate experimentally that the contamination timescale is strikingly shorter for moving contact lines than in the static case. Eventually, we propose a simple poroelastic model capturing the main features of contamination observed in experiments

Elastocapillary deformation of thin elastic ribbons in 2D foam columns

International audienceThe ability of liquid interfaces to shape slender elastic structures provides powerful strategies to control the architecture of mechanical self assemblies. However, elastocapillarity-driven intelligent design remains unexplored in more complex architected liquids - such as foams. Here we propose a model system which combines an assembly of bubbles and a slender elastic structure. Arrangements of soap bubbles in confined environments form well-defined periodic structures, dictated by Plateau’s laws. We consider a 2D foam column formed in a container with square cross-section in which we introduce an elastomer ribbon, leading to architected structures whose geometry is guided by a competition between elasticity and capillarity. In this system, we quantify both experimentally and theoretically the equilibrium shapes, using X-ray micro-tomography and energy minimisation techniques. Beyond the understanding of the amplitude of the wavy elastic ribbon deformation, we provide a detailed analysis of the profile of the ribbon, and show that such setup can be used to grant a shape to a UV-curable composite slender structure, as a foam-forming technique suitable to miniaturisation. In more general terms, this work provides a stepping stone towards an improved understanding of the interactions between liquid foams and slender structures

Capillarity-induced folds fuel extreme shape changes in thin wicked membranes

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Investigating Pore‐Opening of Hydrogel Foams at the Scale of Freestanding Thin Films

International audienceControlling the pore connectivity of polymer foams is key for most of their applications, ranging from liquid uptake, mechanics, and acoustic/thermal insulation to tissue engineering. Despite their importance, the scientific phenomena governing the pore-opening processes remain poorly understood, requiring tedious trial-and-error procedures for property optimization. This lack of understanding is partly explained by the high complexity of the different interrelated, multiscale processes which take place as the foam transforms from an initially fluid foam into a solid foam. To progress in this field, this work takes inspiration from long-standing research on liquid foams and thin films to develop model experiments in a microfluidic “Thin Film Pressure Balance.” These experiments allow the investigation of isolated thin films under well-controlled environmental conditions reproducing those arising within a foam undergoing cross-linking and drying. Using the example of alginate hydrogel films, the evolution of isolated thin films undergoing gelation and drying is correlated with the evolution of the rheological properties of the same alginate solution in bulk. The overall approach is introduced and a first set of results is presented to propose a starting point for the phenomenological description of the different types of pore-opening processes and the classification of the resulting pore-opening types

Soft, skin-interfaced microfluidic systems with integrated immunoassays, fluorometric sensors and impedance measurement capabilities

International audienceSoft microfluidic systems that capture, store, and perform biomarker analysis of microliter volumes of sweat, in situ, as it emerges from the surface of the skin, represent an emerging class of wearable technology with powerful capabilities that complement those of traditional biophysical sensing devices. Recent work establishes applications in the real-time characterization of sweat dynamics and sweat chemistry in the context of sports performance and healthcare diagnostics. This paper presents a collection of advances in biochemical sensors and microfluidic designs that support multimodal operation in the monitoring of physiological signatures directly correlated to physical and mental stresses. These wireless, battery-free, skin-interfaced devices combine lateral flow immunoassays for cortisol, fluorometric assays for glucose and ascorbic acid (vitamin C), and digital tracking of skin galvanic responses. Systematic benchtop evaluations and field studies on human subjects highlight the key features of this platform for the continuous, noninvasive monitoring of biochemical and biophysical correlates of the stress state

Skin-interfaced soft microfluidic systems with modular and reusable electronics for in situ capacitive sensing of sweat loss, rate and conductivity

International audienceStick-on electrodes capacitively coupled to single-use microfluidic channels enable contactless analysis of sweat in a soft wearable format with real-time wireless data collection