Protocol to perform pressurized blister tests on thin elastic films

This work aims to identify common challenges in the preparation of the blister test devices designed for measurement of 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 adhesion energy per unit area of $G = 18 \pm 2$ \mbox{mJ}/{\mbox m}^2 for polystyrene on glass, which is in good agreement with the measurement of $G = 14 \pm 2$ \mbox{mJ}/{\mbox m}^2 found in our independent cleavage test

Generation of silicone poly-HIPES with controlled pore sizes via reactive emulsion stabilization

Macrocellular silicone polymers are obtained after solidification of the continuous phase of a PDMS (polydimethylsiloxane) emulsion, which contains PEG (polyethylene glycol) drops of sub-millimetric dimensions. Coalescence of the liquid template emulsion is prohibited by a reactive blending approach. We investigate in detail the relationship between the interfacial properties and the emulsion stability, and we use micro- and millifluidic techniques to generation macro-cellular polymers with controlled structural properties over a wider range of cell-sizes (0.2-2mm) and volume fractions of the continuous phase (0.1-40%). This approach could easily be transferred to a wide range of polymeric systems

Rescaling the dynamics of evaporating drops

The dynamics of evaporation of wetting droplets has been investigated experimentally in an extended range of drop sizes, in order to provide trends relevant for a theoretical analysis. A model is proposed, which generalises Tanner's law, allowing us to smooth out the singularities both in dissipation and in evaporative flux at the moving contact line. A qualitative agreement is obtained, which represents a first step towards the solution of a very old, complex problem

Water-based peeling of thin hydrophobic films

Inks of permanent markers and water-proof 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 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

Transition from Cassie to Wenzel state in patterned soft elastomer sliding contacts

In this paper, we presented an experimental and theoretical analysis of the formation of the contact between a smooth elastomer lens and an elastomer substrate micropatterned with hexagonal arrays of cylindrical pillars. We show using a JKR model coupled with a full description of the deformation of the substrate between the pillars that the transition between the top to the full contact is obtain when the normal load is increased above a well predicted threshold. We have also shown that above the onset of full contact, the evolution of the area of full contact was obeying a simple scaling.Comment: 4 pages, 6 figures. Submitte

Chemical modification of PDMS surface without impacting the viscoelasticity: Model systems for a better understanding of elastomer/elastomer adhesion and friction

The influence of both viscoelastic and interfacial parameters on the surface properties of elastomers is difficult to study. Here, we describe a simple route to achieve surface modification of PDMS without impacting the viscoelastic properties of the bulk. PEG modified PDMS surfaces were synthesized by two step surface modification based on hydrosilylation. The covalent grafting of PEG on the surface has been evidenced by AFM and ATR-FTIR, and its effect on the hydrophilicity characterized by static and dynamic contact angle. The static water contact angle of the PEG-modified PDMS decreases from 110° (for unmodified PDMS) to 65°. Dynamic contact angles also show a significant decrease in both advancing and receding contact angles, along with a significant increase in the contact angle hysteresis, which can be related to an increase in the surface energy as estimated by JKR measurements. The viscoelastic properties of modified PDMS are found to be quantitatively comparable to those of the unmodified PDMS. This simple method is an efficient way to prepare model materials which can be used to get a better understanding of the exact contribution of the surface chemistry on surface properties of elastomers