Viscoelastic effects and anomalous transient levelling exponents in thin films

We study theoretically the profile evolution of a thin viscoelastic film supported onto a no-slip flat substrate. Due to the nonconstant initial curvature at the free surface, there is a flow driven by Laplace pressure and mediated by viscoelasticity. In the framework of lubrication theory, we derive a thin film equation that contains local viscoelastic stress through the Maxwell model. Then, considering a sufficiently regular small perturbation of the free surface, we linearise the equation and derive its general solution. We analyse and discuss in details the behaviour of this function. We then use it to study the viscoelastic evolution of a Gaussian initial perturbation through its transient levelling exponent. For initial widths of the profile that are smaller than a characteristic length scale involving both the film thickness and the elastocapillary length, this exponent is shown to reach anomalously high values at the elastic-to-viscous transition. This prediction should in particular be observed at sufficiently short times in experiments on thin polymer films.Comment: 4 figure

Wake and wave resistance on viscous thin films

The effect of an external pressure disturbance, being displaced with a constant speed along the free surface of a viscous thin film, is studied theoretically in the lubrication approximation in one- and two-dimensional geometries. In the comoving frame, the imposed pressure field creates a stationary deformation of the interface - a wake - that spatially vanishes in the far region. The shape of the wake and the way it vanishes depend on both the speed and size of the external source and the properties of the film. The wave resistance, namely the force that has to be externally furnished in order to maintain the wake, is analysed in details. For finite-size pressure disturbances, it increases with the speed, up to a certain transition value above which a monotonic decrease occurs. The role of the horizontal extent of the pressure field is studied as well, revealing that for a smaller disturbance the latter transition occurs at higher speed. Eventually, for a Dirac pressure source, the wave resistance either saturates in a 1D geometry, or diverges in a 2D geometry

Flow-injection of branched polymers inside nanopores

Flexible chains (linear or branched) can be forced to enter into a narrow capillary by using a hydrodynamic flow. Here, we correct our earlier description of this problem by considering the progressive nature of the suction process. We find that the critical current for penetration, $J\_c$, is controlled by the entry of a single blob of the capillary size, and that its scaling structure is the same for branched and linear chains.Comment: Submitted to Europhysics Letter

Elastowetting of Soft Hydrogel Spheres

When a soft hydrogel sphere is placed on a rigid hydrophilic substrate, it undergoes arrested spreading by forming an axisymmetric foot near the contact line, while conserving its global spherical shape. In contrast, liquid water (that constitutes greater than 90% of the hydrogel's volume) spreads into a thin film on the same surface. We study systematically this elastowetting of gel spheres on substrates of different surface energies, and find that their contact angle increases as the work of adhesion between the gel and the substrate decreases, as one would observe for drops of pure water - albeit being larger than in the latter case. This difference in the contact angles of gel and water appears to be due to the elastic shear stresses that develop in the gel and oppose its spreading. Indeed, by increasing the elastic modulus of the gel spheres, we find that their contact angle also increases. In addition, the length of the contact foot increases with the work of adhesion and sphere size, while it decreases when the elastic modulus of the gel is increased. We discuss those experimental results in light of a minimal analysis based on energy minimization, volume conservation, and scaling arguments

Self-Similarity and Energy Dissipation in Stepped Polymer Films

The surface of a thin liquid film with nonconstant curvature is unstable, as the Laplace pressure drives a flow mediated by viscosity. We present the results of experiments on one of the simplest variable curvature surfaces: a stepped polymer film. Height profiles are measured as a function of time for a variety of molecular weights. The evolution of the profiles is shown to be self-similar. This self-similarity offers a precise measurement of the capillary velocity by comparison with numerical solutions of the thin film equation. We also derive a master expression for the time dependence of the excess free energy as a function of the material properties and film geometry. The experiment and theory are in excellent agreement and indicate the effectiveness of stepped polymer films to elucidate nanoscale rheological properties.Comment: 5 pages, 4 figures, article accepted for publication in Physical Review Letter