Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userLiquid dewetting under a thin elastic film
121
0
0.0
(
0
)
Added by
Kari Dalnoki-Veress
Publication date
2017
fields
Physics
and research's language is
English
Ask ChatGPT about the research
No Arabic abstract
We study the dewetting of liquid films capped by a thin elastomeric layer. When the tension in the elastomer is isotropic, circular holes grow at a rate which decreases with increasing tension. The morphology of holes and rim stability can be controlled by changing the boundary conditions and tension in the capping film. When the capping film is prepared with a biaxial tension, holes form with a non-circular shape elongated along the high tension axis. With suitable choice of elastic boundary conditions, samples can even be designed such that square holes appear.
rate research
Read More
In this study, thin elastic films supported on a rigid substrate are brought into contact with a spherical glass indenter. Upon contact, adhesive fingers emerge at the periphery of the contact patch with a characteristic wavelength. Elastic films are also pre-strained along one axis before initiation of contact, causing the fingering pattern to become anisotropic and align with the axis along which the strain was applied. This transition from isotropic to anisotropic patterning is characterized quantitatively and a simple model is developed to understand the origin of the anisotropy.
The objective of this work is to study the role of shear on the rupture of ultrathin polymer films. To do so, a finite-difference numerical scheme for the resolution of the thin film equation was set up taking into account capillary and van der Waals (vdW) forces. This method was validated by comparing the dynamics obtained from an initial harmonic perturbation to established theoretical predictions. With the addition of shear, three regimes have then been evidenced as a function of the shear rate. In the case of low shear rates the rupture is delayed when compared to the no-shear problem, while at higher shear rates it is even suppressed: the perturbed interface goes back to its unperturbed state over time. In between these two limiting regimes, a transient one in which shear and vdW forces balance each other, leading to a non-monotonic temporal evolution of the perturbed interface, has been identified. While a linear analysis is sufficient to describe the rupture time in the absence of shear, the nonlinearities appear to be essential otherwise.
Adsorbed molecular films provide two-dimensional systems that show various emergent phenomena that are not observed in bulk counterparts. We have measured the elasticity of thin neon films adsorbed on porous glass down to 1 K by the torsional oscillator technique. The shear modulus of a neon film anomalously increases at low temperatures with excess dissipation. This behavior indicates a crossover from a soft (fluidlike) state at high temperatures to a stiff (solidlike) state at low temperatures. The temperature dependence of the anomaly is qualitatively similar to that of the elastic anomaly of helium films found in our recent study. The dissipation peak temperature, however, becomes constant at about 5 K, contrary to the case of helium, in which it decreases to 0 K at a critical coverage of a quantum phase transition between a gapped localized phase and a mobile (superfluid) phase. It is concluded that neon films behave as a classical system that does not show a quantum phase transition or superfluidity, although the films may be strongly supercooled to temperatures much lower than the bulk triple point, 24.6 K. Our results suggest that the elastic anomaly is a universal phenomenon of atomic or molecular films adsorbed on disordered substrates.
The spontaneous formation of droplets via dewetting of a thin fluid film from a solid substrate allows for materials nanostructuring, under appropriate experimental control. While thermal fluctuations are expected to play a role in this process, their relevance has remained poorly understood, particularly during the nonlinear stages of evolution. Within a stochastic lubrication framework, we show that thermal noise speeds up and substantially influences the formation and evolution of the droplet arrangement. As compared with their deterministic counterparts, for a fixed spatial domain, stochastic systems feature a smaller number of droplets, with a larger variability in sizes and space distribution. Finally, we discuss the influence of stochasticity on droplet coarsening for very long times.
We present results on the leveling of polymer microdroplets on thin films prepared from the same material. In particular, we explore the crossover from a droplet spreading on an infinitesimally thin film (Tanners law regime) to that of a droplet leveling on a film thicker than the droplet itself. In both regimes, the droplets excess surface area decreases towards the equilibrium configuration of a flat liquid film, but with a different power law in time. Additionally, the characteristic leveling time depends on molecular properties, the size of the droplet, and the thickness of the underlying film. Flow within the film makes this system fundamentally different from a droplet spreading on a solid surface. We thus develop a theoretical model based on thin film hydrodynamics that quantitatively describes the observed crossover between the two leveling regimes.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
