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Instability and rupture of sheared viscous liquid nanofilms

Vira Dhaliwal1, Christian Pedersen1, Kheireddin Kadri2, Guillaume Miquelard-Garnier2, Cyrille Sollogoub2, Jorge Peixinho2, Thomas Salez3,*, and Andreas Carlson1,†

  • 1Mechanics Division, Department of Mathematics, University of Oslo, 0316 Oslo, Norway
  • 2Laboratoire PIMM, CNRS, Arts et Métiers Institute of Technology, CNAM, 151 boulevard de l'Hopital, Paris, France
  • 3Univ. Bordeaux, CNRS, LOMA, UMR 5798, F-33405, Talence, France

  • *thomas.salez@cnrs.fr
  • acarlson@math.uio.no

Phys. Rev. Fluids 9, 024201 – Published 8 February, 2024

DOI: https://doi.org/10.1103/PhysRevFluids.9.024201

Abstract

Liquid nanofilms are ubiquitous in nature and technology, and their equilibrium and out-of-equilibrium dynamics are key to a multitude of phenomena and processes. We numerically study the evolution and rupture of viscous nanometric films, incorporating the effects of surface tension, van der Waals forces, thermal fluctuations, and viscous shear. We show that thermal fluctuations create perturbations that can trigger film rupture, but they do not significantly affect the growth rate of the perturbations. The film rupture time can be predicted from a linear stability analysis of the governing thin film equation, by considering the most unstable wavelength and the thermal roughness. Furthermore, applying a sufficiently large unidirectional shear can stabilize large perturbations, creating a finite-amplitude traveling wave instead of film rupture. In three dimensions, unidirectional shear does not inhibit rupture, as perturbations are not suppressed in the direction perpendicular to the applied shear. However, if the direction of shear varies in time, then the growth of large perturbations is prevented in all directions, and rupture can be impeded.

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