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Emergent Strain Stiffening in Interlocked Granular Chains

Denis Dumont, Maurine Houze, Paul Rambach, Thomas Salez, Sylvain Patinet, and Pascal Damman
Phys. Rev. Lett. 120, 088001 – Published 23 February 2018
Physics logo See Focus story: Bead Chains Impersonate Polymer Molecules

Abstract

Granular chain packings exhibit a striking emergent strain-stiffening behavior despite the individual looseness of the constitutive chains. Using indentation experiments on such assemblies, we measure an exponential increase in the collective resistance force F with the indentation depth z and with the square root of the number N of beads per chain. These two observations are, respectively, reminiscent of the self-amplification of friction in a capstan or in interleaved books, as well as the physics of polymers. The experimental data are well captured by a novel model based on these two ingredients. Specifically, the resistance force is found to vary according to the universal relation logFμNΦ11/8z/b, where μ is the friction coefficient between two elementary beads, b is their size, and Φ is the volume fraction of chain beads when semidiluted in a surrounding medium of unconnected beads. Our study suggests that theories normally confined to the realm of polymer physics at a molecular level can be used to explain phenomena at a macroscopic level. This class of systems enables the study of friction in complex assemblies, with practical implications for the design of new materials, the textile industry, and biology.

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  • Received 27 July 2017
  • Revised 16 December 2017

DOI:https://doi.org/10.1103/PhysRevLett.120.088001

© 2018 American Physical Society

Physics Subject Headings (PhySH)

Polymers & Soft Matter

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Bead Chains Impersonate Polymer Molecules

Published 23 February 2018

Chains of metallic beads act a lot like polymer molecules, even though real polymers are in constant motion.

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Authors & Affiliations

Denis Dumont1, Maurine Houze1, Paul Rambach1,2, Thomas Salez2,3,4, Sylvain Patinet5, and Pascal Damman1,*

  • 1Laboratoire Interfaces et Fluides Complexes, Université de Mons, 20 Place du Parc, B-7000 Mons, Belgium
  • 2Laboratoire de Physico-Chimie Théorique, UMR CNRS Gulliver 7083, ESPCI Paris, PSL Research University, 10 rue Vauquelin, 75005 Paris, France
  • 3Université de Bordeaux, CNRS, LOMA, UMR 5798, F-33405 Talence, France
  • 4Global Station for Soft Matter, Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, Japan
  • 5PMMH, ESPCI Paris/CNRS-UMR 7636/Université Paris 6 UPMC/Université Paris 7 Diderot, PSL Research University, 10 rue Vauquelin, 75231 Paris cedex 05, France

  • *pascal.damman@umons.ac.be

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Issue

Vol. 120, Iss. 8 — 23 February 2018

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