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Anisotropic viscoelastic phase separation in polydisperse hard rods leads to nonsticky gelation.

Claudia Ferreiro-CórdovaC Patrick RoyallJeroen Sebastiaan Van Duijneveldt
Published in: Proceedings of the National Academy of Sciences of the United States of America (2020)
Spinodal demixing into two phases having very different viscosities leads to viscoelastic networks-i.e., gels-usually as a result of attractive particle interactions. Here, however, we demonstrate demixing in a colloidal system of polydisperse, rod-like clay particles that is driven by particle repulsions instead. One of the phases is a nematic liquid crystal with a highly anisotropic viscosity, allowing flow along the director, but suppressing it in other directions. This phase coexists with a dilute isotropic phase. Real-space analysis and molecular-dynamics simulations both reveal a long-lived network structure that is locally anisotropic, yet macroscopically isotropic. We show that our system exhibits the characteristics of colloidal gelation, leading to nonsticky gels.
Keyphrases
  • molecular dynamics simulations
  • finite element
  • atomic force microscopy
  • molecular docking
  • signaling pathway
  • genome wide
  • single cell
  • high resolution