GG33 


Rheology of Gels, Glasses and Jammed Systems


Nonaffinity-induced critical slowing down in fibrous networks and dense suspensions


October 11, 2022 (Tuesday) 5:05


Track 3 / Sheraton 5

(Click on name to view author profile)

  1. Shivers, Jordan L. (Rice University, Center for Theoretical Biological Physics)
  2. Sharma, Abhinav (Leibniz Institute for Polymer Research Dresden, Institute Theory of Polymers)
  3. MacKintosh, Fred C. (Rice University, Chemical and Biomolecular Engineering)

(in printed abstract book)
Jordan L. Shivers1, Abhinav Sharma2 and Fred C. MacKintosh3
1Center for Theoretical Biological Physics, Rice University, Houston, TX 77004; 2Institute Theory of Polymers, Leibniz Institute for Polymer Research Dresden, Dresden, Germany; 3Chemical and Biomolecular Engineering, Rice University, Houston, TX 77004


Shivers, Jordan L.


gels; jammed systems; suspensions


Fluid-immersed networks and dense suspensions typically reside near a boundary between soft (or fluid-like) and rigid (or solid-like) mechanical regimes. This boundary can be crossed either by varying the concentration or by deformation. Near the onset or loss of rigidity, dissipation limiting nonaffine rearrangements dominate the macroscopic viscoelastic response, giving rise to diverging relaxation times and power-law rheology. We derive a simple relationship between nonaffinity and excess viscosity in fluid-immersed amorphous materials. We then demonstrate this relationship and its rheological consequences in simulations of stress relaxation in strained filament networks and dense suspensions.