Role of normal stress in the creep dynamics and failure of a biopolymer gel
arXiv:2012.09827 · doi:10.1103/PhysRevLett.125.268006
Abstract
We investigate the delayed rupture of biopolymer gels under a constant shear load by simultaneous dynamic light scattering and rheology measurements. We unveil the crucial role of normal stresses built up during gelation: all samples that eventually fracture self-weaken during the gelation process, as revealed by a partial relaxation of the normal stress concomitant to a burst of microscopic plastic rearrangements. Upon applying a shear stress, weakened gels exhibit in the creep regime distinctive signatures in their microscopic dynamics, which anticipate macroscopic fracture by up to thousands of seconds. The dynamics in fracturing gels are faster than those of non-fracturing gels and exhibit large spatio-temporal fluctuations. A spatially localized region with significant plasticity eventually nucleates, expands progressively, and finally invades the whole sample triggering macroscopic failure.
accepted for publication in Physical Review Letters
References in corpus (5)
- Solvent control of crack dynamics in a reversible hydrogel
- Dilatancy in the flow and fracture of stretched colloidal suspensions
- Fracture of a biopolymer gel as a viscoplastic disentanglement process
- Resolving long-range spatial correlations in jammed colloidal systems using photon correlation imaging
- Instabilities in droplets spreading on gels