Quantitative earthquake-like statistical properties of the flow of soft materials below yield stress.

The flow behavior of soft materials below the yield stress can be rich and is not fully understood. Here, we report shear-stress-induced reorganization of three-dimensional solid-like soft materials formed by closely packed nematic domains of surfactant micelles and a repulsive Wigner glass formed by anisotropic clay nano-discs having ionic interactions. The creep response of both the systems below the yield stress results in angular velocity fluctuations of the shearing plate showing large temporal burst-like events that resemble seismic foreshocks-aftershocks data measuring the ground motion during earthquake avalanches. We find that the statistical properties of the quake events inside such a burst map on to the scaling relations for magnitude and frequency distribution of earthquakes, given by Gutenberg-Richter and Omori laws, and follow a power-law distribution of the inter-occurrence waiting time. In situ polarized optical microscopy reveals that during these events the system self-organizes to a much stronger solid-like state.

Experimental signatures of a nonequilibrium phase transition near the crossover point of a Langmuir monolayer.

We investigate the response of the two-dimensional (2D) continuous non-particulate film of surfactant sorbitan tristearate confined at the air-water interface under oscillatory shear deformation. The time dependence of various rheological parameters show critical-like behavior at a value of strain amplitude close to the crossover point of elastic ([Formula: see text]) and viscous ([Formula: see text]) shear moduli. Imposing oscillatory shear of different strain amplitudes ([Formula: see text]) above and below the crossover strain amplitude ([Formula: see text]) over a large number of cycles, we quantify the temporal dependence of interfacial viscous modulus, phase angle ([Formula: see text]) as well as higher harmonic components of stress. The number of shear cycles ([Formula: see text]) required for these quantities to reach the steady state value diverges near [Formula: see text]. The steady state values of the third harmonic ([Formula: see text]) show order parameter like behavior indicating the importance of higher order harmonics near the nonequilibrium transition. We further show that the energy dissipation per cycle per unit volume has a marked change near [Formula: see text], consistent with continuum level nonequilibrium shear-transformation-zone model of amorphous viscoplasticity.