The influence of an applied shear field on the dynamics of an aging colloidal suspension has been investigated by the dynamic light-scattering determination of the density autocorrelation function. Though a stationary state is never observed, the slow dynamics crosses between two different nonequilibrium regimes as soon as the structural relaxation time τ s approaches the inverse shear rate γ̇ -1. In the shear-dominated regime (at high γ̇ values) the structural relaxation time is found to be strongly sensitive to the shear rate (τ s ∼ γ̇ -α, with α ∼ 1) while aging proceeds at a very slow rate. The effect of the shear on the detailed shape of the density autocorrelation function is quantitatively described, assuming that the structural relaxation process arises from the heterogeneous superposition of many relaxing units, each one independently coupled to shear with a parallel composition rule for time scales: 1/τ→ 1/τ+Aγ̇. © 2005 The American Physical Society.
Aging under shear: Structural relaxation of a non-Newtonian fluid / DI LEONARDO, Roberto; F., Ianni; Ruocco, Giancarlo. - In: PHYSICAL REVIEW E, STATISTICAL, NONLINEAR, AND SOFT MATTER PHYSICS. - ISSN 1539-3755. - 71:1(2005), pp. 011505-1-011505-10. [10.1103/physreve.71.011505]
Aging under shear: Structural relaxation of a non-Newtonian fluid
DI LEONARDO, ROBERTO;RUOCCO, Giancarlo
2005
Abstract
The influence of an applied shear field on the dynamics of an aging colloidal suspension has been investigated by the dynamic light-scattering determination of the density autocorrelation function. Though a stationary state is never observed, the slow dynamics crosses between two different nonequilibrium regimes as soon as the structural relaxation time τ s approaches the inverse shear rate γ̇ -1. In the shear-dominated regime (at high γ̇ values) the structural relaxation time is found to be strongly sensitive to the shear rate (τ s ∼ γ̇ -α, with α ∼ 1) while aging proceeds at a very slow rate. The effect of the shear on the detailed shape of the density autocorrelation function is quantitatively described, assuming that the structural relaxation process arises from the heterogeneous superposition of many relaxing units, each one independently coupled to shear with a parallel composition rule for time scales: 1/τ→ 1/τ+Aγ̇. © 2005 The American Physical Society.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.