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Register a new userTime resolved viscoelastic properties during structural arrest and aging of a colloidal glass
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Evolution of the energy landscape during physical aging of glassy materials can be understood from the frequency and strain dependence of the shear modulus but the non-stationary nature of these systems frustrates investigation of their instantaneous underlying properties. Using a series of time dependent measurements we systematically reconstruct the frequency and strain dependence as a function of age for a repulsive colloidal glass undergoing structural arrest. In this manner, we are able to unambiguously observe the structural relaxation time, which increases exponentially with sample age at short times. The yield stress varies logarithmically with time in the arrested state, consistent with recent simulation results, whereas the yield strain is nearly constant in this regime. Strikingly, the frequency dependence at fixed times can be rescaled onto a master curve, implying a simple connection between the aging of the system and the change in the frequency dependent modulus.
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We employ parallel superposition rheology to study the dynamics of an aging colloidal glass in the presence of a mean field stress. Over a range of intermediate stresses, the loss modulus exceeds the storage modulus at short times but develops a maximum concomitant with a crossover between the two as the system ages. This is attended by a narrowing of the loss peak on increasing stress. We show that this feature is characteristic of the structural arrest in these materials, which is made observable on reasonable timescales by the activating influence of the stress. The arrest time displays an exponential dependence on inverse stress. These results provide experimental validation of the role of stress as an effective temperature in soft glassy systems as has been advanced in recent theoretical frameworks.
We report measurements of the frequency-dependent shear moduli of aging colloidal systems that evolve from a purely low-viscosity liquid to a predominantly elastic glass or gel. Using microrheology, we measure the local complex shear modulus $G^{*}(omega)$ over a very wide range of frequencies (1 Hz- 100 kHz). The combined use of one- and two-particle microrheology allows us to differentiate between colloidal glasses and gels - the glass is homogenous, whereas the colloidal gel shows a considerable degree of heterogeneity on length scales larger than 0.5 micrometer. Despite this characteristic difference, both systems exhibit similar rheological behavior which evolve in time with aging, showing a crossover from a single power-law frequency dependence of the viscoelastic modulus to a sum of two power laws. The crossover occurs at a time $t_{0}$, which defines a mechanical transition point. We found that the data acquired during the aging of different samples can be collapsed onto a single master curve by scaling the aging time with $t_{0}$. This raises questions about the prior interpretation of two power laws in terms of a superposition of an elastic network embedded in a viscoelastic background. Keywords: Aging, colloidal glass, passive microrheology
In this work, we study ageing behavior of aqueous laponite suspension, a model soft glassy material, in creep. We observe that viscoelastic behavior is time dependent and is strongly influenced by the deformation field; the effect is known to arise due to ageing and rejuvenation. We show that irrespective of strength of deformation field (shear stress) and age, when imposed time-scale is normalized with dominating relaxation mode of the system, universal ageing behavior is obtained demonstrating time-stress superposition; the phenomena that may be generic in variety of soft materials.
Motivated by the mean field prediction of a Gardner phase transition between a normal glass and a marginally stable glass, we investigate the off-equilibrium dynamics of three-dimensional polydisperse hard spheres, used as a model for colloidal or granular glasses. Deep inside the glass phase, we find that a sharp crossover pressure $P_{rm G}$ separates two distinct dynamical regimes. For pressure $P < P_{rm G}$, the glass behaves as a normal solid, displaying fast dynamics that quickly equilibrates within the glass free energy basin. For $P>P_{rm G}$, instead, the dynamics becomes strongly anomalous, displaying very large equilibration time scales, aging, and a constantly increasing dynamical susceptibility. The crossover at $P_{rm G}$ is strongly reminiscent of the one observed in three-dimensional spin-glasses in an external field, suggesting that the two systems could be in the same universality class, consistently with theoretical expectations.
Colloidal dispersions of Laponite platelets are known to age slowly from viscous sols to colloidal glasses. We follow this aging process by monitoring the diffusion of probe particles embedded in the sample via dynamic light scattering. Our results show that the time-dependent diffusion of the probe particles scales with their size. This implies that the fluctuation-dissipation theorem can be generalized for this out-of-equilibrium system by replacing the bath temperature with an effective temperature. Simultaneous dynamic rheological measurements reveal that this effective temperature increases as a function of aging time and frequency. This suggests the existence of two regimes: at probed time scales longer than the characteristic relaxation time of the Laponite dispersion, the system thermalizes with the bath, whereas at shorter time scales, the system is out-of-equilibrium with an effective temperature greater than the bath temperature.
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