14 research outputs found

    Universal non-diffusive slow dynamics in aging soft matter

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    We use conventional and multispeckle dynamic light scattering to investigate the dynamics of a wide variety of jammed soft materials, including colloidal gels, concentrated emulsions, and concentrated surfactant phases. For all systems, the dynamic structure factor f(q,t) exhibits a two-step decay. The initial decay is due to the thermally activated diffusive motion of the scatterers, as indicated by the q -2 dependence of the characteristic relaxation time, where q is the scattering vector. However, due to the constrained motion of the scatterers in jammed systems, the dynamics are arrested and the initial decay terminates in a plateau. Surprisingly, we find that a final, ultraslow decay leads to the complete relaxation of f(q,t), indicative of rearrangements on length scales as large as several microns or tens of microns. Remarkably, for all systems the same very peculiar form is found for the final relaxation of the dynamic structure factor: f(q,t)∌exp[-(t/τ s) P], with p ≈ 1.5 and τ s∌q -1, thus suggesting the generality of this behavior. Additionally, for all samples the final relaxation slows down with age, although the aging behavior is found to be sample dependent. We propose that the unusual ultraslow dynamics are due to the relaxation of internal stresses, built into the sample at the jamming transition, and present simple scaling arguments that support this hypothesis

    Multiscale Molecular Simulations of Polymer-Matrix Nanocomposites

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    Dynamics of Weakly Aggregated Colloidal Particles

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    We discuss the behavior of the dynamics of colloidal particles with a weak attractive interparticle interaction that is induced through the addition of polymer to the solvent. We briefly review the description of their behavior in terms of the jamming phase diagram, which parameterized the fluid to solid transition due to changes in volume fraction, attractive energy or applied stress. We focus on a discussion of aging of the solid gels formed by these colloid-polymer mixtures. They exhibit a delayed collapse induced by gravity. The time evolution of the height of the sediment exhibits an unexpected scaling behavior, suggesting a universal nature to this delayed collapse. We complement these measurements of the scaling of the collapse with microscopic investigations of the evolution of the structure of the network using confocal microscopy. These results provide new insight into the origin of this aging behavior. 1

    Universal Non-Diffusive Slow Dynamics in Aging Soft Matter

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    this paper, we present light scattering measurements of the ultraslow dynamics and the aging of several soft matter jammed systems. Remarkably, we find that for all systems the dynamic structure factor exhibit the same very unusual behavior: at long times an ultraslow, " compressedexponential " relaxation, whose characteristic time scales as the inverse scattering vector, leads to the complete loss of correlation of the scattered light. This behavior is in sharp contrast with the di#usive or sub-di#usive, slower-than-exponential relaxation typically observed when approaching the jammed phase from the fluid side. We propose a simple model to explain these uncommon dynamics, based on the relaxation of internal stresses, which are built in the sample at the jamming transition. The observation of the very same dynamics in systems ranging from tenuous colloidal fractal gels to concentrated emulsions, and from lamellar gels to micellar polycrystals suggests the generality of this behavior in disordered, jammed, soft materials, underlying the central role of stress relaxation on the system evolutio

    Dynamics of weakly aggregated colloidal particles - discussion

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    We discuss the behaviour of the dynamics of colloidal particles with a weak attractive interparticle interaction that is induced through the addition of polymer to the solvent. We briefly review the description of their behaviour in terms of the jamming phase diagram, which parametrized the fluid–to–solid transition due to changes in volume fraction, attractive energy or applied stress. We focus on a discussion of ageing of the solid gels formed by these colloid–polymer mixtures. They exhibit a delayed collapse induced by gravity. The time evolution of the height of the sediment exhibits an unexpected scaling behaviour, suggesting a universal nature to this delayed collapse. We complement these measurements of the scaling of the collapse with microscopic investigations of the evolution of the structure of the network using confocal microscopy. These results provide new insight into the origin of this ageing behaviour
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