Density Scaling and Dynamic Correlations in Viscous Liquids

We use a recently proposed method [Berthier L.; Biroli G.; Bouchaud J.P.; Cipelletti L.; El Masri D.; L'Hote D.; Ladieu F.; Pierno M. Science 2005, 310, 1797.] to obtain an approximation to the 4-point dynamic correlation function from derivatives of the linear dielectric response function. For four liquids over a range of pressures, we find that the number of dynamically correlated molecules, Nc, depends only on the magnitude of the relaxation time, independently of temperature and pressure. This result is consistent with the invariance of the shape of the relaxation dispersion at constant relaxation time and the density scaling property of the relaxation times, and implies that Nc also conforms to the same scaling behavior. For propylene carbonate and salol Nc becomes constant with approach to the Arrhenius regime, consistent with the value of unity expected for intermolecularly non-cooperative relaxation.Comment: revisio

Comment on "Constant stress and pressure rheology of colloidal suspensions"

This is a comment on the recent letter by Wang and Brady on "Constant stress and pressure rheology of colloidal suspensions", Phys. Rev. Lett. 115, 158301 (2015).Comment: 1 page; under review -> v2: publishe

Can the jamming transition be described using equilibrium statistical mechanics?

When materials such as foams or emulsions are compressed, they display solid behaviour above the so-called `jamming' transition. Because compression is done out-of-equilibrium in the absence of thermal fluctuations, jamming appears as a new kind of a nonequilibrium phase transition. In this proceeding paper, we suggest that tools from equilibrium statistical mechanics can in fact be used to describe many specific features of the jamming transition. Our strategy is to introduce thermal fluctuations and use statistical mechanics to describe the complex phase behaviour of systems of soft repulsive particles, before sending temperature to zero at the end of the calculation. We show that currently available implementations of standard tools such as integral equations, mode-coupling theory, or replica calculations all break down at low temperature and large density, but we suggest that new analytical schemes can be developed to provide a fully microscopic, quantitative description of the jamming transition.Comment: 8 pages, 6 figs. Talk presented at Statphys24 (July 2010, Cairns, Australia

Nonlinear rheology of colloidal dispersions

Colloidal dispersions are commonly encountered in everyday life and represent an important class of complex fluid. Of particular significance for many commercial products and industrial processes is the ability to control and manipulate the macroscopic flow response of a dispersion by tuning the microscopic interactions between the constituents. An important step towards attaining this goal is the development of robust theoretical methods for predicting from first-principles the rheology and nonequilibrium microstructure of well defined model systems subject to external flow. In this review we give an overview of some promising theoretical approaches and the phenomena they seek to describe, focusing, for simplicity, on systems for which the colloidal particles interact via strongly repulsive, spherically symmetric interactions. In presenting the various theories, we will consider first low volume fraction systems, for which a number of exact results may be derived, before moving on to consider the intermediate and high volume fraction states which present both the most interesting physics and the most demanding technical challenges. In the high volume fraction regime particular emphasis will be given to the rheology of dynamically arrested states.Comment: Review articl

Heterogeneities in systems with quenched disorder

We study the strong role played by structural (quenched) heterogeneities on static and dynamic properties of the Frustrated Ising Lattice Gas in two dimensions, already in the liquid phase. Differently from the dynamical heterogeneities observed in other glass models in this case they may have infinite lifetime and be spatially pinned by the quenched disorder. We consider a measure of local frustration, show how it induces the appearance of spatial heterogeneities and how this reflects in the observed behavior of equilibrium density distributions and dynamic correlation functions.Comment: 8 page

Spatial fluctuations in transient creep deformation

We study the spatial fluctuations of transient creep deformation of materials as a function of time, both by Digital Image Correlation (DIC) measurements of paper samples and by numerical simulations of a crystal plasticity or discrete dislocation dynamics model. This model has a jamming or yielding phase transition, around which power-law or Andrade creep is found. During primary creep, the relative strength of the strain rate fluctuations increases with time in both cases - the spatially averaged creep rate obeys the Andrade law $\epsilon_t \sim t^{-0.7}$, while the time dependence of the spatial fluctuations of the local creep rates is given by $\Delta \epsilon_t \sim t^{-0.5}$. A similar scaling for the fluctuations is found in the logarithmic creep regime that is typically observed for lower applied stresses. We review briefly some classical theories of Andrade creep from the point of view of such spatial fluctuations. We consider these phenomenological, time-dependent creep laws in terms of a description based on a non-equilibrium phase transition separating evolving and frozen states of the system when the externally applied load is varied. Such an interpretation is discussed further by the data collapse of the local deformations in the spirit of absorbing state/depinning phase transitions, as well as deformation-deformation correlations and the width of the cumulative strain distributions. The results are also compared with the order parameter fluctuations observed close to the depinning transition of the 2$d$ Linear Interface Model or the quenched Edwards-Wilkinson equation.Comment: 27 pages, 18 figure

Correlation and response in the Backgammon model: the Ehrenfest legacy

We pursue our investigation of the non-equilibrium dynamics of the Backgammon model, a dynamical urn model which exhibits aging and glassy behavior at low temperature. We present an analytical study of the scaling behavior of the local correlation and response functions of the density fluctuations of the model, and of the associated fluctuation- dissipation ratios, throughout the alpha regime of low temperatures and long times. This analysis includes the aging regime, the convergence to equilibrium, sand the crossover behavior between them.Comment: 30 pages, 2 figures. To appear in Journal of Physics

Kovacs effect and fluctuation-dissipation relations in 1D kinetically constrained models

Strong and fragile glass relaxation behaviours are obtained simply changing the constraints of the kinetically constrained Ising chain from symmetric to purely asymmetric. We study the out-of-equilibrium dynamics of those two models focusing on the Kovacs effect and the fluctuation--dissipation relations. The Kovacs or memory effect, commonly observed in structural glasses, is present for both constraints but enhanced with the asymmetric ones. Most surprisingly, the related fluctuation-dissipation (FD) relations satisfy the FD theorem in both cases. This result strongly differs from the simple quenching procedure where the asymmetric model presents strong deviations from the FD theorem.Comment: 13 pages and 7 figures. To be published in J. Phys.

Crystallization in suspensions of hard spheres: A Monte Carlo and Molecular Dynamics simulation study

The crystallization of a metastable melt is one of the most important non equilibrium phenomena in condensed matter physics, and hard sphere colloidal model systems have been used for several decades to investigate this process by experimental observation and computer simulation. Nevertheless, there is still an unexplained discrepancy between simulation data and experimental nucleation rate densities. In this paper we examine the nucleation process in hard spheres using molecular dynamics and Monte Carlo simulation. We show that the crystallization process is mediated by precursors of low orientational bond-order and that our simulation data fairly match the experimental data sets