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J. M. Brader

Publications and source records attributed to J. M. Brader.

35 records · Page 2Linked to original sources

Residual Stresses in Glasses

The history dependence of the glasses formed from flow-melted steady states by a sudden cessation of the shear rate $\dotγ$ is studied in colloidal suspensions, by molecular dynamics simulations, and mode-coupling theory. In an ideal glass, stresses relax only partially, leaving behind a finite persistent residual stress. For intermediate times, relaxation curves scale as a function of $\dotγt$, even though no flow is present. The macroscopic stress evolution is connected to a length scale of residual liquefaction displayed by microscopic mean-squared displacements. The theory describes this history dependence of glasses sharing the same thermodynamic state variables, but differing static properties.

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Density Functional approach to Nonlinear Rheology

We present a density functional based closure of the pair Smoluchowski equation for Brownian particles under shear flow. Given an equilibrium free energy functional as input the theory provides first-principles predictions for the flow-distorted pair correlation function and associated rheological quantities over a wide range of volume fractions and flow rates. Taking two-dimensional hard-disks under shear flow as an illustrative model we calculate the pair correlation function, viscosity and normal stress difference under both steady and start-up shear.

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First-Principles Constitutive Equation for Suspension Rheology

We provide a detailed derivation of a recently developed first-principles approach to calculating averages in systems of interacting, spherical Brownian particles under time-dependent flow. Although we restrict ourselves to flows which are both homogeneous and incompressible, the time-dependence and geometry (e.g. shear, extension) are arbitrary. The approximations formulated within mode-coupling theory are particularly suited to dense colloidal suspensions and capture the slow relaxation arising from particle interactions and the resulting glass transition to an amorphous solid. The delicate interplay between slow structural relaxation and time-dependent external flow in colloidal suspensions may thus be studied within a fully tensorial theory.

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Schematic Mode Coupling Theory of Glass Rheology: Single and Double Step Strains

Mode coupling theory (MCT) has had notable successes in addressing the rheology of hard-sphere colloidal glasses, and also soft colloidal glasses such as star-polymers. Here, we explore the properties of a recently developed MCT-based schematic constitutive equation under idealized experimental protocols involving single and then double step strains. We find strong deviations from expectations based on factorable, BKZ-type constitutive models. Specifically, a nonvanishing stress remains long after the application of two equal and opposite step strains; this residual stress is a signature of plastic deformation. We also discuss the distinction between hypothetically instantaneous step strains and fast ramps. These are not generally equivalent in our MCT approach, with the latter more likely to capture the physics of experimental `step' strains. The distinction points to the different role played by reversible anelastic, and irreversible plastic rearrangements.

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Three Dimensional Flow of Colloidal Glasses

Recent experiments performed on a variety of soft glassy materials have demonstrated that any imposed shear flow serves to simultaneously fluidize these systems in all spatial directions [Ovarlez \textit{et al.} (2010)]. When probed with a second shear flow, the viscous response of the experimental system is determined by the rate of the primary, fluidizing flow. Motivated by these findings, we employ a recently developed schematic mode-coupling theory [Brader \textit{et al.} (2009)] to investigate the three dimensional flow of a colloidal glass, subject to a combination of simple shear and uniaxial compression. Despite differences in the specific choice of superposed flow, the flow curves obtained show good qualitative agreement with the experimental findings and recover the observed power law describing the decay of the scaled viscosity as a function of the dominant rate. We then proceed to perform a more formal analysis of our constitutive equation for different kind of `mixed' flows consisting of a dominant primary flow subject to a weaker perturbing flow. Our study provides further evidence that the theory of Brader \textit{et al.} (2009) reliably describes the dynamic arrest and mechanical fluidization of dense particulate suspensions.

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Density profiles of a colloidal liquid at a wall under shear flow

Using a dynamical density functional theory we analyze the density profile of a colloidal liquid near a wall under shear flow. Due to the symmetries of the system considered, the naive application of dynamical density functional theory does not lead to a shear induced modification of the equilibrium density profile, which would be expected on physical grounds. By introducing a physically motivated dynamic mean field correction we incorporate the missing shear induced interparticle forces into the theory. We find that the shear flow tends to enhance the oscillations in the density profile of hard-spheres at a hard-wall and, at sufficiently high shear rates, induces a nonequilibrium transition to a steady state characterized by planes of particles parallel to the wall. Under gravity, we find that the center-of-mass of the density distribution increases with shear rate, i.e., shear increases the potential energy of the particles.

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Nonlinear response of dense colloidal suspensions under oscillatory shear: Mode-coupling theory and FT-rheology experiments

Using a combination of theory, experiment and simulation we investigate the nonlinear response of dense colloidal suspensions to large amplitude oscillatory shear flow. The time-dependent stress response is calculated using a recently developed schematic mode-coupling-type theory describing colloidal suspensions under externally applied flow. For finite strain amplitudes the theory generates a nonlinear response, characterized by significant higher harmonic contributions. An important feature of the theory is the prediction of an ideal glass transition at sufficiently strong coupling, which is accompanied by the discontinuous appearance of a dynamic yield stress. For the oscillatory shear flow under consideration we find that the yield stress plays an important role in determining the non linearity of the time-dependent stress response. Our theoretical findings are strongly supported by both large amplitude oscillatory (LAOS) experiments (with FT-rheology analysis) on suspensions of thermosensitive core-shell particles dispersed in water and Brownian dynamics simulations performed on a two-dimensional binary hard-disc mixture. In particular, theory predicts nontrivial values of the exponents governing the final decay of the storage and loss moduli as a function of strain amplitude which are in excellent agreement with both simulation and experiment. A consistent set of parameters in the presented schematic model achieves to jointly describe linear moduli, nonlinear flow curves and large amplitude oscillatory spectroscopy.

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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.

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Glass Rheology: From mode-coupling theory to a dynamical yield criterion

The mode coupling theory (MCT) of glasses, while offering an incomplete description of glass transition physics, represents the only established route to first-principles prediction of rheological behavior in nonergodic materials such as colloidal glasses. However, the constitutive equations derivable from MCT are somewhat intractable, hindering their practical use and also their interpretation. Here, we present a schematic (single-mode) MCT model which incorporates the tensorial structure of the full theory. Using it, we calculate the dynamic yield surface for a large class of flows.

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Effect of mixing and spatial dimension on the glass transition

We study the influence of composition changes on the glass transition of binary hard disc and hard sphere mixtures in the framework of mode coupling theory. We derive a general expression for the slope of a glass transition line. Applied to the binary mixture in the low concentration limits, this new method allows a fast prediction of some properties of the glass transition lines. The glass transition diagram we find for binary hard discs strongly resembles the random close packing diagram. Compared to 3D from previous studies, the extension of the glass regime due to mixing is much more pronounced in 2D where plasticization only sets in at larger size disparities. For small size disparities we find a stabilization of the glass phase quadratic in the deviation of the size disparity from unity.

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Rheology, Structure and Dynamics of Colloid-Polymer Mixtures: from Liquids to Gels

We investigated the viscoelastic properties of colloid-polymer mixtures at intermediate colloid volume fraction and varying polymer concentrations, thereby tuning the attractive interactions. Within the examined range of polymer concentrations, the samples ranged from fluids to gels. Already in the liquid phase the viscoelastic properties significantly changed when approaching the gelation boundary, indicating the formation of clusters and transient networks. This is supported by an increasing correlation length of the density fluctuations, observed by static light scattering and microscopy. At the same time, the correlation function determined by dynamic light scattering completely decays, indicating the absence of dynamical arrest. Upon increasing the polymer concentration beyond the gelation boundary, the rheological properties changed qualitatively again, now they are consistent with the formation of colloidal gels. Our experimental results, namely the location of the gelation boundary as well as the elastic (storage) and viscous (loss) moduli, are compared to different theoretical models. These include consideration of the escape time as well as predictions for the viscoelastic moduli based on scaling relations and Mode Coupling Theories (MCT).

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A First-Principles Constitutive Equation for Suspension Rheology

Using mode-coupling theory, we derive a constitutive equation for the nonlinear rheology of dense colloidal suspensions under arbitrary time-dependent homogeneous flow. Generalizing previous results for simple shear, this allows the full tensorial structure of the theory to be identified. Macroscopic deformation measures, such as the Cauchy-Green tensors, thereby emerge. So does a direct relation between the stress and the distorted microstructure, illuminating the interplay of slow structural relaxation and arbitrary imposed flow. We present flow curves for steady planar and uniaxial elongation and compare these to simple shear. The resulting non-linear Trouton ratios point to a tensorially nontrivial dynamic yield condition for colloidal glasses.

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Structural precursor to freezing: An integral equation study

Recent simulation studies have drawn attention to the shoulder which forms in the second peak of the radial distribution function of hard-spheres at densities close to freezing and which is associated with local crystalline ordering in the dense fluid. We address this structural precursor to freezing using an inhomogeneous integral equation theory capable of describing local packing constraints to a high level of accuracy. The addition of a short-range attractive interaction leads to a well known broadening of the fluid-solid coexistence region as a function of attraction strength. The appearence of a shoulder in our calculated radial distribution functions is found to be consistent with the broadened coexistence region for a simple model potential, thus demonstrating that the shoulder is not exclusively a high density packing effect.

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Structure and phase equilibria of the Widom-Rowlinson model

The Widom-Rowlinson model plays an important role in the statistical mechanics of second order phase transitions and yet there currently exists no theoretical approach capable of accurately predicting both the microscopic structure and phase equilibria. We address this issue using computer simulation, density functional theory and integral equation theory. A detailed study of the pair correlation functions obtained from computer simulation motivates a closure of the Ornstein-Zernike equations which gives a good description of the pair structure and locates the critical point to an accuracy of 2 percent.

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From Equilibrium to Steady State: The Transient Dynamics of Colloidal Liquids under Shear

We investigate stresses and particle motion during the start up of flow in a colloidal dispersion close to arrest into a glassy state. A combination of molecular dynamics simulation, mode coupling theory and confocal microscopy experiment is used to investigate the origins of the widely observed stress overshoot and (previously not reported) super-diffusive motion in the transient dynamics. A link between the macro-rheological stress versus strain curves and the microscopic particle motion is established. Negative correlations in the transient auto-correlation function of the potential stresses are found responsible for both phenomena, and arise even for homogeneous flows and almost Gaussian particle displacements.

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Dense colloidal suspensions under time-dependent shear

We consider the nonlinear rheology of dense colloidal suspensions under a time-dependent simple shear flow. Starting from the Smoluchowski equation for interacting Brownian particles advected by shearing (ignoring fluctuations in fluid velocity) we develop a formalism which enables the calculation of time-dependent, far-from-equilibrium averages. Taking shear-stress as an example we derive exactly a generalized Green-Kubo relation, and an equation of motion for the transient density correlator, involving a three-time memory function. Mode coupling approximations give a closed constitutive equation yielding the time-dependent stress for arbitrary shear rate history. We solve this equation numerically for the special case of a hard sphere glass subject to step-strain.

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