Kinetics of Fragmenting Freely Evolving Granular Gases

We investigate the effect of fragmentation on the homogeneous free cooling of inelastic hard spheres, using Boltzmann kinetic theory and Direct Monte Carlo simulations. We analyze in detail a model where dissipative collisions may subsequently lead to a break-up of the grains. With a given probability, two off-springs are then created from one of the two colliding partners, with conservation of mass, momentum and kinetic energy. We observe a scaling regime characterized by a single collisional average, that quantifies the deviations from Gaussian behaviour for the joint size and velocity distribution function. We also discuss the possibility of a catastrophe whereby the number of particles diverges in a finite time. This phenomenon appears correlated to a ``shattering'' transition marked by a delta singularity at vanishingly small grains for the rescaled size distribution.Comment: 22 pages, 8 figure

Dissipative particle dynamics for interacting systems

We introduce a dissipative particle dynamics scheme for the dynamics of non-ideal fluids. Given a free-energy density that determines the thermodynamics of the system, we derive consistent conservative forces. The use of these effective, density dependent forces reduces the local structure as compared to previously proposed models. This is an important feature in mesoscopic modeling, since it ensures a realistic length and time scale separation in coarse-grained models. We consider in detail the behavior of a van der Waals fluid and a binary mixture with a miscibility gap. We discuss the physical implications of having a single length scale characterizing the interaction range, in particular for the interfacial properties.Comment: 25 pages, 12 figure

Dynamics of Polydisperse Polymer Mixtures

We develop a general analysis of the diffusive dynamics of polydisperse polymers in the presence of chemical potential gradients, within the context of the tube model (with all species entangled). We obtain a set of coupled dynamical equations for the time evolution of the polymeric densities with explicitly derived coefficients. For the case of chemical polydispersity (a set of chains that are identical except for having a continuous spectrum of enthalpic interaction strengths) the coupled equations can be fully solved in certain cases. For these we study the linearised mode spectrum following a quench through the spinodal, with and without a passive (polymeric) solvent. We also study the more conventional case of length polydisperse chains in a poor solvent.Comment: 21 pages, 3 figures,revised versio

A practical density functional for polydisperse polymers

The Flory Huggins equation of state for monodisperse polymers can be turned into a density functional by adding a square gradient term, with a coefficient fixed by appeal to RPA (random phase approximation). We present instead a model nonlocal functional in which each polymer is replaced by a deterministic, penetrable particle of known shape. This reproduces the RPA and square gradient theories in the small deviation and/or weak gradient limits, and can readily be extended to polydisperse chains. The utility of the new functional is shown for the case of a polydisperse polymer solution at coexistence in a poor solvent.Comment: 9 pages, 3 figure

Negative fluctuation-dissipation ratios in the backgammon model

We analyze fluctuation-dissipation relations in the Backgammon model: a system that displays glassy behavior at zero temperature due to the existence of entropy barriers. We study local and global fluctuation relations for the different observables in the model. For the case of a global perturbation we find a unique negative fluctuation-dissipation ratio that is independent of the observable and which diverges linearly with the waiting time. This result suggests that a negative effective temperature can be observed in glassy systems even in the absence of thermally activated processes.Comment: 32 pages, 10 figures. Accepted in PR