ترغب بنشر مسار تعليمي؟ اضغط هنا

Aging in Dense Colloids as Diffusion in the Logarithm of Time

123   0   0.0 ( 0 )
 نشر من قبل Stefan Boettcher
 تاريخ النشر 2009
  مجال البحث فيزياء
والبحث باللغة English
 تأليف S. Boettcher




اسأل ChatGPT حول البحث

The far-from-equilibrium dynamics of glassy systems share important phenomenological traits. A transition is generally observed from a time-homogeneous dynamical regime to an aging regime where physical changes occur intermittently and, on average, at a decreasing rate. It has been suggested that a global change of the independent time variable to its logarithm may render the aging dynamics homogeneous: for colloids, this entails diffusion but on a logarithmic time scale. Our novel analysis of experimental colloid data confirms that the mean square displacement grows linearly in time at low densities and shows that it grows linearly in the logarithm of time at high densities. Correspondingly, pairs of particles initially in close contact survive as pairs with a probability which decays exponentially in either time or its logarithm. The form of the Probability Density Function of the displacements shows that long-ranged spatial correlations are very long-lived in dense colloids. A phenomenological stochastic model is then introduced which relies on the growth and collapse of strongly correlated clusters (dynamic heterogeneity), and which reproduces the full spectrum of observed colloidal behaviors depending on the form assumed for the probability that a cluster collapses during a Monte Carlo update. In the limit where large clusters dominate, the collapse rate is ~1/t, implying a homogeneous, log-Poissonian process that qualitatively reproduces the experimental results for dense colloids. Finally an analytical toy-model is discussed to elucidate the strong dependence of the simulation results on the integrability (or lack thereof) of the cluster collapse probability function.

قيم البحث

اقرأ أيضاً

110 - Imre Varga , Ferenc Kun , 2003
A theoretical study of the structure formation observed very recently [Phys. Rev. Lett. 90, 128303 (2003)] in binary colloids is presented. In our model solely the dipole-dipole interaction of the particles is considered, electrohidrodynamic effects are excluded. Based on molecular dynamics simulations and analytic calculations we show that the total concentration of the particles, the relative concentration and the relative dipole moment of the components determine the structure of the colloid. At low concentrations the kinetic aggregation of particles results in fractal structures which show a crossover behavior when increasing the concentration. At high concentration various lattice structures are obtained in a good agreement with experiments.
Recent experiments and simulations have revealed glassy features in the cytoplasm, living tissues as well as dense assemblies of self propelled colloids. This leads to a fundamental question: how do these non-equilibrium (active) amorphous materials differ from conventional passive glasses, created either by lowering temperature or by increasing density? To address this we investigate the aging behaviour after a quench to an almost arrested state of a model active glass former, a Kob-Andersen glass in two dimensions. Each constituent particle is driven by a constant propulsion force whose direction diffuses over time. Using extensive molecular dynamics simulations we reveal rich aging behaviour of this dense active matter system: short persistence times of the active forcing lead to effective thermal aging; in the opposite limit we find a two-step aging process with active athermal aging at short times followed by activity-driven aging at late times. We develop a dedicated simulation method that gives access to this long-time scaling regime for highly persistent active forces.
Modeling collective motion in non-conservative systems, such as granular materials, is difficult since a general microscopic-to-macroscopic approach is not available: there is no Hamiltonian, no known stationary densities in phase space, not a known small set of relevant variables. Phenomenological coarse-grained models are a good alternative, provided that one has identified a few slow observables and collected a sufficient amount of data for their dynamics. Here we study the case of a vibrofluidized dense granular material. The experimental study of a tracer, dispersed into the media, showed the evidence of many time scales: fast ballistic, intermediate caged, slow superdiffusive, very slow diffusive. A numerical investigation has demonstrated that tracers superdiffusion is related to slow rotating drifts of the granular medium. Here we offer a deeper insight into the slow scales of the granular medium, and propose a new phenomenological model for such a secular dynamics. Based upon the model for the granular medium, we also introduce a model for the tracer (fast and slow) dynamics, which consists in a stochastic system of equations for three coupled variables, and is therefore more refined and successful than previous models.
65 - D. R. Strachan , G. C. Kalur , 2005
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 s how 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.
We present a comprehensive investigation of polymer diffusion in the semidilute regime by fluorescence correlation spectroscopy (FCS) and dynamic light scattering (DLS). Using single-labeled polystyrene chains, FCS leads to the self-diffusion coeffic ient while DLS gives the cooperative diffusion coefficient for exactly the same molecular weights and concentrations. Using FCS we observe a new fast mode in the semidilute entangled concentration regime beyond the slower mode which is due to self-diffusion. Comparison of FCS data with data obtained by DLS on the same polymers shows that the second mode observed in FCS is identical to the cooperative diffusion coefficient measured with DLS. An in-depth analysis and a comparison with current theoretical models demonstrates that the new cooperative mode observed in FCS is due to the effective long-range interaction of the chains through the transient entanglement network.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا