Stability at Random Close Packing

The requirement that packings of hard particles, arguably the simplest structural glass, cannot be compressed by rearranging their network of contacts is shown to yield a new constraint on their microscopic structure. This constraint takes the form a bound between the distribution of contact forces P(f) and the pair distribution function g(r): if P(f) \sim f^{\theta} and g(r) \sim (r-{\sigma})^(-{\gamma}), where {\sigma} is the particle diameter, one finds that {\gamma} \geq 1/(2+{\theta}). This bound plays a role similar to those found in some glassy materials with long-range interactions, such as the Coulomb gap in Anderson insulators or the distribution of local fields in mean-field spin glasses. There is ground to believe that this bound is saturated, offering an explanation for the presence of avalanches of rearrangements with power-law statistics observed in packings

On the dependence of the avalanche angle on the granular layer thickness

A layer of sand of thickness h flows down a rough surface if the inclination is larger than some threshold value theta which decreases with h. A tentative microscopic model for the dependence of theta with h is proposed for rigid frictional grains, based on the following hypothesis: (i) a horizontal layer of sand has some coordination z larger than a critical value z_c where mechanical stability is lost (ii) as the tilt angle is increased, the configurations visited present a growing proportion $_s of sliding contacts. Instability with respect to flow occurs when z-z_s=z_c. This criterion leads to a prediction for theta(h) in good agreement with empirical observations.Comment: 6 pages, 2 figure

Theory of the Jamming Transition at Finite Temperature

A theory for the microscopic structure and the vibrational properties of soft sphere glass at finite temperature is presented. With an effective potential, derived here, the phase diagram and vibrational properties are worked out around the Maxwell critical point at zero temperature $T$ and pressure $p$. Variational arguments and effective medium theory identically predict a non-trivial temperature scale $T^*\sim p^{(2-a)/(1-a)}$ with $a \approx 0.17$ such that low-energy vibrational properties are hard-sphere like for $T \gtrsim T^*$, and zero-temperature soft-sphere like otherwise. However, due to crossovers in the equation of state relating $T$, $p$, and the packing fraction $\phi$, these two regimes lead to four regions where scaling behaviors differ when expressed in terms of $T$ and $\phi$. Scaling predictions are presented for the mean-squared displacement, characteristic frequency, shear modulus, and characteristic elastic length in all regions of the phase diagram.Comment: 8 pages + 3 pages S

Geometric origin of excess low-frequency vibrational modes in amorphous solids

Glasses have a large excess of low-frequency vibrational modes in comparison with crystalline solids. We show that such a feature is a necessary consequence of the geometry generic to weakly connected solids. In particular, we analyze the density of states of a recently simulated system, comprised of weakly compressed spheres at zero temperature. We account for the observed a) constancy of the density of modes with frequency, b) appearance of a low-frequency cutoff, and c) power-law increase of this cutoff with compression. We predict a length scale below which vibrations are very different from those of a continuous elastic body.Comment: 4 pages, 2 figures. Argument rewritten, identical result

Theory for the density of interacting quasi-localised modes in amorphous solids

Quasi-localised modes appear in the vibrational spectrum of amorphous solids at low-frequency. Though never formalised, these modes are believed to have a close relationship with other important local excitations, including shear transformations and two-level systems. We provide a theory for their frequency density, $D_{L}(\omega)\sim\omega^{\alpha}$, that establishes this link for systems at zero temperature under quasi-static loading. It predicts two regimes depending on the density of shear transformations $P(x)\sim x^{\theta}$ (with $x$ the additional stress needed to trigger a shear transformation). If $\theta>1/4$, $\alpha=4$ and a finite fraction of quasi-localised modes form shear transformations, whose amplitudes vanish at low frequencies. If $\theta<1/4$, $\alpha=3+ 4 \theta$ and all quasi-localised modes form shear transformations with a finite amplitude at vanishing frequencies. We confirm our predictions numerically

How collective asperity detachments nucleate slip at frictional interfaces

Sliding at a quasi-statically loaded frictional interface can occur via macroscopic slip events, which nucleate locally before propagating as rupture fronts very similar to fracture. We introduce a novel microscopic model of a frictional interface that includes asperity-level disorder, elastic interaction between local slip events, and inertia. For a perfectly flat and homogeneously loaded interface, we find that slip is nucleated by avalanches of asperity detachments of extension larger than a critical radius $A_c$ governed by a Griffith criterion. We find that after slip, the density of asperities at a local distance to yielding $x_\sigma$ presents a pseudo-gap $P(x_\sigma) \sim (x_\sigma)^\theta$, where $\theta$ is a non-universal exponent that depends on the statistics of the disorder. This result makes a link between friction and the plasticity of amorphous materials where a pseudo-gap is also present. For friction, we find that a consequence is that stick-slip is an extremely slowly decaying finite size effect, while the slip nucleation radius $A_c$ diverges as a $\theta$-dependent power law of the system size. We discuss how these predictions can be tested experimentally

Dynamics of Strongly Deformed Polymers in Solution

Bead spring models for polymers in solution are nonlinear if either the finite extensibility of the polymer, excluded volume effects or hydrodynamic interactions between polymer segments are taken into account. For such models we use a powerful method for the determination of the complete relaxation spectrum of fluctuations at {\it steady state}. In general, the spectrum and modes differ significantly from those of the linear Rouse model. For a tethered polymer in uniform flow the differences are mainly caused by an inhomogeneous distribution of tension along the chain and are most pronounced due to the finite chain extensibility. Beyond the dynamics of steady state fluctuations we also investigate the nonlinear response of the polymer to a {\em large sudden change} in the flow. This response exhibits several distinct regimes with characteristic decay laws and shows features which are beyond the scope of single mode theories such as the dumbbell model.Comment: 7 pages, 3 figure

Contact line motion for partially wetting fluids

We study the flow close to an advancing contact line in the limit of small capillary number. To take into account wetting effects, both long and short-ranged contributions to the disjoining pressure are taken into account. In front of the contact line, there is a microscopic film corresponding to a minimum of the interaction potential. We compute the parameters of the contact line solution relevant to the matching to a macroscopic problem, for example a spreading droplet. The result closely resembles previous results obtained with a slip model

Classification of the nickel-like silver spectrum (AgXX) from a fast capillary discharge plasma

Includes bibliographical references (page 25).A study of the Ni-like silver (AgXX) spectra in the 13:7-20:5 nm wavelength region using a plasma generated by a fast high power capillary discharge is reported. Forty-three AgXX transitions have been identified with the assistance of calculations performed using the Slater-Condon method with generalized least-squares fits of the energy parameters. The average difference between the measured transition wavelengths and the theoretical values is 0.0026 nm