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Register a new userElasticity of soft particles and colloids near Random Close Packing
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Matthieu Wyart
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Assemblies of purely repulsive and frictionless particles, such as emulsions or hard spheres, display very curious properties near their jamming transition, which occurs at the random close packing for mono-disperse spheres. Although such systems do not contain the long and cross-linked polymeric chains characterizing a rubber, they behave macroscopically in a similar way: the shear modulus $G$ can become infinitely smaller than the bulk modulus $B$. After reviewing recent theoretical results on the structure of such packing (in particular their coordination) I will propose an explanation for the observed scaling of the elastic moduli, and explain why the arguments both apply to soft and hard particles.
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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.
Starting from a microscopic model of randomly cross-linked particles with quenched disorder, we calculate the Laudau-Wilson free energy S for arbitrary cross-link densities. Considering pure shear deformations, S takes the form of the elastic energy of an isotropic amorphous solid state, from which the shear modulus can be identified. It is found to be an universal quantity, not depending on any microscopic length-scales of the model.
We perform numerical simulations of purely repulsive soft colloidal particles interacting via a generalized elastic potential and constrained to a two-dimensional plane and to the surface of a spherical shell. For the planar case, we compute the phase diagram in terms of the systems rescaled density and temperature. We find that a large number of ordered phases becomes accessible at low temperatures as the density of the system increases, and we study systematically how structural variety depends on the functional shape of the pair potential. For the spherical case, we revisit the generalized Thomson problem for small numbers of particles N <= 12 and identify, enumerate and compare the minimal energy polyhedra established by the location of the particles to those of the corresponding electrostatic system.
Spatial heterogeneity in the elastic properties of soft random solids is examined via vulcanization theory. The spatial heterogeneity in the emph{structure} of soft random solids is a result of the fluctuations locked-in at their synthesis, which also brings heterogeneity in their emph{elastic properties}. Vulcanization theory studies semi-microscopic models of random-solid-forming systems, and applies replica field theory to deal with their quenched disorder and thermal fluctuations. The elastic deformations of soft random solids are argued to be described by the Goldstone sector of fluctuations contained in vulcanization theory, associated with a subtle form of spontaneous symmetry breaking that is associated with the liquid-to-random-solid transition. The resulting free energy of this Goldstone sector can be reinterpreted as arising from a phenomenological description of an elastic medium with quenched disorder. Through this comparison, we arrive at the statistics of the quenched disorder of the elasticity of soft random solids, in terms of residual stress and Lame-coefficient fields. In particular, there are large residual stresses in the equilibrium reference state, and the disorder correlators involving the residual stress are found to be long-ranged and governed by a universal parameter that also gives the mean shear modulus.
We have made experimental observations of the force networks within a two-dimensional granular silo similar to the classical system of Janssen. Models like that of Janssen predict that pressure within a silo saturates with depth as the result of vertical forces being redirected to the walls of the silo where they can then be carried by friction. By averaging ensembles of experimentally-obtained force networks in different ways, we compare the observed behavior with various predictions for granular silos. We identify several differences between the mean behavior in our system and that predicted by Janssen-like models: We find that the redirection parameter describing how the force network transfers vertical forces to the walls varies with depth. We find that changes in the preparation of the material can cause the pressure within the silo to either saturate or to continue building with depth. Most strikingly, we observe a non-linear response to overloads applied to the top of the material in the silo. For larger overloads we observe the previously reported giant overshoot effect where overload pressure decays only after an initial increase [G. Ovarlez et al., Phys. Rev. E 67, 060302(R) (2003)]. For smaller overloads we find that additional pressure propagates to great depth. This effect depends on the particle stiffness, as given for instance by the Youngs modulus, E, of the material from which the particles are made. Important measures include E, the unscreened hydrostatic pressure, and the applied load. These experiments suggest that when the load and the particle weight are comparable, particle elasticity acts to stabilize the force network, allowing non-linear network effects to be seen in the mean behavior.
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