A granular mixture of particles of two sizes that is shaken vertically will in most cases segregate. If the larger particles accumulate at the top of the sample, this is called the Brazil-nut effect (BNE); if they accumulate at the bottom, it is called the reverse Brazil-nut effect (RBNE). While this process is of great industrial importance in the handling of bulk solids, it is not well understood. In recent years ten different mechanisms have been suggested to explain when each type of segregation is observed. However, the dependence of the mechanisms on driving conditions and material parameters and hence their relative importance is largely unknown. In this paper we present experiments and simulations where both types of particles are made from the same material and shaken under low air pressure, which reduces the number of mechanisms to be considered to seven. We observe both BNE and RBNE by varying systematically the driving frequency and amplitude, diameter ratio, ratio of total volume of small to large particles, and overall sample volume. All our results can be explained by a combination of three mechanisms: a geometrical mechanism called void filling, transport of particles in sidewall-driven convection rolls, and thermal diffusion, a mechanism predicted by kinetic theory.

We prepare packings of frictional tetrahedra with volume fractions ϕ ranging from 0.469 to 0.622 using three different experimental protocols under isobaric conditions. Analysis via x-ray microtomography reveals that the contact number Z grows with ϕ, but does depend on the preparation protocol. While there exist four different types of contacts in tetrahedra packings, our analysis shows that the edge-to-face contacts contribute about 50% of the total increase in Z. The number of constraints per particle C increases also with ϕ and even the loosest packings are strongly hyperstatic, i.e., mechanically overdetermined with C approximately twice the degrees of freedom each particle possesses.

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We investigate how material rigidity acts as a key control parameter for the failure of solids under stress. In both experiments and simulations, we demonstrate that material failure can be continuously tuned by varying the underlying rigidity of the material while holding the amount of disorder constant. As the rigidity transition is approached, failure due to the application of uniaxial stress evolves from brittle cracking to system-spanning diffuse breaking. This evolution in failure behavior can be parameterized by the width of the crack. As a system becomes more and more floppy, this crack width increases until it saturates at the system size. Thus, the spatial extent of the failure zone can be used as a direct probe for material rigidity.failure | metamaterials | jamming | cracks | glasses

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.