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Correlated rigidity percolation in fractal lattices

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 Added by Shae Machlus
 Publication date 2020
  fields Physics
and research's language is English




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Rigidity percolation (RP) is the emergence of mechanical stability in networks. Motivated by the experimentally observed fractal nature of materials like colloidal gels and disordered fiber networks, we study RP in a fractal network. Specifically, we calculate the critical packing fractions of site-diluted lattices of Sierpinski gaskets (SGs) with varying degrees of fractal iteration. Our results suggest that although the correlation length exponent and fractal dimension of the RP of these lattices are identical to that of the regular triangular lattice, the critical volume fraction is dramatically lower due to the fractal nature of the network. Furthermore, we develop a simplified model for an SG lattice based on the fragility analysis of a single SG. This simplified model provides an upper bound for the critical packing fractions of the full fractal lattice, and this upper bound is strictly obeyed by the disorder averaged RP threshold of the fractal lattices. Our results characterize rigidity in ultra-low-density fractal networks.



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Rigidity percolation (RP) occurs when mechanical stability emerges in disordered networks as constraints or components are added. Here we discuss RP with structural correlations, an effect ignored in classical theories albeit relevant to many liquid-to-amorphous-solid transitions, such as colloidal gelation, which are due to attractive interactions and aggregation. Using a lattice model, we show that structural correlations shift RP to lower volume fractions. Through molecular dynamics simulations, we show that increasing attraction in colloidal gelation increases structural correlation and thus lowers the RP transition, agreeing with experiments. Hence colloidal gelation can be understood as a RP transition, but occurs at volume fractions far below values predicted by the classical RP, due to attractive interactions which induce structural correlation.
103 - Kuang Liu , S. Henkes , 2018
We introduce two new concepts, frictional rigidity percolation and minimal rigidity proliferation, to help identify the nature of the frictional jamming transition as well as significantly broaden the scope of rigidity percolation. For frictional rigidity percolation, we construct rigid clusters in two different lattice models using a $(3,3)$ pebble game, while taking into account contacts below and at the Coulomb threshold. The first lattice is a honeycomb lattice with next-nearest neighbors, the second, a hierarchical lattice. For both, we generally find a continuous rigidity transition. Our numerical results suggest that, for the honeycomb lattice, the exponents associated with the transition found with the frictional $(3,3)$ pebble game are distinct from those of a central-force $(2,3)$ pebble game. We propose that localized motifs, such as hinges, connecting rigid clusters that are allowed only with friction could give rise to this new frictional universality class. However, the closeness of the order parameter exponent between the two cases hints at potential superuniversality. To explore this possibility, we construct a bespoke cluster generating algorithm invoking generalized Henneberg moves, dubbed minimal rigidity proliferation. The minimally rigid clusters the algorithm generates appear to be in the same universality class as connectivity percolation, suggesting superuniversality between all three types of transitions. Finally, the hierarchical lattice is analytically tractable and we find that the exponents depend both on the type of force and on the fraction of contacts at the Coulomb threshold. These combined results allow us to compare two universality classes on the same lattice via rigid clusters for the first time to highlight unifying and distinguishing concepts within the set of all possible rigidity transitions in disordered systems.
We study how the dynamics of a drying front propagating through a porous medium are affected by small-scale correlations in material properties. For this, we first present drying experiments in micro-fluidic micro-models of porous media. Here, the fluid pressures develop more intermittent dynamics as local correlations are added to the structure of the pore spaces. We also consider this problem numerically, using a model of invasion percolation with trapping, and find that there is a crossover in invasion behaviour associated with the length-scale of the disorder in the system. The critical exponents associated with large enough events are similar to the classic invasion percolation problem, whereas the addition of a finite correlation length significantly affects the exponent values of avalanches and bursts, up to some characteristic size. This implies that the even a weak local structure can interfere with the universality of invasion percolation phenomena.
Cluster concepts have been extremely useful in elucidating many problems in physics. Percolation theory provides a generic framework to study the behavior of the cluster distribution. In most cases the theory predicts a geometrical transition at the percolation threshold, characterized in the percolative phase by the presence of a spanning cluster, which becomes infinite in the thermodynamic limit. Standard percolation usually deals with the problem when the constitutive elements of the clusters are randomly distributed. However correlations cannot always be neglected. In this case correlated percolation is the appropriate theory to study such systems. The origin of correlated percolation could be dated back to 1937 when Mayer [1] proposed a theory to describe the condensation from a gas to a liquid in terms of mathematical clusters (for a review of cluster theory in simple fluids see [2]). The location for the divergence of the size of these clusters was interpreted as the condensation transition from a gas to a liquid. One of the major drawback of the theory was that the cluster number for some values of thermodynamic parameters could become negative. As a consequence the clusters did not have any physical interpretation [3]. This theory was followed by Frenkels phenomenological model [4], in which the fluid was considered as made of non interacting physical clusters with a given free energy. This model was later improved by Fisher [3], who proposed a different free energy for the clusters, now called droplets, and consequently a different scaling form for the droplet size distribution. This distribution, which depends on two geometrical parameters, has the nice feature that the mean droplet size exhibits a divergence at the liquid-gas critical point.
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