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Register a new userShear dilatancy in marginal solids
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Brian P. Tighe
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Shearing stresses can change the volume of a material via a nonlinear effect known as shear dilatancy. We calculate the elastic dilatancy coefficient of soft sphere packings and random spring networks, two canonical models of marginal solids close to their rigidity transition. We predict a dramatic enhancement of dilatancy near rigidity loss in both materials, with a surprising distinction: while packings expand under shear, networks contract. We show that contraction in networks is due to the destabilizing influence of increasing hydrostatic or uniaxial loads, which is counteracted in packings by the formation of new contacts.
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Paradigmatic model systems, which are used to study the mechanical response of matter, are random networks of point-atoms, random sphere packings, or simple crystal lattices, all of these models assume central-force interactions between particles/atoms. Each of these models differs in the spatial arrangement and the correlations among particles. In turn, this is reflected in the widely different behaviours of the shear (G) and compression (K) elastic moduli. The relation between the macroscopic elasticity as encoded in G, K and their ratio, and the microscopic lattice structure/order, is not understood. We provide a quantitative analytical connection between the local orientational order and the elasticity in model amorphous solids with different internal microstructure, focusing on the two opposite limits of packings (strong excluded-volume) and networks (no excluded-volume). The theory predicts that, in packings, the local orientational order due to excluded-volume causes less nonaffinity (less softness or larger stiffness) under compression than under shear. This leads to lower values of G/K, a well-documented phenomenon which was lacking a microscopic explanation. The theory also provides an excellent one-parameter description of the elasticity of compressed emulsions in comparison with experimental data over a broad range of packing fractions.
Memory encoding by cyclic shear is a reliable process to store information in jammed solids, yet its underlying mechanism and its connection to the amorphous structure are not fully understood. When a jammed sphere packing is repeatedly sheared with cycles of the same strain amplitude, it optimizes its mechanical response to the cyclic driving and stores a memory of it. We study memory by cyclic shear training as a function of the underlying stability of the amorphous structure in marginally stable and highly stable packings, the latter produced by minimizing the potential energy using both positional and radial degrees of freedom. We find that jammed solids need to be marginally stable in order to store a memory by cyclic shear. In particular, highly stable packings store memories only after overcoming brittle yielding and the cyclic shear training takes place in the shear band, a region which we show to be marginally stable.
Shear transformations, as fundamental rearrangement events operating in local regions, hold the key of plastic flow of amorphous solids. Despite their importance, the dynamic features of shear transformations are far from clear. Here, we use a colloidal glass under shear as the prototype to directly observe the shear transformation events in real space. By tracing the colloidal particle rearrangements, we quantitatively determine two basic properties of shear transformations: local shear strain and dilatation (or free volume). It is revealed that the local free volume undergoes a significantly temporary increase prior to shear transformations, eventually leading to a jump of local shear strain. We clearly demonstrate that shear transformations have no memory of the initial free volume of local regions. Instead, their emergence strongly depends on the dilatancy ability of these regions, i.e., the dynamic creation of free volume. More specifically, the particles processing the high dilatancy ability directly participate in subsequent shear transformations. These results experimentally support the Argons statement about the dilatancy nature of shear transformations, and also shed insight into the structural origin of amorphous plasticity.
The holographic principle has proven successful in linking seemingly unrelated problems in physics; a famous example is the gauge-gravity duality. Recently, intriguing correspondences between the physics of soft matter and gravity are emerging, including strong similarities between the rheology of amorphous solids, effective field theories for elasticity and the physics of black holes. However, direct comparisons between theoretical predictions and experimental/simulation observations remain limited. Here, we study the effects of non-linear elasticity on the mechanical and thermodynamic properties of amorphous materials responding to shear, using effective field and gravitational theories. The predicted correlations among the non-linear elastic exponent, the yielding strain/stress and the entropy change due to shear are supported qualitatively by simulations of granular matter models. Our approach opens a path towards understanding complex mechanical responses of amorphous solids, such as mixed effects of shear softening and shear hardening, and offers the possibility to study the rheology of solid states and black holes in a unified framework.
Dense assemblies of self propelled particles, also known as active or living glasses are abundantaround us, covering different length and time scales: from the cytoplasm to tissues, from bacterialbio-films to vehicular traffic jams, from Janus colloids to animal herds. Being structurally disorderedas well as strongly out of equilibrium, these systems show fascinating dynamical and mechanicalproperties. Using extensive molecular dynamics simulation and a number of different dynamicaland mechanical order parameters we differentiate three dynamical steady states in a sheared modelactive glassy system: (a) a disordered phase, (b) a propulsion-induced ordered phase, and (c) ashear-induced ordered phase. We supplement these observations with an analytical theory based onan effective single particle Fokker-Planck description to rationalise the existence of the novel shear-induced orientational ordering behaviour in our model active glassy system that has no explicitaligning interactions,e.g.of Vicsek-type. This ordering phenomenon occurs in the large persistencetime limit and is made possible only by the applied steady shear. Using a Fokker-Planck descriptionwe make testable predictions without any fit parameters for the joint distribution of single particleposition and orientation. These predictions match well with the joint distribution measured fromdirect numerical simulation. Our results are of relevance for experiments exploring the rheologicalresponse of dense active colloids and jammed active granular matter systems.
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