Yield stress materials flow if a sufficiently large shear stress is applied. Although such materials are ubiquitous and relevant for industry, there is no accepted microscopic description of how they yield, even in the simplest situations in which temperature is negligible and in which flow inhomogeneities such as shear bands or fractures are absent. Here we propose a scaling description of the yielding transition in amorphous solids made of soft particles at zero temperature. Our description makes a connection between the Herschel-Bulkley exponent characterizing the singularity of the flow curve near the yield stress Σ c , the extension and duration of the avalanches of plasticity observed at threshold, and the density P(x) of soft spots, or shear transformation zones, as a function of the stress increment x beyond which they yield. We argue that the critical exponents of the yielding transition may be expressed in terms of three independent exponents, θ, d f , and z, characterizing, respectively, the density of soft spots, the fractal dimension of the avalanches, and their duration. Our description shares some similarity with the depinning transition that occurs when an elastic manifold is driven through a random potential, but also presents some striking differences. We test our arguments in an elastoplastic model, an automaton model similar to those used in depinning, but with a different interaction kernel, and find satisfying agreement with our predictions in both two and three dimensions. M any solids will flow and behave as fluids if a sufficiently large shear stress is applied. In crystals, plasticity is governed by the motion of dislocations (1, 2). In amorphous solids, there is no order, and conserved defects cannot be defined. However, as noticed by Argon (3), plasticity consists of elementary events localized in space, called shear transformations, in which a few particles rearrange. This observation supports that there are special locations in the sample, called shear transformation zones (STZs) (4), in which the system lies close to an elastic instability. Several theoretical approaches of plasticity, such as STZ theory (4) or soft glassy rheology (5), assume that such zones relax independently or are coupled to each other via an effective temperature. However, at zero temperature and small applied strain rate _ γ, computer experiments (6-11) and very recent experiments (12, 13) indicate that local rearrangements are not independent: plasticity occurs via avalanches in which many shear transformations are involved, forming elongated structures in which plasticity localizes. If conditions are such that flow is homogeneous (as may occur, for example, in foams or emulsions), one finds that the flow curves are singular at small strain rate and follow a Herschel-Bulkley law Σ − Σ c ∼ _ γ 1=β (14, 15). These features are reproduced qualitatively by elasto-plastic models (16)(17)(18)(19)(20) in which space is discretized. In these models, a site that yields plastically affects the stress in its surroundi...
Connectedness and applied stress strongly affect elasticity in solids. In various amorphous materials, mechanical stability can be lost either by reducing connectedness or by increasing pressure. We present an effective medium theory of elasticity that extends previous approaches by incorporating the effect of compression, of amplitude e, allowing one to describe quantitative features of sound propagation, transport, the boson peak, and elastic moduli near the elastic instability occurring at a compression ec. The theory disentangles several frequencies characterizing the vibrational spectrum: the onset frequency where strongly-scattered modes appear in the vibrational spectrum, the pressure-independent frequency ω* where the density of states displays a plateau, the boson peak frequency ωBP found to scale as , and the Ioffe-Regel frequency ωIR where scattering length and wavelength become equal. We predict that sound attenuation crosses over from ω(4) to ω(2) behaviour at ω0, consistent with observations in glasses. We predict that a frequency-dependent length scale ls(ω) and speed of sound ν(ω) characterize vibrational modes, and could be extracted from scattering data. One key result is the prediction of a flat diffusivity above ω0, in agreement with previously unexplained observations. We find that the shear modulus does not vanish at the elastic instability, but drops by a factor of 2. We check our predictions in packings of soft particles and study the case of covalent networks and silica, for which we predict ωIR ≈ ωBP. Overall, our approach unifies sound attenuation, transport and length scales entering elasticity in a single framework where disorder is not the main parameter controlling the boson peak, in agreement with observations. This framework leads to a phase diagram where various glasses can be placed, connecting microscopic structure to vibrational properties.
Low-frequency vibrational modes play a central role in determining various basic properties of glasses, yet their statistical and mechanical properties are not fully understood. Using extensive numerical simulations of several model glasses in three dimensions, we show that in systems of linear size L sufficiently smaller than a crossover size L_{D}, the low-frequency tail of the density of states follows D(ω)∼ω^{4} up to the vicinity of the lowest Goldstone mode frequency. We find that the sample-to-sample statistics of the minimal vibrational frequency in systems of size L
We study theoretically and numerically how hard frictionless particles in random packings can rearrange. We demonstrate the existence of two distinct unstable non-linear modes of rearrangement, both associated with the opening and the closing of contacts. Mode one, whose density is characterized by some exponent θ , corresponds to motions of particles extending throughout the entire system. Mode two, whose density is characterized by an exponent θ = θ , corresponds to the local buckling of a few particles. Mode one is shown to yield at a much higher rate than mode two when a stress is applied. We show that the distribution of contact forces follows P (f ) ∼ f min(θ ,θ) , and that imposing that the packing cannot be densified further leads to the bounds γ ≥ 1 2+θ, where γ characterizes the singularity of the pair distribution function g(r) at contact. These results extend the theoretical analysis of [1] where the existence of mode two was not considered. We perform numerics that support that these bounds are saturated with γ ≈ 0.38, θ ≈ 0.17 and θ ≈ 0.44. We measure systematically the stability of all such modes in packings, and confirm their marginal stability. The principle of marginal stability thus allows to make clearcut predictions on the ensemble of configurations visited in these out-of-equilibrium systems, and on the contact forces and pair distribution functions. It also reveals the excitations that need to be included in a description of plasticity or flow near jamming, and suggests a new path to study two-level systems and soft spots in simple amorphous solids of repulsive particles.
While the rheology of non-Brownian suspensions in the dilute regime is well understood, their behavior in the dense limit remains mystifying. As the packing fraction of particles increases, particle motion becomes more collective, leading to a growing length scale and scaling properties in the rheology as the material approaches the jamming transition. There is no accepted microscopic description of this phenomenon. However, in recent years it has been understood that the elasticity of simple amorphous solids is governed by a critical point, the unjamming transition where the pressure vanishes, and where elastic properties display scaling and a diverging length scale. The correspondence between these two transitions is at present unclear. Here we show that for a simple model of dense flow, which we argue captures the essential physics near the jamming threshold, a formal analogy can be made between the rheology of the flow and the elasticity of simple networks. This analogy leads to a new conceptual framework to relate microscopic structure to rheology. It enables us to define and compute numerically normal modes and a density of states. We find striking similarities between the density of states in flow, and that of amorphous solids near unjamming: both display a plateau above some frequency scale ω Ã ∼ jz c − zj, where z is the coordination of the network of particle in contact, z c ¼ 2D where D is the spatial dimension. However, a spectacular difference appears: the density of states in flow displays a single mode at another frequency scale ω min ≪ ω Ã governing the divergence of the viscosity. granular flows | jamming | rheology | viscoelasticity S uspensions are heterogeneous fluids containing solid particles. Their viscosity in the dilute regime was computed early on by Einstein and Batchelor (1). However, as the packing fraction ϕ increases, steric hindrance becomes dominant and particles move under stress in an increasingly coordinated way. For non-Brownian particles, the viscosity diverges as the suspension jams into an amorphous solid. This jamming transition is a nonequilibrium critical phenomena: the rheology displays scaling laws (2-8) and a growing length scale (2, 3, 9, 10). Jamming occurs more generally in driven materials made of repulsive particles, such as in aerial granular flows (11) with similar rheological phenomenology (12), and where large eddies are observed as jamming is approached (9). This phenomenology bears similarity with that of the glass transition, where steric hindrance increases upon cooling, and where the dynamics becomes increasingly collective as relaxation times grow (13). In dense granular materials and in supercooled liquids, the physical origin of collective dynamics and associated rheological phenomena remain elusive.Recent progress has been made on a related problem, the unjamming transition where a solid made of repulsive soft particles is isotropically decompressed toward vanishing pressure (14)(15)(16)(17)(18)(19)(20). In this situation, various properties of the ...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.