Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userSoft random solids and their heterogeneous elasticity
208
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
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.
rate research
Read More
The mechanical response of naturally abundant amorphous solids such as gels, jammed grains, and biological tissues are not described by the conventional paradigm of broken symmetry that defines crystalline elasticity. In contrast, the response of such athermal solids are governed by local conditions of mechanical equilibrium, i.e., force and torque balance of its constituents. Here we show that these constraints have the mathematical structure of a generalized electromagnetism, where the electrostatic limit successfully captures the anisotropic elasticity of amorphous solids. The emergence of elasticity from local mechanical constraints offers a new paradigm for systems with no broken symmetry, analogous to emergent gauge theories of quantum spin liquids. Specifically, our $U(1)$ rank-2 symmetric tensor gauge theory of elasticity translates to the electromagnetism of fractonic phases of matter with the stress mapped to electric displacement and forces to vector charges. We corroborate our theoretical results with numerical simulations of soft frictionless disks in both two and three dimensions, and experiments on frictional disks in two dimensions. We also present experimental evidence indicating that force chains in granular media are sub-dimensional excitations of amorphous elasticity similar to fractons.
This paper discusses the elastic behavior of a very long crosslinked polyelectrolyte chain (Debye-Huckel chain), which is weakly charged. Therefore the response of the crosslinked chain (network) on an external constant force $f$ acting on the ends of the chain is considered. A selfconsistent variational computation of an effective field theory is employed. It is shown, that the modulus of the polyelectrolyte network has two parts: the first term represents the usual entropy elasticity of connected flexible chains and the second term takes into account the electrostatic interaction of the monomers. It is proportional to the squared crosslink density and the Debye - screening parameter.
In a recent paper [Phys. Rev. E {bf 104}, 024904] it was shown that mechanical strains in amorphous solids are screened via the formation of plastic events that are typically quadrupolar in nature. At low densities the screening effect is reminiscent of the role of dipoles in dielectrics, while the effect at high density has no immediate electrostatic analog, and is expected to change qualitatively the mechanical response, as seen for example in the displacement field. In this Letter we show that high-density screening results in undulating displacement field that strictly deviate from elasticity theory. We show that theoretical analysis, experimental measurements and numeric simulations of frictional granular amorphous assemblies are in agreement with each other and provide a strong support for the theory.
The vibrational anomalies of glasses, in particular the boson peak, are addressed from the standpoint of heterogeneous elasticity, namely the spatial fluctuations of elastic constants caused by the structural disorder of the amorphous materials. In the first part of this review article a mathematical analogy between diffusive motion in a disordered environment and a scalar simplification of vibrational motion under the same condition is emploited. We demonstrate that the disorder-induced long-time tails of diffusion correspond to the Rayleigh scattering law in the vibrational system and that the cross-over from normal to anomalous diffusion corresponds to the boson peak. The anomalous motion arises as soon as the disorder-induced self-energy exceeds the frequency-independent diffusivity/elasticity. For this model a variational scheme is emploited for deriving two mean-field theories of disorder, the self-consistent Born approximation (SCBA) and coherent-potential approximation (CPA). The former applies if the fluctuations are weak and Gaussian, the latter applies for stronger and non-Gaussian fluctuations. In the second part the vectorial theory of heterogenous elasticity is presented and solved in SCBA and CPA, introduced for the scalar model. Both approaches predict and explain the boson-peak and the associated anomalies, namely a dip in the acoustic phase velocity and a characteristic strong increase of the acoustic attenuation below the boson peak. Explicit expressions for the density of states and the inelastic Raman, neutron and X-ray scattering laws are given. Recent conflicting ways of explaining the boson-peak anomalies are discussed.
We review a new theory of viscoelasticity of a glass-forming viscous liquid near and below the glass transition. In our model we assume that each point in the material has a specific viscosity, which varies randomly in space according to a fluctuating activation free energy. We include a Maxwellian elastic term and assume that the corresponding shear modulus fluctuates as well with the same distribution as that of the activation barriers. The model is solved in coherent-potential approximation (CPA), for which a derivation is given. The theory predicts an Arrhenius-type temperature dependence of the viscosity in the vanishing-frequency limit, independent of the distribution of the activation barriers. The theory implies that this activation energy is generally different from that of a diffusing particle with the same barrier-height distribution. If the distribution of activation barriers is assumed to have Gaussian form, the finite-frequency version of the theory describes well the typical low-temperature alpha relaxation peak of glasses. Beta relaxation can be included by adding another Gaussian with center at much lower energies than that responsible for the alpha relaxation. At high frequencies our theory reduces to the description of an elastic medium with spatially fluctuating elastic moduli (heterogeneous elasticity theory), which explains the occurrence of the boson-peak-related vibrational anomalies of glasses.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
