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Register a new userMapping forces in 3D elastic assembly of grains
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Our understanding of the elasticity and rheology of disordered materials, such as granular piles, foams, emulsions or dense suspensions relies on improving experimental tools to characterize their behaviour at the particle scale. While 2D observations are now routinely carried out in laboratories, 3D measurements remain a challenge. In this paper, we use a simple model system, a packing of soft elastic spheres, to illustrate the capability of X-ray microtomography to characterise the internal structure and local behaviour of granular systems. Image analysis techniques can resolve grain positions, shapes and contact areas; this is used to investigate the materials microstructure and its evolution upon strain. In addition to morphological measurements, we develop a technique to quantify contact forces and estimate the internal stress tensor. As will be illustrated in this paper, this opens the door to a broad array of static and dynamical measurements in 3D disordered systems
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Motivated by a freely suspended graphene and polymerized membranes in soft and biological matter we present a detailed study of a tensionless elastic sheet in the presence of thermal fluctuations and quenched disorder. The manuscript is based on an extensive draft dating back to 1993, that was circulated privately. It presents the general theoretical framework and calculational details of numerous results, partial forms of which have been published in brief Letters (Le Doussal and Radzihovsky 1992). The experimental realization of atom-thin graphene sheets has driven a resurgence in this fascinating subject, making our dated predictions and their detailed derivations timely. To this end we analyze the statistical mechanics of a generalized D-dimensional elastic membrane embedded in d dimensions using a self-consistent screening approximation (SCSA), that has proved to be unprecedentedly accurate in this system, exact in three complementary limits: d --> infinity, D --> 4, and D=d. Focusing on the critical flat phase, for a homogeneous two-dimensional membrane embedded in three dimensions, we predict its universal length-scale dependent roughness, elastic moduli exponents, and a universal negative Poisson ratio of -1/3. We also extend these results to short- and long-range correlated random heterogeneity, predicting a variety of glassy wrinkled membrane states. Finally, we also predict and analyze a continuous crumpling transition in a phantom elastic sheet. We hope that this detailed presentation of the SCSA theory will be useful for further theoretical developments and corresponding experimental investigations on freely suspended graphene.
Random (disordered) components in the surface anchoring of the smectic-A liquid crystalline film in general modify the thermal pseudo-Casimir interaction. Anchoring disorder of the quenched type is in general decoupled from the thermal pseudo-Casimir force and gives rise to an additional disorder-generated interaction, in distinction to the annealed disorder, whose effect on the pseudo-Casimir force is non-additive. We consider the effects of the surface anchoring disorder by assuming that one of the substrates of the film is contaminated by a disorder source, resulting in a Gaussian-weighted distribution of the preferred molecular anchoring orientation (easy axes) on that substrate, having a finite mean and variance or, more generally, a homogeneous in-plane, two-point correlation function. We show that the presence of disorder, either of the quenched or annealed type, leads to a significant reduction in the magnitude of the net thermal fluctuation force between the confining substrates of the film. In the quenched case this is a direct consequence of an additive free energy dependent on the variance of the disorder, while in the annealed case, the suppression of the interaction force can be understood based on a disorder-renormalized, effective anchoring strength.
On the basis of the first principles simulation, the structure, formation enthalpy, and mechanical properties (elastic constant, bulk, and shear modulus and hardness) of five Nb-doped Ni systems are systematically studied. The calculated equilibrium volume increases with the Nb concentration increasing. The computational elastic constants and formation enthalpy indicate that all Nb-doped Ni systems are mechanically and thermodynamically stable in our research. The hardness of these systems also be predicted after the bulk modulus and shear modulus have been accurately calculated. The results show that the hardness increases with the Nb concentration increasing when the Nb concentration below 4.9%, beyond which the hardness will decrease within the scope of our study.
We present a theory of viscoelasticity of amorphous media, which takes into account the effects of confinement along one of three spatial dimensions. The framework is based on the nonaffine extension of lattice dynamics to amorphous systems, or nonaffine response theory. The size effects due to the confinement are taken into account via the nonaffine part of the shear storage modulus $G$. The nonaffine contribution is written as a sum over modes in $k$-space. With a rigorous argument based on the analysis of the $k$-space integral over modes, it is shown that the confinement size $L$ in one spatial dimension, e.g. the $z$ axis, leads to a infrared cut-off for the modes contributing to the nonaffine (softening) correction to the modulus that scales as $L^{-3}$. Corrections for finite sample size $D$ in the two perpendicular dimensions scale as $sim (L/D)^4$, and are negligible for $L ll D$. For liquids it is predicted that $Gsim L^{-3}$ in agreement with a previous more approximate analysis, whereas for amorphous materials $G sim G_{bulk} + beta L^{-3}$. For the case of liquids, four different experimental systems are shown to be very well described by the $L^{-3}$ law.
Hydrated granular packings often crack into discrete clusters of grains when dried. Despite its ubiquity, accurate prediction of cracking remains elusive. Here, we elucidate the previously overlooked role of individual grain shrinkage---a feature common to many materials---in determining crack patterning using both experiments and simulations. By extending the classical Griffith crack theory, we obtain a scaling law that quantifies how cluster size depends on the interplay between grain shrinkage, stiffness, and size---applicable to a diverse array of shrinkable, granular packings.
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