arXiv subjects

Charles K. C. Lieou

Publications and source records attributed to Charles K. C. Lieou.

13 recordsLinked to original sources

arXiv2022

Shear-wave-induced softening and simultaneous compaction in dense granular media through acoustic lubrication at flow heterogeneities

We report the simultaneous softening and compaction of a confined dense granular pack in acoustic resonance experiments. Elastic softening is manifested by a reduction of the shear-wave speed, as the wave amplitude increases beyond some threshold. No macroscopic rearrangement of grains or dilatancy is observed; instead, elastic softening is accompanied by a tiny amount of compaction on the scale of grain asperities. We explain these apparent contradictory observations using a theoretical model, based on shear transformation zones (STZs), of soft spots and slipping contacts. It predicts a linear shear stress-strain response with negligible macro-plastic deformation due to the small-amplitude acoustic oscillation. However, these waves reduce the interparticle friction and contact stiffness through the acoustic lubrication of grain contacts, resulting in an increase in the structural disorder or compactivity and softening of dynamic modulus. The compaction associated with this microscopic friction decrease is consistent with the prediction by an Ising-like correlation between STZs in the subyield regime.

cond-mat.soft↗

arXiv2022

Dynamical heterogeneities in liquid and glass originate from medium-range order

Slow relaxation and plastic deformation in disordered materials such as metallic glasses and supercooled liquids occur at dynamical heterogeneities, or neighboring particles that rearrange in a correlated, cooperative manner. Dynamical heterogeneities have historically been described by a four-point, time-dependent density correlation function $χ_4 (r, t)$. In this paper, we posit that $χ_4 (r, t)$ contains essentially the same information about medium-range order as the Van Hove correlation function $G(r, t)$. In other words, medium-range order is the origin of spatially correlated regions of cooperative particle motion. The Van Hove function is the preferred tool for describing dynamical heterogeneities than the four-point function, for which the physical meaning is less transparent.

cond-mat.stat-mech↗

arXiv2022

Mean-field model for the Curie-Weiss temperature dependence of coherence length in metallic liquids

The coherence length of the medium-range order (MRO) in metallic liquids is known to display a Curie-Weiss temperature dependence; its inverse is linearly related to temperature, and when extrapolated from temperatures above the glass transition, the coherence length diverges at a negative temperature with a critical exponent of unity. We propose a mean-field pseudospin model that explains this behavior. Specifically, we model the atoms and their local environment as Ising spins with antiferromagnetic exchange interactions. We further superimpose an exchange interaction between dynamical heterogeneities, or clusters of atoms undergoing cooperative motion. The coherence length in the metallic liquid is thus the correlation length between dynamical heterogeneities. Our results reaffirm the idea that the MRO coherence length is a measure of point-to-set correlations, and that local frustrations in the interatomic interactions are prominent in metallic liquids.

cond-mat.soft↗

arXiv2020

Thermomechanical conversion in metals: dislocation plasticity model evaluation of the Taylor-Quinney coefficient

Using a partitioned-energy thermodynamic framework which assigns energy to that of atomic configurational stored energy of cold work and kinetic-vibrational, we derive an important constraint on the Taylor-Quinney coefficient, which quantifies the fraction of plastic work that is converted into heat during plastic deformation. Associated with the two energy contributions are two separate temperatures -- the ordinary temperature for the thermal energy and the effective temperature for the configurational energy. We show that the Taylor-Quinney coefficient is a function of the thermodynamically defined effective temperature that measures the atomic configurational disorder in the material. Finite-element analysis of recently published experiments on the aluminum alloy 6016-T4 \citep{neto_2020}, using the thermodynamic dislocation theory (TDT), shows good agreement between theory and experiment for both stress-strain behavior and temporal evolution of the temperature. The simulations include both conductive and convective thermal energy loss during the experiments, and significant thermal gradients exist within the simulation results. Computed values of the differential Taylor-Quinney coefficient are also presented and suggest a value which differs between materials and increases with increasing strain.

cond-mat.mtrl-sci↗

arXiv2019

Thermodynamic theory of crystal plasticity: formulation and application to polycrystal fcc copper

We present a thermodynamic description of crystal plasticity. Our formulation is based on the Langer-Bouchbinder-Lookman thermodynamic dislocation theory (TDT), which asserts the fundamental importance of an effective temperature that describes the state of configurational disorder and therefore the dislocation density of the crystalline material. We extend the TDT description from isotropic plasticity to crystal plasticity with many slip systems. Finite-element simulations show favourable comparison with experiments on polycrystal fcc copper under uniaxial compression, tension, and simple shear. The thermodynamic theory of crystal plasticity thus provides a thermodynamically consistent and physically rigorous description of dislocation motion in crystals. We also discuss new insights about the interaction of dislocations belonging to different slip systems.

cond-mat.mtrl-sci↗

arXiv2018

Strain localization and dynamic recrystallization in polycrystalline metals: thermodynamic theory and simulation framework

We describe a theoretical and computational framework for adiabatic shear banding (ASB) and dynamic recrystallization (DRX) in polycrystalline materials. The Langer-Bouchbinder-Lookman (LBL) thermodynamic theory of polycrystalline plasticity, which we recently reformulated to describe DRX via the inclusion of the grain boundary density or the grain size as an internal state variable, provides a convenient and self-consistent way to represent the viscoplastic and thermal behavior of the material, with minimal ad-hoc assumptions regarding the initiation of yielding or onset of shear banding. We implement the LBL-DRX theory in conjunction with a finite-element computational framework. Favorable comparison to experimental measurements on a top-hat AISI 316L stainless steel sample compressed with a split-Hopkinson pressure bar suggests the accuracy and usefulness of the LBL-DRX framework, and demonstrates the crucial role of DRX in strain localization.

cond-mat.mtrl-sci↗

arXiv2018

Dynamic recrystallization in adiabatic shear banding: effective-temperature model and comparison to experiments in ultrafine-grained titanium

Dynamic recrystallization (DRX) is often observed in conjunction with adiabatic shear banding (ASB) in polycrystalline materials. The recrystallized nanograins in the shear band have few dislocations compared to the material outside of the shear band. In this paper, we reformulate the recently-developed Langer-Bouchbinder-Lookman (LBL) continuum theory of polycrystalline plasticity and include the creation of grain boundaries. While the shear-banding instability emerges because thermal heating is faster than heat dissipation, recrystallization is interpreted as an entropic effect arising from the competition between dislocation creation and grain boundary formation. We show that our theory closely matches recent results in sheared ultrafine-grained titanium. The theory thus provides a thermodynamically consistent way to systematically describe the formation of shear bands and recrystallized grains therein.

cond-mat.mtrl-sci↗

arXiv2016

Deformation in amorphous-crystalline nanolaminates -- an effective-temperature theory and interaction between defects

Experiments and atomic-scale simulations suggest that the transmission of plasticity carriers in deforming amorphous-crystalline nanolaminates is mediated by the biphase interface between the amorphous and crystalline layers. In this paper, we present a micromechanics model for these biphase nanolaminates that describes defect interactions through the amorphous-crystalline interface (ACI). The model is based on an effective-temperature framework to achieve a unified description of the slow, configurational atomic rearrangements in both phases when driven out of equilibrium. We show how the second law of thermodynamics constrains the density of defects and the rate of configurational rearrangements, and apply this framework to dislocations in crystalline solids and shear transformation zones (STZs) in amorphous materials. The effective-temperature formulation enables us to interpret the observed movement of dislocations to the ACI and the production of STZs at the interface as a "diffusion" of configurational disorder across the material. We demonstrate favorable agreement with experimental findings reported in (Kim et al., Adv. Funct. Mater., 2011), and demonstrate how the ACI acts as a sink of dislocations and a source of STZs.

cond-mat.mtrl-sci↗

arXiv2015

Stick-slip instabilities in sheared granular flow: the role of friction and acoustic vibrations

We propose a theory of shear flow in dense granular materials. A key ingredient of the theory is an effective temperature that determines how the material responds to external driving forces such as shear stresses and vibrations. We show that, within our model, friction between grains produces stick-slip behavior at intermediate shear rates, even if the material is rate-strengthening at larger rates. In addition, externally generated acoustic vibrations alter the stick-slip amplitude, or suppress stick-slip altogether, depending on the pressure and shear rate. We construct a phase diagram that indicates the parameter regimes for which stick-slip occurs in the presence and absence of acoustic vibrations of a fixed amplitude and frequency. These results connect the microscopic physics to macroscopic dynamics, and thus produce useful information about a variety of granular phenomena including rupture and slip along earthquake faults, the remote triggering of instabilities, and the control of friction in material processing.

cond-mat.soft↗

arXiv2014

Shear flow of angular grains: acoustic effects and non-monotonic rate dependence of volume

Naturally-occurring granular materials often consist of angular particles whose shape and frictional characteristics may have important implications on macroscopic flow rheology. In this paper, we provide a theoretical account for the peculiar phenomenon of auto-acoustic compaction -- non-monotonic variation of shear band volume with shear rate in angular particles -- recently observed in experiments. Our approach is based on the notion that the volume of a granular material is determined by an effective-disorder temperature known as the compactivity. Noise sources in a driven granular material couple its various degrees of freedom and the environment, causing the flow of entropy between them. The grain-scale dynamics is described by the shear-transformation-zone (STZ) theory of granular flow, which accounts for irreversible plastic deformation in terms of localized flow defects whose density is governed by the state of configurational disorder. To model the effects of grain shape and frictional characteristics, we propose an Ising-like internal variable to account for nearest-neighbor grain interlocking and geometric frustration, and interpret the effect of friction as an acoustic noise strength. We show quantitative agreement between experimental measurements and theoretical predictions, and propose additional experiments that provide stringent tests on the new theoretical elements.

cond-mat.stat-mech↗

arXiv2014

Grain fragmentation in sheared granular flow: weakening effects, energy dissipation, and strain localization

We describe the shear flow of a disordered granular material in the presence of grain fracture using the shear-transformation-zone (STZ) theory of amorphous plasticity adapted to systems with a hard-core inter-particle interaction. To this end, we develop the equations of motion for this system within a statistical-thermodynamic framework analogous to that used in the analysis of molecular glasses. For hard-core systems, the amount of internal, configurational disorder is characterized by the compactivity $X = \partial V / \partial S_C$, where $V$ and $S_C$ are respectively the volume and configurational entropy. Grain breakage is described by a constitutive equation for the temporal evolution of a characteristic grain size $a$, based on fracture mechanics. We show that grain breakage is a weakening mechanism, significantly lowering the flow stress at large strain rates, if the material is rate-strengthening in character. We show in addition that if the granular material is sufficiently aged, spatial inhomogeneity in configurational disorder results in strain localization. We also show that grain splitting contributes significantly to comminution at small shear strains, while grain abrasion becomes dominant at large shear displacements.

cond-mat.soft↗

arXiv2013

Sacrificial bonds and hidden length in biomaterials -- a kinetic, constitutive description of strength and toughness in bone

Sacrificial bonds and hidden length in structural molecules account for the greatly increased fracture toughness of biological materials compared to synthetic materials without such structural features, by providing a molecular-scale mechanism for energy dissipation. One example is in the polymeric glue connection between collagen fibrils in animal bone. In this paper, we propose a simple kinetic model that describes the breakage of sacrificial bonds and the release of hidden length, based on Bell's theory. We postulate a master equation governing the rates of bond breakage and formation. This enables us to predict the mechanical behavior of a quasi-one-dimensional ensemble of polymers at different stretching rates. We find that both the rupture peak heights and maximum stretching distance increase with the stretching rate. In addition, our theory naturally permits the possibility of self-healing in such biological structures.

cond-mat.soft↗

arXiv2012

Non-equilibrium thermodynamics in sheared hard-sphere materials

We combine the shear-transformation-zone (STZ) theory of amorphous plasticity with Edwards' statistical theory of granular materials to describe shear flow in a disordered system of thermalized hard spheres. The equations of motion for this system are developed within a statistical thermodynamic framework analogous to that which has been used in the analysis of molecular glasses. For hard spheres, the system volume $V$ replaces the internal energy $U$ as a function of entropy $S$ in conventional statistical mechanics. In place of the effective temperature, the compactivity $X = \partial V / \partial S$ characterizes the internal state of disorder. We derive the STZ equations of motion for a granular material accordingly, and predict the strain rate as a function of the ratio of the shear stress to the pressure for different values of a dimensionless, temperature-like variable near a jamming transition. We use a simplified version of our theory to interpret numerical simulations by Haxton, Schmiedeberg and Liu, and in this way are able to obtain useful insights about internal rate factors and relations between jamming and glass transitions.

cond-mat.stat-mech↗