Focusing on simulated polymer glasses well below the glass transition, we confirm the validity and the efficiency of the recently proposed simple-average expression $G(t) = μ_A - h(t)$ for the computational determination of the shear stress relaxation modulus $G(t)$. Here, $μ_A = G(0)$ characterizes the affine shear transformation of the system at $t=0$ and $h(t)$ the mean-square displacement of the instantaneous shear stress as a function of time $t$. This relation is seen to be particulary useful for systems with quenched or sluggish transient shear stresses which necessarily arise below the glass transition. The commonly accepted relation $G(t)=c(t)$ using the shear stress auto-correlation function $c(t)$ becomes incorrect in this limit.
A molecular level analysis of segmental trajectories obtained from molecular dynamics simulations is used to obtain the full relaxation time spectrum in aging polymer glasses subject to three different deformation protocols. As in experiments, dynamics can be accelerated by several orders of magnitude, and a narrowing of the distribution of relaxation times during creep is directly observed. Additionally, the acceleration factor describing the transformation of the relaxation time distributions is computed and found to obey a universal dependence on the global strain, independent of age and de…
Using molecular dynamics simulation of a standard coarse-grained polymer glass model we investigate by means of the stress-fluctuation formalism the shear modulus $μ$ as a function of temperature $T$ and sampling time $Δt$. While the ensemble-averaged modulus $μ(T)$ is found to decrease continuously for all $Δt$ sampled, its standard deviation $δμ(T)$ is non-monotonous with a striking peak at the glass transition. Confirming the effective time-translational invariance of our systems, $μ(Δt)$ can be understood using a weighted integral over the shear-stress relaxation modulus $G(t)$. While the …
Semiflexible polymer glasses (SPGs), including those formed by the recently synthesized semiflexible conjugated polymers (SCPs), are expected to be brittle because classical formulas for their craze extension ratio $λ_{\rm craze}$ and fracture stretch $λ_{\rm frac}$ predict that systems with $N_e = C_\infty$ have $λ_{\rm craze} = λ_{\rm frac} = 1$ and hence cannot be deformed to large strains. Using molecular dynamics simulations, we show that in fact such glasses can form stable crazes with $λ_{\rm craze} \simeq N_e^{1/4} \simeq C_\infty^{1/4}$, and that they fracture at $λ_{\rm frac} = (3N_e…
Elucidating the physics of a concentrated suspension of ring polymers, or of an ensemble of ring polymers in a complex environment, is an important outstanding question in polymer physics. Many of the characteristic features of these systems arise due to topological interactions between polymers, or between the polymers and the environment, and it is often challenging to describe this quantitatively. Here we review recent research which suggests that a key role is played by inter-ring threadings (or penetrations), which become more abundant as the ring size increases. As we discuss, the physic…
A derivation is given for the Vogel-Fulcher-Tammann thermal activation law for the glassy state of a bulk polymer. Our microscopic considerations involve the entropy of closed polymer molecular chains (i.e. polymer closed strings). For thin film polymer glasses, one obtains open polymer strings in that the boundary surfaces serve as possible string endpoint locations. The Vogel-Fulcher-Tammann thermal activation law thereby holds true for a bulk polymer glass but is modified in the neighborhood of the boundaries of thin film polymers.
We perform thorough molecular-dynamics simulations to compare elasticity and yielding of atomic crystals and model semicrystalline polymers, the latter characterized by very similar positional ordering with respect to atomic crystals and considerable bond disorder. We find that the elastic modulus, the shear yield strength and the critical yield strain of semicrystalline polymers are higher than (modulus and yield strength), or comparable to (critical strain), the corresponding ones of atomic crystals. The findings suggest that the bond disorder suppresses dislocation-mediated plasticity in po…
Sheared multi-component bulk metallic glasses are characterized by both chemical and structural disorder that define their properties. We investigate the behavior of the local, microstructural elastic modulus across the plastic yielding transition in six Ni-based multi-component glasses, that are characterized by compositional features commonly associated with solid solution formability. We find that elastic modulus fluctuations display consistent percolation characteristics pointing towards universal behavior across chemical compositions and overall yielding sharpness characteristics. Elastic…
Molecular dynamics simulations are used to investigate the effects of deformation on the segmental dynamics in an aging polymer glass. Individual particle trajectories are decomposed into a series of discontinuous hops, from which we obtain the full distribution of relaxation times and displacements under three deformation protocols: step stress (creep), step strain, and constant strain rate deformation. As in experiments, the dynamics can be accelerated by several orders of magnitude during deformation, and the history dependence is entirely erased during yield (mechanical rejuvenation). Agin…
Governing equations are derived for the kinetics of physical aging in polymeric glasses. An amorphous polymer is treated as an ensemble of cooperatively rearranged regions (CRR). Any CRR is thought of as a string of elementary clusters (EC). Fragmentation of the string may occur at random time at any border between ECs. Two string can aggregate at random time to produce a new string. The processes of aggregation and fragmentation are treated as thermally activated, and the rate of fragmentation is assumed to grow with temperature more rapidly than that for coalescence. This implies that only e…
We have derived a universal relaxation function for heterogeneous materials using the maximum entropy principle for nonextensive systems. The power law exponents of the relaxation function are simply related to a global fractal parameter and for large time to the entropy nonextensivity parameter q. For intermediate times the relaxation follows a stretched exponential behavior. The asymptotic power law behaviors both in the time and the frequency domains coincide with those of the Weron generalized dielectric function derived in the stochastic theory from an extension of the Levy central limit …
Glasses exhibit spatially inhomogeneous elastic properties, which can be investigated by measuring their elastic moduli at a local scale. Various methods to evaluate the local elastic modulus have been proposed in the literature. A first possibility is to measure the local stress-local strain curve and to obtain the local elastic modulus from the slope of the curve, or equivalently to use a local fluctuation formula. Another possible route is to assume an affine strain and to use the applied global strain instead of the local strain for the calculation of the local modulus. Most recently a thi…
We probe the Ioffe-Regel limits of glasses with repulsions near the zero-temperature jamming transition by measuring the dynamical structure factors. At zero temperature, the transverse Ioffe-Regel frequency vanishes at the jamming transition with a diverging length, but the longitudinal one does not, which excludes the existence of a diverging length associated with the longitudinal excitations. At low temperatures, the transverse and longitudinal Ioffe-Regel frequencies approach zero at the jamming-like transition and glass transition, respectively. As a consequence, glasses between the glas…
We present computer simulations of concentrated solutions of unknotted nonconcatenated semiflexible ring polymers. Unlike in their flexible counterparts, shrinking involves a strong energetic penalty, favoring interpenetration and clustering of the rings. We investigate the slow dynamics of the centers-of-mass of the rings in the amorphous cluster phase, consisting of disordered columns of oblate rings penetrated by bundles of prolate ones. Scattering functions reveal a striking decoupling of self- and collective motions. Correlations between centers-of-mass exhibit slow relaxation, as expecte…
Simulations are used to examine the microscopic origins of strain hardening in polymer glasses. While traditional entropic network models can be fit to the total stress, their underlying assumptions are inconsistent with simulation results. There is a substantial energetic contribution to the stress that rises rapidly as segments between entanglements are pulled taut. The thermal component of stress is less sensitive to entanglements, mostly irreversible, and directly related to the rate of local plastic arrangements. Entangled and unentangled chains show the same strain hardening when plotted…
Shear yielding of glassy polymers is usually described in terms of the pressure-dependent Tresca or von Mises yield criteria. We test these criteria against molecular dynamics simulations of deformation in amorphous polymer glasses under triaxial loading conditions that are difficult to realize in experiments. Difficulties and ambiguities in extending several standard definitions of the yield point to triaxial loads are described. Two definitions, the maximum and offset octahedral stresses, are then used to evaluate the yield stress for a wide range of model parameters. In all cases, the onset…
We show that in monomeric supercooled liquids and glasses that are plastically flowing at a constant shear stress $σ$ while being deformed with strain rate $\dotε$, the microscopic structural relaxation time $τ_{\rm str}$ is given by the universal relation $σ/G_\infty\dotε$ with $G_\infty$ a modulus. This equality holds for all rheological regimes from temperatures above the glass transition all the way to the athermal limit, and arises from the competing effects of elastic loading and viscous dissipation. In macromolecular (polymeric) glasses, however, the stress decouples from this relaxatio…
We study the effect of physical aging on the mechanical properties of a model polymer glass using molecular dynamics simulations. The creep compliance is determined simultaneously with the structural relaxation under a constant uniaxial load below yield at constant temperature. The model successfully captures universal features found experimentally in polymer glasses, including signatures of mechanical rejuvenation. We analyze microscopic relaxation timescales and show that they exhibit the same aging characteristics as the macroscopic creep compliance. In addition, our model indicates that th…
We examine how the distribution of contour lengths and the high-stretch stiffening of individual chain segments affect the macroscopic shear modulus of flexible polymer gels, using a 2D numerical model, in which polymer segments form a triangular network and disorder is introduced by varying their contour lengths. We show that in the relevant parameter range: (i) the non-affine contribution to the shear modulus is negligible, i.e. the Born approximation is satisfactory; (ii) the shear modulus is dominated by the contribution originating from equilibrium chain tensions. Moreover, mechanical equ…
Simulations on a Lennard-Jones computer glass are performed to study effects arising from defects in glasses at low temperatures. The numerical analysis reveals that already a low concentration of defects may dramatically change the low temperature properties by giving rise to extrinsic double-well potentials (DWP's). The main characteristics of these extrinsic DWP's are (i) high barrier heights, (ii) high probability that a defect is indeed connected with an extrinsic DWP, (iii) highly localized dynamics around this defect, and (iv) smaller deformation potential coupling to phonons. Designing…
We explore the link between soft vibrational modes and local relaxation events in polymer glasses during physical aging, active deformation at constant strain rate, and subsequent recovery. A softness field is constructed out of the superposition of the amplitudes of the lowest energy normal modes, and found to predict up to 70% of the rearrangements. Overlap between softness and rearrangements increases logarithmically during aging and recovery phases as energy barriers rise due to physical aging, while yielding rapidly rejuvenates the overlap to that of a freshly prepared glass. In the strai…
The excess low-frequency vibrational spectrum, called boson peak, and non-affine elastic response are the most important particularities of glasses. Herein, the vibrational and mechanical properties of polymeric glasses are examined by using coarse-grained molecular dynamics simulations, with particular attention to the effects of the bending rigidity of the polymer chains. As the rigidity increases, the system undergoes a glass transition at a higher temperature (under a constant pressure), which decreases the density of the glass phase. The elastic moduli, which are controlled by the decreas…
The dynamics of structural relaxation in a model polymer glass subject to spatially-homogeneous, time-periodic shear deformation is investigated using molecular dynamics simulations. We study a coarse-grained bead-spring model of short polymer chains below the glass transition temperature. It is found that at small strain amplitudes, the segmental dynamics is nearly reversible over about $10^4$ cycles, while at strain amplitudes above a few percent, polymer chains become fully relaxed after a hundred cycles. At the critical strain amplitude, the transition from slow to fast relaxation dynamics…
In metallic glasses a clear correlation had been established between plasticity or ductility with the Poisson ratio and alternatively the ratio of the elastic bulk modulus to the shear modulus, K/G. Such a correlation between these two macroscopic mechanical properties is intriguing and is challenging to explain from the dynamics on a microscopic level. Such a microscopic explanation is provided in this paper.
We examine the vitrification and melting of asymmetric star polymers mixtures by combining rheological measurements with mode coupling theory. We identify two types of glassy states, a {\it single} glass, in which the small component is fluid in the glassy matrix of the big one and a {\it double} glass, in which both components are vitrified. Addition of small star polymers leads to melting of {\it both} glasses and the melting curve has a non-monotonic dependence on the star-star size ratio. The phenomenon opens new ways for externally steering the rheological behavior of soft matter systems.
We derive expressions for the shear modulus of deeply-quenched, glassy solids, in terms of a Cauchy-Born free energy expansion around a rigid (quenched) reference state, following the approach due to Alexander [Alexander, Phys. Rep. 296, 1998]. Continuum-limit explicit expressions of the shear modulus are derived starting from the microscopic Hamiltonians of central and bond-bending interactions. The applicability of the expressions to dense covalent glasses as well as colloidal glasses with strongly attractive and adhesive bonds is discussed.
We compute the shear modulus of amorphous hard and soft spheres, using the exact solution in infinite spatial dimensions that has been developed recently. We characterize the behavior of this observable in the whole phase diagram, and in particular around the glass and jamming transitions. Our results are consistent with other theoretical approaches, that are unified within this general picture, and they are also consistent with numerical and experimental results. Furthermore, we discuss some properties of the out-of-equilibrium dynamics after a deep quench close to the jamming transition, and…
By combining molecular dynamics simulations and topological analyses with scaling arguments, we obtain analytic expressions that quantitatively predict the entanglement length $N_e$, the plateau modulus $G$, and the tube diameter $a$ in melts that span the entire range of chain stiffnesses for which systems remain isotropic. Our expressions resolve conflicts between previous scaling predictions for the loosely entangled [Lin-Noolandi: $G\ell_K^3/k_\textrm{B}T \sim (\ell_K/p)^3$], semiflexible [Edwards/de Gennes: $G\ell_K^3/k_\textrm{B}T \sim (\ell_K/p)^2$], and tightly-entangled [Morse: $G\ell…
The effects of entanglement and chain orientation on strain hardening in glassy polymers are separated by examining mixtures of chains with different lengths. Simulations show that the orientation of a molecule of a given chain length is the same in monodisperse systems and bidisperse mixtures, even when entangled and unentangled chains are mixed. In addition, the stress in mixtures is equal to the weighted average of the stresses in monodisperse systems. These results indicate that chains contribute independently to strain hardening, that chain orientation is determined by local interactions …
This paper is an attempt to predict the thickness and modulus at the nanometric interphase region with the knowledge on the macroscopic Young's modulus in the polymer-clay nanocomposites. First, a systematic design of 20160 linear elastic finite element simulations are used to derive an analytical equation between the interphase thickness, the interphase modulus, the nanoclay content and the macroscopic Young's modulus of the nanocomposite. Four calibration parameters in this equation are calculated based on the reported data about NYLON6-MMT nanocomposite. Next, an analytical nanoscale equati…
Amorphous materials exhibit peculiar mechanical and vibrational properties, including non-affine elastic responses and excess vibrational states, i.e., the so-called boson peak. For polymer glasses, these properties are considered to be affected by the bending rigidity of the constituent polymer chains. In our recent work [Tomoshige, et al., Sci. Rep. 9 19514 (2019)], we have revealed simple relationships between the variations of vibrational properties and the global elastic properties: the response of the boson peak scales only with that of the global shear modulus. This observation suggests…
We investigate the viscoelastic properties of entangled networks of semiflexible polymers. At intermediate time scales the elastic response of these networks to shear deformation is described by the plateau modulus $G$. Different scaling laws with polymer concentration $c$ have been proposed based on the assumption that the deformation field is affine on all length scales. We develop a numerical approach that allows to calculate the modulus via free energy changes for both affine and non-affine deformations. The non-affine deformation field is obtained by a free energy minimization. Our findin…
We construct a linear response theory of applying shear deformations from boundary walls in the film geometry in Kubo's theoretical scheme. Our method is applicable to any solids and fluids. For glasses, we assume quasi-equilibrium around a fixed inherent state. Then, we obtain linear-response expressions for any variables including the stress and the particle displacements, even though the glass interior is elastically inhomogeneous. In particular, the shear modulus can be expressed in terms of the correlations between the interior stress and the forces from the walls. It can also be expresse…
The relation between elasticity and yielding is investigated in a model polymer solid by Molecular-Dynamics simulations. By changing the bending stiffness of the chain and the bond length, semicrystalline and disordered glassy polymers - both with bond disorder - as well as nematic glassy polymers with bond ordering are obtained. It is found that in systems with bond disorder the ratio Ty/G between the shear yield strength Ty and the shear modulus G is close to the universal value of the atomic metallic glasses. The increase of the local nematic order in glasses leads to the increase of the sh…
In a recent letter, Govaert et al. examined the relationship between strain hardening modulus $G_r$ and flow stress $σ_{flow}$ for five different glassy polymers. In each case, results for $G_r$ at different strain rates or different temperatures were linearly related to the flow stress. They suggested that this linear relation was inconsistent with simulations. Data from previous publications and new results are presented to show that simulations also yield a linear relation between modulus and flow stress. Possible explanations for the change in the ratio of modulus to flow stress with tempe…
Constitutive equations are derived for enthalpy recovery in polymeric glasses after thermal jumps. The model is based on the theory of cooperative relaxation in a version of the trapping concept. It is demonstrated that some critical temperature and some critical degree of crystallinity exist above which the energy landscape becomes homogeneous and structural relaxation ceases.
In this paper we focus on the mechanical properties of oligomeric glasses (waxes), employing a microscopic model that provides, via numerical simulations, information about the shear modulus of such materials, the failure mechanism via plastic instabilities and about the geometric responses of the oligomers themselves to a mechanical load. We present a microscopic theory that explains the numerically observed phenomena, including an exact theory of the shear modulus and of the plastic instabilities, both local and system spanning. In addition we present a model to explain the geometric changes…
We study the dynamics of the phase behavior of a polymer blend in the presence of shear flow. By adopting a two fluid picture and using a generalization of the concept of material derivative, we construct kinetic equations that describe the phase behavior of polymer blends in the presence of external flow. A phenomenological form for the shear modulus for the blend is proposed. The study indicates that a nonlinear dependence of the shear modulus of the blend on the volume fraction of one of the species is crucial for a shift in the stability line to be induced by shear flow.
Because the theory of SER is still a work in progress, the phenomenon itself can be said to be the oldest unsolved problem in science, as it started with Kohlrausch in 1847. Many electrical and optical phenomena exhibit SER with probe relaxation I(t) ~ exp[-(t/τ)β], with 0 < β < 1. Here τ is a material-sensitive parameter, useful for discussing chemical trends. The "shape" parameter β is dimensionless and plays the role of a non-equilibrium scaling exponent; its value, especially in glasses, is both practically useful and theoretically significant. The mathematical complexity of SER is such th…
Simulations are used to examine the microscopic origins of strain hardening in polymer glasses. While stress-strain curves for a wide range of temperature can be fit to the functional form predicted by entropic network models, many other results are fundamentally inconsistent with the physical picture underlying these models. Stresses are too large to be entropic and have the wrong trend with temperature. The most dramatic hardening at large strains reflects increases in energy as chains are pulled taut between entanglements rather than a change in entropy. A weak entropic stress is only obser…
The problem of effective shear and bulk moduli, of an effective Poison's ratio and of an effective dielectric response in microcomposites of the ferroelastic-dielectric type was studied by us recently. Recently one of us, M. Hudak, studied static mechanical properties of the EVA material theoretically and experimentally. We extend our mentioned study of mechanical response of microcomposites of the type ferrolastics - dielectrics to study of Young modulus and shear wave velocity.
Fracture initiation in glassy polymers with no notch is studied together with the evolution at zero stress in the glassy state. Confocal microscopy observations and auto-correlation methods are used to characterize specimens of polymethyl methacrylate (PMMA) loaded at room temperature and subsequently unloaded. The evolution of the morphology and the location of the cracking submitted to elongation rate up to 8% are reported and analyzed during the zero-stress relaxation. The crackling (longitudinal crack, transverse crack and crazes) takes place mainly within a 10micron thickness layer from t…
Max Planck Institute for the Physics of Complex Systems（马克斯·普朗克复杂系统物理研究所）；School of Science, Constructor University（康斯坦茨大学理学院）；Department of Physics, Massachusetts Institute of Technology（麻省理工学院物理系）
Based upon the resistor analogy and using the ideal loop gas approximation(ILGA) it is shown that only pending loops reduce the modulus of an otherwise perfect network made of monodisperse strands and junctions of identical functionality. Thus, the cycle rank of the network with pending structures removed (cyclic and branched) is sufficient to characterize modulus, if the resistor analogy can be employed. It is further shown that it is impossible to incorporate finite cycles into a polymer network such that individual network strands are at equilibrium conformations while maintaining simultane…
Many structural glasses feature static and dynamic mechanical properties that can depend strongly on glass formation history. The degree of universality of this history-dependence, and what it is possibly affected by, are largely unexplored. Here we show that the variability of elastic properties of simple computer glasses under thermal annealing depends strongly on the strength of attractive interactions between the glasses' constituent particles -- referred to here as glass `stickiness'. We find that in stickier glasses the stiffening of the shear modulus with thermal annealing is strongly s…
The emergence of nanoscience has increased the importance of experiments able to probe the very local structure of materials, especially for disordered and heterogeneous systems. This is technologically important; for example, the nanoscale structure of glassy polymers has a direct correlation with their macroscopic physical properties. We have discovered how a local, high frequency dynamic process can be used to monitor and even predict macroscopic behavior in glassy polymers. Polyvinylethylenes vitrified by different chemical and thermodynamic pathways exhibit different densities in the glas…
We review the nature of glass transitions and the glasses arising from a square-well potential with a narrow and deep well. Our discussion is based on the Mode Coupling Theory, and the predictions of glasses that we make refer to the `ideal' glasses predicted by that theory. We believe that the square well system well represents colloidal particles with attractive interactions produced by grafted polymers, or depletion interactions. It has been recently shown that two types of glass, an attractive and a repulsive one, are predicted by MCT for this model. The former can form at quite low densit…
Glassy polymers show strain hardening: at constant extensional load, their flow first accelerates, then arrests. Recent experiments under such loading have found this to be accompanied by a striking dip in the segmental relaxation time. This can be explained by a minimal nonfactorable model combining flow-induced melting of a glass with the buildup of stress carried by strained polymers. Within this model, liquefaction of segmental motion permits strong flow that creates polymer-borne stress, slowing the deformation enough for the segmental (or solvent) modes to then re-vitrify. Here we presen…
We investigate by means of molecular dynamics simulation a coarse-grained polymer glass model focusing on (quasi-static and dynamical) shear-stress fluctuations as a function of temperature T and sampling time $Δt$. The linear response is characterized using (ensemble-averaged) expectation values of the contributions (time-averaged for each shear plane) to the stress-fluctuation relation $μ_{sf}$ for the shear modulus and the shear-stress relaxation modulus $G(t)$. Using 100 independent configurations we pay attention to the respective standard deviations. While the ensemble-averaged modulus $…
We report measurements of the frequency-dependent shear moduli of aging colloidal systems that evolve from a purely low-viscosity liquid to a predominantly elastic glass or gel. Using microrheology, we measure the local complex shear modulus $G^{*}(ω)$ over a very wide range of frequencies (1 Hz- 100 kHz). The combined use of one- and two-particle microrheology allows us to differentiate between colloidal glasses and gels - the glass is homogenous, whereas the colloidal gel shows a considerable degree of heterogeneity on length scales larger than 0.5 micrometer. Despite this characteristic dif…
A number of strange results have been reported for the twist elasticity of a semiflexible filament, actin. In particular dynamic and static methods for determining the torsional twist modulus give very different results. I show here that internal losses (friction) in a semiflexible filament could be an important cause of dissipation and that the interpretation of dynamic experiments should be made in terms of a storage and loss modulus for actin proteins.
