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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…

软凝聚态物质 · 物理学 2009-11-13 Robert S. Hoy , Mark O. Robbins

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.…

材料科学 · 物理学 2009-11-13 Robert S. Hoy , Mark O. Robbins

Glassy polymers show strain hardening: at constant extensional load, their flow first accelerates, then arrests. Recent experiments have found this to be accompanied by a striking and unexplained dip in the segmental relaxation time. Here…

软凝聚态物质 · 物理学 2015-05-30 S. M. Fielding , R. G. Larson , M. E. Cates

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…

软凝聚态物质 · 物理学 2015-05-14 Robert S. Hoy , Mark O. Robbins

In a recent letter, Govaert et al. examined the relationship between strain hardening modulus $G_r$ and flow stress $\sigma_{flow}$ for five different glassy polymers. In each case, results for $G_r$ at different strain rates or different…

软凝聚态物质 · 物理学 2015-05-13 M. O. Robbins , R. S. Hoy

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.…

软凝聚态物质 · 物理学 2015-06-11 S. M. Fielding , R. L. Moorcroft , R. G. Larson , M. E. Cates

Molecular dynamic simulation enables one to correlate the evolution of the micro-structure with anisotropic stress when a material is subject to strain. The anisotropic stress due to a constant strain-rate load in a cross-linked polymer is…

软凝聚态物质 · 物理学 2011-05-05 Prashant Kumar Srivastava , Kartik Venkatraman

Constitutive equations are derived for the viscoelastoplastic response of amorphous glassy polymers at isothermal loading with small strains. A polymer is treated as an ensemble of cooperatively relaxing regions (CRR) which rearrange at…

材料科学 · 物理学 2007-05-23 Aleksey D. Drozdov

We study shear yielding and steady state flow of glassy materials with molecular dynamics simulations of two standard models: amorphous polymers and bidisperse Lennard-Jones glasses. For a fixed strain rate, the maximum shear yield stress…

软凝聚态物质 · 物理学 2009-11-10 Joerg Rottler , Mark O. Robbins

Amorphous elastomers exhibit significant rate-stiffening and unique viscous flow characteristics across a wide range of strain rates, often undergoing glass transition above a strain rate threshold. We have developed a…

软凝聚态物质 · 物理学 2026-05-26 Bibekananda Datta , Sushan Nakarmi , Nitin P. Daphalapurkar

We study with molecular dynamics simulations of a generic bead-spring model the cyclic crazing behaviour of glassy polymers. The aim is to elucidate the mechanical response of sole fibrillated craze matter as well as its interaction with…

软凝聚态物质 · 物理学 2024-06-21 Tobias Laschuetza , Ting Ge , Thomas Seelig , Joerg Rottler

Using molecular dynamics simulations, we show that a widely-accepted theoretical prediction for glassy-polymeric strain hardening moduli ($G_R \propto \rho_e$, where $\rho_e$ is the entanglement density) fails badly for semiflexible…

软凝聚态物质 · 物理学 2025-11-24 Robert S. Hoy

The deformation kinetics for glassy polymers confined in microscopic domain at very low temperature regime was investigated using a transition-rate-state dependent model considering the shear thinning behavior which means, once material…

软凝聚态物质 · 物理学 2009-04-09 Guanghua Zhu

We report on an extensive study of craze formation in glassy polymers. Molecular dynamics simulations of a coarse-grained bead-spring model were employed to investigate the molecular level processes during craze nucleation, widening, and…

材料科学 · 物理学 2009-11-10 Joerg Rottler , Mark O. Robbins

A simple theory for glassy polymeric mechanical response which accounts for large scale chain relaxation is presented. It captures the crossover from perfect-plastic response to strong strain hardening as the degree of polymerization $N$…

软凝聚态物质 · 物理学 2015-05-18 Robert S. Hoy , Corey S. O'Hern

The structural properties of a linear polymer and its evolution in time have a strong bearing on its anisotropic stress response. The mean-square bond length and mean bond angle are the critical parameters that influence the time-varying…

软凝聚态物质 · 物理学 2010-12-30 Prashant Kumar Srivastava , Kartik Venkatraman

The stress-strain relations and the yield behavior of model glass (a 80:20 binary Lennard-Jones mixture) is studied by means of MD simulations. First, a thorough analysis of the static yield stress is presented via simulations under imposed…

软凝聚态物质 · 物理学 2009-11-10 F. Varnik , L. Bocquet , J. -L. Barrat

In this Perspective, I describe recent work on systems in which the traditional distinctions between (i) unentangled vs. well-entangled systems and (ii) melts vs. glasses seem least useful, and argue for the broader use in glassy polymer…

软凝聚态物质 · 物理学 2015-05-27 Robert S. Hoy

The polymer relaxation dynamic of a sample, stretched up to the stress hardening regime, is measured, at room temperature, as a function of the strain $\lambda$ for a wide range of the strain rate $\dot\gamma$, by an original dielectric…

软凝聚态物质 · 物理学 2020-03-11 R. Sahli , J. Hem , C. Crauste-Thibierge , F. Clément , D Long , S. Ciliberto

Atomistic deformation simulations in the nominally elastic regime are performed for a model binary glass with strain rates as low as $10^{4}$/sec (corresponding to 0.01 shear strain per 1$\mu$sec). A robust elasticity is revealed that…

软凝聚态物质 · 物理学 2020-11-21 P. M. Derlet , R. Maass
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