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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

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

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

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

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

We perform molecular dynamics simulations under uniaxial tension to investigate the micromechanisms underlying strain hardening in glassy polymers. By decomposing the stress into virial components associated with pair, bond, and angle…

软凝聚态物质 · 物理学 2024-11-13 Wuyang Zhao

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 investigate the mechanical properties of amorphous polymers by means of coarse-grained simulations and nonaffine lattice dynamics theory. A small increase of polymer chain bending stiffness leads first to softening of the material, while…

软凝聚态物质 · 物理学 2017-09-14 Christopher Ness , Vladimir V. Palyulin , Rico Milkus , Robert Elder , Timothy Sirk , Alessio Zaccone

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

We present a unified theory for the longitudinal dynamic response of a stiff polymer in solution to various external perturbations (mechanical excitations, hydrodynamic flows, electrical fields, temperature quenches ...) that can be…

软凝聚态物质 · 物理学 2007-05-23 Oskar Hallatschek , Erwin Frey , Klaus Kroy

We report the mechanical response of a model nanocomposite system of poly(styrene) (PS)-silica to large-amplitude oscillatory shear deformations. Nonlinear behavior of PS nanocomposites is discussed with the changes in particle dispersion…

软凝聚态物质 · 物理学 2013-01-14 Erkan Senses , Pinar Akcora

Chemical reactions inside cells are typically subject to the effects both of the cell's confining surfaces and of the viscoelastic behavior of its contents. In this paper, we show how the outcome of one particular reaction of relevance to…

软凝聚态物质 · 物理学 2015-06-04 Pinaki Bhattacharyya , Rati Sharma , Binny J. Cherayil

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…

软凝聚态物质 · 物理学 2014-01-10 Nikolai V. Priezjev

Constitutive equations are derived for the time-dependent behavior of particle-reinforced elastomers at isothermal loading with finite strains. A rubbery polymer is modelled as a network of macromolecules bridged by junctions which can slip…

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

I develop a kinetic mechanism to explain chain folding in polymer crystallization which is based on the competition between the formation of stems, which is due to frequent occupations of trans states along the chains in the supercooled…

软凝聚态物质 · 物理学 2014-09-23 S. Stepanow

We report on the linear viscoelastic properties of mixtures comprising multiarm star (as model soft colloids) and long linear chain homopolymers in a good solvent. In contrast to earlier works, we investigated symmetric mixtures (with a…

软凝聚态物质 · 物理学 2020-07-01 Daniele Parisi , Domenico Truzzolillo , Vishnu D. Deepak , Mario Gauthier , Dimitris Vlassopoulos

Constitutive equations are derived for the viscoelastic response of rubbery polymers at finite strains. A polymer is thought of as a network of long chains connected to temporary junctions. At a random time, a chain detaches from a…

软凝聚态物质 · 物理学 2007-05-23 Aleksey D. Drozdov , Al Dorfmann

Using molecular dynamics simulations we examine the dynamics of a family of model polymers with varying chain length and torsional potential barriers. We focus on features of the dynamics of polymers that are seen experimentally but absent…

软凝聚态物质 · 物理学 2019-06-11 Daniel Fragiadakis , C. Michael Roland

We investigate, using numerical simulations and analytical arguments, a simple one dimensional model for the swelling or the collapse of a closed polymer chain of size N, representing the dynamical evolution of a polymer in a \Theta-solvent…

凝聚态物理 · 物理学 2009-10-31 E. Pitard , J. -P. Bouchaud

Using molecular dynamics simulations, we provide chain-level insights into the dissimilarities in rearrangements of polymers under uniaxial tensile and compressive deformation in glassy and semicrystalline samples of varying chain lengths.…

软凝聚态物质 · 物理学 2019-01-23 Sara Jabbari-Farouji , Damien Vandembroucq
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