Search results for "MECHANICS"

showing 10 items of 9361 documents

Nanoparticle dynamics in semidilute polymer solutions: Rings versus linear chains

2021

We study the dynamics of nanoparticles in semidilute solutions of ring and linear polymers using hybrid molecular dynamics–multiparticle collision dynamics simulations. The dynamics of the monomers, the polymer centers-of-mass, and the nanoparticles coincide for these two architectures for solutions of the same monomer concentration. The long time diffusivities of the nanoparticles follow the predictions of a polymer coupling theory [Cai et al., Macromolecules 44, 7853–7863 (2011)], suggesting that nanoparticle dynamics are coupled to segmental relaxations for both polymer architectures examined here. At intermediate time scales, the nanoparticle dynamics are characterized by subdiffusive e…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceMechanical EngineeringDiffusionNanoparticlePolymerCondensed Matter PhysicsRing (chemistry)Thermal diffusivityCondensed Matter::Soft Condensed MatterCoupling (physics)chemistry.chemical_compoundMonomerchemistryMechanics of MaterialsChemical physicsGeneral Materials ScienceMacromoleculeJournal of Rheology
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Frictional drag between polymer bearing surfaces

2002

Some fundamental features of friction between two polymer bearing surfaces in relative sliding motion are investigated by molecular dynamics simulations. End-tethered and adsorbed polymers are considered under good and poor solvent conditions. The shear stress is measured while varying the solvent's viscosity, surface separation, degree of polymerization and grafting density. For all systems we observe shear thinning that is attributed to the orientation of the chains along the shear direction. This effect is particularly strong for brushes, for which the shear stress during the steady sliding state is mainly determined by the degree of overlap between the brushes.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceShear thinningGeneral Physics and AstronomyPolymerDegree of polymerizationPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterMolecular dynamicsClassical mechanicsAdsorptionShear (geology)chemistryHardware and ArchitectureDragShear stressComposite materialComputer Physics Communications
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Structure of bottle-brush polymers in solution: A Monte Carlo test of models for the scattering function

2008

Extensive Monte Carlo results are presented for a lattice model of a bottle-brush polymer under good solvent or Theta solvent conditions. Varying the side chain length, backbone length, and the grafting density for a rigid straight backbone, both radial density profiles of monomers and side chain ends are obtained, as well as structure factors describing the scattering from a single side chain and from the total bottle-brush polymer. To describe the structure in the interior of a very long bottle-brush, a periodic boundary condition in the direction along the backbone is used, and to describe effects due to the finiteness of the backbone length, a second set of simulations with free ends of…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceStatistical Mechanics (cond-mat.stat-mech)ScatteringMonte Carlo methodTheta solventGeneral Physics and AstronomyFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterMolecular physicsConvolutionCondensed Matter::Soft Condensed MatterchemistrySide chainPeriodic boundary conditionsSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryCondensed Matter - Statistical MechanicsLattice model (physics)
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Stochastic dynamics of polymer brushes under shear deformation

1998

The dynamical properties of polymer brushes under shear deformation have been studied by computer simulation. Both the local and the global dynamic properties at various shear rates have been calculated. The distribution of orientational and translational mobilities of the different monomers along the chain have been obtained. It was shown that the local mobility of the brushes changes very slowly with increasing of shear rates up to the largest rates. Increase in grafting density leads to an increasingly step like dependence of the correlation times as a function of shear rate.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMineralogy02 engineering and technologyPolymerMechanics010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed MatterSimple shearShear rateStochastic dynamicschemistryShear (geology)Materials ChemistryCeramics and Composites0210 nano-technologyJournal of Non-Crystalline Solids
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Phase transitions of single polymer chains and of polymer solutions: insights from Monte Carlo simulations

2008

The statistical mechanics of flexible and semiflexible macromolecules is distinct from that of small molecule systems, since the thermodynamic limit can also be approached when the number of (effective) monomers of a single chain (realizable by a polymer solution in the dilute limit) is approaching infinity. One can introduce effective attractive interactions into a simulation model for a single chain such that a swollen coil contracts when the temperature is reduced, until excluded volume interactions are effectively canceled by attractive forces, and the chain conformation becomes almost Gaussian at the theta point. This state corresponds to a tricritical point, as the renormalization gro…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPhase transitionMonte Carlo methodThermodynamicsStatistical mechanicsPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterTricritical pointchemistryPhase (matter)Thermodynamic limitExcluded volumeGeneral Materials ScienceJournal of Physics: Condensed Matter
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Competition between liquid-crystalline ordering and glassy freezing in melts of semiflexible polymers: A monte carlo simulation

1999

We present results of a Monte Carlo simulation of dense melts of semiflexible polymers using the bond-fluctuation model. The chosen Hamiltonian increases the chain stiffness upon cooling which in turn leads to glass-transition like freezing of the polymer mobility. Employing an efficient simulation algorithm, which is able to equilibrate the simulated systems to lower temperature than the Rouse-type algorithm showing the glassy freezing, we are able to observe an isotropic-nematic phase transition. This transition lies above the glass transition temperature one would extrapolate from the observed freezing behavior.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPhase transitionPolymers and PlasticsChemistryLiquid crystallineOrganic ChemistryMonte Carlo methodThermodynamicsStiffnessPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed Mattersymbols.namesakeSimulation algorithmMaterials Chemistrymedicinesymbolsmedicine.symptomHamiltonian (quantum mechanics)Glass transitionMacromolecular Symposia
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Monte-Carlo Simulation of 3-Dimensional Glassy Polymer Melts: Reptation Versus Single Monomer Dynamics

1995

A polymer melt is simulated at finite temperature by the Monte-Carlo method. We use a coarse-grained model for the polymer system, the bond-fluctuation model. Static properties of the melt can be obtained by generating configurations not with single-monomer- dynamics which moves individual monomers locally, but reptation-dynamics which allows collec- tive motion of the chains. This algorithm can produce equilibrated configurations much faster. It is demonstrated that static properties do not differ from those obtained by single-monomer- dynamics. Values of the radius of gyration, the mean square bond length and similar quantities for different temperatures and densities are presented.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPhysics and Astronomy (miscellaneous)Dynamics (mechanics)Monte Carlo methodGeneral EngineeringThermodynamicsPolymerAtomic and Molecular Physics and OpticsCondensed Matter::Soft Condensed MatterBond lengthchemistry.chemical_compoundReptationMonomerchemistryRadius of gyrationStatistical physicsPolymer meltJournal de Physique II
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Monte Carlo simulations of the polymer glass transition: From the test of theories to material modeling

1997

We present results on the glass transition in polymer melts using Monte Carlo simulations of the bond fluctuation lattice model. There are two questions we address in this work. What is the temperature dependence of the entropy density in such a model polymer melt and how well is it described by theories like the Gibbs-DiMarzio theory of the glass transition? And to what degree is one able to map the Hamiltonian of such an abstract lattice model onto a specific polymer material and use it to model the large scale and long time properties of a realistic polymer melt?

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed Mattersymbols.namesakeEntropy densitychemistryMaterials ChemistrysymbolsHamiltonian (quantum mechanics)Glass transitionPolymer meltMacromolecular Symposia
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Frictional Drag Mechanisms between Polymer-Bearing Surfaces

2001

The fundamental features of friction between two polymer-bearing surfaces in relative sliding motion are investigated by molecular dynamics simulation. Adsorbed and grafted polymers are considered in good and bad solutions. The solvent is not treated explicitly but indirectly in terms of a Langevin thermostat. In both systems, we observe shear thinning that is attributed to an orientation of the radius of gyration along the sliding direction. This effect is particularly strong for surfaces bearing polymer brushes. In this case, the shear stresses are mainly determined by the degree of the interpenetration of brushes.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesShear thinningMaterials scienceSurfaces and InterfacesPolymerCondensed Matter PhysicsThermostatlaw.inventionCondensed Matter::Soft Condensed MatterMolecular dynamicsClassical mechanicsShear (geology)chemistryDraglawElectrochemistryRadius of gyrationGeneral Materials ScienceComposite materialSpectroscopyLangmuir
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Electronic structure of polysilanes: influence of substitution and conformation

1993

Abstract The valence effective Hamiltonian (VEH) quantum-chemical approach is used to investigate the electronic properties of polysilane. The valence band structure calculated for this fully saturated polymer is analyzed in terms of orbital contributions and compared to that of the closely related carbon polymer, polyethylene. The effects of alkyl substitution and silicon backbone conformation are studied by elucidating the modifications that these structural changes induce on the electronic valence band structure of all-trans unsubstituted polysilane. The VEH results predict a decrease of the band gap upon alkyl substitution and on going from helical to all-trans conformations.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesValence (chemistry)SiliconBand gapMechanical EngineeringMetals and Alloyschemistry.chemical_elementPolymerElectronic structurePolyethyleneCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundsymbols.namesakeCrystallographychemistryMechanics of MaterialsComputational chemistryMaterials ChemistrysymbolsPolysilaneHamiltonian (quantum mechanics)Synthetic Metals
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