Search results for "dynamics."

showing 10 items of 9637 documents

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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Polymer droplets on substrates with striped surface domains: molecular dynamics simulations of equilibrium structure and liquid bridge rupture

2005

The structure of a polymer nanodroplet adsorbed on a flat lyophobic substrate chemically decorated with a lyophilic stripe of width 2RD is studied by molecular dynamics simulation of a coarse-grained bead–spring model of short macromolecules (containing N = 20 effective monomers). Varying the stripe width, the strength of the monomer–wall attraction and the temperature, the equilibrium morphology of the resulting droplets is studied and discussed in terms of current phenomenological theories. In the second part, the behaviour of a liquid bridge connecting two such lyophilic stripes a distance L apart is analysed. It is shown that for large enough L such free-standing films are unstable and …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMorphology (linguistics)NanotechnologyPolymerSubstrate (electronics)Condensed Matter PhysicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicsMonomerAdsorptionchemistryChemical physicsGeneral Materials ScienceThin filmMacromoleculeJournal of Physics: Condensed Matter
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On the thermodynamic treatment of poly(vinylidene fluoride)/polystyrene blend under liquid—liquid phase separation conditions

1995

Abstract This paper deals with experimental and theoretical investigations on the compatibility of binary of polymer blends in solution. The experimental phase boundary of a crystalline polymer such as poly(vinylidene fluoride) with polystyrene (an amorphous polymer) in dimethylformamide as solvent has been determined by size-exclusion chromatography at 25°C. The composition of the coexisting phases has been used to calculate interaction parameters by means of the Flory—Huggins-type function for the free energy of mixing, including composition dependence of the polymer-polymer interaction parameter and a first correction term denoted as ternary interaction parameter. The calculation of thes…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPhase boundaryTernary numeral systemPolymers and PlasticsOrganic ChemistryThermodynamicsPolymerFlory–Huggins solution theoryCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryPolystyrenePolymer blendTernary operationPhase diagramPolymer
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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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Biomolecular-solvent stereodynamic coupling probed by deuteration.

1983

Thermodynamic interpretation of experiments with isotopically perturbed solvent supports the view that solvent stereodynamics is directly relevant to thermodynamic stability of biomolecules. According with the current understanding of the structure of the aqueous solvent, in any stereodynamic configuration of the latter, connectivity pathways are identifiable for their topologic and order properties. Perturbing the solvent by isotopic substitution or, e.g., by addition of co-solvents, can therefore be viewed as reinforcing or otherwise perturbing these topologic structures. This microscopic model readily visualizes thermodynamic interpretation. In conclusion, the topologic stereodynamic str…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPhysics::Biological PhysicsAqueous solutionBiomoleculeMolecular ConformationStereoisomerismGeneral MedicineDeuteriumCondensed Matter::Soft Condensed MatterSolventCoupling (physics)Order (biology)chemistryModels ChemicalStructural BiologyComputational chemistryPhase spaceSolventsMoleculeThermodynamicsChemical stabilityPhysics::Chemical PhysicsMolecular BiologyJournal of biomolecular structuredynamics
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Static and Dynamic Properties of Adsorbed Chains at Surfaces:  Monte Carlo Simulation of a Bead-Spring Model

1996

The adsorption of flexible polymers from dilute solution in good solvents at attractive walls is studied by Monte Carlo simulation of a coarse-grained off-lattice model, varying chain length N and ...

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodThermodynamicsPolymerSpring (mathematics)Condensed Matter::Soft Condensed MatterInorganic ChemistryBead (woodworking)Chain lengthAdsorptionMaterials ChemistryStatistical physicsPhysics::Chemical PhysicsMacromolecules
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Brownian dynamics simulation of grafted polymer brushes

1995

We present results of computer simulations by the method of Brownian dynamics of polymeric brushes attached to impenetrable planes. For testing both model and method we have used one polymer brush attached to a repulsive plane and compare some results with Monte Carlo results of Lai and Binder on the bond fluctuation model. We have also studied two polymeric brushes attached to two parallel planes at different distances between planes, and investigate the interplay between the interpenetration of the brushes and the configurational properties of the grafted chains.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsChemistryPlane (geometry)Organic ChemistryMonte Carlo methodPolymerCondensed Matter PhysicsPolymer brushdigestive systemCondensed Matter::Soft Condensed MatterInorganic ChemistryComputer Science::GraphicsIntermolecular interactionChemical physicsMaterials ChemistryBrownian dynamicsStatistical physicsStructure factorBond fluctuation modelMacromolecular Theory and Simulations
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Association Equilibria Theory for Polymers in Mixed Solvents with Specific Interactions

2004

Hydrogen bonding plays an important role in determining the physical and thermodynamic properties of polar fluids. Theoretical and experimental aspects of polymers, in mixed solvents with hydrogen-bonding-specific interactions, are investigated using a simple association model based on the theory of association equilibria developed by Pouchly et al. The thermodynamic non-idealities are accounted for using a modified Flory-Huggins theory with effective g ij parameters. The entropic term of the above formalism has been formulated taking into account the pplymer segment-solvent as well as the solvent-solvent hydrogen-bond formation. Four equilibrium constants are introduced to make a realistic…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsHydrogen bondChemistryOrganic ChemistrySolvationThermodynamicsSorptionPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterInorganic ChemistryVirial coefficientMaterials ChemistryPhysical chemistryPhysics::Chemical PhysicsSolvent effectsTernary operationEquilibrium constantMacromolecular Theory and Simulations
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