Search results for " Plastics"

showing 10 items of 2628 documents

Stochastic dynamics simulation of grafted polymer brushes under shear deformation

1998

We present results of computer simulations of polymer brushes (layers of polymer chains attached at one end onto an impermeable planar surface) under shear deformation at constant shear rate. As the first stage of calculations the behavior of a single brush was studied. The monomer density profile, the distribution of the chain ends, the positions and orientations of different monomers along the chain were calculated. Dimensions of the polymer chains as functions of the shear rate were obtained for different grafting densities. An increase in the brush thickness over the grafting plane with an increase in the shear rate as predicted by the theory of Barrat was observed. However, the magnitu…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsOrganic ChemistryBrushPolymerCondensed Matter Physicslaw.inventionCondensed Matter::Soft Condensed MatterInorganic ChemistryShear ratechemistry.chemical_compoundMonomerStochastic dynamicsPlanarchemistrylawPolymer chemistryMaterials ChemistryComposite material
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Comb-Branched Polymers:  Monte Carlo Simulation and Scaling

1996

The Monte Carlo simulation technique (the bond fluctuation model) has been used for the study of the equilibrium conformations of comb-branched polymers consisting of a long flexible main chain and side chains grafted at a regular separation onto the main chain. The solvent has been supposed to be good (athermal) for the main and side chains. The global conformation and the gyration radius of the polymer, as well as the local conformational structure of the comb, have been analyzed as functions of the length of the side chains and spacers. The effect of induced rigidity of the comb due to the interaction between side chains has been observed. We have found the results of the simulation to b…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsOrganic ChemistryMonte Carlo methodPhysics::OpticsPolymerGyrationCondensed Matter::Soft Condensed MatterInorganic ChemistryRigidity (electromagnetism)chemistryChemical physicsMaterials ChemistrySide chainRadius of gyrationStatistical physicsScalingBond fluctuation modelMacromolecules
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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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Brownian dynamics of grafted polymer chains: time dependent properties

1995

Results of computer simulations of polymer layers consisting of chains grafted by one end on an unpenetrable plane are presented. Characteristics of translational and rotational motion of different chain segments and correlation functions of chain radii were calculated both for single layers at different grafting densities s and for two interacting layers at different distances D between parallel grafting planes. Two values of grafting density were used in the latter case. The behavior of different correlation times as function of s and D and the interplay between the interpenetration of the brushes and rotational and translational motion are discussed. Both relaxation functions and mean sq…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsPlane (geometry)Organic ChemistryRelaxation (NMR)Rotation around a fixed axisFunction (mathematics)PolymerCondensed Matter PhysicsMolecular physicsExponential functionCondensed Matter::Soft Condensed MatterInorganic ChemistrychemistryChain (algebraic topology)Materials ChemistryBrownian dynamicsPhysical chemistryMacromolecular Theory and Simulations
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Toluene self-diffusion in solutions of linear and crosslinked polystyrene

1995

Toluene self-diffusion coefficients in solutions of linear and crosslinked polystyrene (PS) at concentrations up to 30 wt% polymer have been determined over the temperature range 143–230 K using the1H n.m.r. static gradient stimulated echo method. At similar polymer concentrations, the diffusion coefficient values of toluene were higher for mixtures with crosslinked PS than for solutions containing linear PS. On cooling and approaching the solution glass transition, the amplitude decays in diffusion and spin-relaxation measurements become non-exponential and are interpreted in terms of a two-component decomposition. The estimated fraction of the toluene motionally bound to polymer increases…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesSelf-diffusionPolymers and PlasticsDiffusionOrganic ChemistryAnalytical chemistryConcentration effectPolymerAtmospheric temperature rangeTolueneCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryPolystyreneGlass transitionPolymer
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Adsorption and structure formation of semiflexible polymers on spherical surfaces

2018

Abstract Rigid spheres with a short-range attractive potential are taken as a coarse-grained model of vesicles, which contain a solution of semiflexible polymers in their interior. Assuming good solvent conditions with an implicit description of the solvent, effective monomers experience bond-length and bond-angle potentials as well as excluded-volume interaction. Due to the attractive vesicle surface, phase separation occurs between a thin shell of adsorbed monomers at the surface and a rather dilute, and therefore, disordered polymer solution in the sphere interior. While at a planar attractive surface the wormlike chains would exhibit liquid crystalline (nematic and smectic) order, the c…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesStructure formationMaterials sciencePolymers and PlasticsOrganic ChemistryShell (structure)02 engineering and technologyPolymer021001 nanoscience & nanotechnologyCurvature01 natural sciencesCondensed Matter::Soft Condensed MatterchemistryLiquid crystalChemical physics0103 physical sciencesMonolayerMaterials ChemistrySPHERESDensity functional theory010306 general physics0210 nano-technologyPolymer
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A thermodynamic analysis on the coincidence of extrema conditions in the sorption equilibrium for ternary polymer systems

1993

Flory-Huggins theory of polymer solutions has been used to express the condition of extrema values in the total sorption, as well as the inversion point in the preferential adsorption parameters for termary polymer systems. Two approaches have been followed, the first considers the binary and ternary interaction parameters independent of polymer concentration and solvent composition. In the second one, this dependence has been introduced. Our attention is focused on the volume fraction of solvent mixture dependence of the above parameters, in order to confirm or not the coincidence between the extrema values and the inversion point. Several cosolvent and cononsolvent ternary polymer systems…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesTernary numeral systemPolymers and PlasticsChemistryThermodynamicsSorptionPolymerCoincidenceCondensed Matter::Soft Condensed MatterMaxima and minimaColloid and Surface ChemistryVolume fractionMaterials ChemistryPhysical and Theoretical ChemistrySolvent effectsTernary operationColloid & Polymer Science
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Prediction of maxima and minima in the curve of total sorption parameter in ternary polymer systems. Influence of ternary interaction parameter

1993

Flory-Huggins theory modified by Pouchly has been applied to predict maxima and minima in the curve of total sorption in ternary polymer systems formed by a polymer and two liquids. In this work, different diagrams based on experimental magnitudes easily obtained such as the difference in affinities of liquids, solvents and non solvents, and the solvent molar volume ratio. Total sorption parameter has been considered to be the decisive magnitude to define extrema conditions in both cosolvent and cononsolvent ternary polymer systems. The theoretical prediction is not altered by the inclusion of ternary interactions. Different examples of ternary systems dealing with vinyl polymers and polydi…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesTernary numeral systemPolymers and PlasticsThermodynamicsSorptionPolymerFlory–Huggins solution theoryVinyl polymerCondensed Matter::Soft Condensed MatterMaxima and minimaColloid and Surface ChemistryMolar volumechemistryMaterials ChemistryPhysical and Theoretical ChemistryTernary operationColloid & Polymer Science
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A comparative study between cosolvent and cononsolvent ternary polymer systems through the preferential adsorption coefficient

1993

Sorption equilibrium of polystyrene and poly (dimethyl siloxane) in mixed solvents has been monitored by means of the preferential adsorption coefficient experimentally determined from intensity light scattering measurements. The pairs of solvents used to dissolve each polymer sample have been selected for the purpose to perform cosolvent and cononsolvent ternary polymer systems. Flory-Huggins formalism including ternary interactions has been used to predict the sorption equilibrium for the cosolvent system and, for the first time, for cononsolvent ones. Moreover, the proportionality between binary and ternary interactions, recognized by Pouchly, is also corroborated for both ternary polyme…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesTernary numeral systemPolymers and PlasticsThermodynamicsSorptionPolymerGibbs free energyCondensed Matter::Soft Condensed MatterSolventchemistry.chemical_compoundsymbols.namesakeColloid and Surface ChemistrychemistryMaterials ChemistrysymbolsOrganic chemistryPolystyrenePhysics::Chemical PhysicsPhysical and Theoretical ChemistrySolvent effectsTernary operationColloid and Polymer Science
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Spinodal demixing, percolation and gelation of biostructural polymers

1990

We present a variety of new experiments which concern the self-assembly of a polymeric network from homogeneous solutions of Agarose, a representative biostructural polysaccharide used for previous studies at our laboratories. They allow deriving a semi-quantitative phase diagram in the T, C plane. The diagram includes both the spinodal and gelation lines. Below a value of about 2% w/v, concentration is not sufficient for direct gelation; however, quenching of the sol from high temperatures to below the spinodal line initiates the spinodal demixing. The latter generates two sets of regions having respectively, higher- and lower-than-average polymer concentrations. In the higher-concentratio…

chemistry.chemical_classificationQuenchingSpinodalMaterials sciencePolymers and PlasticsPlane (geometry)Organic ChemistryDiagramKineticsPolymerCondensed Matter PhysicsCrystallographychemistryChemical physicsPercolationMaterials ChemistryPhase diagramMakromolekulare Chemie. Macromolecular Symposia
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