Search results for "Cooling"

showing 10 items of 470 documents

Monte Carlo simulation of the glass transition in polymer melts: An application of MCT

1995

Abstract This paper reviews the results of a large scale Monte Carlo simulation for the dynamics of a supercooled polymer melt. The dynamics of the melt was studied by means of the time evolution of the incoherent intermediate scattering function φs q(t), which was monitored over seven decades in time. In an intermediate time window it is possible to describe the decay of φs q(t) quantitatively in the framework of mode-coupling theory, provided the extended version of the theory is used.

chemistry.chemical_classificationMaterials scienceScale (ratio)Applied MathematicsMonte Carlo methodTime evolutionGeneral Physics and AstronomyThermodynamicsTransportationStatistical and Nonlinear PhysicsPolymerCondensed Matter::Soft Condensed MatterchemistryTime windowsDynamic Monte Carlo methodStatistical physicsGlass transitionSupercoolingMathematical PhysicsTransport Theory and Statistical Physics
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Correlations of the nonexponentiality and state dependence of mechanical relaxations with bond connectivity in Ge-As-Se supercooled liquids

1992

We have studied the mechanical responses of supercooled Ge-As-Se liquids to flexural strains and temperature steps. The departures from exponential relaxation correlate well with the variations in connectivity. The structural state dependence of the mechanical relaxation, detected in pure and weakly cross-linked Se, is suppressed completely at the rigidity percolation threshold {l angle}{ital r}{sub {ital c}}{r angle}, where the liquid fragility is a minimum. The shapes of the decay functions of samples with the same {l angle}{ital r}{sub {ital c}}{r angle} but different compositions are not universal at {ital T}{sub {ital g}} probably because of chemical effects near the binary edges of th…

chemistry.chemical_classificationMaterials scienceTernary numeral systemchemistryFlexural strengthChemical bondComputer Science::Information RetrievalState dependenceThermodynamicsPercolation thresholdSupercoolingInorganic compoundExponential functionPhysical Review B
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I. Glass Transition. Theoretical concepts on the glass transition of polymers and their test by computer simulation

1996

Various organic molecules, in particular polymers, are extremely good glass formers and allow the study of supercooled melts near the glass transition in metastable equilibrium. Theories of the glass transition imply such an equilibrium (e.g. mode-coupling theory, or Gibbs-di Marzio theory) and can hence be tested in these systems. Simplified lattice models for polymer melts (e.g. the bond fluctuation model) have been developed that can very efficiently be studied by Monte-Carlo simulation, and although they fail to accurately describe the local structure, they describe many features of the experiments very well. In this model, the mechanism of the glass transition is a competition between …

chemistry.chemical_classificationPhase transitionMaterials scienceGeneral Chemical Engineeringmedia_common.quotation_subjectConfiguration entropyFrustrationThermodynamicsPolymerCondensed Matter::Soft Condensed MatterchemistryGravitational singularitySupercoolingGlass transitionmedia_commonEntropy (order and disorder)Berichte der Bunsengesellschaft für physikalische Chemie
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Static and dynamic properties of supercooled thin polymer films

2004

The dynamic and static properties of a supercooled (non-entangled) polymer melt are investigated via molecular-dynamics (MD) simulations. The system is confined between two completely smooth and purely repulsive walls. The wall-to-wall separation (film thickness), D, is varied from about 3 to about 14 times the bulk radius of gyration. Despite the geometric confinement, the supercooled films exhibit many qualitative features which were also observed in the bulk and could be analyzed in terms of mode-coupling theory (MCT). Examples are the two-step relaxation of the incoherent intermediate scattering function, the time-temperature superposition property of the late time alpha-process and the…

chemistry.chemical_classificationPhysicsCondensed matter physicsScale of temperatureBiophysicsSurfaces and InterfacesGeneral ChemistryPolymerCondensed Matter::Soft Condensed MatterSuperposition principlechemistryRadius of gyrationRelaxation (physics)General Materials ScienceSoft matterSupercoolingStructure factorBiotechnologyThe European Physical Journal E
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Publisher’s Note: “Polymer-specific effects of bulk relaxation and stringlike correlated motion in the dynamics of a supercooled polymer melt” [J. Ch…

2004

a! Present address: Department of Physics, Wesleyan University, Middletown, CT 06459. b!Author to whom correspondence should be addressed. Electronic mail: baschnag@ics.u-strasbg.fr c!Author to whom correspondence should be addressed. Electronic mail: sglotzer@umich.edu FIG. 8. Temperature dependence of the ratio of ^sseg(tstr )& and ^s(tstr )&. tstr max is the peak time of ^sseg& and ^s& at different temperatures. TMCT 50.45. JOURNAL OF CHEMICAL PHYSICS VOLUME 120, NUMBER 14 8 APRIL 2004

chemistry.chemical_classificationPhysicschemistryGeneral Physics and AstronomyThermodynamicsMotion (geometry)Relaxation (physics)PolymerPhysical and Theoretical ChemistrySupercoolingPolymer meltElectronic mailThe Journal of Chemical Physics
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Monte carlo simulation of the glass transition of polymer melts

2007

The bond fluctuation model of polymer melts is presented as a reasonable compromise between simulation efficiency and realistic chemical detail. It is shown that inclusion of a potential energy that depends on the length of the effective bonds connecting the effective monomers easily creates a conflict between configurational entropy of dense packing and the energetic tendency of the bonds to stretch. This competition leads to a glass transition of the model, which very well describes many features of real systems.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodConfiguration entropyThermodynamicsPolymerPotential energyCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerchemistryGlass transitionSupercoolingBond fluctuation model
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Monte Carlo simulation studies of the interfaces between polymeric and other solids as models for fiber-matrix interactions in advanced composite mat…

1996

As a coarse-grained model for dense amorphous polymer systems interacting with solid walls (i.e., the fiber surface in a composite), the bond fluctuation model of flexible polymer chains confined between two repulsive surfaces is studied by extensive Monte Carlo simulations. Choosing a potential for the length of an effective bond that favors rather long bonds, the full temperature region from ordinary polymer melts down to the glass transition is accessible. It is shown that in the supercooled state near the glass transition an “interphase” forms near the walls, where the structure of the melt is influenced by the surface. This “interphase” already shows up in static properties, but also h…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodMineralogyPolymerCondensed Matter PhysicsGyrationAmorphous solidCondensed Matter::Soft Condensed MatterInorganic ChemistrychemistryChemical physicsMaterials ChemistryRadius of gyrationSupercoolingGlass transitionConfined spaceMacromolecular Theory and Simulations
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Polymer-specific effects of bulk relaxation and stringlike correlated motion in the dynamics of a supercooled polymer melt

2003

We analyze dynamical heterogeneities in a simulated “bead-spring” model of a nonentangled, supercooled polymer melt. We explore the importance of chain connectivity on the spatially heterogeneous motion of the monomers. We find that when monomers move, they tend to follow each other in one-dimensional paths, forming strings as previously reported in atomic liquids and colloidal suspensions. The mean string length is largest at a time close to the peak time of the mean cluster size of mobile monomers. This maximum string length increases, roughly in an exponential fashion, on cooling toward the critical temperature TMCT of the mode-coupling theory, but generally remains small, although large…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceScatteringGeneral Physics and Astronomy02 engineering and technologyPolymer021001 nanoscience & nanotechnology01 natural sciencesExponential functionCondensed Matter::Soft Condensed MatterCrystallographychemistry.chemical_compoundMonomerchemistryChain (algebraic topology)Chemical physics0103 physical sciencesRelaxation (physics)Physical and Theoretical Chemistry010306 general physics0210 nano-technologySupercoolingGlass transitionThe Journal of Chemical Physics
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Interfacial properties of glassy polymer melts: A Monte Carlo study

1996

The properties of the interface between a polymer melt and a solid wall are studied over a wide range of temperatures by dynamic Monte Carlo simulations. It is shown that in the supercooled state near the glass transition of the melt an “interphase” forms, the structure of which is influenced by the wall. The thickness of this interphase is determined from the monomer density profile near the surface and is strongly temperature dependent. At low glass-like temperatures it is larger than the bulk radius of gyration of the chains.

chemistry.chemical_classificationRange (particle radiation)Materials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerCondensed Matter PhysicsCondensed Matter::Disordered Systems and Neural NetworksCondensed Matter::Soft Condensed MatterCrystallographychemistry.chemical_compoundMonomerchemistryMaterials ChemistryRadius of gyrationInterphaseSupercoolingGlass transitionMacromolecular Symposia
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Influence of“controlled processing conditions” on the solidification of iPP, PET and PA6

2002

In this work reliable experimental data for three semicrystalline polymers (iPP, PA6, PET) crystallised under pressure and high cooling rates are supplied. These results were achieved on the basis of a model experiment where drastic controlled solidification conditions are applied. The final objective was to quantify the effect of two typical operating conditions (pressure and cooling rate) on the final properties and morphology of the obtained product. The influence of processing conditions on some macroscopically relevant properties, such as density and micro hardness is stressed, together with the influence of processing conditions on the product morphology, investigated by means of Wide…

chemistry.chemical_classificationWork (thermodynamics)Materials scienceMorphology (linguistics)Polymers and PlasticsScatteringOrganic ChemistryMineralogyPolymerCondensed Matter PhysicsIndentation hardnessCrystallinityCooling ratechemistryPressure increaseMaterials ChemistryComposite materialMacromolecular Symposia
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