Search results for "dynamics."

showing 10 items of 9637 documents

Computer simulations of undercooled fluids and the glass transition

2000

Abstract Two model studies are presented that attempt to describe the static and dynamic properties of glass-forming fluids via molecular dynamics simulations: The first model is an atomistically realistic model of SiO 2 , the second model provides a coarse-grained description of polymer liquids, i.e., typical `fragile' glassformers, while SiO 2 is the prototype of a `strong glassformer'. For both models, attention is given to the questions as to which range of temperatures are properties in equilibrium, and whether such simulations can help to interpret experiments and/or check theoretical predictions. While in the simulation of SiO 2 using the potential of van Beest, Kramer and van Santen…

chemistry.chemical_classificationThermodynamicsSodium silicatePolymerAtmospheric temperature rangeCondensed Matter PhysicsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMolecular dynamicsMonomerchemistryMaterials ChemistryCeramics and CompositesGlass transitionPolymer meltMacromoleculeJournal of Non-Crystalline Solids
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Nonisothermal elongational behavior of blends with liquid crystalline polymers

1994

Measurements of melt strength and breaking stretching ratio of several blends of thermoplastic polymers with liquid crystalline polymers are presented. The melt strength behavior depends not only on the viscosity of the blends but also on the temperature dependence of the viscosity. In particular, even if the viscosities of the blends are, at the extrusion temperature, lower than that of the thermoplastic matrices, the melt strength can be larger than that of the pure thermoplastics if its viscosity-temperature curve exceeds that of the matrices far from the solidification temperature. This behavior allows one to spin or film blow these blends despite the low viscosity.

chemistry.chemical_classificationThermoplasticMaterials sciencePolymers and PlasticsLiquid crystallineGeneral ChemistryPolymerPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterViscositychemistryLiquid crystalMaterials ChemistryExtrusionComposite materialThermoplastic polymerPolymer Engineering and Science
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Shear flow characterization of blends containing liquid crystal polymers

1992

A simple phenomenological approach is proposed in order to predict the presence of minima in the viscosity-composition curves of blends of thermoplastic with liquid crystal polymer (LCP). When the viscosity of the liquid crystal polymer is larger than that of the thermoplastic matrix, a minimum is observed. A possible explanation of the presence of yield stress in the flow curves of these blends is also given.

chemistry.chemical_classificationThermoplasticMaterials sciencePolymers and PlasticsOrganic ChemistryFlow (psychology)PolymerCondensed Matter PhysicsCharacterization (materials science)Condensed Matter::Soft Condensed MatterPhysics::Fluid DynamicsViscositychemistryLiquid crystalMaterials ChemistryThermoplastic matrixComposite materialShear flowMakromolekulare Chemie. Macromolecular Symposia
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Time–carbonyl groups equivalence in photo-oxidative aging of virgin/recycled polymer blends

2004

AbstractThe photo-oxidation behaviour of polymers is strongly dependent on the initial amount of carbonyl groups along the chains. The growing use of recycled post-consumer polymers coming from products used outdoors and then photo-oxidised, both pure and blended with the same virgin polymer, gives rise to an unpredictable behaviour of weathering resistance of products made with these materials. The present work shows that the carbonyl group–exposure time curves can be shifted along the time axis to give a single generalised master plot. It is then possible to predict the formation of the new carbonyl groups by knowing only the initial amount of the same carbonyl groups. The same shift fact…

chemistry.chemical_classificationUnpredictable behaviourWork (thermodynamics)Materials sciencePolymers and PlasticsGeneral Chemical EngineeringPolymerShift factorchemistryPHOTO-OXIDATION RECYCLED POLYMERS TIME CARBONYL GROUPS EQUIVALENCE VIRGIN/RECYCLED POLYMER BLENDSMaterials ChemistryCeramics and CompositesPolymer blendComposite materialPlastics, Rubber and Composites
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1979

chemistry.chemical_classificationViscosityMaterials scienceTemperature dependence of liquid viscositychemistryRelative viscosityIntrinsic viscosityInherent viscosityThermodynamicsPolymerPressure dependenceDie Makromolekulare Chemie
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Pressure influences on the viscosity of polymer solutions

1982

Of all physico-chemical quantities characterizing the behavior of liquids, the viscosity coefficient η is normally most sensitive to pressure. Early measurements of η(p) date back almost 100 years [1] but they were carried out with very different objectives [2]. Currently, one is particularly interested in polymer solutions, for instance because of the additives to motor oils and of oil recovery. The present paper reports on measurements with polystyrenes of high molecular uniformity in eight different solvents. It confines itself to zero-shear viscosities and discusses the possibilities of discovering the influence of pressure via the molecular structure of the solvent and via its thermody…

chemistry.chemical_classificationViscosityMaterials sciencechemistryTemperature dependence of liquid viscosityRelative viscosityIntrinsic viscosityInherent viscosityThermodynamicsViscosity indexPolymerReduced viscosity
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Experimental organic matter maturation at 2kbar: Heat-up effect to low temperatures on vitrinite reflectance

2012

Abstract An experimental study was performed to evaluate the effect of heat-up to various low temperatures on vitrinite reflectance ( VR ) at 2 kbar employing the same previously used heat-up procedures, starting material and apparatus. Heat-up is the isobaric experimental procedure consisting of the increase in temperature of the laboratory vitrinite maturation from room temperature to the desired run temperature T end of heat-up at which the isobaric-isothermal maturation starts. Experiments employed cold-seal pressure vessels with classical heat-up devices and were carried out on wet (water added) xylite of swamp cypress. Confined system maturation experiments were conducted at 2 kbar an…

chemistry.chemical_classificationVitrinite reflectance020209 energyStratigraphyKinetic analysisThermodynamicsMineralogyGeology02 engineering and technologyRate equation010502 geochemistry & geophysicsKinetic energy01 natural sciencesIsothermal processFuel Technologychemistry0202 electrical engineering electronic engineering information engineeringIsobaric processEconomic GeologyOrganic matterVitrinite0105 earth and related environmental sciencesInternational Journal of Coal Geology
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Vapor–liquid equilibria in dendrimer and hyperbranched polymer solutions: experimental data and modeling using UNIFAC-FV

2004

Abstract This work evaluates the potential of the group contribution method universal functional activity coefficients-free-volume (UNIFAC-FV) to predict vapor–liquid equilibria (VLE) in dendrimer-solvent and hyperbranched polymer-solvent systems. The VLE of hydroxyl-functional dendritic polymers (polyethers, polyesters, polyamidoamine), dissolved in polar solvents (ethanol and/or water) are studied both experimentally and theoretically. A new approach is suggested to account for the contribution of selected types of polymer structural units (i.e. linear, dendritic and terminal units) to the solvent residual activity. The results of calculations are in a good agreement with experiment. Furt…

chemistry.chemical_classificationWork (thermodynamics)General Chemical EngineeringGeneral Physics and AstronomyExperimental dataThermodynamicsPolymerGroup contribution methodPolyesterSolventchemistryDendrimerOrganic chemistryPhysical and Theoretical ChemistryUNIFACFluid Phase Equilibria
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Frontispiece: Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers

2018

chemistry.chemical_classificationWork (thermodynamics)Hierarchy (mathematics)media_common.quotation_subjectOrganic ChemistryGeneral ChemistryHelicityAsymmetryCatalysisSupramolecular polymersSelf sortingchemistryChain (algebraic topology)Chemical physicsHelixmedia_commonChemistry - A European Journal
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LARGE DEFORMATION CREEP BEHAVIOR OF A SOLID POLYMER.

1981

Abstract The effect of loading rate and strain on the creep behavior after sample yielding has been studied in previous communications (14–15) for Mylar in tension and for Lexan in compression. In this work the creep behavior of Lexan samples previously elongated is considered both in tension and in compression. A procedure which collects all the data independently of both loading rate and initial creep strain is proposed.

chemistry.chemical_classificationWork (thermodynamics)Large deformationMaterials sciencePolymers and PlasticsTension (physics)General Chemical EngineeringDiffusion creepPolymerCompression (physics)Analytical ChemistrychemistryCreepLoading rateComposite material
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