Search results for "THERMODYNAMICS"

showing 10 items of 2774 documents

Determination of χ from liquid-liquid phase data in ternary polymer systems (solvent/polymer/polymer) with hydrogen bonding

2008

Two different models accounting for the dependences of χ and g interaction parameters on both temperature and composition have been applied to different ternary polymer systems (TPS) solvent(1)/polymer(2)/polymer(3). The ana- lyzed TPS have consisted on ten different polymer mixtures in chloroform as common solvent that can specifically interact via hydrogen bond. Experimental ternary phase diagrams determined by liquid chromatography were taken from literature. The application of the two models to the experimental data have served to obtain χij and gij interaction parameters for all the binary ij (ij = 12, 13, 23) interactions established between the three components of the system, with si…

chemistry.chemical_classificationMaterials scienceChloroformPolymers and PlasticsHydrogen bondGeneral Chemical EngineeringOrganic ChemistryThermodynamicsPolymerSolventchemistry.chemical_compoundchemistryPhase (matter)Materials ChemistryLiquid liquidOrganic chemistryTernary phase diagramPhysical and Theoretical ChemistryTernary operationExpress Polymer Letters
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Shear influences on the solubility of LDPE in ethene

1998

Abstract The influence of shear on the demixing pressures of the binary system ethene/polyethene was determined viscometrically in the temperature range 147–195°C up to pressures of 1400 bar at polymer concentrations of 18.4, 22.5 and 27.4 wt%, respectively. Autoclaves were used to prepare the solutions and to measure cloud points for the stagnant system. A high-pressure viscometer was used to perform experiments at shear rates γ up to 1500 s −1 . Under all conditions investigated here the two-phase area grows as γ becomes larger and the demixing pressures increase up to 23 bar. This observation is in contrast to theoretical expectation according to which it should be the one-phase region w…

chemistry.chemical_classificationMaterials scienceChromatographyGeneral Chemical EngineeringViscometerThermodynamicsPolymerAtmospheric temperature rangeCondensed Matter PhysicsLow-density polyethylenechemistryShear (geology)Binary systemPhysical and Theoretical ChemistrySolubilityThe Journal of Supercritical Fluids
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Tracer diffusion in polymer and organic liquids close to the glass transition studied by forced rayleigh scattering

2007

Translational diffusion coefficients D of photochronic dye molecules have been measured by forced Rayleigh scattering in polymer diluent systems at compositions from pure polymer to pure diluent. D could be measured down to below the glass transition temperature T g. In the pure diluent, D(T g) was found typically about two decades below that in the pure polymer but still far above the Stokes-Einstein prediction extrapolated from high temperatures. Some experimental results are in contrast with predictions from free-volume theory.

chemistry.chemical_classificationMaterials scienceDiffusionPlasticizerThermodynamicsPolymerDiluentCondensed Matter::Soft Condensed MatterchemistryTRACEROrganic chemistryForced Rayleigh scatteringMoleculePhysics::Chemical PhysicsGlass transition
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Statistical properties of linear-hyperbranched graft copolymers prepared via "hypergrafting" of AB(m) monomers from linear B-functional core chains: …

2015

The reaction of ABm monomers (m = 2, 3) with a multifunctional Bf-type polymer chain ("hypergrafting") is studied by coarse-grained molecular dynamics simulations. The ABm monomers are hypergrafted using the slow monomer addition strategy. Fully dendronized, i.e., perfectly branched polymers are also simulated for comparison. The degree of branching of the molecules obtained with the "hypergrafting" process critically depends on the rate with which monomers attach to inner monomers compared to terminal monomers. This ratio is more favorable if the ABm monomers have lower reactivity, since the free monomers then have time to diffuse inside the chain. Configurational chain properties are also…

chemistry.chemical_classificationMaterials scienceHydrodynamic radiusGeneral Physics and AstronomyThermodynamicsPolymerBranching (polymer chemistry)Molecular dynamicschemistry.chemical_compoundMonomerchemistryPolymer chemistryCopolymerRadius of gyrationPolymer blendPhysical and Theoretical ChemistryThe Journal of chemical physics
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Effects of pressure and of thermal history on the structural phase transition of KCN

1992

The cubic-noncubic structural phase transition of a KCN single crystal is studied as a function of thermal history and of hydrostatic pressure up to 2 kbar. The standard sequence of phases is cubic-monoclinic-orthorhombic on cooling and orthorhombic-cubic on heating. The monoclinic phase is also absent in first cooling runs at low pressures (p≦250 bar). The width of the monoclinic field inp, T phase diagram is increased in second cooling runs. The effects are discussed in terms of a martensitic transformation behavior and random strain fields.

chemistry.chemical_classificationMaterials scienceHydrostatic pressureThermodynamicsCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials SciencePolymorphism (materials science)chemistryDiffusionless transformationX-ray crystallographyCondensed Matter::Strongly Correlated ElectronsGeneral Materials ScienceSingle crystalInorganic compoundMonoclinic crystal systemPhase diagramZeitschrift f�r Physik B Condensed Matter
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Crystallization Behaviour at High Cooling Rates of Two Polypropylenes

1993

Phase distribution of quenched samples of two isotactic polypropylenes, having different molecular weight distributions, was evaluated by a deconvolution procedure of WAXD spectra. The dependence on cooling rate of the two resins shows the low molecular weights rich polymer is characterized by a faster kinetics with an α-monoclinic to mesomorphic transition taking place at higher cooling rates.

chemistry.chemical_classificationMaterials scienceKineticsThermodynamicsCooling ratesPolymerSpectral linelaw.inventionchemistrylawPhase (matter)TacticityMolar mass distributionCrystallization
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Combined main chain/side chain polymers. A new class of liquid crystalline polymers with unusual structural, thermodynamic and dynamic properties

1990

Abstract Combined main chain/side chain polymers carry rigid rod-like mesogenic units both in the side chain and along the chain backbone. The properties of such combined systems are expected to be controlled by the competition of the interactions between the mesogenic units in the side and main chains as well as the tendency of the chain backbones to maximize their entropy. The thermodynamic, structural and dynamic properties of such combined main chain/side chain liquid-crystalline polymers were investigated for various chain architectures. The combined systems were found to display properties corresponding in many cases to a favourable superposition of properties characteristic of both m…

chemistry.chemical_classificationMaterials scienceLiquid crystallineMesogenThermodynamicsGeneral ChemistryPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterSuperposition principlechemistryLiquid crystalSide chainOrganic chemistryGeneral Materials ScienceEntropy (order and disorder)Liquid Crystals
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Elastic Properties of Liquid Crystal Elastomer Balloons

2001

We introduce a method to measure elastic properties of smectic liquid crystalline elastomers. Freely suspended smectic polymer films containing photoreactive groups are inflated to spherical bubbles and crosslinked by UV light irradiation. After crosslinking, the balloon volume is varied and elastic properties of the material are determined from the relation between radius and inner excess pressure. The influence of the network topology on the elastic behaviour is discussed.

chemistry.chemical_classificationMaterials scienceLiquid crystallinebusiness.industryLight irradiationLiquid crystal elastomerRadiusPolymerCondensed Matter PhysicsElastomerCondensed Matter::Soft Condensed MatterOpticsVolume (thermodynamics)chemistryComposite materialbusinessElastic modulusMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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Interfacial Tensions from Drop Retraction versus Pendant Drop Data and Polydispersity Effects

2004

Interfacial tensions sigma were measured by means of both methods for the following polymer pair: polyisobutylene (PIB 3) plus poly(dimethylsiloxane) (PDMS 152) and poly(dimethyl-co-methylphenylsiloxane) (CoP26*) plus PDMS 48. The numbers after the abbreviation state the molar masses in kilograms; the homopolymers exhibit polydispersities on the order of 2. The reliability of the method of drop retraction is backed up by systematic measurements, which demonstrate that it is possible to study the time evolution of sigma. Because of the free choice of the phases (drop or matrix) and the possibility to vary the overall composition of the system in a wide range, drop retraction yields more info…

chemistry.chemical_classificationMaterials scienceMolar massDrop (liquid)DispersityTime evolutionThermodynamicsSurfaces and InterfacesPolymerCondensed Matter PhysicsDrop methodSurface tensionchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceSpectroscopyLangmuir
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Penetrant diffusion in frozen polymer matrices: A finite-size scaling study of free volume percolation

1996

The diffusion of penetrant particles in frozen polymer matrices is investigated by means of Monte Carlo simulations of the bond fluctuation model. By applying finite-size scaling to data obtained from very large systems it is demonstrated that the diffusion process takes place on a percolating free volume cluster describable by a correlated site percolation model which falls into the same universality class as random percolation. The diverging correlation length entails a pronounced dependence of the diffusion constant on the size of the simulated system. It is shown that this dependence is appreciable for a wide range of parameters around the transition. \textcopyright{} 1996 The American …

chemistry.chemical_classificationMaterials sciencePenetrant (mechanical electrical or structural)Condensed matter physicschemistryDiffusion processMonte Carlo methodThermodynamicsPolymerRenormalization groupScalingBond fluctuation modelFick's laws of diffusionPhysical Review E
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