Search results for "Fluid Dynamics"

showing 10 items of 1005 documents

Rheological behavior of a semirigid liquid crystal polymer

1993

The rheological behavior of liquid crystal polymers is still far from completely clarified from both experimental and theoretical points of view. In this paper, the shear flow and the non-isothermal elongation flow behavior of a semi-rigid liquid crystal copolyester is discussed. The viscosity strongly decreases when the test temperature is increased above the crystal-nematic transition temperature; below this temperature the viscosity is very high. The thermal history strongly affects the shear viscosity. The elongational flow behavior depends also on temperature. Above the crystal-nematic transition temperature and the mesophase is easily spinnable, whereas below this temperature, the spi…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsTransition temperatureMesophaseGeneral ChemistryPolymerCopolyesterPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterViscositychemistryRheologyLiquid crystalPolymer chemistryMaterials ChemistryComposite materialShear flow
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Microfluidic Pumping by Micromolar Salt Concentrations

2017

An ion-exchange-resin-based microfluidic pump is introduced that utilizes trace amounts of ions to generate fluid flows. We show experimentally that our pump operates in almost deionized water for periods exceeding 24h and induces fluid flows of um/s over hundreds of um. This flow displays a far-field, power-law decay which is characteristic of two-dimensional (2D) flow when the system is strongly confined and of three-dimensional (3D) flow when it is not. Using theory and numerical calculations we demonstrate that our observations are consistent with electroosmotic pumping driven by umol/L ion concentrations in the sample cell that serve as 'fuel' to the pump. Our study thus reveals that t…

chemistry.chemical_classificationMaterials scienceTrace AmountsMicrofluidicsFlow (psychology)Analytical chemistryFluid Dynamics (physics.flu-dyn)Salt (chemistry)FOS: Physical sciencesPhysics - Fluid Dynamics02 engineering and technologyGeneral ChemistryCondensed Matter - Soft Condensed Matter010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesIonchemistrySoft Condensed Matter (cond-mat.soft)Charge carrier0210 nano-technology
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Controlling the wetting properties of the Asakura-Oosawa model and applications to spherical confinement.

2012

We demonstrate for the Asakura-Oosawa model and an extension of this model that uses continuous rather than hard potentials, how wetting properties at walls can be easily controlled. By increasing the interaction range of the repulsive wall potential acting on the colloids (while keeping the polymer-wall interactions constant) polymers begin to substitute colloids at walls and the system can be driven from complete wetting of colloids via partial wetting to complete wetting of polymers. As an application, we discuss the morphology and wetting behavior of colloid-polymer mixtures in spherical confinement. We apply the recently developed 'ensemble switch method' where the Hamiltonian is exten…

chemistry.chemical_classificationMaterials sciencedigestive oral and skin physiologyNanotechnologyPolymerCondensed Matter PhysicsPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterContact anglesymbols.namesakeColloidGibbs isothermchemistryWetting transitionChemical physicssymbolsGeneral Materials ScienceWettingHamiltonian (quantum mechanics)Interaction rangeJournal of physics. Condensed matter : an Institute of Physics journal
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No-flow temperature and solidification in injection molding simulation

2011

The no‐flow temperature (NFT) is a parameter representing the rheological solidification temperature of a polymer. A polymer, during injection molding filling stage, can stop its flow because of its high viscosity, although it is not yet fully solidified by means of glass transition or crystallization. The NFT is used in most of injection molding simulation packages: with this simple parameter it is possible to reduce the errors deriving from viscosity extrapolation at relatively low temperatures. The viscosity measurements for polymers are usually carried out at high temperatures, and the viscosity models can fail in prediction at temperatures close to the glass transition or crystallizati…

chemistry.chemical_classificationMaterials scienceinjection molding simulationMolding (process)Polymerlaw.inventionAmorphous solidPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterViscosityTemperature dependence of liquid viscositychemistryRheologylawfilling stageCrystallizationComposite materialsolidificationGlass transition
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1988

Phase diagrams were calculated for flowing solutions of polystyrene in trans-decahydronaphthalene assuming that the energy (Es) stored in the sheared state has to be added to the Gibbs energy of mixing; Es is computed from viscometric data (flow curves). The resulting phase diagrams exhibit two maxima in most of the cases instead of only one for the stagnant solutions. A comparison with experimental data (Part 1) shows that the calculated demixing behaviour agrees well for moderate shear rates and concentrations of the polymer. Deviations in the semidilute region, particularly for higher values, are a consequence of the fact that so far no reliable theoretical relation has been given for th…

chemistry.chemical_classificationMineralogyThermodynamicsPolymerGibbs free energyPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Mattersymbols.namesakechemistry.chemical_compoundShear (geology)chemistryPolymer chemistryStored energysymbolsPolystyreneMaximaDissolutionPhase diagramDie Makromolekulare Chemie
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Structure and phase transitions of a liquid crystalline polymer

1981

The structures, textures as well as thermodynamic properties of a side chain polymer exhibiting a liquid crystalline phase in addition to a partially crystalline state and the isotropic fluid state were investigated. Furthermore the kinetics of phase transitions between these states were analyzed. It was found that the properties of this polymer are intermediate between that of low molecular weight liquid crystals and common polymers. In particular it was observed that the relation between the liquid crystalline texture and the structure is different from that of low molecular weight liquid crystals and that the properties of the crystalline and liquid crystalline state depend strongly on t…

chemistry.chemical_classificationPhase transitionMaterials sciencePolymers and PlasticsKineticsPolymereye diseasesPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterCondensed Matter::Materials ScienceCrystallographyColloid and Surface ChemistrychemistryChemical physicsLiquid crystalTacticityPhase (matter)Materials ChemistrySide chainsense organsTexture (crystalline)Physical and Theoretical ChemistryColloid and Polymer Science
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Phase Behaviour of Dye-Containing Liquid Crystalline Copolymers and their Mixtures with Low Molecular Weight Liquid Crystals

1985

Liquid crystalline side-chain polymers can be obtained by connecting the mesogenic groups and the polymer chain via a flexible spacer. The liquid crystalline polymers combine the well-known properties of low molecular weight liquid crystals with those of polymers.1

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceLiquid crystallineMesogenPolymereye diseasesPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterCondensed Matter::Materials SciencechemistryLiquid crystalPhase (matter)Polymer chemistryCopolymersense organs
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Frictional drag between polymer bearing surfaces

2002

Some fundamental features of friction between two polymer bearing surfaces in relative sliding motion are investigated by molecular dynamics simulations. End-tethered and adsorbed polymers are considered under good and poor solvent conditions. The shear stress is measured while varying the solvent's viscosity, surface separation, degree of polymerization and grafting density. For all systems we observe shear thinning that is attributed to the orientation of the chains along the shear direction. This effect is particularly strong for brushes, for which the shear stress during the steady sliding state is mainly determined by the degree of overlap between the brushes.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceShear thinningGeneral Physics and AstronomyPolymerDegree of polymerizationPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterMolecular dynamicsClassical mechanicsAdsorptionShear (geology)chemistryHardware and ArchitectureDragShear stressComposite materialComputer Physics Communications
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Phase Behavior of the System Linear Polyglycerol + Methanol + Carbon Dioxide

2011

To compare the phase behavior of linear and hyperbranched polymers, the phase envelopes of the ternary system linear polyglycerol + methanol + carbon dioxide were determined for polymers of varying molar mass. Phase changes were detected by a static synthetic method using the Cailletet setup for temperatures between 331 K and 421 K and pressures up to 13.1 MPa. Besides the vapor–liquid and liquid–liquid equilibria, also the vapor–liquid to vapor–liquid–liquid and vapor–liquid–liquid to liquid–liquid phase boundaries are reported. The experimental results are similar to systems with hyperbranched polymers (rather than linear polymers). For the systems with linear polymers, however, the bubbl…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesTernary numeral systemMolar massChemistryGeneral Chemical EngineeringBubbleGeneral ChemistryPolymerLower critical solution temperaturePhysics::Fluid DynamicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundChemical engineeringPhase (matter)Carbon dioxidePolymer chemistryMethanolJournal of Chemical & Engineering Data
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Scattering function and the dynamics of phase separation in polymer mixtures under shear flow

1988

The phenomenological mean-field theory describing concentration fluctuations and spinodal decomposition of binary mixtures of long flexible macromolecules is generalized to mixtures under steady shear flow. This shear flow leads to a partial orientation and stretching of the coils, as well as to an anisotropic deformation of concentration fluctuations. Generalizing the approach of Onuki and Kawasaki, we obtain the collective scattering function describing these concentration fluctuations in the mixture under shear flow. Both the steady-state situation in the one-phase region and the initial stages of spinodal decomposition for concentrations inside of the spinodal curve are considered.

chemistry.chemical_classificationScattering functionSpinodalPolymers and PlasticsSpinodal decompositionChemistryDynamics (mechanics)ThermodynamicsPolymerPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterColloid and Surface ChemistryMaterials ChemistryField theory (psychology)Physical and Theoretical ChemistryShear flowStructure factorColloid & Polymer Science
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