Search results for " effect"

showing 10 items of 7524 documents

Branched Versus Linear Polyisoprene: Flory-Huggins Interaction Parameters for their Solutions in Cyclohexane

2009

Flory-Huggins interaction parameters were determined as a function of composition for solutions of linear and of branched polyisoprene in cyclohexane (CH) at 25, 45, and 65 °C by means of vapor pressure measurements (moderate to concentrated solutions) and by vapor pressure osmometry (dilute solutions). The results demonstrate that CH is a considerably worse solvent for branched polyisoprene than for the linear analog at all temperatures and at all compositions. This observation corroborates the expectation based on a recent phenomenological approach, which accounts explicitly for the incapability of the segments of an individual polymer molecule to spread out over the entire volume of the …

chemistry.chemical_classificationPolymers and PlasticsCyclohexaneVapor pressureVapor pressure osmometryOrganic ChemistryConcentration effectPolymerFlory–Huggins solution theoryCondensed Matter Physicschemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryMoleculeBinary systemPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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PEO/CHCl3. Crystallinity of the Polymer and Vapor Pressure of the Solvent. Equilibrium and Nonequilibrium Phenomena

2003

Vapor pressures were measured for the system CHCl3/PEO 1000 (PEO stands for poly(ethylene oxide) and 1000 for Mw in kg/mol) at 25 °C as a function of the weight fraction w of the polymer by means of a combination of headspace sampling and gas chromatography. The establishment of thermodynamic equilibria was assisted by employing thin polymer films. The degrees of crystallinity α of the pure PEO and of the solid polymer contained in the mixtures were determined via DSC. An analogous degree of polymer insolubility β was calculated from the vapor pressures measured in this composition range. The experiments demonstrate that both quantities and their concentration dependence are markedly affect…

chemistry.chemical_classificationPolymers and PlasticsEthylene oxideVapor pressureOrganic Chemistrytechnology industry and agricultureConcentration effectPolymerFlory–Huggins solution theoryAmorphous solidInorganic Chemistrychemistry.chemical_compoundCrystallinitychemistryChemical engineeringMaterials ChemistryOrganic chemistryBinary systemMacromolecules
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Polymerization of long chain alkyl glycidyl ethers: a platform for micellar gels with tailor-made melting points

2018

Controlled polymerization of long-chain alkyl glycidyl ethers (AlkGE) under anionic ring opening polymerization conditions is enabled by the addition of a crown ether (18-crown-6, K+). Homopolymers with molecular weights in the range of 4000 to 9000 g mol−1 and side chain melting temperatures of 14 °C (C12-AlkGE) and 43 °C (C16-AlkGE), respectively were synthesized. Furthermore, a series of amphiphilic ABA polyether triblock copolymers with polyethylene glycol (PEG) as the hydrophilic central block (Mn = 6k, 10k, and 20k g mol−1) with total molecular weights in the range of 7000 to 28 000 g mol−1 and narrow dispersity (1.12 to 1.34) were prepared. Separate melting endotherms of the triblock…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryDispersityBioengineering02 engineering and technologyPolyethylene glycol010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryRing-opening polymerization0104 chemical sciencesHydrophobic effectchemistry.chemical_compoundchemistryPolymerizationChemical engineeringCopolymerSide chain0210 nano-technologyAlkylPolymer Chemistry
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Composition-dependent Flory-Huggins parameters: molecular weight influences at high concentrations

1995

Flory-Huggins interaction parameters X were determined by means of equilibrium vapor pressures (measured via a combination of a head-space sampler with a gas chromatograph) and light scattering as a function of composition and temperature for the systems cyclohexanone/polystyrene [CHO/PS] and cyclohexanone/poly(butyl methacrylate) [CHO/PBMA]. The investigation of molecular weight influences on X with the system CHO/PBMA demonstrates that they persist almost up to the pure polymer. In order to rationalize this result, it is postulated (in accord with experimental findings and theoretical predictions) that the dimensions of polymer chains may vary upon the addition of solvent even in highly c…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryEnthalpyCyclohexanoneConcentration effectPolymerFlory–Huggins solution theoryCondensed Matter PhysicsLight scatteringSolventchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryPolystyrenePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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On the viscosity of moderately concentrated solutions of poly(ether imide) in a mixed solvent of marginal quality

2000

Abstract Viscosities η were measured for moderately concentrated (15.5 wt%) solutions of poly(ether imide) (PEI) as a function of the composition of the cosolvent tetrahydrofuran (THF) plus γ-butyrolactone (γ-BL). The solutions are almost by a factor of four less viscous when THF predominates than when γ-BL is the major component of the solvent mixture. Furthermore, the viscosity passes a minimum as the composition of the mixed solvent is varied. Both observations can be well understood in terms of the viscosities of the mixed solvents and the hydrodynamic interaction between the polymer molecules. The pronounced dissymmetry of η as a function of the composition of the mixed solvent η resul…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryEtherPolymerSolventchemistry.chemical_compoundViscositychemistryPolymer chemistryMaterials ChemistryPhysical chemistryMoleculeSolvent effectsImideTetrahydrofuranPolymer
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Poly(4-vinylbenzoyl azide): A New Isocyanato Group Generating Polymer

2007

4-Vinylbenzoyl azide was synthesized from p-vinylbenzoic acid and polymerized by free radical polymerization. The obtained polymer contained acyl azide groups which were thermally transformed to the corresponding isocyanato groups. Reactions on these polymers with ethanol, hydroxyethyl methacrylate and 1-pyrene-butanol proceeded quantitatively. Time-resolved FT-IR studies of the reactions with ethanol were carried out by varying the concentration and temperature. The effect of the solvent polarity on the Curtius rearrangement was investigated.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationPolymer(Hydroxyethyl)methacrylateAcyl azidechemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryAzideSolvent effectsCurtius rearrangementMacromolecular Rapid Communications
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Influence of morphology and chemical structure on the inverse response of polypropylene to gamma radiation under vacuum

1999

Abstract In this work the influence of the chemical structure and of the morphology on the gamma-radiation effects on polypropylene based polymers is studied on the basis of a previously discussed kinetic model [1] . For this aim an isotactic polypropylene and a random ethylene–propylene copolymer were irradiated under vacuum at one dose rate and several absorbed doses after well defined solidification conditions. We show that the model is reliable varying both the chemical structure and the morphology of the polypropylene based polymer. An inversion of the response of the material to gamma radiation under vacuum is always observed, and the inversion conditions depend on the irradiation par…

chemistry.chemical_classificationPolypropyleneMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerRadiationRadiation effectchemistry.chemical_compoundchemistryTacticityPhase (matter)Absorbed dosePolymer chemistryMaterials ChemistryIrradiationComposite material
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Solvent-Induced Length Variation of Cylindrical Brushes

2001

Communication: Polymacromonomers with a main chain much larger than the side-chain length adopt the form of cylindrical brush polymers the contour length per mainchain monomer of which depends on the side-chain length. In the present investigation it is demonstrated that the length per monomer also depends on the solvent quality, i.e., the cylinders are shorter in a poor solvent as compared to a good solvent. It is argued that the repulsion of the side chains represents the extension force, which acts against the entropic contraction force of the main chain. Thus, cylindrical brushes may be suitable as responsive materials for sensors, actuators or soft machines.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesHydrodynamic radiusPolymers and PlasticsPolymer scienceOrganic ChemistryBrushPolymerlaw.inventionCondensed Matter::Soft Condensed MatterSolventchemistry.chemical_compoundMonomerchemistrylawChemical physicsMaterials ChemistrySide chainRadius of gyrationSolvent effectsMacromolecular Rapid Communications
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Interactions between polymer brush-coated spherical nanoparticles: the good solvent case.

2011

The interaction between two spherical polymer brushes is studied by molecular dynamics simulation varying both the radius of the spherical particles and their distance, as well as the grafting density and the chain length of the end-grafted flexible polymer chains. A coarse-grained bead-spring model is used to describe the macromolecules, and purely repulsive monomer-monomer interactions are taken throughout, restricting the study to the good solvent limit. Both the potential of mean force between the particles as a function of their distance is computed, for various choices of the parameters mentioned above, and the structural characteristics are discussed (density profiles, average end-to…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceGeneral Physics and AstronomyNanoparticleInteraction energyPolymerPolymer brushCondensed Matter::Soft Condensed MatterMolecular dynamicschemistryComputational chemistryChemical physicsDensity functional theoryPhysical and Theoretical ChemistryPotential of mean forceSolvent effectsThe Journal of chemical physics
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Pressure-Induced Formation of Diblock Copolymer "Micelles" in Supercritical Fluids. A Combined Study by Small Angle Scattering Experiments and Mean-F…

2004

We developed a simple mean-field theory to describe polymer and AB diblock copolymer phase separation in supercritical (SC) fluids. The highly compressible SC fluid has been described by using a phenomenological hole theory, properly extended to consider the solvent/polymer/vacancy pseudoternary mixture. The model has been applied to describe the phase behavior of AB-diblock copolymers under the assumption of a strong solvent selectivity for just one copolymer chain. In our model the solvent selectivity is a strong function of the external pressure because in compressible fluids vacancies reduce the number of favorable solvent-polymer contacts. The combined effect of the pressure on the ave…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceSmall-angle X-ray scatteringGeneral Physics and AstronomyThermodynamicsPolymerSupercritical fluid extraction Carbon dioxide dispersion polymerizationSupercritical fluidCondensed Matter::Soft Condensed MatterMean field theorychemistryPhase (matter)CopolymerOrganic chemistryPolymer blendPhysical and Theoretical ChemistrySolvent effects
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