Search results for "PLASTICS"

showing 10 items of 2724 documents

N-Isopropylacrylamide andN-Isopropylmethacryl-amide: Cloud Points of Mixtures and Copolymers

2001

The cloud point curve of aqueous solutions of poly(N-isopropylacrylamide), poly(N-isopropylmethacrylamide) and their statistical copolymers were determined turbidimetrically. All the Systems demix upon heating at the cloud point temperature and mix reversibly upon cooling. The cloud points are independent of the total concentration of the solutions (dilute range) and of the sample thickness. Mixtures of the homopolymers poly(N-isopropylacrylamide) and poly(N-isopropylmethacrylamide) in water (ternary systems) exhibit two cloud points, which are nearly the same as the cloud points of the two binary systems homopolymer/water. A quantitative correlation was found between the cloud point temper…

Cloud pointMaterials scienceTernary numeral systemAqueous solutionPolymers and Plasticsbusiness.industryOrganic ChemistryCloud computingCondensed Matter PhysicsQuantitative correlationchemistry.chemical_compoundchemistryAmidePolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistrybusinessTernary operationMacromolecular Chemistry and Physics
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Phase diagrams of the system tetrahydrofuran/γ-butyrolactone/poly(ether imide) and determination of interaction parameters

1998

Abstract The thermodynamic interactions in the ternary mixture tetrahydrofuran/γ-butyrolactone/poly(ether imide) (THF/γ-BL/PEI) are investigated from 30 to 50°C. This is a membrane-forming system with a high He-selectivity. Cloud point measurements show that the two binary polymer solutions THF/PEI and γ-BL/PEI exhibit miscibility gaps which close towards the centre of the ternary phase diagram where the mixtures become homogeneous (cosolvency). Vapour pressures were determined for the subsystem THF/γ-BL. For the theoretical calculations the Gibbs energy of mixing is formulated according to the Flory-Huggins theory and the interaction parameter χ THF γ-BL calculated from the vapour pressure…

Cloud pointPolymers and PlasticsOrganic ChemistryEtherFlory–Huggins solution theoryMiscibilityGibbs free energychemistry.chemical_compoundsymbols.namesakechemistryMaterials ChemistrysymbolsPhysical chemistryOrganic chemistryTernary operationTetrahydrofuranPhase diagramPolymer
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Pressure Effects on the Thermodynamics oftrans-Decahydronaphthalene/Polystyrene Polymer Solutions: Application of the Sanchez-Lacombe Lattice Fluid T…

2003

The cloud-point temperatures (T-cl's) of trans-decahydronaphthalene(TD)/polystyrene (PS, (M) over bar (w) = 270 000) solutions were determined by light scattering measurements over a range of temperatures (1-16degreesC), pressures (100-900 bar), and compositions (4.2-21.6 vol.-% polymer). The system phase separates upon cooling and T-cl was found to increase with rising pressure for constant composition. In the absence of special effects, this finding indicates positive excess volume for the mixing. Special attention was paid to the demixing temperatures as a function of pressure for different polymer solutions and the plots in the T-phi plane (where phi signifies volume fractions). The clo…

Cloud pointSpinodalPolymers and PlasticsChemistryOrganic ChemistryThermodynamicsFlory–Huggins solution theoryCondensed Matter PhysicsEnthalpy of mixingCritical point (thermodynamics)Phase (matter)Materials ChemistryCompressibilityPhysical and Theoretical ChemistryPhase diagramMacromolecular Chemistry and Physics
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Shear influence on the phase separation of oligomer blends

1994

Shear influences on the phase separation behaviour of four different blends of ethylene glycol/propylene glycol oligomers, exhibiting upper critical solution temperatures, were investigated. Cloud point curves at rest (turbidity measurements) are reported for all systems, spinodal conditions (light scattering) and tie-lines (analysis of the coexisting phases) are given for some examples. Phase diagrams under shear were obtained from rheological data. They demonstrate that the demixing temperatures of systems where both glycols bear OH end-groups are lowered up to ca. 1°C by shear rates of 1000s−1; the critical composition, generalized to the non-equilibrium conditions of flow, is markedly s…

Cloud pointSpinodalPolymers and PlasticsOrganic Chemistrytechnology industry and agricultureThermodynamicsCondensed Matter PhysicsLight scatteringGibbs free energyCondensed Matter::Soft Condensed Mattersymbols.namesakechemistry.chemical_compoundchemistryShear (geology)Polymer chemistryMaterials ChemistrysymbolsOrganic chemistryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryShear flowEthylene glycolPhase diagramMacromolecular Chemistry and Physics
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Preparation, characterization and hydrolytic degradation of PLA/PCL co-mingled nanofibrous mats prepared via dual-jet electrospinning

2017

Abstract PLA/PCL co-mingled nanofibrous mats were prepared via multi-jet electrospinning. The concentration of PLA and PCL in the co-mingled mats were controlled by changing the flow rate of the two polymer solutions. The amount of PLA and PCL in the co-mingled nanofibrous mats was monitored by UV–Vis measurements through a colored dye added to PLA and by FTIR-ATR analysis. Morphology and mechanical properties of the nanofibrous mats were respectively examined by scanning electron microscopy (SEM) and tensile tests. Water contact angles measurements were also carried out in order to investigate the wettability of the materials. Finally, the hydrolytic degradation of the mats in buffer solut…

Co-mingled nanomatCo-electrospinningMaterials scienceHydrolytic degradationPolymers and PlasticsScanning electron microscopeGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciencesContact anglechemistry.chemical_compoundPhysics and Astronomy (all)Polymer degradationUltimate tensile strengthMaterials ChemistryComposite materialchemistry.chemical_classificationPolymers and PlasticpH dependent degradationOrganic ChemistryPolymerBuffer solutionPolymer degradation021001 nanoscience & nanotechnologyElectrospinning0104 chemical scienceschemistryChemical engineeringDual-jet electrospinningWetting0210 nano-technology
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Bimodal drop size distributions during the early stages of shear induced coalescence

2005

Drop sizes and drop size distributions were determined by means of an optical shear cell in combination with an optical microscope for the systems polyisobutylene/poly(dimethylsiloxane) (I) and poly(dimethyl-co-methylphenylsiloxane)/poly(dimethylsiloxane) (II) at low concentrations of the suspended phases and at different constant shear rates ranging from 10 to 0.5 s-1 . After pre-shearing the two-phase mixtures (I: 50 s-1; II: 100 s-1) for the purpose of producing small drop radii, the shear rate was abruptly reduced to the preselected value and coalescence was studied as a function of time. In all cases one approaches dead end drop radii, i.e. breakup is absent. The drop size distribution…

Coalescence (physics)Condensed Matter - Materials ScienceMaterials sciencePolymers and PlasticsDrop (liquid)Organic ChemistryMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesCondensed Matter - Soft Condensed MatterBreakupMolecular physicslaw.inventionPhysics::Fluid DynamicsShear rateOptical microscopeShear (geology)lawPolymer chemistryMaterials ChemistrySoft Condensed Matter (cond-mat.soft)Polymer blendShear flowPolymer
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Morphology of PEO/PDMS blends during shear: Coexistence of two droplet/matrix structures and additive effects

2005

Abstract The morphologies of blends of polyethyleneoxide (PEO 37) and poly(dimethylsiloxane)s (PDSM), with viscosity ratios, λ , of approximately one (PDMS 230) or 2.8 (PDMS 314, being the component of higher viscosity) and interfacial tensions on the order of 10 mN/m, were investigated at 70 °C as a function of shear rate (up to 10 s −1 ) and of time. For the system PEO 37/PDMS 230 we have also studied the influence of the compatibilizer dimethyl–ethyleneoxide–copolymer (PDMS- co -PEO), which is only reasonably soluble in PEO. To investigate the morphologies we have used an optical shear cell in combination with a light microscope. The most important observation consists in the formation o…

Coalescence (physics)Materials sciencePolymers and PlasticsOrganic ChemistryConcentration effectlaw.inventionShear rateShear (geology)Optical microscopeChemical engineeringlawPolymer chemistryMaterials ChemistryCopolymerPolymer blendShear flowPolymer
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Structuring of polymer blends in simple shear flow

1990

A simplified model for the formation of steady state structure of discrete domains in polymer blends is established for simple shear flow. It is assumed that the domain size distribution, which results from an equilibrium between breakup processes and coalescence processes, may be divided in small and stable spherical domains and large and unstable ellipsoidal domains. Based on simplified rate balances and an expression for domain deformation rate the volume fraction of large domains and the large and small semiaxes of the ellipsoids are expressed as functions of volume fraction and shear rate/shear stress. The ability of the model to simulate actual behaviour is tested against quantitative…

Coalescence (physics)Materials sciencePolymers and PlasticsOrganic ChemistryMechanicsCondensed Matter PhysicsBreakupEllipsoidShear rateSimple shearVolume fractionMaterials ChemistryShear stressPolymer blendMakromolekulare Chemie. Macromolecular Symposia
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On the Role of Drop Break Up for Coalescence Processes and Morphology Development in Polymer Blends under Shear

2005

Drop sizes and drop-size distributions were determined as a function of time at constant shear rates, γ, by means of an optical shear cell in combination with an optical light microscope after preshearing the samples at high γ. The systems under investigation were PIB 3/PDMS 152 (PIB:  polyisobutylene, PDMS:  poly(dimethylsiloxane), numbers:  average molar masses in kg/mol) and COP 26*/PDMS 48 (COP:  poly(dimethyl-co-methylphenylsiloxane), asterisk:  apparent molar mass); all measurements refer to 25 °C. Systems and conditions were chosen such that shear rates in the vicinity of the intersection of the coalescence and the break up curves become experimentally accessible. Under these conditi…

Coalescence (physics)Molar massPolymers and PlasticsBreak-UpChemistryDrop (liquid)Organic ChemistryThermodynamicslaw.inventionInorganic ChemistryShear (geology)Optical microscopelawPolymer chemistryMaterials ChemistryPolymer blendShear flowMacromolecules
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Effect of kind and content of organo-modified clay on properties of PET nanocomposites

2011

In this work we report the properties of nanocomposite based on PET with two different samples of organically modified montmorillonites. In particular, we studied the effect of the filler concentration on morphology, rheology, and mechanical performance, focusing our attention on the effect of the degradation phenomena of the clay modifiers. The results indicate that at low clay level the morphology achieved is mainly intercalated. On increasing the filler level, coalescence and/or bad defragmentation phenomena induce a coarser morphology, as confirmed by XRD, SEM, and TEM observations. When a more polar organic modifier is used to modify the clay, the particle adhesion and distribution is …

Coalescence (physics)NanocompositeMaterials scienceMorphology (linguistics)nanocompositePolymers and PlasticsIntrinsic viscosityorganic modifierModulusGeneral Chemistrycomplex mixturesSurfaces Coatings and FilmsCrystallinityPETRheologyMaterials ChemistryComposite materialElongationdegradationJournal of Applied Polymer Science
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