Search results for "polymer blend"

showing 10 items of 219 documents

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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Relation of Interdiffusion and Self-Diffusion in Polymer Mixtures

1986

From different assumptions one obtains linear relationships either between the interdiffusion coefficient and the self-diffusion coefficients or between the inverse interdiffusion coefficient and the inverse self-diffusion coefficients. The nature of these assumptions and possible experiments for discriminating between them are discussed.

Condensed Matter::Soft Condensed Matterchemistry.chemical_classificationCondensed Matter::Materials ScienceSelf-diffusionLiquid stateChemistryInverseThermodynamicsPhysical chemistryPolymerPolymer blendComputer Science::Other
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Making Floryr–Huggins Practical: Thermodynamics of Polymer-Containing Mixtures

2010

The theoretical part of this article demonstrates how the original Flory–Huggins theory can be extended to describe the thermodynamic behavior of polymer-containing mixtures quantitatively. This progress is achieved by accounting for two features of macromolecules that the original approach ignores: the effects of chain connectivity in the case of dilute solutions, and the ability of polymer coils to change their spatial extension in response to alterations in their molecular environment. In the general case, this approach leads to composition-dependent interaction parameters, which can for most binary systems be described by means of two physically meaningful parameters; systems involving …

Condensed Matter::Soft Condensed Matterchemistry.chemical_classificationQuantitative Biology::BiomoleculesChain (algebraic topology)ChemistryPhase (matter)Binary numberThermodynamicsPolymer blendPolymerFlory–Huggins solution theoryTernary operationPhase diagram
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Solubility of Polymers

2011

Detailed knowledge concerning the phase state (homogeneous or coexistence of two or more condensed phases) of polymer containing mixtures is indispensible in virtually any area related to the production or application of macromolecules. In addition to this qualitative information it is for many purposes highly desirable to dispose of quantitative data regarding solvent quality or, more generally, with respect to the thermodynamic interaction between the components of the mixtures. This contribution starts with a brief presentation of the thermodynamic criteria deciding on the phase state and presents the experimental methods used in this area. The next section gives an overview on typical b…

Condensed Matter::Soft Condensed Matterchemistry.chemical_classificationQuantitative Biology::BiomoleculesHildebrand solubility parameterMaterials sciencechemistryPhase stateHomogeneousThermodynamicsPolymerPolymer blendSolubilityExperimental methods
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Analysis of the crystallization behaviour of PBT-rich PBT/PET blends under processing conditions

2007

Among the high‐performance polyesters blends PBT/PET blends are expected to exhibit remarkable properties as far as the crystallization behaviour is concerned. The solidification behaviour of a 60/40 w/w PBT/PET blend was studied in a wide range of cooling conditions, according to a Continuous Cooling Transformation (CCT) procedure developed by the authors, aiming to emulate the typical conditions encountered in polymer processing. A set of several samples characterized by an homogeneous structure was prepared by solidification from the melt through spray cooling, and the resulting structure and properties were evaluated by density, Micro Hardness (MH), Wide Angle X‐ray Diffraction (WAXD) m…

Diffractionchemistry.chemical_classificationMaterials sciencePolymerContinuous cooling transformationIndentation hardnesslaw.inventionPolyesterNatural rubberchemistrylawvisual_artvisual_art.visual_art_mediumPolymer blendCrystallizationComposite material
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The role of crystalline, mobile amorphous and rigid amorphous fractions in the performance of recycled poly (ethylene terephthalate) (PET)

2012

[EN] The action of thermo-mechanical degradation induced by mechanical recycling of poly(ethylene terephthalate) was simulated by successive injection moulding cycles. Degradation reactions provoked chain scissions and a reduction in molar mass mainly driven by the reduction of diethyleneglycol to ethylene glycol units in the flexible domain of the PET backbone, and the formation of -OH terminated species with shorter chain length. The consequent microstructural changes were quantified taking into account a three-fraction model involving crystalline, mobile amorphous (MAF) and rigid amorphous fractions (RAF). A remarkable increase of RAF, to a detriment of MAF was observed, while the percen…

EthyleneSolucions polimèriquesPolymers and PlasticsInjection mouldingDifferential scanning calorimetry (DSC)Crystalline fractionsMechanical propertiesThermo-mechanical degradationchemistry.chemical_compoundDegradationAmorphous materialsPolymer blendsMaterials ChemistryMechanical recyclingRecyclingComposite materialDiethyleneglycolPoly(ethylene terephthalate) (PET)Injection moldingMolar massMechanical featureRecycled poly(ethylene terephthalate)Microstructural changesCondensed Matter PhysicsChain scissionRigid-amorphous fractionMechanics of MaterialsMAQUINAS Y MOTORES TERMICOSPolymer blendMaterials scienceMechanical performanceViscoelasticityEthyleneDifferential scanning calorimetrySegmental dynamicsInfrared analysis (FT-IR)Degradation reactionDifferential scanning calorimetryInjection mouldingPolyethylene terephthalatesEthylene glycolTermoplàsticsCrystalline materialsShorter chainsAmorphous solidchemistryGlass-rubber relaxationProcessing cyclesEthylene glycol
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Recycling of a starch-based biodegradable polymer

2002

A new starch-based polymeric system, ZI1OU from Novamont, mainly composed of starch and polycaprolactone, was reprocessed several times in an extruder to investigate the recyclability of this biodegradable polymer. A previous investigation of the thermomechanical degradation in a mixer has been also done. The degradation is mostly due to the thermal stress but the presence of the mechanical stress strongly increases the degradation kinetic. During melt processing two concurrent processes take place: the first is the degradation, i.e. the breaking and shortening of polymeric chains, mostly occurring in the PCL phase; the second is the formation of some crosslinked structure in the starch pha…

Extrusion mouldingMaterials sciencePolymers and PlasticsMaterBi biodegradable polymer recycling processingStarchOrganic ChemistryPlastics extrusionmacromolecular substancesCondensed Matter PhysicsBiodegradable polymerchemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryPolycaprolactoneMaterials ChemistryDegradation (geology)ExtrusionPolymer blendComposite materialMacromolecular Symposia
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Processing and mechanical properties of organic filer-polypropylene composites

2005

The addition of organic fillers into thermoplastic polymers is an interesting issue, which has had growing consideration and experimentation during the last years. It can give rise to several advantages. First, the cost of these fillers is usually very low. Also, the organic fillers are biodegradable (thus contributing to an improved environmental impact), and finally, some mechanical and thermomechanical properties can be enhanced. In this study, the effect of the addition of different organic fillers on the mechanical properties and processability of an extrusion-grade polypropylene were investigated. The organic fillers came from natural sources (wood, kenaf, and sago) and were compared …

Extrusion mouldingPolypropyleneMaterials sciencePolymers and PlasticsbiologyGlass fiberIzod impact strength testGeneral Chemistryengineering.materialbiology.organism_classificationKenafSurfaces Coatings and Filmschemistry.chemical_compoundchemistryFiller (materials)Materials ChemistryengineeringPolymer blendComposite materialNatural fiber
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Using organoclay to promote morphology refinement and co-continuity in high-density polyethylene/polyamide 6 blends – Effect of filler content and po…

2010

We investigate the gradual changes of the microstructure of two blends of high-density polyethylene (HOPE) and polyamide 6 (PA6) at opposite composition filled with increasing amounts of an organo-modified clay. The filler locates preferentially inside the polyamide phase, bringing about radical alterations in the micron-scale arrangement of the polymer phases. When the host polyamide represents the major constituent, a sudden reduction of the average sizes of the polyethylene droplets was observed upon addition of even low amounts of organoclay. A morphology refinement was also noticed at low filler contents when the particles distributes inside the minor phase. In this case, however, keep…

Filler (packaging)NanocompositeMaterials scienceNanocompositeImmiscible blendPolymers and PlasticsImmiscible blendsOrganic ChemistryPolyethylenechemistry.chemical_compoundNanocomposite; Immiscible blends; MicrostructurechemistryPhase (matter)PolyamideMaterials ChemistryOrganoclayHigh-density polyethylenePolymer blendComposite materialNanocomposite Immiscible blends MicrostructureMicrostructure
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Heat-Resistant Fully Bio-Based Nanocomposite Blends Based on Poly(lactic acid)

2013

Poly(lactic acid) (PLA) is melt mixed with polyamide 11 (PA11) to obtain a heat-resistant fully bio-based blend with PLA as the dominant component. The goal is achieved by adding small amounts of organoclay (OMMT), which is used to manipulate the blend microstructure. The selective positioning of the OMMT inside the PA11 and at the PLA/PA11 interface turns the blend morphology from drop/matrix into co-continuous at high PLA content (70 wt%). The OMMT-rich PA11 framework that interpenetrates the major PLA phase effectively contributes to bear stresses, and the nanocomposite blend keeps its structural integrity up to ≈160 °C, i.e., about 100 °C above the PLA glass transition.

Heat resistantNanocompositeMaterials sciencenanocompositePolymers and PlasticsBIOPOLYMERSGeneral Chemical EngineeringDrop (liquid)Organic Chemistrybiodegradable polymerMicrostructureNANOCOMPOSITESLactic acidchemistry.chemical_compoundPOLYMER BLENDSchemistryPolyamideMaterials ChemistryPLAOrganoclayComposite materialGlass transitionMacromolecular Materials and Engineering
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