Search results for "Polymer blend"

showing 10 items of 219 documents

Thermomechanical degradation of polyethylene/polyamide 6 blend-clay nanocomposites

2014

Abstract Polymer nanocomposites are gaining a growing interest both in the academia and in the industrial field, because of some specific properties they can assure. However, the rise in the attention from the industry is also leading to concerns about their processing, which can involve issues which are not present in traditional polymers processing; furthermore, additional issues can arise when nanocomposites are based on a polymer blend rather than a single polymer. In this work, a systematic study on thermomechanical degradation and reprocessing behaviour of LDPE/PA6/Cloisite 15A systems has been performed. The characterization was based on rheological, mechanical and morphological anal…

chemistry.chemical_classificationNanocompositeMaterials sciencePolymers and PlasticsPolymer nanocompositePolymerPolyethyleneCondensed Matter PhysicsLow-density polyethylenechemistry.chemical_compoundchemistryRheologyMechanics of MaterialsPolyamideMaterials ChemistryPolymer blendComposite materialPolymer Degradation and Stability
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Selective localization of organoclay and effects on the morphology and mechanical properties of LDPE/PA11 blends with distributed and co-continuous m…

2010

A study was made on the effect of small amounts of organically modified clay on the morphology and mechanical properties of blends of low-density polyethylene and polyamide 11 at different compositions. The influence of the filler on the blend morphology was investigated using wide angle X-ray diffractometry, scanning and transmission electron microscopy and selective extraction experiments. The filler was found to locate predominantly in the more hydrophilic polyamide phase. Although such uneven distribution does not have a significant effect on the onset of phase co-continuity of the polymer components, it brings about a drastic refinement of the microstructure for the blends both with dr…

chemistry.chemical_classificationNanocompositeMaterials sciencePolymers and PlasticsPolymerCondensed Matter PhysicsMicrostructureLow-density polyethylenechemistryPhase (matter)PolyamideMaterials ChemistryOrganoclayPolymer blendPhysical and Theoretical ChemistryComposite materialJournal of Polymer Science Part B: Polymer Physics
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Compatibilization of a polyethylene/polyamide 6 blend nanocomposite

2014

Polymer blends of incompatible components need to be compatibilized to give rise to a blend with good properties. At the same way, polymer/clay nanocomposites show the same problem because of different chemical nature of the polymer matrix and of the clay. Compatibilization is then necessary if an incompatible polymer blend is filled with an organomodified clay. In this work a polyethylene/polyamide 6 blend filled with an organomodified clay has been compatibilized with a maleic anyhidride grafted SEBS (styrene-ethylene-butylene-styrene) copolymer and a glicidylmethacrylate-ethylene copolymer. The results show that compatibilization improves the mechanical properties in terms of elongation …

chemistry.chemical_classificationNanocompositeMaterials sciencenanocompositeCompatibilizationPolymerPolyethylenechemistry.chemical_compoundchemistryPolyamideCopolymerPolymer blendElongationComposite materialAIP Conference Proceedings
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Controlled solvent vapour annealing for polymer electronics

2009

Solvent vapour annealing (SVA) is demonstrated as an attractive method to anneal polymer blend and block copolymer thin films at low temperatures. It is especially suitable for organic electronics, where sensitive materials with strong intermolecular interactions are used. We demonstrate the effect of solvent vapour exposure on the film properties of a perylene bisimide acrylate (PPerAcr) side-chain polymer with strong crystallinity at the perylene bisimide moieties. We record the film thickness, light absorption and fluorescence as a function of the relative solvent vapour pressure. At a certain threshold of relative solvent vapour pressure, we observe a disruption of the π–π stacking, whi…

chemistry.chemical_classificationOrganic electronicsMaterials scienceAnnealing (metallurgy)General ChemistryPolymerCondensed Matter PhysicsSolventchemistry.chemical_compoundCrystallinitychemistryChemical engineeringPolymer chemistryPolymer blendThin filmPeryleneSoft Matter
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On the compatibilization of PET/HDPE blends through a new class of copolyesters

2000

Polyethyleneterephthalate (PET) and polyethylene are incompatible polymers and their blends show, in general, poor properties. Compatibilization is then a necessary step to obtain blends with good mechanical and barrier properties. In this work different compatibilizing agents were used, i.e. a maleic anhydride elastomer and some new products containing graft-copolymers having polyester segments grafted onto polyethylene backbone chains. Both the functionalized elastomer and the new products drastically improve the morphology and the ductility of the blend. In the case of the modified elastomer the compatibilizing action has been attributed to the formation of H-bonds whereas the copolymers…

chemistry.chemical_classificationPOLYETHYLENEMaterials sciencecompatibilizationPolymers and PlasticsOrganic ChemistryPET/HDPE blendsMaleic anhydridePolymerCompatibilizationPolyethyleneElastomercopolyestersLIQUID-CRYSTALLINE POLYMERPolyesterchemistry.chemical_compoundPET/HDPE blends; copolyesters; compatibilization; LIQUID-CRYSTALLINE POLYMER; POLYETHYLENEchemistryChemical engineeringMaterials ChemistryPolymer blendHigh-density polyethyleneComposite materialPolymer
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Shear induced mixing/demixing: blends of homopolymers, of homopolymers plus copolymers, and blends in solution

2000

Shear may shift the phase boundary towards the homogeneous state (shear induced mixing, SIM), or in the opposite direction (shear induced demixing, SID). SIM is the typical behavior of mixtures of components of low molar mass and polymer solutions, SID can be observed with solutions of high molar mass polymers and polymer blends at higher shear rates. The typical sequence with increasing shear rate is SIM, then occurrence of an isolated additional immiscible area (SLD), melting of this island into the main miscibility gap, and finally SIM again. A three phase line originates and ends in two critical end points. Raising pressure increases the shear effects. For copolymer containing systems S…

chemistry.chemical_classificationPhase boundaryMolar massMaterials sciencePolymers and PlasticsSpinodal decompositionOrganic ChemistryThermodynamicsPolymerCondensed Matter PhysicsShear ratechemistryShear (geology)Materials ChemistryCopolymerOrganic chemistryPolymer blendMacromolecular Symposia
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1995

Surfaces have a profound effect on the structure and related properties of multiphase polymeric materials, such as polymer mixtures and block copolymer mesophases. In particular, phase transitions in the bulk (unmixing, microphase separation, etc.) may be complemented by surface-induced transitions (formation of wetting layers, surface-directed spinodal decomposition, surface-induced ordering). This review gives a brief introduction to the phenomenological theories of such phenomena, emphasizing the simplest approach based on Flory—Huggins—de Gennes free energy functionals and associated Monte Carlo simulations. More sophisticated theories and recent experiments are mentioned briefly.

chemistry.chemical_classificationPhase transitionPolymers and PlasticsSpinodal decompositionGeneral Chemical EngineeringMonte Carlo methodMineralogyThermodynamicsPolymerCondensed Matter::Soft Condensed MatterchemistryMean field theoryPhenomenological modelWettingPolymer blendActa Polymerica
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Characterization and Processability of Blends of Polylactide Acid with a New Biodegradable Medium-Chain-Length Polyhydroxyalkanoate

2015

In this work the processability and the mechanical performance of polylactide acid (PLA) based blends with a sample of a new biodegradable medium-chain-length poly (hydroxyalkanoate) (PHA) were investigated. The two polymers are incompatible with scarce adhesion and with the dispersed PHA particles size increasing with the PHA content. Rheological tests in shear flow indicate that adding PHA improves the processability of the matrix by increasing the content of this second component in the blend, as observed also for the torque curves, due to the very low viscosity of this new sample of PHA. The processability is only slightly worsened in non-isothermal elongational flow as the melt strengt…

chemistry.chemical_classificationPolylactide acid (PLA)Environmental EngineeringMaterials sciencePolymers and Plasticstechnology industry and agriculturePlasticizerchemical and pharmacologic phenomenaPolymer blendPolymerPolyhydroxyalkanoatesSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryRheologyMaterials ChemistryPolyhydroxyalkanoate (PHA)Polymer blendLubricantElongationComposite materialMechanical propertieElastic modulusJournal of Polymers and the Environment
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Recent Developments in Monte Carlo Simulations of Lattice Models for Polymer Systems

2008

A brief review is given of methodological advances made during the past decade with the Monte Carlo sampling of equilibrium properties of simple lattice models of polymer systems, and representative applications of these new algorithms are summarized. These algorithms include Wang−Landau (WL) sampling, the pruned-enriched Rosenbluth method (PERM), and topology violating dynamic Monte Carlo algorithms such as combinations of local moves, slithering snake moves, and “double bridging” moves for the bond fluctuation model. The applications mentioned concern phase-transition-like phenomena of single chains (collapse and crystallization in bad solvents; interplay of collapse and adsorption; escap…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodBinary numberPolymerCondensed Matter::Soft Condensed MatterInorganic ChemistryIntramolecular forceLattice (order)Materials ChemistryDynamic Monte Carlo methodStatistical physicsPolymer blendBond fluctuation modelMacromolecules
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Interfaces between coexisting phases in polymer mixtures: What can we learn from Monte Carlo simulations?

1999

Symmetric binary polymer mixtures are studied by Monte Carlo simulation of the bond fluctuation model, considering both interfaces between coexisting bulk phases and interfaces confined in thin films. It is found that the critical behavior of interfacial tension and width is compatible with that of the Ising model, as expected from the universality principle. In the strong segregation limit, only qualitative but not quantitative agreement with the self-consistent field (SCF) theory is found. It is argued that the SCF theory requires √ 6 X √D for short-range forces, in agreement with experiment.

chemistry.chemical_classificationPolymers and PlasticsCondensed matter physicsOrganic ChemistryMonte Carlo methodBinary numberPolymerCondensed Matter PhysicsUniversality (dynamical systems)Condensed Matter::Soft Condensed MatterSurface tensionchemistryMaterials ChemistryIsing modelPolymer blendStatistical physicsThin filmMacromolecular Symposia
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