Search results for "blend"

showing 10 items of 421 documents

Tuning of biodegradation rate of PLLA scaffolds via blending with PLA

2009

Blends of Poly-L-Lactic Acid (PLLA) with Poly-Lactic Acid (PLA) in different proportions (95/5, 90/10, 80/20, 70/30 and 60/40) were utilized in order to realize biodegradable and biocompatible scaffolds for soft tissue engineering applications. The scaffolds were produced via thermally induced phase separation (TIPS) starting from ternary systems where dioxane was the solvent and water the non-solvent. Morphology was evaluated by Scanning Electron Microscopy (average pore size and interconnection). Foams’ apparent density was also evaluated (porosity ranges from 87% to 92%). Moreover an in vitro biodegradation test of scaffolds was set-up in order to verify the rate of degradation of the va…

chemistry.chemical_classificationMorphology (linguistics)Materials scienceScanning electron microscopePolymerBiodegradationSolventTissue engineeringchemistryDegradation (geology)lipids (amino acids peptides and proteins)General Materials ScienceTissue engineering Scaffold PLA PLLA Blends BiodegradationComposite materialPorosityInternational Journal of Material Forming
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The role of organoclay in promoting co-continuous morphology in high-density poly(ethylene)/poly(amide) 6 blends

2008

The effect of organically modified clay on the morphology, rheology and mechanical properties of high-density polyethylene (HDPE) and polyamide 6 (PA6) blends (HDPE/PA6 ¼ 75/25 parts) is studied. Virgin and filled blends were prepared by melt compounding the constituents using a twin-screw extruder. The influence of the organoclay on the morphology of the hybrid was deeply investigated by means of wide-angle X-ray diffractometry, transmission and scanning electron microscopies and quantitative extraction experiments. It has been found that the organoclay exclusively places inside the more hydrophilic polyamide phase during the melt compounding. The extrusion process promotes the formation o…

chemistry.chemical_classificationNanocomposite polymer blendNanocompositeMaterials sciencenanocompositePolymers and PlasticsPolymer nanocompositepolymer blends; nanocomposites; morphologyOrganic ChemistryCo-continuity Morphology Nanocomposite polymer blendPolymerpolymer blendchemistryCo-continuityPhase (matter)nanocompositesmorphologyPolyamideMaterials ChemistryOrganoclayHigh-density polyethylenePolymer blendComposite materialpolymer blendsPolymer
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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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Properties and morphology of PMMA/ABN blends obtained via MMA in situ polymerisation through γ-rays

2001

Abstract Methylmethacrylate polymerisation in the presence of 4 wt% butadiene-acrylonitrile rubber was carried out at fixed dose-rate and temperature. The effect of irradiation was investigated with respect to the mechanical and dynamic-mechanical properties in the solid state. A general increase of the “compatibilisation” on irradiation is obtained. In fact both rubber and polymethylmethacrylate glass transition temperatures, determined through dynamic-mechanical analysis, reveal the presence of strong interactions between the components. Furthermore an improvement of the mechanical tensile properties of the blends is observed when irradiation is continued after polymerisation, at least un…

chemistry.chemical_classificationNuclear and High Energy PhysicsMaterials scienceMorphology (linguistics)γ-rayPMMA/ABN blendPolymerMethacrylateSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNatural rubberChemical engineeringPolymerizationchemistryCompatibilisationvisual_artPolymer chemistryUltimate tensile strengthvisual_art.visual_art_mediumPolymerisationIrradiationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieGlass transitionInstrumentation
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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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Reactions Occurring during the Melt Mixing of Nylon 6 and Oxazoline−Cyclophosphazene Units

2009

Specific reactions of amino and carboxyl end groups of Nylon 6 with the reactive oxazoline groups belonging to a cyclophosphazene compound (referred as CP20XA) were carried out at 240 °C for different times, under inert atmosphere. Ny6 polymers terminated with one specific reactive chain end (-COOH or NH2) were reacted with different amounts of CP20XA to study the kinetic order of the reactions. All Ny6-CP20XA reacted products soluble in trifluoroethanol (TFE) were well characterized by MALDI-TOF MS, FT-IR and ( 1H and 13C) NMR techniques. The MALDI-TOF results show that the oxazoline rings react with the carboxyl chain ends of Ny6 following second-order kinetics. The reactions with amino c…

chemistry.chemical_classificationOxazolineReaction mechanismPolymers and PlasticsOrganic ChemistryKineticsSide reactionPolymerOxazolineReactive BlendingInorganic Chemistrychemistry.chemical_compoundEnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon6Nylon 6chemistrycyclophosphazenes polyamide end-functionalization MALDI-TOFMaterials ChemistryOrganic chemistryInert gasMALDIMacromolecules
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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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