Search results for "Density"

showing 10 items of 4402 documents

On the Improvement of the Processability of UHMW-HDPE by Adding a Liquid Crystalline Polymer and a Fluoroelastomer

2001

Ultra-high molecular weight polyethylene possesses many interesting properties but a very bad processability. This material is not usually processed in conventional devices but only by compression moulding and RAM extrusion. Low molecular weight polyethylene can be used to improve the processability. In this work small amounts of a fluoroelastomer and of a liquid crystalline polymer have been used as processing aids to improve the extrudability of this polymer. In fact, the die pressure decreases whereas the output flow rate slightly increases with increasing concentration of the processing aids. Solution viscosity data shows that reduction of the mechanical stress during extrusion decrease…

chemistry.chemical_classificationMaterials sciencebusiness.product_categoryPolymers and PlasticsGeneral Chemical EngineeringOrganic ChemistryPolymerPolyethylenechemistry.chemical_compoundViscositychemistryPolymer chemistryMaterials ChemistryDie (manufacturing)FluoroelastomerExtrusionPolymer blendHigh-density polyethyleneComposite materialbusinessMacromolecular Materials and Engineering
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Melt Strength and Extensibility of High-Density Polyethylene

1984

The extensional flow of polymer melts has been extensively studied because of its importance in many technological processing operations and, from a more fundamental point of view, because the tensile properties of the polymer melts cannot be correlated directly with shear viscosity behavior.1–5

chemistry.chemical_classificationMaterials sciencechemistryShear viscosityUltimate tensile strengthFlow (psychology)Molar mass distributionPoint (geometry)High-density polyethylenePolymerComposite materialExtensibility
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Crystallization kinetics of LDPE/Ny6 blends

1988

The crystallization behaviour of low density polyethylene/nylon 6 blends has been investigated as a function of the composition. The melting points of the polymers are almost uninfluenced by the presence of the other homopolymers except for blends with a nylon content of 75–90%. Blends with 10% nylon content do not exhibit the crystallization peak during the cooling step probably because of the low concentration and high viscosity of the low density polyethylene matrix. The crystallinity degree of the polyethylene is independent of the composition, while some variations are shown by the polyamide. Finally the rate of nucleation is strongly affected by the composition, in particular for the …

chemistry.chemical_classificationMaterials sciencetechnology industry and agricultureNucleationPolymerPolyethylenelaw.inventionLow-density polyethylenechemistry.chemical_compoundCrystallinityNylon 6chemistryChemical engineeringlawPolymer chemistryMelting pointCrystallizationJournal of thermal analysis
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Morphology and Rheology of HDPE/LCP Blends Compatibilized by a Novel PE-g-LCP Copolymer

1999

A novel graft copolymer (PE-g-LCP) consisting of polyethylene (PE) backbones and liquid crystalline polymer (LCP) branches was synthesized via reactive blending of an acrylic acid-functionalized PE (Escor 5000 by Exxon) with a semiflexible LCP (SBH 1 : 1 : 2 by Eniricerche S.p.A.). The crude reactive blending product (COP) was shown by investigation of the fractions soluble in boiling toluene and xylene and of the residue to contain unreacted Escor and SBH, together with the graft copolymer forming the interphase. The compatibilizing activity of COP for PE/SBH blends, compared to that of pure Escor, was investigated using two PE grades. The COP addition into 80/20 PE/SBH blends caused a muc…

chemistry.chemical_classificationMolar massMaterials sciencePolymers and PlasticsGeneral ChemistryCompatibilizationPolymerPolyethyleneSurfaces Coatings and Filmschemistry.chemical_compoundRheologychemistryChemical engineeringPolymer chemistryMaterials ChemistryCopolymerHigh-density polyethylenePolymer blend
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Viscometry of polyelectrolyte solutions: Star-like versus linear poly[[2-(methacryloyloxy)ethyl] trimethylammonium iodide] and specific salt effects

2017

Abstract The intrinsic viscosities, [η], of the 3-arm star polyelectrolyte in pure water are for a given molar mass considerably lower than for the linear product because of the higher monomer concentration and charge density in isolated coils. These effects are much more pronounced than in the case of uncharged macromolecules. Extra salt (NaCl, NaI, CaCl2) reduces the solution viscosities of the 3-arm star polymer less than of the linear product. The transition of [η] from the value in pure water to the minimum saturation value at high salt concentrations follows a Boltzmann sigmoid. In saline solvents the changes of the viscosities with rising polymer concentration depend strongly on the …

chemistry.chemical_classificationMolar massPolymers and PlasticsOrganic ChemistryIodideGeneral Physics and AstronomyThermodynamicsViscometerSalt (chemistry)Charge density02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPolyelectrolyte0104 chemical scienceschemistry.chemical_compoundMonomerchemistryMaterials ChemistryOrganic chemistry0210 nano-technologyEuropean Polymer Journal
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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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Thermo-Mechanical Degradation of LDPE-Based Nanocomposites

2007

Thermo-mechanical degradation of LDPE-based nanocomposites was studied by mainly investigating the rheological properties. For all of the investigated processing conditions, the viscosity of the nanocomposites was higher than that of the pure-LDPE matrix, but on increasing the severity of the mixing conditions, the difference between the viscosity of the nano-filled polymer and that of the pure LDPE decreased. The X-ray traces of the nanocomposites suggest that intercalation has been achieved during the melt, when less-severe processing conditions were used. At severe processing conditions (longer mixing time, high temperature and shear stress) the thermo-mechanical degradation was accelera…

chemistry.chemical_classificationNanocompositeMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringOrganic ChemistryPolymerchemistry.chemical_compoundLow-density polyethyleneViscosityMontmorillonitechemistryRheologyMaterials ChemistryShear stressOrganoclayComposite materialMacromolecular Materials and Engineering
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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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Understanding the origin of the asynchronicity in bond-formation in polar cycloaddition reactions. A DFT study of the 1,3-dipolar cycloaddition react…

2012

The origin of the asynchronicity in bond-formation in polar cycloadditions has been studied by an ELF analysis of the electron reorganisation along the 1,3-dipolar cycloaddition of Padwa's carbonyl ylide 4 with the 1,2-benzoquinone 8. This reaction presents an unexpected asynchronous bond-formation, which is initialised through the nucleophilic attack of Padwa's carbonyl ylide on the carbonyl oxygen atom of the strongly electrophilically activated 1,2-benzoquinone. The present study allows for the establishment that along an asynchronous bond-formation, the more favourable two-center interaction begins at the most electrophilic center, which is the center with the highest spin density achie…

chemistry.chemical_classificationNucleophileChemistryYlideGeneral Chemical EngineeringElectrophile13-Dipolar cycloadditionPolarGeneral ChemistrySpin densityBond formationPhotochemistryCycloadditionRSC Adv.
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