Search results for " Polyethylene"

showing 10 items of 229 documents

Interactions between aroma and edible films. 1. Permeability Of methylcellulose and low-density polyethylene films to methyl ketones.

1998

This work contributes to the study of aroma transfers through edible and plastic packaging films. Permeability, sorption, and diffusivity of three methyl ketones (2-heptanone, 2-octanone, and 2-nonanone) in and through low-density polyethylene and methylcellulose-based edible films have been determined. Permeability was measured using a dynamic method coupled with a gas chromatograph. The methyl ketone permeability of polyethylene films mainly depends on diffusivity of the penetrant in the polymer. In the case of 2-heptanone, a saturation of the polymer network is observed at high vapor concentrations. The formation of clusters could take place when concentrations are higher in the vapor ph…

chemistry.chemical_classificationMaterials sciencebiologyPlasticizerfood and beveragesSorptionGeneral ChemistryPolymerPolyethyleneKetonesMethylcelluloseThermal diffusivitybiology.organism_classificationPermeabilitychemistry.chemical_compoundLow-density polyethylenechemistryChemical engineeringPermeability (electromagnetism)Organic chemistryPolyethylenesGeneral Agricultural and Biological SciencesAromaJournal of agricultural and food chemistry
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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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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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Stabilisation of LDPE cross-linked in the presence of peroxides III. Mass spectrometric study of chemical changes taking place in the n-octadecane–di…

2000

Abstract An attempt was made to identify the products of the reaction between dicumyl peroxide and Irganox 1081, carried out in n -octadecane (saturated hydrocarbon), in conditions of fast decomposition of the peroxide (180°C, 5 min). Mass spectrometry (MS) was employed to find m/z values of molecular and fragment ions in analyses of the components ( n -octadecane, dicumyl peroxide, Irganox 1081) and of the following systems: n -octadecane–dicumyl peroxide, n -octadecane–Irganox 1081 and n -octadecane–dicumyl peroxide–Irganox 1081, after holding them at a temperature of 180°C for 5 min. The tendency of sulphur in Irganox 1081 to oxidise, specifically in the presence of dicumyl peroxide, was…

chemistry.chemical_classificationOrganic peroxidePolymers and PlasticsChemistryConcentration effectCondensed Matter PhysicsMass spectrometryDecompositionPeroxidechemistry.chemical_compoundLow-density polyethyleneHydrocarbonOctadecaneMechanics of MaterialsPolymer chemistryMaterials ChemistryPolymer Degradation and Stability
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