Search results for "Concentration effect"

showing 10 items of 80 documents

The role of organoclay and matrix type in photo-oxidation of polyolefin/clay nanocomposite films

2009

Abstract In this paper the photo-oxidation behaviour of polyolefin/clay nanocomposite films was studied; in particular, the effect of the amount of organo-modifier and the matrix polarity on the photo-oxidation was investigated. Two different organo-modified clays and compositions of LDPE/EVA blend films were used and the photo-oxidation was followed by mechanical and spectroscopic analyses. The organoclay and matrix type strongly influence the photo-oxidative behaviour of nanocomposite films. The films filled with CL15A show a faster loss of mechanical performance and higher carbonyl formation with respect to the films filled with the CL20A. Additionally, the LDPE based nanocomposite under…

Materials scienceNanocompositePolymers and PlasticsConcentration effectPolyethyleneCondensed Matter PhysicsPolyolefinLow-density polyethylenechemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiMontmorillonitePhoto-oxidation nanocomposites Polyethylene Poly(ethylene-co-vinyl acetate)chemistryMechanics of MaterialsMaterials ChemistryOrganoclayPolymer blendComposite materialPolymer Degradation and Stability
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Modelling the Influence of Nanoparticles in the Phase Behaviour of an Epoxy/Polystyrene Mixture, 2

2007

The influences of nanoparticle size and concentration on the thermodynamic behaviour of epoxy/polystyrene blends are evaluated in the framework of Ginzburg's simple analytical theory. Two approaches have been employed: NPEPO (for particles coated with epoxy groups) and NPFEN (for particles coated with phenyl groups). Using NPEPO, the particles are found to prefer the phase richer in epoxy, whereas the opposite occurs for NPFEN. The particles size significantly influences blend compatibility. When the particle radius Rp is about the same size as the radius of gyration R g of PS, the compatibility of blends increases with particle concentration, whereas for R p > R g , higher particle concent…

Materials sciencePolymers and PlasticsOrganic ChemistryConcentration effectNanoparticleEpoxyCondensed Matter PhysicsInorganic Chemistrychemistry.chemical_compoundchemistryChemical engineeringvisual_artPhase (matter)Polymer chemistryMaterials Chemistryvisual_art.visual_art_mediumRadius of gyrationParticleParticle sizePolystyreneMacromolecular Theory and Simulations
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Effect of the additive level and of the processing temperature on the re-building of post consumer pipes from polyethylene blends

2007

Abstract One of the main shortcomings of the mechanical recycling is that the properties of the secondary materials are generally sensibly inferior with respect to the virgin ones. This feature implies, for sure, that they cannot be used for the same technological application but also other uses of the secondary material are impossible. The aim of this work is to study the re-building of recycled post-consumer pipes, made of a blend of different polyethylenes, by re-processing in the presence of a nitroxyl compound as radical generator. The processing temperature and the additive concentration have been varied in order to study the effect of these parameters on the final properties. The mec…

Materials sciencePolymers and PlasticsOrganic ChemistryGeneral Physics and AstronomyConcentration effectIzod impact strength testPolyethylenechemistry.chemical_compoundCrystallinityRheologychemistryMaterials ChemistryExtrusionPolymer blendComposite materialElastic modulusPolypropylenes Extrusion density polyethylene
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Viscoelastic behavior of epoxy prepolymer/organophilic montmorillonite dispersions

2008

Dispersions of a bisphenol A-based epoxy resin with an organophilic montmorillonite (Nanofil 919) were studied by X-ray diffraction and oscillatory shear rheometry. X-ray studies reveal that the clay is intercalated by the epoxy and forms stable dispersions. The viscoelastic behavior of the nanodispersions was measured as a function of the Nanofil concentration and temperature. An increase in both G′ and G″ moduli was detected as the concentration increases. Furthermore, a transition from a liquid-like behavior, at low temperatures, to a solid-like behavior, at higher temperatures, was observed for all the samples. This transition is accounted for the formation of a percolated structure of …

Materials sciencePolymers and PlasticsPolymer nanocompositeRheometryConcentration effectEpoxyCondensed Matter PhysicsViscoelasticitychemistry.chemical_compoundMontmorillonitechemistryRheologyvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryComposite materialPrepolymerJournal of Polymer Science Part B: Polymer Physics
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Kinetic interpretation of influence of sodium chloride concentration and temperature on xanthan gum dispersion flow model

2001

The present study derives a fixed-concentration (0.4%) xanthan gum dispersion flow model for different molar concentrations of sodium chloride (0–0.25M) and different temperatures (20–70°C). The Ostwald–de Waele model is used in all cases. A temperature rise reduces the shear-thinning characteristics of the systems, although the power law index is much less sensitive to changes in temperature when NaCl is added, even in very small amounts. The lowest consistency values correspond to the dispersions formulated in the absence of salt, the highest values are observed for molar values of ≥0.15, and there are decreases in consistency upon raising the temperature in all cases. The viscous behavio…

Molar concentrationPolymers and PlasticsSodiumThermodynamicschemistry.chemical_elementConcentration effectGeneral ChemistrySurfaces Coatings and FilmsViscosityVolume (thermodynamics)chemistryMaterials ChemistrymedicineEyring equationDispersion (chemistry)Xanthan gummedicine.drugJournal of Applied Polymer Science
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Intrinsic Viscosity of Aqueous Solutions of Carboxymethyl Guar in the Presence and in the Absence of Salt

2008

Intrinsic viscosities were determined for solutions of CMG in pure water and 0.9 wt.-% aqueous NaCl. To avoid the 0/0-type extrapolation typical for Huggins plots, a new procedure was used. For CMG and pure water, this requires only two adjustable parameters: the specific hydrodynamic volume of the polymer in the limit of infinite dilution and a hydrodynamic interaction parameter. The intrinsic viscosity of CMG (no salt) at room temperature is 6 050 mL · g -1 ; approximately half as large as that of Na-PSS of comparable molar mass. The ratio of the intrinsic viscosities with and without salt is ≈7 for CMG, as compared to >100 for Na-PSS. The reasons for the different behaviors of the two ty…

Molar massGuar gumAqueous solutionPolymers and PlasticsChemistryIntrinsic viscosityOrganic ChemistryConcentration effectFlory–Huggins solution theoryCondensed Matter PhysicsPolyelectrolyteDilutionPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Injection moldability and properties of compatibilized PA6/LDPE blends

2004

An ethylene-acrylic acid copolymer (EAA), either alone or combined with a low molar mass bis-oxazoline compound (PBO), has been used as a compatibilization promoter for blends of polyamide-6 (PA6) with low-density polyethylene (LDPE). The effect of compatibilization on blend processability in injection molding operations and on the properties of the molded specimens has been studied. In the absence of compatibilization, the injection molded articles were shown to have low-quality surface appearance and poor mechanical properties. Both these characteristics were appreciably improved as a result of reactive compatibilization of the blends with EAA and, even more, with the EAA-PBO couple. In f…

Molar massMaterials sciencePolymers and Plasticstechnology industry and agricultureConcentration effectGeneral ChemistryCompatibilizationMolding (process)Polyethylenechemistry.chemical_compoundLow-density polyethylenechemistryMaterials ChemistryCopolymerPolymer blendComposite material
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Comparative Study of Different Maleic Anhydride Grafted Compatibilizer Precursors toward LDPE/PA6 Blends: Morphology and Mechanical Properties

2005

The study deals with the effectiveness of maleic anhydride grafted styrene-b-ethylene-co-propylene copolymer (SEPMA) as compatibilizer precursor (CP) for blends of low density polyethylene (LDPE) with polyamide-6 (PA). The CP was produced by grafting MA onto SEP in the melt. The specific interactions between the CP and the blends components have been investigated through characterizations of the binary LDPE/CP and PA/CP blends. The compatibilizing efficiency of the MA-grafted SEP, as revealed by the thermal properties and the morphology of the compatibilized blends, has been shown to be excellent. The morphology, as well as the mechanical properties of the compatibilized with SEPMA 75/25 w/…

Morphology (linguistics)Materials sciencePolymers and PlasticsOrganic ChemistryMaleic anhydrideConcentration effectGraftingmorphology and mechanical propertiesLDPE/PA6 blendchemistry.chemical_compoundLow-density polyethylenechemistryChemical engineeringMA-functionalized compatibilizer precursorMaterials ChemistryCopolymerPolymer blendHigh-density polyethyleneComposite material
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About entangled networks of worm-like micelles: a rejected hypothesis

1996

We report new results from small-angle neutron scattering on d(1 2)-cyclohexane/lecithin/water micellar solutions performed as a function of the water content (w(o)), temperature (T) and dispersed phase volume fraction (phi). The data from dilute samples are interpretable in terms of the existence of giant cylindrical reverse micelles and are well fit with a core-shell model (that provides the micelle structure and dimensions) with values of 28 and 45 Angstrom for the inner core and the outer shell radii, almost independent on temperature and concentration. Such a result could appear consistent with the current idea that worm-like micelles are living polymers. On the contrary, the appearanc…

ORGANOGELSPolymers and PlasticsSANSChemistryInner coreForm factor (quantum field theory)Concentration effectThermodynamicsMineralogyliving polymersNeutron scatteringgelsSmall-angle neutron scatteringMicelleLIGHT-SCATTERINGCondensed Matter::Soft Condensed MatterColloid and Surface ChemistryMICROEMULSIONSMicellar solutionsMaterials Chemistryreverse micellesPhysical and Theoretical ChemistryStructure factorLECITHIN REVERSE MICELLESColloid and Polymer Science
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Stabilisation of LDPE cross-linked in the presence of peroxidesII. FTIR study of chemical changes taking place in the LDPE–dicumyl peroxide–Irganox 1…

2000

Abstract The chemical changes taking place in the systems: LDPE–Irganox 1081, LDPE–dicumyl peroxide and LDPE–Irganox 1081–dicumyl peroxide, after homogenisation (in a rolling mill at 130°C) and after homogenisation and cross-linking (at 180°C and 5.0 MPa for 20 min) were investigated by FTIR. It was found that the OH groups in Irganox 1081 were in a bound form, and were most probably linked to the sulphur co-ordination centre. Further, the presence of dicumyl peroxide without Irganox 1081 in LDPE resulted in the formation of hydroperoxide groups at a temperature of 130°C, which were replaced by free hydroxy and carbonyl groups of a ketonic type after cross-linking. Simultaneous addition of …

Organic peroxidePolymers and PlasticsPotassium bromideConcentration effectPolyethyleneCondensed Matter PhysicsPeroxideLow-density polyethylenechemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMaterials ChemistryOrganic chemistryPartial oxidationFourier transform infrared spectroscopyPolymer Degradation and Stability
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