Search results for "angle"

showing 10 items of 1921 documents

Preparation and determination of the structure of high-performance polymer blends by small-angle neutron scattering

1995

Amorphous blends from a deuterated polyaryletherketone and a polyetherimide have been prepared and investigated by neutron scattering. The used components differ remarkably in their structure antheir solution properties. The blends on the other hand are combinatorial mixtures : the scattering quantity Φ 1 Φ 2 /S(q) is independent of the composition of the blends if the polymer chains have the same length

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsScatteringOrganic ChemistryAnalytical chemistryPolymerNeutron scatteringFlory–Huggins solution theoryPolyetherimideSmall-angle neutron scatteringchemistry.chemical_compoundchemistryPolyaryletherketoneMaterials ChemistryRadius of gyrationComposite materialMacromolecular Rapid Communications
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Small angle X-ray scattering from amorphous polymers arising from heterogeneities

1973

The small angle X-ray scattering of glassy polymers (PET, PC, PVC, PMMA) and of polymer melts (PE) was studied. The dependence of the intensity scattered at small angles on the sample treatment suggests that neither the inherent structure of the pure polymer phase nor microholes are the origin of the scattering. In agreement with all experimental facts the scattering can be attributed to foreign particles such as for instance stabilizers in the polymer matrix. The consequence of this result is discussed with respect to the nodular structure of the amorphous phase and with respect to structural models of the amorphous phase. The nodular structure is not related to regions of different densit…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsScatteringSmall-angle X-ray scatteringPolymerAmorphous solidCondensed Matter::Soft Condensed MatterMatrix (mathematics)CrystallographyColloid and Surface ChemistrychemistryChemical physicsPhase (matter)Materials ChemistryPhysical and Theoretical ChemistryWide-angle X-ray scatteringIntensity (heat transfer)Kolloid-Zeitschrift und Zeitschrift für Polymere
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Processing and adjusting the hydrophilicity of poly(oxymethylene) (co)polymers: nanoparticle preparation and film formation

2016

Handling the insoluble POM: the preparation of nanoparticles based on hyperbranched-linear-hyperbranched ABA triblock copolymers with variable hydrophilicity and composed of short hyperbranched polyglycerol (hbPG) as the A-blocks and linear poly(oxymethylene) (POM) as a B-block is described. The POM-hbPG-nanoparticles with diameters in the range of 190 to 250 nm were generated in a convenient process, combining the solvent evaporation process with the miniemulsion technique, a water borne handling for POM-copolymers. Furthermore, the film formation properties of the nanoparticles were investigated by deposition on silicon and subsequent sintering, which leads to films with a thickness in th…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSiliconOrganic ChemistryNanoparticleSinteringchemistry.chemical_elementBioengineering02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesContact angleMiniemulsionchemistryChemical engineeringPolymer chemistryCopolymerDeposition (phase transition)0210 nano-technology
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1995

Redoxactive liquid crystalline (LC) side group polymers were prepared by copolymerization of liquid crystalline acrylates and ferrocene-containing acrylates. The corresponding liquid crystalline ionomers were synthesized by a reversible redox reaction. The incorporation of tetra-alkylated ferrocene derivatives leads to LC polymers with reduced redox potential. These polymers can be oxidized under mild conditions to the corresponding ionomers, which are much more stable in solution than LC ionomers containing monoalkylated ferrocenium ions. Dynamic mechanical measurements and small angle X-ray scattering (SAXS) perfomed on LC ionomers prove the existence of ionic superstructures (clusters) w…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSmall-angle X-ray scatteringGeneral Chemical EngineeringIonic bondingPolymerchemistry.chemical_compoundchemistryLiquid crystalPhase (matter)Polymer chemistryPolymer blendPendant groupIonomerActa Polymerica
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Morphology, rheology, and mechanical properties of a new nanobiocomposite

2015

Nanobiocomposites are a new class of biodegradable polymer materials with an ultrafine phase dispersion of the order of a few nanometers in a biodegradable polymer matrix that shows very interesting properties often very different from those of conventional filled polymers. In this work the morphology and the rheological and mechanical properties of a new nanobiocomposite made of a biodegradable copolyester based blend with an organomodified montmorillonite have been investigated to evaluate its possible use in several applications. SAXS diffractograms and TEM micrographs show that the in both the adopted processing conditions an hybrid intercalated/exfoliated morphology is observed. Rheolo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSmall-angle X-ray scatteringGeneral ChemistryPolymerBiomaterialBiodegradable polymerCopolyesterSurfaces Coatings and Filmschemistry.chemical_compoundMontmorillonitechemistryRheologyPhase (matter)Properties and characterizationMaterials ChemistryNanostructured polymerComposite materialRheologyElastic modulusJournal of Applied Polymer Science
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Dynamics of supramolecular associative polymer networks at the interplay of chain entanglement, transient chain association, and chain‐sticker cluste…

2019

The dynamic mechanical properties of supramolecular associative polymer networks depend on the average number of entanglements along the network‐forming chains, Nₑ, and on their content of associative groups, f. In addition, there may be further influence by aggregation of the associative groups into clusters, which, in turn, is influenced by the chemical structure of these groups, and again by Nₑ and f of the polymer. Therefore, the effects of these parameters are interdependent. To conceptually understand this interdependency, we study model networks in which (a) Nₑ, (b) f, and (c) the chemical structure of the associative groups are varied systematically. Each network is probed by rheolo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSupramolecular chemistry02 engineering and technologyQuantum entanglementPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesTurn (biochemistry)Chain (algebraic topology)chemistryChemical physicsMaterials ChemistryCluster (physics)Physical and Theoretical Chemistry0210 nano-technologyCluster analysisAssociative propertyJournal of Polymer Science Part B: Polymer Physics
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Superhydrophobic TiO2/Fluorinated Polysiloxane Hybrid Coatings with Controlled Morphology for Solar Photocatalysis

2021

Abstract Technological applications of polysiloxane coatings have been influenced by their intrinsic low surface energy, which increases their water repellence. Accurate control of composition and interfacial properties through the introduction of perfluorinated moieties further lowers the polysiloxane surface energy, while mixing with metal oxide nanoparticles enhances roughness, resulting in a great potential in the development of superhydrophobic materials for photocatalysis. Herein, a series of hydrophobic and superhydrophobic hybrid coatings were prepared by dehydrocoupling and hydrosilylation reactions of polymethylhydrosiloxane with 1H,1H,2H,2H‐perfluorooctyltriethoxysilane and 1,3-d…

chemistry.chemical_classificationMaterials sciencePolymethylhydrosiloxaneHydrosilylationtitanium dioxidePMHSPolymerSurface energyContact anglechemistry.chemical_compoundColloid and Surface Chemistryhybrid coatingschemistryChemical engineeringPhotocatalysisfluorinated polysiloxanesWettingFourier transform infrared spectroscopyphotocatalysissuperhydrophobicitySettore CHIM/02 - Chimica Fisica
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Switching of Polymer Brushes

1999

Polymer coatings of brushlike monolayers composed of two different polymers, polystyrene and poly(2-vinylpyridine), are grafted by radical polymerization on the surface of silicon wafers. Thickness, grafting density, molecular weight of grafted chains, and the composition of the coatings were regulated by grafting time, monomer concentration, and additional initiator in solution. A typical dry film thickness is between 10 and 100 nm, and the molecular weights of the components range from 100 to 300 kg/mol. The fabricated coatings turn out to be sensitive to the composition of the environment. For instance after exposition to toluene the layer becomes hydrophobic and the top of the layer is …

chemistry.chemical_classificationMaterials scienceRadical polymerizationSurfaces and InterfacesPolymerCondensed Matter PhysicsContact anglechemistry.chemical_compoundMonomerChemical engineeringchemistryX-ray photoelectron spectroscopyMonolayerElectrochemistryGeneral Materials SciencePolystyreneLayer (electronics)SpectroscopyLangmuir
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2019

Abstract The preparation method of a polymer composite and the filler loading are amongst the factors that influence the properties of the final composites. This article studies the effect of these factors on the thermal stability and thermal degradation kinetics of poly(methyl methacrylate) (PMMA)/mesoporous silica (MCM-41) composites filled with small amounts of MCM-41. The PMMA/MCM-41 composites were prepared through in situ polymerisation and melt mixing methods, with MCM-41 loadings of 0.1, 0.3, and 0.5 wt.%. The presence of MCM-41 increased the thermal stability of PMMA/MCM-41 composites prepared by melt mixing, but in the case of the in situ polymerised samples, the MCM-41 accelerate…

chemistry.chemical_classificationMaterials scienceRenewable Energy Sustainability and the EnvironmentSmall-angle X-ray scattering02 engineering and technologyPolymerActivation energyMesoporous silica010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPoly(methyl methacrylate)0104 chemical sciencesBiomaterialschemistry.chemical_compoundPolymerizationchemistryvisual_artCeramics and Compositesvisual_art.visual_art_mediumThermal stabilityMethyl methacrylateComposite material0210 nano-technologyWaste Management and DisposalEmergent Materials
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The structure of high-performance polymer blends by small-angle neutron scattering

1997

Abstract Amorphous blends from a deuterated polyaryletherketone and a polyetherimide have been prepared and investigated by small-angle neutron scattering (SANS). The blends are combinatorial mixtures: the scattering quantity Φ1Φ2/S(q) is independant of the composition of the blends.

chemistry.chemical_classificationMaterials scienceScatteringPolymerNeutron scatteringCondensed Matter PhysicsPolyetherimideSmall-angle neutron scatteringElectronic Optical and Magnetic MaterialsAmorphous solidchemistry.chemical_compoundchemistryDeuteriumPolyaryletherketoneElectrical and Electronic EngineeringComposite materialPhysica B: Condensed Matter
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