Search results for "POWDER"

showing 10 items of 437 documents

Synthesis and thermoelectric characterisation of bismuth nanoparticles

2009

An effective method of preparation of bismuth nanopowders by thermal decomposition of bismuth dodecyl-mercaptide Bi(SC12H25)3 and preliminary results on their thermoelectric properties are reported. The thermolysis process leads to Bi nanoparticles due to the efficient capping agent effect of the dodecyl-disulfide by-product, which strongly bonds the surface of the Bi clusters, preventing their aggregation and significantly reducing their growth rate. The structure and morphology of the thermolysis products were investigated by differential scanning calorimetry, thermogravimetry, X-ray diffractometry, 1H nuclear magnetic resonance spectroscopy, scanning electron microscopy, and energy dispe…

Materials scienceSettore AGR/13 - Chimica AgrariaNanopowderAnalytical chemistryEnergy-dispersive X-ray spectroscopyNanoparticlechemistry.chemical_elementBioengineeringSemimetal–semiconductor transitionBismuthDifferential scanning calorimetrySeebeck coefficientbismuthThermoelectric effectSettore CHIM/01 - Chimica AnaliticaGeneral Materials SciencenanotechnologyBismuth nanoparticleThermoelectric characteristicThermal decompositionSettore CHIM/05 - Scienza E Tecnologia Dei Materiali PolimericiGeneral ChemistryCondensed Matter Physicsthermoelectric propertiesAtomic and Molecular Physics and OpticsThermogravimetrychemistryModeling and SimulationMercaptide thermolysinanoparticlesJournal of Nanoparticle Research
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Structural evolution of CO2 filled pure silica LTA zeolite under high-pressure high-temperature conditions

2017

[EN] The crystal structure of CO2-filled pure-SiO2 LTA zeolite has been studied at high pressures and temperatures using synchrotron-based X-ray powder diffraction. Its structure consists of 13 CO2 guest molecules, 12 of them accommodated in the large alpha-cages and one in the beta-cages, giving a SiO2/CO2 stoichiometric ratio smaller than 2. The structure remains stable under pressure up to 20 GPa with a slight pressure-dependent rhombohedral distortion, indicating that pressure-induced amorphization is prevented by the insertion of guest species in this open framework. The ambient temperature lattice compressibility has been determined. In situ high-pressure resistive-heating experiments…

Materials scienceSiliconGeneral Chemical EngineeringAnalytical chemistrychemistry.chemical_elementFOS: Physical sciences02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesChemical reactionNegative thermal expansionPhysics - Chemical PhysicsMaterials ChemistryMoleculeZeoliteChemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceMaterials Science (cond-mat.mtrl-sci)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographychemistry0210 nano-technologyStoichiometryPowder diffraction
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MoSi2 Formation Mechanisms during a Spark Plasma Synthesis from Mechanically Activated Powder Mixture

2010

Materials scienceSpark (mathematics)MetallurgyPlasmaMechanism (sociology)Powder mixture
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Temperature control during Spark Plasma Sintering and application to up-scaling and complex shaping

2013

International audience; The determination and the homogeneity of the sample temperature during consolidation of powders by Spark Plasma Sintering (SPS) are addressed. Densifications were carried out in three different facilities differing by their constructors and their size. A structural transformation activated in a TiAl alloy was used as a marker of the sample temperature and finite element modeling were performed to evaluate the temperature at each point of the set-up. A good agreement between experimental and simulated data is exhibited. Alloys with identical microstructures were sintered and the homogeneity of the microstructure was better in the largest machines or when the sample wa…

Materials scienceUp scalingAlloySpark plasma sintering02 engineering and technologyengineering.materialIndustrial and Manufacturing Engineering0203 mechanical engineeringHomogeneity (physics)TIAL-BASED ALLOYSFIELDPOWDERTemperature controlConsolidation (soil)MetallurgyMetals and AlloysMECHANICAL-PROPERTIES021001 nanoscience & nanotechnologyMicrostructureFinite element methodComputer Science Applications020303 mechanical engineering & transportsModeling and SimulationCeramics and Compositesengineering0210 nano-technology
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Anomalous Valence Contrast of Metal Transition in Nanocrystalline Ferrite

2001

Materials scienceValence (chemistry)Condensed matter physicsAnomalous scatteringRietveld refinementMechanical EngineeringBeta ferriteCondensed Matter PhysicsNanocrystalline materialMetalCrystallographyMechanics of Materialsvisual_artvisual_art.visual_art_mediumGeneral Materials SciencePowder diffractionMaterials Science Forum
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Mixed-Valence Defect Ferrites : a New Family of Fine Powders and Thin Films of Spinel Ferrites

1997

When highly divided spinel ferrites become reactive enough with oxygen, to allow the oxidation of the Fe 2+ ions at low temperature and of substitute cations too, when these cations are capable of different valence states. We prepared fine particles of spinel ferrites substituted by Mn, Mo, Cu, by chimie douce, especially from oxalate precursors and used them to reveal and to study the oxido-reduction phenomena occurring in these finely divided materials. It was shown that the oxidation created a new family of spinel ferrites : the mixed-valence defect ferrites, having specific characteristics and properties. The ferrites of this type can be fine powders prepared at low temperature, or grou…

Materials scienceValence (chemistry)SpinelMetallurgyGeneral Physics and Astronomychemistry.chemical_element02 engineering and technologyengineering.material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxygenOxalate0104 chemical sciencesIonchemistry.chemical_compoundFine powderChemical engineeringchemistry[PHYS.HIST]Physics [physics]/Physics archivesChemical preparationengineeringThin film0210 nano-technology
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Physical chemistry of the powder metallurgy of beryllium: Chemical characterization of the powder in relation to its granularity

1996

Combining the systematic quantitative chemical analysis of the light impurities H, C, N, and O, the quantitative thermal desorption of molecular H2O and H2, and X ray diffractometry of various size fractions of a commercial Be powder (SP-65 grade from Brush-Wellman) allowed the precise de-termination of the mean composition and equivalent mean thickness of the surface impurity phases in the passivation-contamination layer on the surface of the particles. The overall surface stoichi-ometry is as follows: 0.2 BeOcrystallized, 0.8 [BeO - 0.59 H2O]amorphous, 0.14 H2Oads The result of the elemental analysis by X-ray photoelectron spectroscopy of the unetched surface of a powder pellet is compare…

Materials scienceX-ray photoelectron spectroscopyMechanics of MaterialsImpurityElemental analysisPowder metallurgyMetals and AlloysIntermetallicAnalytical chemistryMetal powderParticle sizeCondensed Matter PhysicsChemical compositionMetallurgical and Materials Transactions A
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Electron diffraction tomography and X-ray powder diffraction on photoredox catalyst PDI

2019

N,N-Bis(2,6-diisopropylphenyl)-perylene-3,4,9,10-bis(dicarboximide) (PDI-iPr) is starting to be widely used as a metal-free homogeneous photoredox catalyst. The crystal structure was determined by a combination of electron diffraction tomography and X-ray powder diffraction and further validated by DFT-D calculations. Surprisingly, the molecular geometry of PDI-iPr leads to voids in the packing.

Materials scienceX-ray02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesCatalysisCrystallographyMolecular geometryElectron diffractionHomogeneousGeneral Materials ScienceTomography0210 nano-technologyPowder diffractionCrystEngComm
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Co-precipitation synthesis of neodymium-doped yttrium aluminium oxides nanopowders: Quantitative phase investigation as a function of joint isotherma…

2007

Abstract Neodymium-doped yttrium aluminium nanopowders with nominal Nd:Y:Al ratio equal to X:3–X:5 (where X = 0, 0.006, 0.012, 0.024, 0.048, 0.081, 0.096, 0.171, 0.192, 0.384, 0.540 and 0.720) were prepared by the co-precipitation method and subjected to five cumulative stages of isothermal treatment in the temperature range from 900 to 1050 °C. The phase evolution of the oxides were investigated quantitatively by the X-ray powder diffraction approach using the Rietveld method of analysis. An almost single phase cubic garnet structure was attained at temperatures as low as 900 °C for specimens with neodymium loading less than ca. 6 at.% with respect to total (Nd + Y) atoms. Isothermal treat…

Materials scienceXRDAnalytical chemistrychemistry.chemical_elementNeodymiumIsothermal processInorganic ChemistryYttrium aluminium oxides powdersPhase (matter)Electrical and Electronic EngineeringPhysical and Theoretical ChemistrySpectroscopySettore CHIM/02 - Chimica FisicaPerovskite (structure)Aluminium oxidesYAG nanopowderOrganic ChemistryMetallurgyRietveld methodMetastable phaseAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialschemistryOrthorhombic crystal systemPowder diffractionMonoclinic crystal systemOptical Materials
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Microstructure-oxidation resistance relationship in Ti3AlC2 MAX phase

2020

International audience; Spark Plasma Sintering and Hot Isostatic Pressing were used to synthesize coarse-grained and fine-grained Ti3AlC2 specimens. Moreover, Spark Plasma Sintering processing parameters were modified in order to vary the TiC, Al2O3 and TixAly impurity and the porosity contents in the fine-grained samples. The influence of the Ti3AlC2 microstructure on the oxidation resistance was assesed. It is demonstrated that the grain size can drastically modify the oxidation resistance. The higher density of grain boundaries, in fine-grained specimens, increases the number of Al diffusion paths and leads to the formation of a protective alumina scale. In coarse-grained sample, Al diff…

Materials science[PHYS.MPHY]Physics [physics]/Mathematical Physics [math-ph]OxideSpark plasma sinteringSPS02 engineering and technology010402 general chemistry01 natural sciences[SPI.AUTO]Engineering Sciences [physics]/Automaticchemistry.chemical_compound[SPI]Engineering Sciences [physics][PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Powder metallurgyHot isostatic pressingPowder metallurgyOxidationMaterials Chemistry[PHYS.MECA.MEFL]Physics [physics]/Mechanics [physics]/Fluid mechanics [physics.class-ph][PHYS.MECA.BIOM]Physics [physics]/Mechanics [physics]/Biomechanics [physics.med-ph]Composite materialPorosityMicrostructureComputingMilieux_MISCELLANEOUS[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph][PHYS.MECA.VIBR]Physics [physics]/Mechanics [physics]/Vibrations [physics.class-ph][SPI.FLUID]Engineering Sciences [physics]/Reactive fluid environmentMechanical Engineering[SPI.NRJ]Engineering Sciences [physics]/Electric powerMetals and Alloys[CHIM.MATE]Chemical Sciences/Material chemistry[PHYS.MECA.MSMECA]Physics [physics]/Mechanics [physics]/Materials and structures in mechanics [physics.class-ph]021001 nanoscience & nanotechnologyMicrostructureGrain sizeGrain size[PHYS.MECA.ACOU]Physics [physics]/Mechanics [physics]/Acoustics [physics.class-ph]0104 chemical sciences[SPI.ELEC]Engineering Sciences [physics]/Electromagnetism[CHIM.POLY]Chemical Sciences/PolymerschemistryMechanics of Materials[PHYS.MECA.THER]Physics [physics]/Mechanics [physics]/Thermics [physics.class-ph]MAX phaseGrain boundary0210 nano-technology
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