Search results for "Composites"

showing 10 items of 1905 documents

Energetics of conformational conversion between 1,1,2-trichloroethane polymorphs

2008

Pressure-induced transformations between gauche-, gauche+ and transoid conformations have been evidenced by X-ray single-crystal diffraction for 1,1,2-trichloroethane, and the energies of intermolecular interactions, conformational conversion, and the latent heat have been determined.

Diffraction112-TrichloroethaneEnergeticsIntermolecular forceMolecular ConformationMetals and AlloysGeneral ChemistryCrystallography X-RayCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryComputational chemistryLatent heatMaterials ChemistryCeramics and CompositesTrichloroethanesChemical Communications
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High-pressure powder x-ray diffraction study of EuVO4

2015

The high-pressure structural behavior of europium orthovanadate has been studied using in-situ, synchrotron based, high-pressure x-ray powder diffraction technique. Angle-dispersive x-ray diffraction measurements were carried out at room temperature up to 34.7 GPa using a diamond-anvil cell, extending the pressure range reported in previous experiments. We confirmed the occurrence of zircon-scheelite phase transition at 6.8 GPa and the coexistence of low- and high-pressure phases up to 10.1 GPa. In addition, clear evidence of a scheelite-fregusonite transition is found at 23.4 GPa. The fergusonite structure remains stable up to 34.7 GPa, the highest pressure reached in the present measureme…

DiffractionChemical Physics (physics.chem-ph)Phase transitionCondensed Matter - Materials ScienceChemistrychemistry.chemical_elementMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesCrystal structureCondensed Matter PhysicsFergusoniteSynchrotronElectronic Optical and Magnetic Materialslaw.inventionInorganic ChemistryCrystallographylawPhysics - Chemical PhysicsX-ray crystallographyMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryEuropiumPowder diffraction
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In situ and time resolved study of the - transition in nanometric particles

2007

In situ and real-time study of the {gamma} to {alpha}-Fe{sub 2}O{sub 3} transition is carried out on the H10 beamline at LURE (France). {gamma}-Fe{sub 2}O{sub 3} particles are synthesized by soft chemistry. These particles have an average diameter evaluated by X-ray diffraction of 9{+-}1nm and a specific surface area of 116m{sup 2}g{sup -1}. The size of produced {alpha}-Fe{sub 2}O{sub 3} particles is determined by in situ and time resolved X-ray diffraction measurements at different temperatures. An amazing evolution of size with time is revealed: an abrupt doubling of the {alpha}-Fe{sub 2}O{sub 3} particle size is observed whatever the heating temperature. Some assumptions are given in ord…

DiffractionCoalescence (physics)Phase transitionChemistryMaghemiteengineering.materialCondensed Matter PhysicsSurface energySoft chemistryElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystallographyX-ray crystallographyMaterials ChemistryCeramics and CompositesengineeringParticle sizePhysical and Theoretical ChemistryJournal of Solid State Chemistry
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Thermal evolution and structural study of 2:1 mullite from monophasic gels

2006

Abstract Single phase mullite gels with composition 2Al 2 O 3 ·SiO 2 (2:1) were prepared by the slow hydrolysis method using aluminium nitrate nonahydrate and tetraethylorthosilicate as reagents. The evolution to mullite from gels was studied by infrared (IR) spectroscopy and X-ray diffraction (XRD). Gels thermally treated under fast schedules showed mullite formation below 900 °C. Compositional and microstructural changes in 2:1 mullites through the range of temperature from 900 to 1600 °C were determined by the measurement of lattice parameters and field emission scanning electron microscopy. The alumina-rich mullites formed at low temperatures become almost the nominal 2:1 at 1600 °C. Th…

DiffractionMaterials scienceInfraredMulliteAluminium nitrateGrain sizeCrystallographyHydrolysischemistry.chemical_compoundChemical engineeringchemistryReagentMaterials ChemistryCeramics and CompositesSpectroscopyJournal of the European Ceramic Society
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X-ray diffraction microstructure analysis of mullite, quartz and corundum in porcelain insulators

2005

Abstract The X-ray diffraction microstructure analysis has been performed on commercial samples of the silica and alumina porcelain insulators obtained at 1300 °C, with the same time of firing. The study was carried out on mullite, corundum and quartz by applying several integral breadth methods (i.e. the Williamson–Hall analysis, the Langford method and the Halder–Wagner approximation) and the Fourier analysis (Warren–Averbach method). The apparent crystallite sizes determined for the mullite are direction-dependent (anisotropic) and within each group of samples, on average, the greatest values are obtained along the direction [0 0 1]. With regard to the microstructure of the corundum and …

DiffractionMaterials scienceMineralogyCorundumMulliteengineering.materialMicrostructureFlexural strengthX-ray crystallographyMaterials ChemistryCeramics and CompositesengineeringCrystalliteComposite materialQuartzJournal of the European Ceramic Society
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Which tool to distinguish transient alumina from alpha alumina in thermally grown alumina scales?

2005

International audience; Alumina scales constitute excellent protective barriers when they form on alumina-forming steels. If they keep tightly adherent to the underlying substrate, they isolate it from the surrounding aggressive atmosphere at high temperature. The protectiveness of the alumina scale is highly dependant upon its growth mechanism. The nucleation and transformation of transient alumina (mainly g-Al2O3 and y-Al2O3) is known to play an important role on alumina scale formation. It is therefore fundamental to characterise these transient alumina especially during the early stages of the oxidation process. The morphology of the transient alumina was observed by scanning electron m…

DiffractionMaterials scienceMorphology (linguistics)Scanning electron microscopeNucleation[ PHYS.COND.CM-MS ] Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Substrate (electronics)02 engineering and technologyMass spectrometry01 natural sciencesX-ray photoelectron spectroscopy0103 physical sciencesMaterials Chemistrytransient alumina010302 applied physicsMechanical Engineeringtechnology industry and agricultureMetals and Alloysthermally grown alumina scalesequipment and supplies021001 nanoscience & nanotechnologyCondensed Matter Physics[PHYS.COND.CM-MS] Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]CrystallographyChemical engineeringTransmission electron microscopyMechanics of Materials[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]alpha aluminaCeramics and Composites0210 nano-technologyMaterials at High Temperatures
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Time-resolved XRD experiments for a fine description of mechanisms induced during reactive sintering

2005

The control of Mechanically Activated Field Activated Pressure Assisted Synthesis hereafter called the MAFAPAS process is the main objective to be achieved for producing nanostructure materials with a controlled consolidation level. Consequently, it was essential to develop characterization tools "in situ" such as the Time Resolved X-ray Diffraction (TRXRD), with an X-ray synchrotron beam (H10, LURE Orsay) coupled to an infrared thermography to study simultaneously structural transformations and thermal evolutions. From the 2003 experiments, we took the opportunity to modify the sample-holder in order to reproduce the better synthesis conditions of the MAFAPAS process, but without the conso…

DiffractionMaterials scienceNanostructureConsolidation (soil)reaction sintering mechanical activationMetals and AlloysSinteringNanotechnologylcsh:Chemical technologyCondensed Matter PhysicsMicrostructureSynchrotronlaw.inventionnanostructure materialslawThermographyThermalMaterials ChemistryCeramics and Compositeslcsh:TP1-1185field activationpressure assisted synthesisScience of Sintering
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Short and long range order of Half-Heusler phases in (Ti,Zr,Hf)CoSb thermoelectric compounds

2016

Abstract The structural properties of (Ti,Zr,Hf)CoSb thermoelectric Half-Heusler compounds were investigated by synchrotron radiation based techniques. The short-range order, in particular the environment of the Co atoms, was studied by extended X-Ray absorption fine structure spectroscopy and the long range order by powder X-Ray diffraction. Structural models were obtained for the single phase materials TiCoSb0.85Sn0.15, ZrCoSb0.85Sn0.15, and HfCoSb0.85Sn0.15. These models were transferred for the phase-separated material Ti0.5Hf0.5CoSb0.85Sn0.15. As a result, proving that each Half-Heusler phase was well ordered, apart from the intermixing of Ti and Hf on its designated crystallographic l…

DiffractionMaterials sciencePolymers and PlasticsExtended X-ray absorption fine structureMetals and AlloysSynchrotron radiation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyThermoelectric materials01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyPhase (matter)Lattice (order)Thermoelectric effectCeramics and Composites0210 nano-technologySpectroscopyActa Materialia
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In situ synchrotron characterization of mechanically activated self-propagating high-temperature synthesis applied in Mo–Si system

1999

Abstract An original experiment was designed to monitor structural and thermal evolutions during the MASHS (Mechanically Activated Self-propagating High-temperature Synthesis) process in the Mo–Si system. Time-Resolved X-Ray Diffraction (TRXRD) coupled with an infrared imaging technique was performed to study, in situ, the formation of the α-MoSi2 phase in the combustion front. Despite a temporal resolution of 50 ms between two consecutive diffractograms, no intermediate phase was observed during the passage of the combustion front. The only reaction responsible for the self-sustentation is Mo+2Si→MoSi2 in the primary zone inside the combustion wave. The mechanical activation was found to i…

DiffractionNanostructureMaterials sciencePolymers and PlasticsMetals and AlloysSelf-propagating high-temperature synthesisAnalytical chemistryMicrostructureCombustionElectronic Optical and Magnetic MaterialsTemperature gradientCrystallographyPhase (matter)Ceramics and CompositesFront velocityActa Materialia
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Mechanisms at structural phase transitions

2007

Abstract Structural phase transitions in crystalline solids are accompanied with the change of symmetry. After EHRENFEST [Ehrenfest, P., Phasenumwandlungen im ublichen und erweiterten Sinn, klassifiziert nach den entsprechenden Singularitaten des thermodynamischen Potentials. Proc. Kon., Amsterdam Acad., 1933, 36(Suppl 75b), 153–157] they can be distinguished between first and second order transitions. Two examples for first and second order transitions will be discussed in order two elaborate the characteristic features. The statements are verified by diffraction experiments; the second order transitions will be discussed on the basis of the LANDAU [Landau, L. and Lifshitz, E.M., Lehrbuch …

DiffractionPhase transitionMaterials scienceTransition pointCondensed matter physicsPhase (matter)Materials ChemistryCeramics and CompositesStructure (category theory)Order (group theory)Superstructure (condensed matter)Symmetry (physics)Journal of the European Ceramic Society
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