Search results for " diffraction"

showing 10 items of 896 documents

Neutron Diffraction Study of the in Situ Oxidation of UO2

2009

This paper discusses uranium oxide crystal structure modifications that are observed during the low-temperature oxidation which transforms UO(2) into U(3)O(8). The symmetries and the structural parameters of UO(2), beta-U(4)O(9), beta-U(3)O(7), and U(3)O(8) were determined by refining neutron diffraction patterns on pure single-phase samples. Neutron diffraction patterns were also collected during the in situ oxidation of powder samples at 483 K. The lattice parameters and relative ratios of the four pure phases were measured during the progression of the isothermal oxidation. The transformation of UO(2) into U(3)O(8) involves a complex modification of the oxygen sublattice and the onset of…

In situKineticsNeutron diffractionchemistry.chemical_element02 engineering and technologyCrystal structure[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxygenIsothermal process0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryLattice (order)Physical chemistryUranium oxidePhysical and Theoretical Chemistry0210 nano-technology
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In-situ high-pressure x-ray diffraction study of zinc ferrite nanoparticles

2016

We have studied the high-pressure structural behavior of zinc ferrite (ZnFe2O4) nanoparticles by powder X-ray diffraction measurements up to 47 GPa. We found that the cubic spinel structure of ZnFe2O4 remains up to 33 GPa and a phase transition is induced beyond this pressure. The high-pressure phase is indexed to an orthorhombic CaMn2O4-type structure. Upon decompression the low- and high-pressure phases coexist. The compressibility of both structures was also investigated. We have observed that the lattice parameters of the high-pressure phase behave anisotropically upon compression. Further, we predict possible phase transition around 55 GPa. For comparison, we also studied the compressi…

In situMaterials scienceNanostructurePHASE TRANSITIONSCiencias FísicasNanoparticle02 engineering and technologyCrystal structure01 natural sciencesCRYSTAL STRUCTURE0103 physical sciencesGeneral Materials ScienceOXIDES010306 general physicsX-RAY DIFFRACTIONNANOSTRUCTUREGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsAstronomíaZinc ferriteCrystallographyHigh pressureX-ray crystallography0210 nano-technologyCIENCIAS NATURALES Y EXACTASSolid State Sciences
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A new cell for the study of in situ chemical reactions using X-ray absorption spectroscopy

2005

An in situ cell for reductive and oxidative treatments at different temperatures that allows the possibility of recording data as a function of temperature has been designed and constructed for X-ray absorption experiments at the GILDA beamline BM08 of ESRF. The cell is linked to a mass quadrupole spectrometer providing control of the reaction gases and monitoring of the products. The apparatus allows measurements to be performed both in transmission and fluorescence geometry. The cell was tested by studying the CO oxidation reaction promoted by a Pt/ceria-zirconia-supported catalyst. The CO(2) yield is correlated with the structural results confirming the existence of a strong metal-suppor…

In situNuclear and High Energy PhysicsAnalytical chemistryChemical reactionRedoxCatalysisSpecimen HandlingCatalysisthree-way catalystX-Ray DiffractionAbsorption (electromagnetic radiation)InstrumentationPlatinumX-ray absorption spectroscopyRadiationSpectrometerChemistryTemperatureSpectrometry X-Ray EmissionCarbon Dioxidein situ EXAFSOxygenYield (chemistry)Flow Injection AnalysisZirconiumOxidation-Reductionstrong metal support interaction
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ChemInform Abstract: Neutron Diffraction Study of the in situ Oxidation of UO2.

2009

This paper discusses uranium oxide crystal structure modifications that are observed during the low-temperature oxidation which transforms UO2 into U3O8. The symmetries and the structural parameters of UO2, β-U4O9, β-U3O7, and U3O8 were determined by refining neutron diffraction patterns on pure single-phase samples. Neutron diffraction patterns were also collected during the in situ oxidation of powder samples at 483 K. The lattice parameters and relative ratios of the four pure phases were measured during the progression of the isothermal oxidation. The transformation of UO2 into U3O8 involves a complex modification of the oxygen sublattice and the onset of complex superstructures for U4O…

In situchemistry.chemical_compoundChemistryLattice (order)KineticsNeutron diffractionUranium oxidePhysical chemistrychemistry.chemical_elementGeneral MedicineCrystal structureOxygenIsothermal processChemInform
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Coordination polymer flexibility leads to polymorphism and enables a crystalline solid-vapour reaction: a multi-technique mechanistic study.

2015

Despite an absence of conventional porosity, the 1D coordination polymer [Ag4 (O2 C(CF2 )2 CF3 )4 (TMP)3 ] (1; TMP=tetramethylpyrazine) can absorb small alcohols from the vapour phase, which insert into AgO bonds to yield coordination polymers [Ag4 (O2 C(CF2 )2 CF3 )4 (TMP)3 (ROH)2 ] (1-ROH; R=Me, Et, iPr). The reactions are reversible single-crystal-to-single-crystal transformations. Vapour-solid equilibria have been examined by gas-phase IR spectroscopy (K=5.68(9)×10(-5) (MeOH), 9.5(3)×10(-6) (EtOH), 6.14(5)×10(-5) (iPrOH) at 295 K, 1 bar). Thermal analyses (TGA, DSC) have enabled quantitative comparison of two-step reactions 1-ROH→1→2, in which 2 is the 2D coordination polymer [Ag4 (O2 …

In situporosityin situ diffractionCoordination polymerStereochemistrygas-phase spectroscopyInfrared spectroscopyCatalysislaw.inventionpolymorphismchemistry.chemical_compoundOptical microscopelawQDThermal analysisTP155chemistry.chemical_classificationChemistryOrganic ChemistryGeneral ChemistryPolymerCoordination PolymersFull PapersCrystallographyPolymorphism (materials science)microscopysolid-state reactionsPowder diffractionthermal analysisChemistry (Weinheim an der Bergstrasse, Germany)
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Gold(I)-catalysed cascade reactions in the synthesis of 2,3-fused indole derivatives.

2015

A gold(I)-catalysed hydroaminative/arylative cascade for the efficient synthesis of a variety of indole-fused skeletons has been developed. Factors controlling the catalyst loading required in these transformations involving 1,3-unsubstituted indole intermediates have been revealed, allowing isolation of an unprecedented 1,3-dimetallated 3H-indole gold complex characterized by X-ray diffraction.

Indole testIndolesChemistryMetals and AlloysGeneral ChemistryCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisX-Ray DiffractionCascadeMaterials ChemistryCeramics and CompositesOrganic chemistryGoldChemical communications (Cambridge, England)
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Solid-State Pyrolyses of Metal Phthalocyanines: A Simple Approach towards Nitrogen-Doped CNTs and Metal/Carbon Nanocables

2006

Solid-state pyrolysis of organometallic precursors has emerged as an alternative method for preparing carbon nanostructures such as carbon nanotubes (CNT) and carbon anions. The morphology of the tubes can be controlled by the nature of the precursors and the pyrolysis procedures, and micrometer long nanotubes, composed of metal carbide wires encased in a graphitic sheath. Cobalt phthalocyanine (CoPc) as well as iron phthalocyanine were pyrolyzed at different temperatures to obtain CNTs. HRTEM and energy-dispersion X-Ray analysis disclosed that the core consisted of long, iron-containing single crystals and that the core was fully surrounded by crystallized graphic carbon. Iron-filled carbo…

IndolesMaterials scienceNitrogenSelective chemistry of single-walled nanotubesMetal Nanoparticleschemistry.chemical_elementElectronsNanotechnologyCarbon nanotubeIsoindolesCarbidelaw.inventionBiomaterialschemistry.chemical_compoundMicroscopy Electron TransmissionX-Ray DiffractionlawElectrochemistryNanotechnologyGeneral Materials ScienceNanotubes CarbonCarbon nanofiberTemperatureGeneral ChemistryFerrocenechemistryChemical engineeringSpectrophotometryFrit compressionMicroscopy Electron ScanningCarbonPyrolysisBiotechnologySmall
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The structural versatility of proton sponge bismuth halides

2022

Hybrid halometalates containing lead, tin, bismuth and antimony and organic cations have recently shown a bevy of interesting photophysical properties. Aiming at finding chemically stable and thermally inert species, three halobismutate species of this class, crystallized with proton sponge-derived cations (PRSH), have been isolated as microcrystalline powders by mixing 1,8-bis(dimethylamino)-naphthalene (proton sponge, or PRS) and bismuth oxide in concentrated HX acids (X ​= ​Cl, Br and I). The two isomorphous (PRSH)3Bi2X9 (X ​= ​Br, I) species, containing isolated [Bi2X9]3- anions, are triclinic at room temperature and convert upon heating into a monoclinic structure through a displacive …

Inorganic ChemistryBismuth halidesPowder diffractionSettore CHIM/03 - Chimica Generale E InorganicaCrystal structureProton spongeSynchrotron X-raysMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryCondensed Matter PhysicsElectronic Optical and Magnetic Materials
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An Investigation of the Pressure-Induced Structural Phase Transition of Nanocrystalline alpha-CuMoO4

2022

The structural behavior of nanocrystalline α-CuMoO4 was studied at ambient temperature up to 2 GPa using in situ synchrotron X-ray powder diffraction. We found that nanocrystalline α-CuMoO4 undergoes a structural phase transition into γ-CuMoO4 at 0.5 GPa. The structural sequence is analogous to the behavior of its bulk counterpart, but the transition pressure is doubled. A coexistence of both phases was observed till 1.2 GPa. The phase transition gives rise to a change in the copper coordination from square-pyramidal to octahedral coordination. The transition involves a volume reduction of 13% indicating a first-order nature of the phase transition. This transformation was…

Inorganic ChemistryCondensed Matter::Materials Sciencehigh pressure; phase transition; synchrotron radiation; X-ray diffractionGeneral Chemical EngineeringFísicaGeneral Materials ScienceCondensed Matter PhysicsMaterials
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Crystalline Non‐Equilibrium Phase of a Cobalt(II) Complex with Tridentate Ligands

2015

In six-coordinate complexes, flexible tridentate ligands enable mer, cis-fac, and trans-fac stereoisomers. With labile metal ions of the first transition metal series, typically only the final thermodynamic product is available because of the rapid isomerization processes. Here we report on the structural characterization of a so far elusive kinetic intermediate of [Co(ddpd)2](BF4)2 (1; ddpd = N,N′-dimethyl-N,N′-dipyridine-2-yl-pyridine-2,6-diamine). Microcrystals of the cis-fac isomer of 1 were obtained by rapid precipitation. The solid-state structure of cis-fac-1 was determined from electron diffraction data.

Inorganic ChemistryCrystallographyEquilibrium phaseElectron diffractionTransition metalChemistryPrecipitation (chemistry)Metal ions in aqueous solutionchemistry.chemical_elementKinetic energyCobaltIsomerizationEuropean Journal of Inorganic Chemistry
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