Search results for "Diffraction"

showing 10 items of 1584 documents

Testing the shape-similarity hypothesis between partide-size distribution and water retention for sicilian soils

2012

Application of the Arya and Paris (AP) model to estimate the soil water retention curve requires a detailed description of the particlesize distribution (PSD) but limited experimental PSD data are generally determined by the conventional sieve-hydrometer (SH) method. Detailed PSDs can be obtained by fitting a continuous model to SH data or performing measurements by the laser diffraction (LD) method. The AP model was applied to 40 Sicilian soils for which the PSD was measured by both the SH and LD methods. The scale factor was set equal to 1.38 (procedure AP1) or estimated by a logistical model with parameters gathered from literature (procedure AP2). For both SH and LD data, procedure AP2 …

Arya and Paris modelSoil water retention curveLaser diffraction methodSettore AGR/08 - Idraulica Agraria E Sistemazioni Idraulico-ForestaliParticle size distribution
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Structural properties of the quaternary Heusler alloy Co2Cr1−xFexAl

2007

The quarternary substitutional series Co2Cr1?xFexAl was investigated by means of surface and bulk sensitive techniques in order to exploit its structural and compositional properties. Both bulk and powder samples of the alloy series were investigated to obtain specific information about this material.The long range order was determined by means of x-ray diffraction and neutron diffraction, while the site specific (short range) order was proved by extended x-ray absorption fine structure spectroscopy. The magnetic structure was investigated by M?ssbauer spectroscopy in transmission and scattering modes in order to compare and separate powder and bulk properties. The chemical composition was …

Auger electron spectroscopyAcoustics and UltrasonicsMagnetic structureChemistryNeutron diffractionOxideCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyChemical physicsEmission spectrumThin filmAbsorption (electromagnetic radiation)SpectroscopyJournal of Physics D: Applied Physics
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Reactivity of H2S and H2S/H2 Mixture With Molybdenum Oxide Thin Films Epitaxied on CoO (100) : Characterization by Rheed and Auger Spectroscopy

2010

Molybdenum-Cobalt composite oxide films were prepared by the evaporation of molybdenum trioxide on a fresh cleaved CoO (100) surface (Thickness = 10 A). The MoO3-CoO interface has been characterized simultaneously by reflexion high electron diffraction (RHEED) and Auger Electron Spectroscopy (AES). The thin film structure and composition depend on the annealing temperature. After a 300°C treatment, metallic cobalt islands nucleate at the interface thin film - CoO (100) and crystallize with the cubic FCC symmetry. After a 700°C treatment cobalt molybdate (a CoMoO4) islands grow. The metastable crystallites are epitaxied on CoO (100). After a 900°C treatment, the thin film consists of flat tw…

Auger electron spectroscopyCrystallographychemistry.chemical_compoundReflection high-energy electron diffractionChemistrychemistry.chemical_elementGeneral ChemistryCrystalliteThin filmMolybdateCobaltAmorphous solidMolybdenum trioxideBulletin des Sociétés Chimiques Belges
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Effect of the surface stoichiometry on the interaction of Mo with TiO2 (110)

2000

Abstract Molydenum has been deposited at room temperature on (110) TiO2 surfaces with different stoichiometries, roughnesses and crystallinities. Whatever the substrate preparation is, in-situ Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS) studies as well as ex-situ atomic force microscopy (AFM) and reflexion high-energy electron diffraction (RHEED) studies reveal a Stranski–Krastanov growth mode: the completion of three monolayers followed by islands growth is observed in every case. The three monolayers are always composed of amorphous molybdenum oxide with an oxidation state of molybdenum less than IV. The oxidation of the molybdenum layers generates Ti3+ an…

Auger electron spectroscopyReflection high-energy electron diffractionChemistryAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesSubstrate (electronics)Condensed Matter PhysicsElectron beam physical vapor depositionSurfaces Coatings and FilmsCrystallographyX-ray photoelectron spectroscopyElectron diffractionMolybdenumMonolayerMaterials ChemistrySurface Science
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Influence of the grain orientation spread on the pitting corrosion resistance of duplex stainless steels using electron backscatter diffraction and c…

2013

Abstract The corrosion behavior of UNS S32202 duplex stainless steel was studied by combining electron backscatter diffraction (EBSD) measurements and critical pitting temperature tests at the microscale. The grain orientation spread (GOS) value was determined in grains of both phases from EBSD data. It was shown that austenitic sites containing extremely small ferrite grains having a GOS value greater than 1.3° were precursor sites for pitting in 4 M NaCl. The critical pitting temperature range was 45–90 °C. All the other sites of both phases remained passive up to 100 °C.

AusteniteMaterials scienceDual-phase steelElectron diffractionGeneral Chemical EngineeringMetallurgyPitting corrosionGeneral Materials ScienceGeneral ChemistryAtmospheric temperature rangeMicrostructureCorrosionElectron backscatter diffractionCorrosion Science
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Passive properties of lean duplex stainless steels after long-term ageing in air studied using EBSD, AES, XPS and local electrochemical impedance spe…

2013

Abstract Passivity of duplex stainless steel was studied after long-term ageing in air using local electrochemical impedance spectroscopy, AES, XPS and EBSD. After mechanical polishing, the passive film was homogeneous and had a capacitive behaviour described by the CPE. After long-term ageing, a small thickening was detected and O2−/OH− was significantly higher in the austenite than in the ferrite. Austenite behaved as a blocking electrode whereas two capacitive loops were observed in the ferrite (low value of O2−/OH). The loop at high frequencies was related with the oxygen reduction and the loop at low frequencies was connected with the passive film.

AusteniteMaterials scienceGeneral Chemical EngineeringCapacitive sensingMetallurgyGeneral ChemistryDielectric spectroscopyCorrosionX-ray photoelectron spectroscopyFerrite (iron)ElectrodeGeneral Materials ScienceComposite materialElectron backscatter diffractionCorrosion Science
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Influence of friction on the local mechanical and electrochemical behaviour of duplex stainless steels.

2006

International audience; The electrochemical behaviour of ferritic and austenitic phases in duplex stainless steel (UNS S32304) and the modifications induced by straining during sliding were studied by potentiodynamic polarisation curves determined at the microscale in a 1MNaCl (pH 3) solution, using an electrochemical microcell. The mechanical properties and stress state of each phase were determined by microhardness and X-ray microdiffraction measurements, before and after straining. The results show that sliding generates elastic straining of the ferrite and plastic deformation of the austenite. The electrochemical behaviour of these phases is dramatically altered, inducing a reduction of…

AusteniteMaterials sciencePassivationFrictionMetallurgyMicrodiffractionSurfaces and InterfacesCondensed Matter PhysicsElectrochemistryStressIndentation hardnessSurfaces Coatings and FilmsCorrosion[SPI]Engineering Sciences [physics]Local electrochemistryMechanics of MaterialsDuplex (building)MicrohardnessFerrite (iron)Duplex steelsMaterials Chemistry[ SPI ] Engineering Sciences [physics]Microscale chemistry
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MZ-35, a new layered pentasil borosilicate synthesized in the presence of large alkali cations

2013

Abstract A new layered borosilicate has been synthesized in the presence of cesium and sodium cations and its structure has been solved by a combination of automated diffraction tomography (ADT) and X-ray powder diffraction (XRPD). MZ-35 has a composition NaCs 2 [BSi 7 O 16 (OH) 2 ](OH) 2 ·4H 2 O and features space group P-4m2. The unusually small unit cell ( a 7.3081 A, c 10.7520 A) is shared by two random-stacked configurations of the structure: a network of connected pentasil units related to the layer of RUB-18 and a bidimensional checkerboard of intersecting ladders of 4-membered rings. The two configurations are related by the simple face-sharing inversion of a hydroxyl-bearing tetrah…

Automated electron diffraction tomography; Rietveld structure refinement; Layered borosilicate; 4-MR ladders; Face-sharing terahedraMaterials science4-MR laddersSodiumchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesDiffraction tomographyFace-sharing terahedraGroup (periodic table)General Materials ScienceRietveld structure refinementLayered borosilicateBorosilicate glassAutomated electron diffraction tomographyGeneral Chemistry4-MR ladders; Automated electron diffraction tomography; Face-sharing terahedra; Layered borosilicate; Rietveld structure refinement[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsAlkali metal4-MR ladders; Automated electron diffraction tomography; Face-sharing terahedra; Layered borosilicate; Rietveld structure refinement;0104 chemical sciencesCrystallographychemistryMechanics of MaterialsCaesiumTetrahedron0210 nano-technologyPowder diffraction
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4-hydroxy-ONN-azoxybenzene

2000

The oxidation of 4-hydroxy­azo­benzene provided a mixture of two azoxy compounds, which were separated by column chromatography. The isomer with the higher melting point appeared to belong to the α (ONN) series, as determined by X-ray diffraction. The mol­ecule, C12H10N2O2, is almost planar. The benzene rings are twisted by 11.7 (2) (substituted) and 4.1 (1)° (unsubstituted) with respect to the ONN plane. The mol­ecules are connected to one another by strong O—H⋯O hydrogen bonds forming chains extended along [001], which are bound by much weaker C—H⋯O hydrogen bonds forming layers in the bc plane.

AzoxyDiffractionPlane (geometry)Hydrogen bondStereochemistryGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundCrystallographyColumn chromatographychemistryMelting pointBenzeneActa crystallographica. Section C, Crystal structure communications
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Orthorhombic polymorphs of twotrans-4-aminoazoxybenzenes

2002

The two isomeric compounds 4-amino-ONN-azoxybenzene [or 1-(4-aminophenyl)-2-phenyldiazene 2-oxide], i.e. the alpha isomer, and 4-amino-NNO-azoxybenzene [or 2-(4-aminophenyl)-1-phenyldiazene 2-oxide], i.e. the beta isomer, both C(12)H(11)N(3)O, crystallized from a polar solvent in orthorhombic space groups, and their crystal and molecular structures have been determined using X-ray diffraction. There are no significant differences in the bond lengths and valence angles in the two isomers, in comparison with their monoclinic polymorphs. However, the conformations of the molecules are different due to rotation along the Ar-N bonds. In the alpha isomer, the benzene rings are twisted by 31.5 (2)…

AzoxyValence (chemistry)X ray diffractionHydrogen bondStereochemistryCrystal structureChemical bondsGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular BiologyConformationsIsomersBond lengthCrystallographychemistry.chemical_compoundchemistryQuantum theoryMoleculeOrthorhombic crystal systemMolecular structureMonoclinic crystal systemActa Crystallographica Section C Crystal Structure Communications
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