Search results for "vanadium"

showing 10 items of 260 documents

Spark Plasma Sintering (SPS)-Assisted Synthesis and Thermoelectric Characterization of Magnéli Phase V6O11

2018

The Magneli phase V6O11 was synthesized in gram amounts from a powder mixture of V6O11/V7O13 and vanadium metal, using the spark plasma sintering (SPS) technique. Its structure was determined with synchrotron X-ray powder diffraction data from a phase-pure sample synthesized by conventional solid-state synthesis. A special feature of Magneli-type oxides is a combination of crystallographic shear and intrinsic disorder that leads to relatively low lattice thermal conductivities. SPS prepared V6O11 has a relatively low thermal conductivity of κ = 2.72 ± 0.06 W (m K)-1 while being a n-type conductor with an electrical conductivity of σ = 0.039 ± 0.005 (μΩ m)-1, a Seebeck coefficient of α = -(3…

ChemistryAnalytical chemistryVanadiumchemistry.chemical_elementSpark plasma sintering02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic ChemistryThermal conductivityElectrical resistivity and conductivitySeebeck coefficientThermoelectric effectPhysical and Theoretical Chemistry0210 nano-technologyPowder diffractionPowder mixtureInorganic Chemistry
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Experimental set up for determining the temperature-oxygen partial pressure conditions during synthesis of spinel oxide nanoparticles

1997

Abstract Nanometric spinel oxide powders, Fe 3− x M x O 4 , where M is a transition element, have been synthetized by soft chemistry. This method generally leads to a non-stoichiometric phase, Fe 3− x M x O 4+δ where δ is the deviation from stoichiometry so that further annealing at low temperatures around 450°C and low oxygen partial pressure around 10 −25 Pa given by N 2 /H 2 /H 2 O gas mixtures is required: this enables a stoichiometric compound to be obtained and a nanometric size to be maintained. The complete set up consisting of a gas mixer, a thermogravimetric apparatus and a preparative furnace is described. Some results concerning the conditions of temperature and oxygen partial p…

ChemistryInorganic chemistrySpinelOxideAnalytical chemistryVanadiumchemistry.chemical_elementGeneral ChemistryPartial pressureengineering.materialCondensed Matter PhysicsOxygenSoft chemistrychemistry.chemical_compoundTransition metalengineeringGeneral Materials ScienceStoichiometry
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Structural Evolution and Vanadium Distribution in the Preparation of V4+-ZrSiO4 Solid Solutions from Gels

2004

Vanadium-containing ZrSiO4-gel precursors with nominal compositions Vx-ZrSiO4 with x= 0.0, 0.002, 0.004, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.1, and 0.2 were prepared using a previously reported procedure and thermally treated over a range of temperature up to the formation of the V4+-ZrSiO4 solid solution. The structural evolution and the V4+ location and its homogenous distribution were followed using powder X-ray diffractometry and electron spin resonance spectroscopy (ESR). Our experiments showed that a tetragonal form of V4+-ZrO2 was the first crystalline phase obtained on heating the gels. On further heating, a phase transformation to the monoclinic form of V4+-ZrO2 took place. Final…

ChemistryInorganic chemistryVanadiumchemistry.chemical_elementAmorphous solidTetragonal crystal systemLattice constantPhase (matter)Materials ChemistryCeramics and CompositesPhysical chemistrySolubilitySolid solutionMonoclinic crystal systemJournal of the American Ceramic Society
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Oxidative dehydrogenation of propane and n-butane on V-Mg based catalysts

1994

Abstract The catalytic properties of vanadium supported catalysts for the oxidative dehydrogenation of propane and n-butane has been studied. Natural Sepiolite and magnesium oxalate were used as starting support materials. Large differences in the type of crystalline phases were detected on the calcined catalysts depending on the vanadium content and nature of the support. The active and selective sites for the oxidative dehydrogenation of propane and n-butane, are related with isolated V 5+ with atetrahedral coordination. The presence of vanadium species with coordination higher than 4 negatively influence the selectivity to dehydrogenation products.

ChemistryInorganic chemistryVanadiumchemistry.chemical_elementButaneMedicinal chemistryCatalysislaw.inventionchemistry.chemical_compoundlawPropaneCalcinationDehydrogenationSelectivityMagnesium oxalate
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A Superoxovanadium(V) Complex Linking the Peroxide and Dioxygen Chemistry of Vanadium.

2001

A missing link: A superoxovanadium(V) complex is the first reaction intermediate in the oxidative conversion of a peroxovanadium(V) complex into a vanadyl(IV) complex and molecular oxygen. The superoxo species appears also to play an essential role in the formation of the peroxovanadium(V) complex from the vanadyl(IV) complex and molecular oxygen.

ChemistryRadicalVanadiumchemistry.chemical_elementGeneral MedicineGeneral ChemistryReaction intermediateOxidative phosphorylationPhotochemistryPeroxideOxygenCatalysischemistry.chemical_compoundMolecular oxygenAngewandte Chemie (International ed. in English)
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Colorimetric method for the determination of vanadium with tannic acid in water and oils

1994

A new spectrophotometric method was developed to determine vanadium using tannic acid as a complexing reagent to form a coloured reaction product which can easily be extracted by 1-pentanol in the presence of cetylpyridinium. The developed method can successfully be applied to determine trace levels of 10 ng/ml of vanadium in natural waters without any preconcentration step. It can also determine less than 1 mg/kg of vanadium in edible oils and petroleum products.

Chromatographymedicine.diagnostic_testChemistrybusiness.industryNatural waterVanadiumchemistry.chemical_elementCetylpyridiniumBiochemistryAnalytical Chemistrychemistry.chemical_compoundPetroleum productLiquid–liquid extractionReagentSpectrophotometryTannic acidmedicinebusinessFresenius' Journal of Analytical Chemistry
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Statistical characterisation of heavy metal contents inParacentrotus lividusfrom Mediterranean Sea

2014

This work focuses on the estimation of Hg, As, Cr, Ni, Cu, V, Cd and Pb by inductively coupled plasma mass spectrometry in 135 adult specimens of Paracentrotus lividus collected in different coastal areas of Sicily (Gela, Punta Secca, Ragusa (RG), Siracusa, Priolo, Catania, Messina, Milazzo, Brolo and Filicudi), in order to monitor the Mediterranean marine ecosystem by use of sea urchin as bioindicator. Moreover, the paper deals with the statistical classification of the tested samples according to the sampling area based on metal concentrations. The descriptive statistics findings were obtained and, a starting multivariate matrix was built. Data-sets were subjected to Kruskal-Wallis test t…

ChromiumMediterranean climatePrincipal Components AnalysisPlant ScienceBiochemistryParacentrotus lividusArsenicsea urchinAnalytical Chemistrysea urchin; Bioindicator; Mediterranean sea; heavy metals; Principal Components AnalysisMediterranean seaNickelPrincipal components analysiMetals Heavybiology.animalAnimalsMarine ecosystemheavy metalsSicilyInductively coupled plasma mass spectrometrySea urchinbiologyBioindicatorOrganic ChemistryVanadiumHeavy metalsSettore CHIM/06 - Chimica OrganicaMercurybiology.organism_classificationFisheryHeavy metalLeadEnvironmental chemistryMediterranean seaParacentrotusEnvironmental scienceBioindicatorCopperWater Pollutants ChemicalCadmiumNatural Product Research
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Gas-phase selective oxidation of chloro- and methoxy-substituted toluenes on TiO2–Sepiolite supported vanadium oxides

2009

Abstract Catalytic behaviour of vanadium oxide systems (5–20 wt.% V2O5) supported on TiO2–Sepiolite (with titania loading around the theoretical monolayer, 12 wt.%, 12Ti–Sep) and, as reference, on Sepiolite calcined (Sepc) in the p-substituted toluene derivatives selective oxidation was studied. In all the catalysts studied p-chloro (p-ClBA) and p-methoxybenzaldehyde (p-MeOBA) were the main products. The yields to benzaldehydes obtained with %V/12Ti–Sep are comparable with some of those reported in the literature under similar kinetically controlled experimental conditions (Sp-ClBA = 70% and X = 19% were obtained at 653 K on 20 V/12Ti–Sep). The activity for benzaldehyde derivatives formatio…

Concerted reactionProcess Chemistry and TechnologyInorganic chemistryVanadiumchemistry.chemical_elementMedicinal chemistryTolueneCatalysisVanadium oxideCatalysisBenzaldehydechemistry.chemical_compoundchemistryPartial oxidationMethyl groupApplied Catalysis A: General
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Synthesis and characterization of vanadyl(IV) complexes of Schiff bases derived from anthranilic acid and salicylaldehyde (or its derivatives) or ace…

1997

Anhydrous, dimeric vanadyl(IV) complexes of Schiff bases derived from [1+1] condensation of salicylaldehyde (or its derivatives) and anthranilic acid, have been synthesized from CH3CN and were characterized by elemental analysis, FTIR, EPR, absorption, TGA, cyclic voltammetry and room temperature magnetic susceptibility measurements. These complexes were found to be oxidized by air in polar solvents like MeOH and DMF to V-V products. The E(1/2) values were found to be around 660 mV indicating that the carboxylate group favours vanadyl(IV) binding when compared to the alkoxo-bound vanadium complexes. Oxidative instability of these complexes are dependent on the substituent on the salicylalde…

Coordination sphereAcetylacetoneDimeric Vanadyl(Iv)Inorganic chemistryDecavanadateVanadiumchemistry.chemical_elementRedoxSingle Crystal X-RayInorganic Chemistrychemistry.chemical_compoundOxidationPyridinePolymer chemistryMaterials ChemistryAnthranilic acidPhysical and Theoretical ChemistrySchiff BasesSchiff baseReactivityVanadiumBindingMononuclear Octahedral Vo3+chemistrySalicylaldehydeDecavanadatesPyridiniumOxidative InstabilityOxovanadium(Iv)Polyhedron
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Synthesis and Stability Region of Stoichiometric Nanocrystalline Vanadium−Iron Spinel Powders

2000

Vanadium-iron spinels with nanometric sizes have been synthesized by a soft chemistry route. This way of elaboration consists of a coprecipitation followed by thermal treatments at low temperatures. The last thermal annealing is performed under a reducing atmosphere in order to obtain the exact oxygen stoichiometry (four oxygen atoms for three metal atoms in AB 2 O 4 ). Because of the low temperatures used, very low oxygen partial pressures (between 10 -20 and 10 -30 Pa) have to be applied. For this purpose, a reducing setup has been used. It consists of H 2 /N 2 /H 2 O gas mixtures, creating a reducing atmosphere with low oxygen partial pressure. This atmosphere can be applied to a sample …

CoprecipitationGeneral Chemical EngineeringReducing atmosphereSpinelInorganic chemistryVanadiumchemistry.chemical_elementGeneral ChemistryPartial pressureengineering.materialNanocrystalline materialSoft chemistrychemistryMaterials ChemistryengineeringStoichiometryChemistry of Materials
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