Search results for "Vanadium"

showing 10 items of 260 documents

Retention of Vanadium(V), Molybdenum(VI) and Tungsten(VI) by Kaolin

1993

Abstract The ability of kaolin (approximately H2Al2Si2O8 · H2O), a well known clay mineral constituent, to retain V(V) andMo(VI) species from 10−5 and 10−4 M solutions, and W(VI) species from 10−4 M solutions was investigated in the pH range 2–7.5 using a solid/liquid ratio 1:100 (w:v). The equilibration time in the adsorption studies was 72 h, and the shaking time in the desorption studies was 17 h. 0.02 M KCl was used as ionic medium and desorbing liquid. V(V), Mo(VI) and W(VI) were all retained by kaolin to some extent, and the amounts of the elements which could be washed away from kaolin with 0.02 M KCl were very small. The pH dependence of the adsorption was considerable: when added a…

AdsorptionChemistryMolybdenumDesorptionInorganic chemistrySoil Sciencechemistry.chemical_elementKaoliniteIonic bondingVanadiumTungstenClay mineralsAgronomy and Crop ScienceActa Agriculturae Scandinavica, Section B - Soil & Plant Science
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On the influence of the acid-base character of catalysts on the oxidative dehydrogenation of alkanes

1996

Vanadium oxides supported on metal oxide, i.e. Al2O3, MgO and Mg-Al mixed oxide, and V-containing microporous materials (VAPO-5 and MgVAPO-5) have been tested in the oxidative dehydrogenation of C2-C4 alkanes. In all cases, tetrahedral vanadium species (isolated and/or associated) were mainly observed from51V-NMR and diffuse reflectance spectroscopies. The reducibility of V5+-species, determined from the onset-reduction temperature, decreases as follows: VOx/AL > VAPO-5 > MgVAPO-5 =VOx/MG > VOx/MG + AL. The acid character of catalysts, determined from the FTIR spectra of pyridine adsorbed, decreases as: MgVAPO-5 > VOx/AL > VAPO-5 > VOx/MG + AL > VOx/MG. A similar trend between V-reducibilit…

Alkanechemistry.chemical_classificationInorganic chemistryOxideVanadiumchemistry.chemical_elementGeneral ChemistryCatalysisCatalysischemistry.chemical_compoundchemistryPyridineMixed oxideDehydrogenationSelectivity
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The Effect of Electronic Properties of Anodized and Hard Anodized Ti and Ti6Al4V on Their Reactivity in Simulated Body Fluid

2022

The electronic properties of barrier and porous layers on Ti and Ti6Al4V were studied. Barrier anodic oxides grown to 40 V on Ti and on Ti6Al4V are both n-type semiconductors with a band gap of 3.3 eV and 3.4 eV respectively, in agreement with the formation of amorphous TiO2. Anodizing to 200 V at 20 mA cm−2 in calcium acetate and β-glycerol phosphate disodium pentahydrate leads to the formation of Ca and P containing porous films with a photoelectrochemical behaviour dependent on the metallic substrate. A band gap of 3.2 eV and the flat band potential of −0.5 V vs Ag/AgCl were measured for the porous oxide on Ti, while optical transitions at 2.15 eV and a significantly more positive flat b…

Aluminum alloyAnodic oxidationPorous layerGlycerol phosphateAnodizingFlat-band potentialBarrier layerOxide surface layerMaterials ChemistryElectrochemistryPentahydrateOxide surface layer Electrochemical Measurments AnodizingTernary alloyN-type semiconductorPorous oxideRenewable Energy Sustainability and the EnvironmentVanadium alloys Anodic oxideSimulated body fluids Electronic propertiesCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnergy gapSettore ING-IND/23 - Chimica Fisica ApplicataElectrochemical MeasurmentsTitanium dioxideTitanium alloyBody fluidSubstrateCalcium acetate
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Templated growth of smart coatings: Hybrid chemical vapour deposition of vanadyl acetylacetonate with tetraoctyl ammonium bromide

2009

Hybrid aerosol assisted and atmospheric pressure chemical vapour deposition methodology has been utilised to produce thin films of vanadium dioxide from vanadyl acetylacetonate. Tetraoctyl ammonium bromide (TOAB) was used in the aerosol precursor solution. The films were analysed by X-ray diffraction, scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy. Their optical and thermochromic behaviour was also determined. It was found that the use of TOAB had a templating effect that led to a halving in the particle size and that this consequently led to a significant decrease in the thermochromic transition temperature of the films to 34 8C.

Ammonium bromideMaterials scienceScanning electron microscopeInorganic chemistryGeneral Physics and AstronomyVanadiumchemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryChemical vapor depositionCondensed Matter PhysicsSurfaces Coatings and FilmsThermochromic thin film Chemical vapor deposition CVDchemistry.chemical_compoundchemistryTransition metalX-ray photoelectron spectroscopyVanadyl acetylacetonateThin filmApplied Surface Science
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Templated growth of smart nanocomposite thin films: Hybrid aerosol assisted and atmospheric pressure chemical vapour deposition of vanadyl acetylacet…

2009

Hybrid aerosol assisted and atmospheric pressure chemical vapour deposition methodology has been utilised to produce nanocomposite thin films of gold nanoparticles and vanadium dioxide from vanadyl acetylacetonate and auric acid. The addition of tetraoctyl ammonium bromide (TOAB) to the precursor Solution gave control of the size and distribution of gold nanoparticles in the vanadium oxide matrix. These reactions led to vanadium dioxide films with reduced crystallite sizes and enhanced thermochromic properties. The films were analysed by X-ray diffraction, scanning electron microscopy and X-ray photoelectron spectroscopy. Their optical and thermochromic behaviour was also determined, This h…

Ammonium bromideNanocompositeInorganic chemistryOxideSettore ICAR/10 - Architettura TecnicaChemical vapor depositionVanadium oxideInorganic Chemistrychemistry.chemical_compoundCVD Nanocomposite Thermochromism Aerosol HybridSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryX-ray photoelectron spectroscopyChemical engineeringColloidal goldMaterials ChemistryChemical Vapor Deposition CVD Vanadium dioxide thermochromic coatingsPhysical and Theoretical ChemistryVanadyl acetylacetonate
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Selective oxidation of propane over alkali-doped Mo-V-Sb-O catalysts

2009

[EN] Alkali metal-doped MoVSbO catalysts have been prepared by impregnation of a MoVSbO-mixed oxide (prepared previously by a hydrothermal synthesis) and finally activated at 500 or 600 degrees C in N-2. The catalysts have been characterized and tested for the selective oxidation of propane and propylene. Alkali-doped catalysts improved in general the catalytic performance of MoVSbO, resulting more selective to acrylic acid and less selective to acetic acid than the corresponding alkali-free MoVSbO catalysts. However, the specific behaviour strongly depends on both the alkali metal added and/or the final activation temperature. At isoconversion conditions, catalysts activated at 600 degrees…

AntimonyCarboxylic acidIndustrial catalystsInorganic chemistryLithiumHeterogeneous catalysisAcetic acidCatalysisCatalysisPropeneAcrylic acidchemistry.chemical_compoundAcetic acidTransition metalAcrylic acidchemistry.chemical_classificationMolybdenumSodiumVanadiumGeneral ChemistryCaesiumchemistryPotassiumMetal oxidesPropane oxidation
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Study on the sensitive and selective adsorption voltammetry of vanadium with antipyrylazo III (APA III)

1994

The sensitive and selective adsorption voltammetric determination of the vanadium(V)-antipyrylazoIII complex in HAc-NaAc solution is investigated. The V-complex is strongly adsorbed onto a stationary Hg-electrode and is reduced at a potential more negative than that corresponding to the reduction of its ligand. The conditions for determining vanadium are investigated and the mechanism of the reduction peak of the vanadium complex is discussed, as also the influence of foreign ions on the determination of vanadium. An at least 20-fold excess of foreign ions does not cause any interference. The detection limit is 4×10−10 mol/l V with 3 min enrichment time.

Antipyrylazo IIIDetection limitAdsorptionchemistryLigandSelective adsorptionInorganic chemistryVanadiumchemistry.chemical_elementBiochemistryVoltammetryAnalytical ChemistryIonFresenius' Journal of Analytical Chemistry
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Influence of Phase Modifiers on the Degradation of Tri-n-octylamine/dodecane Extracting Mixture by an Acidic Solution of Vanadium (V)

2012

The kinetics of degradation of a mixture of tri-n-octylamine (extractant) and various alcoholic phase modifiers in n-dodecane in contact with acidic aqueous sulfate solutions containing vanadium (V) has been investigated. The nature of the modifier influences the kinetics of degradation and an improvement of the resistance against the chemical degradation is obtained when secondary alcohol (2-nonanol) or tertiary alcohols such as 9-octyl-9-heptadecanol are used as phase modifiers instead of 1-tridecanol. For instance, the kinetic constant of degradation is divided by one half when 9-octyl-9-heptadecanol is used as phase modifier instead of 1-tridecanol. On the contrary, the alcohols contain…

Aqueous solutionDodecaneGeneral Chemical EngineeringKineticsInorganic chemistryVanadiumchemistry.chemical_elementAlcoholGeneral ChemistrySolventchemistry.chemical_compoundchemistryPhase (matter)Chemical decompositionSolvent Extraction and Ion Exchange
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Preparation, characterization and catalytic properties of vanadium oxides supported on calcined Mg/Al-hydrotalcite

1995

Abstract Vanadium oxide supported on calcined hydrotalcite has been investigated for the oxidehydrogenation of n-butane in the 500–550°C temperature interval. Hydrotalcite (Mg/Al atomic ratio of 2.77), consisting of a single phase only, has been employed as a support precursor. The vanadium catalysts (0–50, referred as wt.-% V 2 O 5 ) were prepared by impregnation of calcined hydrotalcite (450°C) with ammonium metavanadate (in an aqueous solution) or vanadyl acetylacetonate (in a methanolic solution), and then calcined at 600°C for 4 h. During the impregnation step, the support is transformed into hydrotalcite if aqueous solutions are used. However, it is not modified if methanolic solution…

Aqueous solutionHydrotalciteChemistryProcess Chemistry and TechnologyInorganic chemistryVanadiumchemistry.chemical_elementCatalysisVanadium oxidelaw.inventionCatalysischemistry.chemical_compoundAmmonium metavanadatelawCalcinationVanadyl acetylacetonateApplied Catalysis A: General
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Microheterogeneous electrocatalytic chiral recognition at monoclinic vanadium-doped zirconias: enantioselective detection of glucose.

2007

Synthetic tetragonal and monoclinic vanadium-doped zirconias (t- and m-VxZr1-xO2, 0.005x0.150) exert an effective catalytic effect toward the electrochemical oxidation of glucose in aqueous alkaline media. The catalytic effect of monoclinic specimens attached to carbon and fluorine-doped tin oxide electrodes exhibits a remarkable enantioselectivity, so that catalytic currents for the oxidation of L-glucose at +0.92 V vs AgCl/Ag are considerably larger than those obtained for the oxidation of D-glucose. This enantioselectivity can be associated with the existence of a noncentrosymmetric coordination of vanadium centers in the monoclinic crystalline form of zirconia. From the electrochemical …

Aqueous solutionMolecular StructureChemistryInorganic chemistryVanadiumchemistry.chemical_elementElectronsStereoisomerismVanadiumElectrocatalystTin oxideElectrochemistryCatalysisAnalytical ChemistryCatalysisGlucoseMicroscopy Electron TransmissionCalibrationElectrochemistryMicroscopy Electron ScanningCubic zirconiaZirconiumOxidation-ReductionMonoclinic crystal systemAnalytical chemistry
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