Search results for "vanadium"

showing 10 items of 260 documents

Synthesis of new molybdenum–tungsten, vanadium–tungsten and vanadium–molybdenum–tungsten oxynitrides from freeze-dried precursors

2004

Abstract Interstitial molybdenum–tungsten, vanadium–tungsten and vanadium–molybdenum–tungsten oxynitrides in the solid solution series Mo1−zWz(OxNy) and V1−zWz(OxNy) (z=0, 0.2, 0.4, 0.5, 0.6, 0.8, 1), and V1−u−zMouWz(OxNy) (u, z=0.2, 0.33, 0.4, 0.6; u+z

Aqueous solutionScanning electron microscopeInorganic chemistrychemistry.chemical_elementVanadiumNitrideTungstenCondensed Matter PhysicsMicrostructureElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystallographychemistryMolybdenumMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistrySolid solutionJournal of Solid State Chemistry
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Thermodynamics of titanium and vanadium reduction in non-aqueous environment calculated at various levels of theory.

2012

Reduction of titanium and vanadium compounds is a process accompanying the activation of coordinative olefin polymerization catalysts. Four density functional theory (DFT) functionals, coupled cluster with single, double, and perturbative triple excitations method CCSD(T) as well as complete active-space second-order perturbation theory method CASPT2 with a complete active-space self-consistent field CASSCF reference wave function were applied to investigate the thermodynamics of titanium and vanadium reduction. The performance of these theoretical methods was assessed and compared with experimental values. The calculations indicate that vanadium(IV) chloride is more easily reduced by trime…

Aqueous solutionchemistry.chemical_elementThermodynamicsVanadiumChlorideCatalysisMetalCoupled clusterchemistryvisual_artmedicinevisual_art.visual_art_mediumPhysical chemistryDensity functional theoryPhysical and Theoretical ChemistryTitaniummedicine.drugThe journal of physical chemistry. A
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V2O5 nanowires with an intrinsic iodination activity leading to the formation of self-assembled melanin-like biopolymers

2011

V2O5 nanowires act as biomimetic catalysts resembling vanadium haloperoxidases (V-HPO). The nanowires display iodinating activity as confirmed by a colorimetric assay using thymol blue (TB), UV/Vis spectrophotometry and mass spectrometry (FD-MS). In the presence of dopamine these nanowires catalyze the fast and efficient synthesis of melanin-like biopolymers under mild conditions (aqueous solution, neutral pH and room temperature). The resulting melanin-like biopolymer obtained by the V2O5 nanowire catalysts was characterized by scanning electron microscopy (SEM), X-ray diffraction, UV-Vis, FT-IR and electric conductivity resembling the natural biopolymer both in its chemical and morphologi…

Aqueous solutionmedicine.diagnostic_testChemistryScanning electron microscopeNanowireVanadiumchemistry.chemical_elementGeneral ChemistryThymol blueengineering.materialPhotochemistryCatalysischemistry.chemical_compoundSpectrophotometryMaterials ChemistrymedicineengineeringOrganic chemistryBiopolymerJournal of Materials Chemistry
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Chemisorption of hydrogen on a V5+ cluster

1996

Abstract The binding between V 5 + and hydrogen is studied by collision induced dissociation of the cluster-adsorbate V 5 + H 2 . Vanadium clusters are produced by laser vaporization and injected into an electromagnetic ion trap. After mass separation of V 5 + , the pulsed addition of hydrogen yields V 5 + H 2 . The desorption of hydrogen is studied by acceleration of V 5 + H 2 with variable rf voltages and collisions with argon atoms. From the threshold voltage necessary for dissociation a binding energy of H 2 on V 5 + of 2.4 ± 0.3 eV is estimated. This value is consistent with a dissociative chemisorption of hydrogen.

ArgonchemistryHydrogenCollision-induced dissociationChemisorptionBinding energyAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementVanadiumIon trapPhysical and Theoretical ChemistryDissociation (chemistry)Chemical Physics Letters
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Corrosion Resistance of Alloys in IGCC Environment

2001

IGCC recovery boiler materials are subject to severe corrosion in environments composed of a gas mixture (CO-H 2 -H 2 O-CO 2 -H 2 S) and vanadium-containing fly-ash resulting from the combustion of oil residues. This paper presents a study of the corrosion behaviour of two Fe-Ni-Cr austenitic alloys in a typical IGCC environment at 400°C. The alloy composition influences the vanadium incorporated in the corrosion scales during the test, which affects the scale growth process. The valence state (determined by micro-XANES) and the amount of the incorporated vanadium is modified by a subsequent air flow at 400°C.

AusteniteMaterials scienceMechanical EngineeringHydrogen sulfideMetallurgyBoiler (power generation)Vanadiumchemistry.chemical_elementCondensed Matter PhysicsCombustionCorrosionchemistry.chemical_compoundchemistryMechanics of MaterialsIntegrated gasification combined cycleRecovery boilerGeneral Materials ScienceMaterials Science Forum
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Experimental calibration and implications of olivine-melt vanadium oxybarometry for hydrous basaltic arc magmas

2018

The strong dependence of vanadium partitioning between olivine and silicate melt (DVOl-M) on redox conditions (fO2) can be used as sensitive oxybarometer in magmatic systems. Here we extend the experimental database on DVOl-M, obtained so far at high temperatures (mainly above 1250 °C), to lower temperatures that are typical for island-arc basalts. Crystallization experiments were performed using a composition from Mutnovsky volcano (Kamchatka), and the investigated temperature, pressure, and oxygen fugacity ranges were 1025–1150 °C, 0.1 and 0.3 GPa, and ΔQFM of –0.5 to +3.2, respectively. The water content in melts ranged from 0.6 to ∼6.5 wt% H2O. The data demonstrate a strong negative cor…

BasaltMaterials scienceOlivine010504 meteorology & atmospheric sciencesAnalytical chemistryVanadiumchemistry.chemical_elementengineering.material010502 geochemistry & geophysics01 natural sciencesSilicatelaw.inventionchemistry.chemical_compoundGeophysicschemistryGeochemistry and PetrologylawMineral redox bufferengineeringPhenocrystCrystallization0105 earth and related environmental sciencesMelt inclusionsAmerican Mineralogist
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Improved composite materials for rechargeable lithium metal polymer batteries

1999

Abstract The performance of several polymer electrolytes for lithium metal batteries for electric vehicle applications are reported. The best performing electrolyte is the composite PEO 20 LiCF 3 SO 3 –γLiAlO 2 , which was prepared by a solvent-free procedure. It showed coulombic efficiency values of the lithium deposition–stripping process of 94%–96%. Electrochemical tests of lithium polymer battery (LPB) prototypes based on a 3 V LiMn 2 O 4 composite cathode material laminated together with the PEO 20 LiCF 3 SO 3 –γLiAlO 2 electrolyte gave promising results for electric vehicle applications. Even under non-optimized battery design, the prototypes delivered, at the C/3 rate and at 94°C, 40…

Battery (electricity)Materials scienceLithium vanadium phosphate batteryRenewable Energy Sustainability and the EnvironmentComposite numberEnergy Engineering and Power Technologychemistry.chemical_elementLithium polymer batteryElectrolyteElectrochemistrychemistryLithiumElectrical and Electronic EngineeringPhysical and Theoretical ChemistryComposite materialFaraday efficiency
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Atomic Layer Deposition of Spinel Lithium Manganese Oxide by Film-Body-Controlled Lithium Incorporation for Thin-Film Lithium-Ion Batteries

2013

Lithium manganese oxide spinels are promising candidate materials for thin-film lithium-ion batteries owing to their high voltage, high specific capacity for storage of electrochemical energy, and minimal structural changes during battery operation. Atomic layer deposition (ALD) offers many benefits for preparing all-solid-state thin-film batteries, including excellent conformity and thickness control of the films. Yet, the number of available lithium-containing electrode materials obtained by ALD is limited. In this article, we demonstrate the ALD of lithium manganese oxide, LixMn2O4, from Mn(thd)3, Li(thd), and ozone. Films were polycrystalline in their as-deposited state and contained le…

Battery (electricity)Materials scienceta114Lithium vanadium phosphate batterySpinelInorganic chemistrychemistry.chemical_elementengineering.materialElectrochemical energy conversionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAtomic layer depositionGeneral EnergychemistryImpurityengineeringLithiumCrystallitePhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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Vanadium pentoxide nanoparticles mimic vanadium haloperoxidases and thwart biofilm formation

2012

Marine biofouling—the colonization of small marine microorganisms on surfaces that are directly exposed to seawater, such as ships' hulls—is an expensive problem that is currently without an environmentally compatible solution1. Biofouling leads to increased hydrodynamic drag, which, in turn, causes increased fuel consumption and greenhouse gas emissions. Tributyltin-free antifouling coatings and paints1, 2, 3, 4 based on metal complexes or biocides have been shown to efficiently prevent marine biofouling. However, these materials can damage5 the environment through metal leaching (for example, of copper and zinc)6 and bacteria resistance7. Here, we show that vanadium pentoxide nanowires ac…

BromidesBiocideVanadium CompoundsBiofoulingBiomedical Engineeringchemistry.chemical_elementVanadiumBioengineeringZincBiofoulingchemistry.chemical_compoundHypobromous acidHumansPentoxideSeawaterGeneral Materials ScienceElectrical and Electronic EngineeringHydrogen peroxideShipsSinglet OxygenNanowiresChemistryHydrogen PeroxideCondensed Matter PhysicsCopperAtomic and Molecular Physics and OpticsAnti-Bacterial AgentsPeroxidasesChemical engineeringBiofilmsNanoparticlesNature Nanotechnology
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The role of molybdenum in Mo-doped V–Mg–O catalysts during the oxidative dehydrogenation of n-butane

1999

Abstract A detailed study on the influence of the addition of molybdenum ions on the catalytic behaviour of a selective vanadium–magnesium mixed oxide catalyst in the oxidation of n-butane has been performed. The catalysts have been prepared by impregnation of a calcined V–Mg–O mixed oxides (23.8 wt% of V2O5) with an aqueous solution of ammonium heptamolybdate, and then calcined, and further characterised by several physico-chemical techniques, i.e. SBET, XRD, FTIR, FT-Raman, XPS, H2-TPR. MgMoO4, in addition to Mg3V2O8 and MgO, have been detected in all the Mo-doped samples. The incorporation of molybdenum modifies not only the number of V5+-species on the catalyst surface and the reducibil…

ChemistryAmmonium heptamolybdateProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementVanadiumButaneCatalysisCatalysislaw.inventionchemistry.chemical_compoundlawMolybdenumMixed oxideDehydrogenationCalcinationApplied Catalysis A: General
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