Search results for "vanA"

showing 10 items of 345 documents

L'incesto della parola. Lingua e scrittura in Silvana Grasso

2009

Marina Castiglione in questo saggio – il primo interamente dedicato a Silvana Grasso, importante voce della letteratura contemporanea – mette in luce come i romanzi dell’autrice siciliana si presentino mutuamente intellegibili alla luce di un materiale linguistico e stilistico (oltre che tematico) che rimbalza dall’uno all’altro anche a notevoli distanze temporali. L’esposizione consente di far emergere, ai diversi livelli della scrittura, costanti, modifiche e variabili che danno all’intero corpus unitarietà nelle intenzioni e una assoluta inscindibilità tra lingua e fabula. Lingua e identità sono, infatti, una bussola certa nell’orizzonte frastagliato delle realtà rappresentate. Il ricors…

Analisi linguistica testualeSilvana Grasso
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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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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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