Search results for "vanadium"

showing 10 items of 260 documents

Vanadium complex with tetradentate [O,N,N,O] ligand supported on magnesium type carrier for ethylene homopolymerization and copolymerization

2009

Immobilization of 1,2-cyclohexylenebis(5-chlorosalicylideneiminato)vanadium dichloride on the magnesium support obtained in the reaction of MgCl 2 .3.4EtOH with Et 2 AlCl gives a highly active precursor for ethylene homopolymerization and its copolymerization with 1-octene. This catalyst exhibits the highest activity in conjunction with MAO, but it is also highly active with AlMe 3 as a cocatalyst. On the other hand, when combined with chlorinated alkylaluminum compounds, Et 2 AlCl and EtAlCl 2 , it gives traces of polyethylene. Moreover, its catalytic activity is strongly affected by the reaction temperature: it increased with rising polymerization temperature from 20 °C to 60 °C, The kine…

EthylenePolymers and PlasticsChemistryMagnesiumOrganic Chemistrychemistry.chemical_elementVanadiumPolyethyleneCatalysischemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistryCopolymerTitaniumJournal of Polymer Science Part A: Polymer Chemistry
researchProduct

Organometallic vanadium‐based heterogeneous catalysts for ethylene polymerization. Study of the deactivation process

1998

Slurry polymerizations of ethylene over vanadium catalysts (based on VCl4 and VOCl3) and their MgCl2(THF)2-supported equivalents were studied. Unsupported vanadium catalysts were found to be unstable while the vanadium active sites deposited on the MgCl2(THF)2 complex are stable. A sharply outlined correlation was found between the concentration of vanadium(III) and catalyst productivity. The high activity and stability of the vanadium catalyst when supported on the magnesium complex is attributed to the increase of resistance to reduction of active vanadium(III) to inactive vanadium(II) by an organoaluminium co-catalyst.

EthylenePolymers and PlasticsMagnesiumOrganic ChemistryInorganic chemistryVanadiumchemistry.chemical_elementPolyethyleneCatalysischemistry.chemical_compoundchemistryEthylene polymerizationMaterials ChemistrySlurryHigh activityMacromolecular Rapid Communications
researchProduct

Dichlorovanadium(IV) diamine-bis(phenolate) complexes for ethylene (co)polymerization and 1-olefin isospecific polymerization

2018

Abstract Two vanadium complexes bearing amine-bis(phenolate) ligands with the amino side-arm donor, [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)2}Cl2] (1) and [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)(CH2-2-O-C6H4)}Cl2] (2), were synthesised and characterized by FTIR and 1H NMR spectroscopy. Upon activation with Al(iBu)3/Ph3CB(C6F5)4, these complexes became active catalysts for 1-octene polymerization giving highly stereoregular polymers (mmmm ∼ 90%) having regioirregularly arranged units. The catalytic activity of the catalysts in ethylene homo- and copolymerization, and their ability to incorporate a comonomer were highly dependent on both the activator type and the complex structure. 1/EtAlCl2 exhi…

EthylenemicrostructureDispersityZiegler-Natta polymerization010402 general chemistry01 natural sciencesCatalysisTREFchemistry.chemical_compoundDiaminediamine-bis(phenolate) ligandPolymer chemistryethyleneCopolymerPhysical and Theoretical Chemistrychemistry.chemical_classificationOlefin fiber010405 organic chemistryChemistryComonomerPolymer0104 chemical sciencescopolymerizationVanadium catalystPolymerization1-octeneJournal of Catalysis
researchProduct

Automation of the determination of hydrogen peroxide, dichromate, formaldehyde and bicarbonate in milk by flow injection analysis

1992

Automatic flow injection methods for the determination of hydrogen peroxide, dichromate, formaldehyde and bicarbonate in dairy products are proposed. They are based on reaction with vanadium pentoxide, diphenyl-carbazide, fuchsine-sulphur dioxide and alizarin, respectively. Sample pre-treatment (paper and membrane filtration, dialysis) is widely discussed for on-line incorporation. The usefulness of these methods was tested by applying them to different commercial samples, satisfactory results being obtained in all instances.

Flow injection analysisChromatographyBicarbonateFormaldehydeAnalytical chemistryVanadiumchemistry.chemical_elementAlizarinBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryPentoxideSample preparationHydrogen peroxideFresenius' Journal of Analytical Chemistry
researchProduct

Predicting breakthrough of vanadium in fixed-bed absorbent columns with complex groundwater chemistries: A multi-component granular ferric hydroxide−…

2020

Granular ferric hydroxide (GFH) is often used for fixed bed adsorbent (FBA) columns in groundwater purification units around the world to remove arsenate contaminations. Groundwater can contain also other toxic (e.g., antimonite and vanadate) and non-toxic oxo-anions (phosphate and silicic acid) that are known to affect FBA lifetimes. Therefore, understanding the breakthrough of toxic compounds intended for removal by FBA is essential to their design, and is important to predict accurately breakthrough curves (BTCs) for FBAs in waterworks to plan future operating costs. Rapid small-scale column tests (RSCCT) and pilot-scale FBA were used to simulate vanadate BTCs for complex groundwater che…

Full PaperChemistryEcological ModelingInorganic chemistryArsenateVanadiumchemistry.chemical_elementPollutionlcsh:TD1-1066HSDMchemistry.chemical_compoundRSCCTAdsorptionCD-MUSICMass transferVanadateFBAFreundlich equationVanadateAdsorptionSilicic acidlcsh:Environmental technology. Sanitary engineeringWaste Management and DisposalGroundwaterWater Science and TechnologyWater Research X
researchProduct

Vanadium‐Doped Zircon and Zirconia Materials Prepared from Gel Precursors as Site‐Selective Electrochemical Sensors

2003

Abstract Polymer film electrodes incorporating vanadium‐doped zircon (V x ZrSiO4, 0.00 < x < 0.10) and vanadium‐doped monoclinic and tetragonal zirconias (V x ZrO2, 0.00 < x < 0.15), prepared by heat treatment of gel precursors, exhibit a significant site‐selective electrocatalytic activity towards the oxidation of amino acids, polyalcohols, and polyhydroxycarboxylic acids in alkaline media. Catalysis of the oxidation of carboxylate and alcohol groups involves a relatively slow chemical reaction between the substrate and vanadium centers, while the oxidation of thiolate in cysteine can be attributed to the oxidation of an adduct formed by vanadium centers and the substrate.

General Chemical EngineeringInorganic chemistrySubstrate (chemistry)Vanadiumchemistry.chemical_elementElectrocatalystElectrochemistryCatalysischemistry.chemical_compoundchemistryCubic zirconiaCarboxylateInstrumentationGeneral Environmental ScienceSol-gelInstrumentation Science &amp; Technology
researchProduct

Dissimilar laser welding of AISI 316L stainless steel to Ti6–Al4–6V alloy via pure vanadium interlayer

2015

Abstract Successful continuous laser joining of AISI 316L stainless steel with Ti6Al4V titanium alloy through pure vanadium interlayer has been performed. Three welding configurations were tested: one-pass welding involving all three materials and two pass and double spot welding involving creation of two melted zones separated by remaining solid vanadium. For the most relevant welds, the investigation of microstructure, phase content and mechanical properties has been carried out. In case of formation of a single melted zone, the insertion of steel elements into V-based solid solution embrittles the weld. In case of creation of two separated melted zones, the mechanical resistance of the j…

Heat-affected zoneMaterials scienceMechanical EngineeringMetallurgyAlloyLaser beam weldingVanadiumchemistry.chemical_elementTitanium alloyWeldingengineering.materialCondensed Matter PhysicsMicrostructurelaw.inventionchemistryMechanics of MaterialslawengineeringGeneral Materials ScienceSpot weldingMaterials Science and Engineering: A
researchProduct

Investigation of the hyperfine structure of weak atomic Vanadium lines by means of Fourier transform spectroscopy

2015

In continuation of our work on the investigation of the hyperfine structure (HFS) of atomic vanadium, we analyzed weak spectral lines in a Fourier transform spectrum that have not been investigated up to now. The main objective of this work was the determination of the magnetic dipole HFS constant A of the energy level at 15 103.784 cm−1, which was the only energy level with unknown A value up to the energy of 28 000 cm−1. Additionally, other gaps in the data of magnetic dipole HFS could be filled in. The spectrum of vanadium–argon plasma in a hollow cathode lamp is recorded in the spectral range from 12 500 to 26 000 cm−1 or 800 to 380 nm, respectively. The HFS of 42 weak atomic vanadium l…

Hollow-cathode lampPhysicsVanadiumchemistry.chemical_elementPlasmaCondensed Matter PhysicsAtomic and Molecular Physics and OpticsSpectral lineFourier transform spectroscopylaw.inventionsymbols.namesakeFourier transformchemistrylawsymbolsPhysics::Atomic PhysicsAtomic physicsHyperfine structureMagnetic dipoleJournal of Physics B: Atomic, Molecular and Optical Physics
researchProduct

Synthesis and Characterization of New Keggin-Based Structure Tungstocobaltates: K9[Co3+W11O39] and its Vanadium Derivatives, K8[Co2+W11V4+O40], K7[Co…

1995

Abstract Good yield synthesis of the potassium salts of four new interrelated : olyoxometalates, [Co3+W11O39]9-(I), [Co2+W11V4+O4]8-(II), [Co2+W11V5+O40]7-(III), and [Co3+W11V5+O40]6-(IV), are reported. The title compounds have been characterized by IR and UV-Vis.-NIR spectroscopies, cyclic voltammetry and magnetic measurements. IR spectra confirm that I has the lacunary structure of an undecatungstate anion, while II through IV have a substituted α-Keggin structure with the vanadium atom located at an octahedral site replacing one tungsten atom. Optical data confirm the oxidation states for both, the Co and V atoms, as formulated for I through IV.

Inorganic ChemistryCrystallographychemistryOctahedronPotassiumYield (chemistry)Infrared spectroscopychemistry.chemical_elementVanadiumPhysical and Theoretical ChemistryCyclic voltammetryLacunary functionIonSynthesis and Reactivity in Inorganic and Metal-Organic Chemistry
researchProduct

Synthesis, Structure, and Properties of BaVO2(AsO4):  a New Vanadium Arsenate Containing the V2O42+ Core

1997

The new vanadium arsenate BaAsVO6 has been synthesized hydrothermally and structurally characterized by single-crystal X-ray diffraction, IR spectroscopy, and magnetic susceptibility measurements. It crystallizes in the monoclinic system, space group P21/c with unit cell parameters a = 5.645(1) A, b = 10.243(1) A, c = 8.945(1) A, β = 90.60(1)°, and Z = 2. The layered structure is built up from V2O42+ units and AsO43- anions, the AsO43- ligands being coordinated to two (V2O4)2+ units in both, terminal and bridging μ2-AsO43- fashion. The [VO2(AsO4)]2- layers are separated by Ba2+ cations. The V2O42+ unit has no precedence in oxo-vanadium chemistry.

Inorganic ChemistryDiffractionchemistry.chemical_compoundCrystallographyChemistryArsenateVanadiumchemistry.chemical_elementInfrared spectroscopyPhysical and Theoretical ChemistryMagnetic susceptibilityMonoclinic crystal systemLayered structureInorganic Chemistry
researchProduct