Search results for "Voltammetry"

showing 10 items of 404 documents

Vanadium and molybdenum concentrations in particulate from Palermo (Italy): analytical methods using voltammetry

2014

The main purpose of this work was to develop a reliable method for the determination of vanadium (V) and molybdenum (Mo) in atmosphere particles or aerosols because they can not be readily measured using conventional techniques. For this research, 30 particulate samples were collected from five different stations located at Palermo, Italy. We used the catalytic adsorptive stripping voltammetry and differential pulsed voltammetry to measure Vand Mo in atmospheric particulate, respectively. The represented method includes advantages of high sensitivity, high selectivity, simplicity, reproducibility, speed and low costs. The quantification limits for V and Mo are, respectively, 0.57 and 0.80 n…

Detection limitReproducibilityRelative standard deviationAnalytical chemistrychemistry.chemical_elementVanadiumParticulatesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturalichemistryMolybdenumEnvironmental chemistryvanadium molybdenum particulate voltammetry PalermoAdsorptive stripping voltammetrySettore CHIM/01 - Chimica AnaliticaVoltammetryGeneral Environmental Science
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Voltammetric behavior and assay of the contraceptive drug levonorgestrel in bulk, tablets, and human serum at a mercury electrode.

2004

The cyclic voltammograms of levonorgestrel (LNG) in Britton-Robinson buffers of pH 2-11 at the hanging mercury drop electrode showed a single two-electron irreversible cathodic peak over the whole pH range. This peak may be attributed to the reduction of the 3-keto-delta-4-group in the A-ring of the LNG molecule. The interfacial adsorptive character of levonorgestrel onto the surface of the hanging mercury drop electrode was identified by means of both cyclic voltammetry and chronocoulometry techniques. A simple, sensitive, and selective square-wave adsorptive cathodic stripping voltammetric procedure was developed for the quantitation of levonorgestrel. Under the optimized operational cond…

Detection limitendocrine systemChromatographyChemistrychemistry.chemical_elementPharmaceutical formulationDropping mercury electrodeAnalytical ChemistryMercury (element)Hanging mercury drop electrodeCathodic stripping voltammetrymedicineLevonorgestrelCyclic voltammetrymedicine.drugTalanta
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Dialkyl(butadiene)cyclopentadienylmolybdenum(III) Complexes. Synthesis, Characterization, and Reactivity

2000

International audience; Treatment of CpMo(η4-diene)Cl2 (diene = 1,3-butadiene, C4H6, 1‘; isoprene, C5H8, 1‘ ‘; 2,3-dimethyl-1,3-butadiene, C6H10, 1‘ ‘) in diethyl ether at low temperature with 2 equiv of alkylmagnesium RMgX reagents affords the corresponding dialkyl complexes CpMo(η4-1,3-diene)R2 (2, 2‘, 2‘ ‘, R = CH3, a; CH2Ph, b; CH2SiMe3, c). These species are isolable in moderate yields and have been fully characterized by EPR, elemental analyses, and cyclic voltammetry. They all show a reversible reduction process at relatively low potentials and an irreversible oxidation. The structure of 2‘ ‘a was confirmed by single-crystal X-ray diffraction. The mixed complex CpMo(η4-C4H6)Cl(CH3), …

DieneStereochemistryReaction productsLigands010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compound[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryRedistribution (chemistry)Redox reactionsPhysical and Theoretical ChemistryIsoprene010405 organic chemistryLigandArylOrganic ChemistryAlkyls0104 chemical scienceschemistryReagentCyclic voltammetryDiethyl etherElectron paramagnetic resonance spectroscopyOrganometallics
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Electrochemical reduction properties of A-frame compounds and crystal structure of Pd2(dppm)2(Me)2(Br)+ dimer

2006

Abstract Two series of A-frame complexes, [Pd2(dppm)2(R)2(μ-X)]+ (R = Me and X = Cl, Br, I, H; R = Mes and X = Br, I), were investigated by cyclic voltammetry (CV). The 2-electron reduction potentials for the first series increase from I (−1.10), Br (−1.17), Cl (−1.25) to H (−1.65 V versus SCE, in CHCl3), as well as in the second series; Br (−1.35) and I (−1.38 V versus SCE, in THF). The nature of the LUMO where the electron reduction takes place is qualitatively addressed by DFT on the corresponding model complexes [Pd2(H2PCH2PH2)2(R)2(μ-X)]+. The LUMO and (LUMO + 1) of the halide derivatives exhibit the presence of Pd d x 2 - y 2 atomic orbitals interacting in an anti-bonding fashion with…

DimerCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryReactivity (chemistry)Molecular orbitalA-framePhysical and Theoretical ChemistryHOMO/LUMOComputingMilieux_MISCELLANEOUSX-ray crystallography010405 organic chemistryChemistrymolecular orbitals[ CHIM.INOR ] Chemical Sciences/Inorganic chemistrypalladium0104 chemical sciences3. Good healthCrystallographyelectrochemistryX-ray crystallographyCyclic voltammetryInorganica Chimica Acta
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Versatile redox reactivity of triaryl-meso-substituted Ni(ii) porphyrin

2014

The electrochemical oxidation of nickel(II) 5,15-p-ditolyl-10-phenylporphyrin (1-Ni) leads to the formation of different coupling products, with the distribution depending on the nature of the solvent (CH2Cl2–CH3CN, CH2Cl2, DMF), the cell configuration (2 or 3 compartments) and the number of electrons abstracted. In a two compartment configuration (anode and cathode in the same compartment) in a CH2Cl2–CH3CN mixture, nickel(II) 5-chloro-10,20-p-ditolyl-15-phenylporphyrin (1-Ni-Cl) was isolated in good yield and its mechanism of formation is proposed. Switching to the three compartment configuration, the meso-β/meso-β doubly fused dimer (3-Ni) is detected as the major product whereas in pure…

DimerInorganic chemistrychemistry.chemical_elementRedoxInorganic ChemistryNickelchemistry.chemical_compoundchemistryYield (chemistry)Polymer chemistryReactivity (chemistry)PhosphoniumCyclic voltammetryTriphenylphosphineDalton Trans.
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Cobalt-Containing Silicotungstate Sandwich Dimer [{Co3(B-β-SiW9O33(OH))(B-β-SiW8O29(OH)2)}2]22-

2005

The 6-cobalt-substituted [{Co3(B-beta-SiW9O33(OH))(B-beta-SiW8O29(OH)2)}2]22- has been characterized by IR and UV-vis spectroscopy, elemental analysis, magnetic studies, electrochemistry, and gel filtration chromatography. A single-crystal X-ray analysis was carried out on K10Na12[{Co3(B-beta-SiW9O33(OH))(B-beta-SiW8O29(OH)2)}2].49H2O (KNa-1), which crystallizes in the monoclinic system, space group P2(1)/n, with a=19.9466(8) A, b=24.6607(10) A, c=34.0978(13) A, beta=102.175(1) degrees, and Z=2. Polyanion 1 represents a novel class of asymmetric sandwich-type polyanions. It contains three cobalt ions, which are encapsulated between an unprecedented (B-beta-SiW9O34) fragment and a (B-beta-Si…

DimerSize-exclusion chromatographyAnalytical chemistrySolid-statechemistry.chemical_elementElectrochemistryInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPhysical and Theoretical ChemistryCyclic voltammetrySpectroscopyCobaltMonoclinic crystal systemInorganic Chemistry
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Electrochemical reduction of graphene oxide and its in situ spectroelectrochemical characterization

2012

The electrochemical properties of self-assembled films of graphene oxide (GO) on mercaptoethylamine (MEA) modified rough Au-surfaces were studied. The film deposition process on MEA primed gold was followed by surface plasmon resonance measurements and the film morphology on 3-aminopropyltriethoxysilane primed Si(100)-surface was studied by atomic force microscopy. The deposited few layer thick GO films on gold were electrochemically reduced by cyclic voltammetry simultaneously as the structural changes in the film were recorded by in situ vibrational spectroscopies. In situ surface enhanced infrared spectroscopy results indicate that the effect of the applied potential on the GO structure …

Double layer (biology)Materials scienceGrapheneAnalytical chemistryOxideGeneral Physics and AstronomyInfrared spectroscopyElectrochemistrylaw.inventionchemistry.chemical_compoundChemical engineeringchemistrylawPhysical and Theoretical ChemistryCyclic voltammetrySurface plasmon resonanceLayer (electronics)
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A comparative evaluation of palladium and platinum nanoparticles as catalysts in proton exchange membrane electrochemical cells

2008

The goal of the present study is the development and comparative characterisation of carbon-supported and nanostructured Pd- and Pt-based electrocatalysts for hydrogen oxidation in Proton Exchange Membrane (PEM) H2/O2(air) fuel cells and proton reduction in PEM water electrolysers. Catalysts have been synthesised in a solution using a combined impregnation/reduction polyol method. They have been characterised using X-ray Diffraction (XRD) analysis, Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA) and cyclic voltammetry. NanoPt, nanoPd and nanoPt-Pd catalysts deposited onto a carbon carrier have been used to prepare Membrane-Electrode Assemblies (MEAs) which, in turn,…

ElectrolysisMaterials scienceElectrolysis of waterElectrolytic celllawInorganic chemistryProton exchange membrane fuel cellCyclic voltammetryElectrochemistryDirect-ethanol fuel cellElectrochemical celllaw.inventionInternational Journal of Nuclear Hydrogen Production and Applications
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Experimental analysis of materials in proton exchange membrane electrolysis cells

2019

Abstract An accelerated supply and demand of energy has resulted in an increased need for efficient energy storage options, where storing energy in hydrogen gas emerges as one of the most attractive. In this study, a singular proton exchange membrane (PEM) electrolysis cell was designed using adequately low-cost materials, and tested using polarisation curves, cyclic voltammetry and AC impedance. A comparative study of various micro porous layer (MPL) materials was performed in an effort to find suitable options which are able to steadily operate under anodic conditions. The best performance was achieved using carbon cloth, however this material was unstable. Untreated porous titanium and n…

ElectrolysisMaterials scienceHydrogenRenewable Energy Sustainability and the EnvironmentElectrolytic cellEnergy Engineering and Power Technologychemistry.chemical_elementProton exchange membrane fuel cell02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesEnergy storage0104 chemical scienceslaw.inventionAnodeFuel TechnologyChemical engineeringchemistrylawCyclic voltammetry0210 nano-technologyCarbonInternational Journal of Hydrogen Energy
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Electrochemical incineration of 1,2-dichloroethane: Effect of the electrode material

2008

The electrochemical incineration of 1,2-dichloroethane (EDC) at Pt, Au, boron-doped diamond (BDD), Ebonex, stainless steel, Ti/IrO2–Ta2O5 and PbO2 has been studied in acid media by cyclic voltammetry and bulk electrolysis. It has been shown that the performances of the process dramatically depend on the anodic material. Higher current efficiencies were obtained at BDD. In particular, at proper values of applied current density, it is possible to obtain the almost complete conversion of EDC to CO2 at BDD with current efficiencies higher than 40%.

ElectrolysisMaterials scienceSynthetic diamondGeneral Chemical EngineeringInorganic chemistryelectrochemial incinerationSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistrydichloroethanelaw.inventionAnodeDichloroethanelawElectrodeElectrochemistryBulk electrolysisCyclic voltammetryElectrochimica Acta
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