Search results for "electrochemistry"

showing 10 items of 1918 documents

Electrochemical characterization of cobalt cordierites attached to paraffin-impregnated graphite electrodes

2004

The electrochemistry of α, β and μ cobalt-containing cordierites (Co2Al4Si5O18) attached to paraffin-impregnated graphite electrodes has been studied by linear scan and cyclic voltammetries in HCl+NaCl and NaOH electrolytes. This electrochemistry is compared with that of vitreous cobalt cordierite, cobalt(II) oxide and cobalt spinel aluminate (CoAl2O4), the two last taken as reference materials. Electrochemical processes involve the site-characteristic reduction of Co(II) species to cobalt metal near to −0.5 V vs. SCE and their oxidative dissolution near +0.3 V, accompanied by solid state interconversion between Co(II) and Co(III) at potentials above +0.45 V. Cordierite-modified electrodes …

inorganic chemicalsAluminateInorganic chemistryOxidechemistry.chemical_elementElectrolyteCondensed Matter PhysicsElectrochemistrychemistry.chemical_compoundchemistryElectrodeElectrochemistryGeneral Materials ScienceElectrical and Electronic EngineeringCobaltDissolutionVoltammetryJournal of Solid State Electrochemistry
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Multi-channel receptors based on thiopyrylium functionalised with macrocyclic receptors for the recognition of transition metal cations and anions.

2010

We report herein the synthesis and characterization of a family of ligands containing different cation binding sites covalently connected to a thiopyrylium signalling reporter. The receptors L1–L6 are able to signal the presence of certain metal cations via three different channels; i.e. electrochemically, fluorogenically and chromogenically. An acetonitrile solution of L1–L6 shows a bright blue colour due to a charge-transfer band in the 575–585 nm region. The colour variation in acetonitrile of L1–L6 in the presence of the metal cations Ag+, Cd2+, Cu2+, Fe3+, Hg2+, Ni2+, Pb2+ and Zn2+ has been studied. A selective hypsochromic shift of the blue band was found for the systems L4-Pb2+ and L…

inorganic chemicalsAnionsCation bindingBinding SitesInorganic chemistryElectrochemical TechniquesThiophenesPhotochemistryElectrochemistryRedoxInorganic ChemistryMetalchemistry.chemical_compoundSpectrometry FluorescenceTransition metalchemistryvisual_artCationsvisual_art.visual_art_mediumTransition ElementsQualitative inorganic analysisHypsochromic shiftAcetonitrileDalton transactions (Cambridge, England : 2003)
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The reduction of molecular oxygen by iron porphyrins

2002

Abstract Molecular assemblies have been synthesised to reproduce the structure of the cytochrome c oxidase (C c O) active site and to explore the roles played by its different features. It was discovered that a single iron porphyrin, adsorbed at the surface of a graphite electrode, is a selective catalyst for the four-electron reduction of dioxygen to water, at pH 7. To cite this article: D. Ricard et al., C. R. Chimie 5 (2002) 33–36

inorganic chemicalsCytochromebiology010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryActive sitechemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistryElectrocatalyst01 natural sciencesPorphyrinOxygen[ CHIM ] Chemical Sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistry[CHIM] Chemical Sciencesbiology.proteinCytochrome c oxidase[CHIM]Chemical SciencesGraphite
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Synthesis, Characterization, and Cu(2+) Coordination Studies of a 3-Hydroxy-4-pyridinone Aza Scorpiand Derivative.

2016

The synthesis, acid-base behavior, and Cu(2+) coordination chemistry of a new ligand (L1) consisting of an azamacrocyclic core appended with a lateral chain containing a 3-hydroxy-2-methyl-4(1H)-pyridinone group have been studied by potentiometry, cyclic voltammetry, and NMR and UV-vis spectroscopy. UV-vis and NMR studies showed that phenolate group was protonated at the highest pH values [log K = 9.72(1)]. Potentiometric studies point out the formation of Cu(2+) complexes of 1:2, 2:2, 4:3, 1:1, and 2:1 Cu(2+)/L1 stoichiometries. UV-vis analysis and electrochemical studies evidence the implication of the pyridinone moieties in the metal coordination of the 1:2 Cu(2+)/L1 complexes. L1 shows …

inorganic chemicalsMagnetic Resonance SpectroscopyStereochemistryPyridinesPyridonesPotentiometric titrationProtonationChemistry Techniques Synthetic010402 general chemistry010403 inorganic & nuclear chemistryElectrochemistryCrystallography X-Ray01 natural sciencesMedicinal chemistryAntioxidantsCoordination complexInorganic Chemistrychemistry.chemical_compoundStructure-Activity RelationshipCoordination ComplexesHumansChelationPhysical and Theoretical ChemistryCell ProliferationChelating Agentschemistry.chemical_classificationLigandHydrogen-Ion Concentration0104 chemical scienceschemistryPotentiometrySpectrophotometry UltravioletCyclic voltammetryDerivative (chemistry)CopperHeLa CellsInorganic chemistry
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Investigation of Activities for Pt-M Bimetallic Nanoparticles Catalysts on the Oxygen Reduction Reaction

2015

Bi-metallic Pt3Ni/C and Pt3Co/C electrocatalysts were successfully synthesized by a solvent free chemical vapour deposition method with a narrow particle size distribution. The results showed that the electrochemical surface area was increased by adding the additional Ni or Co to a pure Pt catalyst. Pt3Ni/C catalyst exhibited a significant enhancement of oxygen reduction reaction activity. The catalysts were characterized by EDS, XRD, HRTEM and electrochemical activity was determined using cyclic voltammetry.

inorganic chemicalsMaterials scienceChemical engineeringNanoparticleChemical vapor depositionCyclic voltammetryCondensed Matter PhysicsElectrocatalystHigh-resolution transmission electron microscopyElectrochemistryBimetallic stripElectronic Optical and Magnetic MaterialsCatalysisFerroelectrics
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Determination of the Boron/Lead Ratio in Ceramic Materials Based on Electrochemical Quartz Crystal Microbalance

2004

A method for quantitatively determining the relationship boron/lead in ceramic materials is presented. It is based on the attachment of microsamples of ceramic frits to an electrochemical quartz crystal microbalance (EQCM). After a reductive deposition step in the � 0.25 to � 0.85 V (vs. AgCl/Ag) potential range, well-defined stripping peaks are recorded in 0.10 M NaCl plus 0.10 M mannitol. The deposition of boron and lead from suspensions of solid materials, and its subsequent oxidative dissolution can be monitorized at the EQCM. The quotient between the maximum mass gain and the corresponding charge passed enables for a direct quantitation of the boron/lead molar ratio in ceramic material…

inorganic chemicalsMaterials scienceStripping (chemistry)chemistry.chemical_elementQuartz crystal microbalanceCeramic materialsElectrochemistryAnalytical Chemistrychemistryvisual_artElectrochemistryvisual_art.visual_art_mediumDeposition (phase transition)CeramicBoronVoltammetryDissolutionElectroanalysis
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Studies of the initial oxidation of cobalt in alkaline solutions using scanning electrochemical microscope

1998

Studies of the initial oxidation of cobalt in alkaline solutions using scanning electrochemical microscope

inorganic chemicalsMicroscopechemistryChemical engineeringlawAnalytical chemistrychemistry.chemical_elementGeneral Materials ScienceGeneral ChemistryElectrochemistryCobaltlaw.inventionApplied Physics A: Materials Science & Processing
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An unexpected ring carboxylation in the electrocarboxylation of aromatic ketones

2006

The electrocarboxylation of various aromatic ketones, carried out in N-methyl-2-pyrrolidone (NMP) in a diaphragmless cell equipped with a carbon cathode and an aluminium sacrificial anode, yielded, among the products, the target hydroxy acids, the corresponding alcohols and pinacols and, quite surprisingly, detectable amounts of substituted benzoic acids and cycloexene carboxylic acids. These compounds arise from a never reported before electrocarboxylation on the aromatic ring, respectively, for substitution of an aromatic hydrogen and from an addition reaction. For example, the electrocarboxylation of acetophenone gave rise to the substituted benzoic acids in ortho, para and meta position…

inorganic chemicalschemistry.chemical_classificationAddition reactionKetoneorganic chemicalsGeneral Chemical EngineeringReaction intermediateSettore ING-IND/27 - Chimica Industriale E TecnologicaHydrogen atom abstractionchemistry.chemical_compoundMeta-chemistryCarboxylationElectrochemistryOrganic chemistryElectrocarboxylationRing carboxylationKetonesCarbon dioxideUndivided cellsBenzoic acidAcetophenone
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Monte Carlo Simulations of Parallel Charged Platelets as an Approach to Tactoid Formation in Clay

2013

The free energy of interaction between parallel charged platelets with divalent counterions has been calculated using Monte Carlo simulations to investigate the electrostatic effects on aggregation. The platelets are primarily intended to represent clay particles. With divalent counterions, the free energy for two platelets or two tactoids (clusters of parallel platelets) shows a minimum at a short separation due to the attraction caused by ion-ion correlations. In a salt-free system, the free energy of interaction has a long-range repulsive tail beyond the minimum. The repulsion increases for tactoids with larger aggregation numbers, whereas the depth of the free-energy minimum is graduall…

inorganic chemicalschemistry.chemical_classificationQuantitative Biology::BiomoleculesMonte Carlo method02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesDivalentCondensed Matter::Soft Condensed MatterchemistryChemical physicsComputational chemistryElectrochemistryGeneral Materials SciencePlatelet[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Counterion0210 nano-technologySpectroscopyComputingMilieux_MISCELLANEOUS
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ORR Activity and Stability of Co-N/C Catalysts Based on Silicon Carbide Derived Carbon and the Impact of Loading in Acidic Media

2018

This work was supported by the EU through the European Regional Development Fund under projects TK141 “Advanced materials and high-technology devices for energy recuperation systems” (2014-2020.4.01.15-0011), NAMUR ”Nanomaterials - research and applications” (3.2.0304.12-0397) and by the Estonian institutional research grant No. IUT20-13.

inorganic chemicalschemistry.chemical_element02 engineering and technology010402 general chemistryElectrochemistry01 natural sciences7. Clean energyCatalysisElectron transferchemistry.chemical_compoundX-ray photoelectron spectroscopy:NATURAL SCIENCES:Physics [Research Subject Categories]Materials ChemistryElectrochemistrySilicon carbideheterocyclic compoundsRenewable Energy Sustainability and the EnvironmentChemistryorganic chemicals021001 nanoscience & nanotechnologyCondensed Matter PhysicsNitrogen0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringDegradation (geology)0210 nano-technologyCarbonJournal of The Electrochemical Society
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