Search results for " electrolyte"

showing 10 items of 106 documents

Electrochemical dating of archaeological gold based on refined peak current determinations and Tafel analysis

2020

Abstract This report proposes a refined method to date archaeological gold samples based on the Tafel analysis of the ascending part of voltammetric curves corresponding to the oxidation of surface flakes of gold in contact with hydrochloric acid aqueous electrolyte. This allows estimating the equilibrium potential of gold oxidation correcting for irreversibility effects. This equilibrium potential can be correlated with the coverage of adsorbed oxygen species and hence the estimated age of the gold samples. A satisfactory potential/time calibration graph was constructed from a set of archaeological samples including two sets of samples from the Mapungubwe Gold Collection, South Africa (120…

Tafel equationCalibration curveGeneral Chemical EngineeringPeak current02 engineering and technologyAqueous electrolyte010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesArchaeology0104 chemical sciencesElectrochemistryEquilibrium potential0210 nano-technologyGeologyElectrochimica Acta
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Template-assisted electrodeposition of cerium oxy-hydroxide nanostructures in aqueous and organic electrolytes

2008

Template-assisted electrodeposition cerium oxy-hydroxide nanostructures aqueous and organic electrolytes
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Effect of ammonium hydroxide addition in the anodizing electrolyte on the electronic properties of anodic oxides on Niobium

2010

ammonium hydroxide addition in the anodizing electrolyte electronic properties anodic oxides Niobium
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Bi2Se3 Nanostructured Thin Films as Perspective Anodes for Aqueous Rechargeable Lithium-Ion Batteries

2022

This research was funded by the European Regional Development Fund Project (ERDF) No. 1.1.1.1/19/A/139. Y.R. acknowledges the support of post-doctoral ERDF project No. 1.1.1.2/VIAA/4/20/694. V.L. also acknowledges the support of “Strengthening of the capacity of doctoral studies at the University of Latvia within the framework of the new doctoral model”, identification No. 8.2.2.0/20/I/006. A.S. acknowledges the support from the Institute of Solid State Physics, University of Latvia, which, as the Center of Excellence, has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2.

anodeaqueous rechargeable lithium-ion batteries (ARLIBs)bismuth oxide (Bi2O3)bismuth selenide (Bi<sub>2</sub>Se<sub>3</sub>); anode; aqueous rechargeable lithium-ion batteries (ARLIBs); solid electrolyte interphase (SEI); bismuth oxide (Bi<sub>2</sub>O<sub>3</sub>); electrochemical performanceElectrochemistryelectrochemical performanceEnergy Engineering and Power Technology:NATURAL SCIENCES::Physics [Research Subject Categories]Electrical and Electronic Engineeringsolid electrolyte interphase (SEI)bismuth selenide (Bi2Se3)
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Electrochemical and Spectroelectrochemical Properties of Free-Base Pyridyl- and N -Alkyl-4-Pyridylporphyrins in Nonaqueous Media

2015

International audience; Twelve structurally related pyridyl and meso-N-methylpyridylporphyrin derivatives are investigated electrochemically in different nonaqueous media. The UV/Vis spectrum of each newly investigated porphyrin was measured before and after electro-reduction and, based on this data, the site of electron transfer is proposed. An interaction occurs between the meso-pyridyl or meso-N-alkyl-4-pyridyl substituents and the porphyrin p-ring system, the magnitude of which depends upon the number of linked pyridyl or N-alkyl-4-pyridyl groups in the compound, the solvent, the supporting electrolyte, and/or other anions added to the solution.

bindingSupporting electrolyteInorganic chemistrycationic porphyrinreductiondnanElectrochemistryporphyrinsdimethylformamide[ CHIM ] Chemical SciencesCatalysischemistry.chemical_compoundElectron transferPolymer chemistry[CHIM]Chemical SciencesAlkylchemistry.chemical_classificationnonaqueous mediacomplex-formationChemistryn-dimethylformamidespectral characterizationaggregationFree basespectroelectrochemistryPorphyrinSolventinteracting centerspotentialselectrochemistry
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Electrochemical ecology: VIMP monitoring of plant defense against external stressors

2015

The use of the voltammetry of immobilized particles (VIMP) approach, by means of the voltammetric response of microparticulate films from ethanolic leaf extracts in contact with aqueous electrolytes and direct contact probe leaf voltammetry, to monitor the defense of plants against external stressors is described. This approach is applied to study the chemical communication between plants of Peperomia obtusifolia A. Dietr. submitted to herbivory by the beetle Monoplatus sp.

biologyChemistryGeneral Chemical EngineeringEcology (disciplines)General ChemistryAqueous electrolyteMonoplatusElectrochemistrybiology.organism_classificationChemical communicationVOLTAMETRIAEnvironmental chemistryPlant defense against herbivoryPeperomia obtusifoliaVoltammetryRSC Advances
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Die aufschlußfreie Bestimmung von Schwermetallen (Zn, Cd, Pb, Cu) in Getränken (Wein) durch inverse Voltammetrie in einer Durchflußzelle

1987

Digestion-free determination of trace-metals (Zn, Cd, Pb, Cu) in beverages by inverse voltammetry in a flow-through cell equipped with a mercury film-electrode is described. Optimal enrichment potentials are obtained by inspection of the pseudopolarograms of the elements in the original diluted sample solution. After the deposition step in the untreated sample solution stripping is effected in a proper supporting electrolyte after medium exchange. Values obtained by this techniques with various samples compare well with those obtained by usual procedures including wet digestion of the samples.

chemistrySupporting electrolyteWet digestionClinical BiochemistryAnalytical chemistrychemistry.chemical_elementGeneral Materials ScienceGeneral MedicineVoltammetryAnalytical ChemistryMercury (element)Fresenius' Zeitschrift für analytische Chemie
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Synthesis of cyanoacetic acid by carbon dioxide and electrogenerated acetonitrile anion in undivided cells equipped with sacrificial anodes

2008

The electrochemical synthesis of cyanoacetic acid was performed by cathodic reduction of tetraalkylammonium salts (R4NX) in acetonitrile in undivided cells equipped with sacrificial anodes with concomitant or subsequent addition of carbon dioxide. These syntheses avoid the use of dangerous reagents, yield cyanoacetic acid in moderate faradic yields and confirm that the cathodic reduction of tetraalkylammonium salts in the presence of acetonitrile leads to the formation of the anion CNCH2-.

chemistry.chemical_classificationCHLOROACETONITRILE electrocarboxylationNitrileSupporting electrolyteGalvanic anodecathodic reduction of alkyl ammonium saltsGeneral Chemical EngineeringCarboxylic acidInorganic chemistrycarbon dioxideSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryAnalytical Chemistrychemistry.chemical_compoundsupporting electrolyteSettore ING-IND/22 - Scienza E Tecnologia Dei Materialialkyl ammonium saltCyanoacetic acidchemistryReagentElectrochemistrycyanoacetic acidAcetonitrilesacrificial anodeJournal of Electroanalytical Chemistry
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Electrochemical technology for the treatment of real washing machine effluent at pre-pilot plant scale by using active and non-active anodes

2018

Abstract Real effluent of washing machine is one of the major sources of microplastics and fabrics in municipal and surface water. The effluents constitute large volume of wastewater with different surfactants since every household and industries nowadays use washing machine rather than traditional hand washing. In this work, a real effluent of washing machine was treated by electrooxidation (EO) in a pre-pilot plant scale electrochemical flow reactor using active (Ti/Pt) or non-active (boron doped diamond (BDD)) anodes and Ti cathode. The effect of anode material (Ti/Pt or BDD) and the applied current density (16.6, 33.3 and 66.6 mA cm−2) on the decay of the organic matter, in terms of che…

chemistry.chemical_classificationChemistrySupporting electrolyteGeneral Chemical EngineeringChemical oxygen demand02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyPulp and paper industry01 natural sciencesCathodeAnalytical ChemistryAnodelaw.inventionPilot plantWastewaterlawElectrochemistryOrganic matter0210 nano-technologyEffluent0105 earth and related environmental sciencesJournal of Electroanalytical Chemistry
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Electrochemical synthesis of sulfamides.

2021

Herein we demonstrate the first electrochemical synthesis protocol of symmetrical sulfamides directly from anilines and SO2 mediated by iodide. Sulfamides are an emerging functional group in drug design. Highlights are the direct use of SO2 from a stock solution and no necessity of any supporting electrolyte. Overall, the reaction has been demonstrated for 15 examples with yields up to 93%.

chemistry.chemical_classificationChemistrySupporting electrolyteIodideMetals and AlloysGeneral ChemistryElectrochemistrycomplex mixturesCombinatorial chemistryCatalysisrespiratory tract diseasesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundFunctional groupMaterials ChemistryCeramics and CompositesStock solutionChemical communications (Cambridge, England)
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