Search results for "Applied potential"

showing 6 items of 6 documents

Passive and transpassive behaviour of Alloy 31 in a heavy brine LiBr solution

2013

The passive and transpassive behaviour of Alloy 31, a highly alloyed austenitic stainless steel (UNS N08031), has been investigated in a LiBr heavy brine solution (400 g/l) at 25 °C using potentiostatic polarisation combined with electrochemical impedance spectroscopy and Mott–Schottky analysis. The passive film formed on Alloy 31 has been found to be p-type and/or n-type in electronic character, depending on the film formation potential. The thickness of the film formed at potentials within the passive region increases linearly with applied potential. The film formed at transpassive potentials is thinner and more conductive than the film formed within the passive region. These observations…

EISMaterials scienceGeneral Chemical EngineeringPassive filmAlloyMetallurgyMott schottkyengineering.materialApplied potentialINGENIERIA QUIMICAStainless steelDielectric spectroscopyElectroquímicaMott–SchottkyBrineElectrochemistryengineeringAcer CorrosióAustenitic stainless steelElectrical conductorTranspassivityElectrochimica Acta
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Calcium binding and ionic conduction in single conical nanopores with polyacid chains: model and experiments.

2012

Calcium binding to fixed charge groups confined over nanoscale regions is relevant to ion equilibrium and transport in the ionic channels of the cell membranes and artificial nanopores. We present an experimental and theoretical description of the dissociation equilibrium and transport in a single conical nanopore functionalized with pH-sensitive carboxylic acid groups and phosphonic acid chains. Different phenomena are simultaneously present in this basic problem of physical and biophysical chemistry: (i) the divalent nature of the phosphonic acid groups fixed to the pore walls and the influence of the pH and calcium on the reversible dissociation equilibrium of these groups; (ii) the asym…

General Physics and AstronomyIonic bondingFunctionalizedDissociation (chemistry)Conical nanoporeNanoscale regionschemistry.chemical_compoundNanoporesI - V curveIonic conductivityGeneral Materials ScienceConical nanoporesPhosphonate groupCalcium concentrationChemistryGeneral EngineeringPH effectsPartition functionsIonic channelsIon equilibriumReversible dissociationChemical physicsFunctional groupsThermodynamicsDesalination membranesIon bindingPorosityDissociationBiophysical chemistryDissociation equilibriaInorganic chemistrychemistry.chemical_elementWater filtrationCalciumIonNernst-Planck equationsApplied potentialsIon bindingCarboxylationPhosphonic acidsComputer SimulationCarboxylateParticle SizeControlled drug releaseCurrent voltage curveIonsBinding SitesFixed charge densityPH sensitiveCarboxylic acidsDesalinationPhosphonic acid groupsPoly acidsElectric ConductivityCarboxylic acid groupsFixed ChargesNanostructuresCell membranesCurrent-voltage curvesModels ChemicalQuantum theoryFISICA APLICADACalciumBiological ion channelsCalcium bindingIonic currentCytologyPore wallStatistical mechanicsAcidsACS nano
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Metallic Nanoparticles Linked to Molecular Switches as Signal Processing Devices

2009

We explore theoretically the use of nanoscale switches whose conductance can be varied between two states by an external stimulus to implement signal processing devices. The building block is formed by a metallic nanoparticle linked to two electrodes by an organic ligand and a molecular switch. The system implementation exploits the sharp current resonance of the system that occurs when the frequencies of the applied potential and the induced variation on the switch conductance coincide.

Molecular switchSignal processingMaterials sciencebusiness.industryBiomedical EngineeringConductanceNanoparticleBioengineeringGeneral ChemistryApplied potentialCondensed Matter PhysicsElectrodeOptoelectronicsGeneral Materials SciencebusinessMetal nanoparticlesNanoscopic scaleJournal of Nanoscience and Nanotechnology
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Iron oxide nanostructures for photoelectrochemical applications: Effect of applied potential during Fe anodization

2019

[EN] In photoelectrochemistry, a suitable photoanode leading to high efficiencies in photocatalytic processes is a research challenge. Iron oxide nanostructures are promising materials to be used as photoanodes. In this work, different potentials during iron anodization were applied to study the properties of the synthesized nanostructures. Results revealed that nanostructures anodized at 50V presented well-defined nanotubular structures with open-tube tops, and they achieved values of photocurrent density of 0.11 mA cm(-2) at 0 rpm and 0.14 mA cm(-2) at 1000 rpm (measured at 0.50 V-Ag/Agcl), corresponding to the oxygen evolution reaction from water, i.e. 2H(2)O+4h(+)-> 4H(+)+O-2, demonstra…

NanostructureMaterials scienceNanostructureGeneral Chemical EngineeringPhotoelectrochemistryIron oxide02 engineering and technologyApplied potential010402 general chemistry01 natural sciencesINGENIERIA QUIMICAPhotoelectrochemistrychemistry.chemical_compoundIron oxidePhotocurrentNanoestructuresAnodizingOxygen evolution021001 nanoscience & nanotechnology0104 chemical sciencesElectroquímicachemistryChemical engineeringPhotocatalysisAnodizationPotential0210 nano-technologyJournal of Industrial and Engineering Chemistry
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The passivation of steel in sodium sulphate solution studied by CEMS and aes

1990

The passive layer formed on standard steel by anodic oxidation in 0.5 M sodium sulphate solution was found to contain iron only in the trivalent state. The thickness of the layer increases with the applied potential as well as with the time the passivating potential is applied to the sample. These results, compared with the electrochemical data, lead to the suggestion that the passive behaviour is not due to the whole oxidic layer but due to a thin, low lying interfacial layer with a structural disorder.

Nuclear and High Energy PhysicsMaterials sciencePassivationAnodic oxidationSodiumInorganic chemistrychemistry.chemical_elementApplied potentialCondensed Matter PhysicsElectrochemistryAtomic and Molecular Physics and OpticschemistryPhysical and Theoretical ChemistryLayer (electronics)Hyperfine Interactions
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A photoelectrochemical characterization of passive films on stainless steels

1986

Abstract Passive films on stainless steels for sea water service have been studied by means of photocurrent measurements. Four experimental ELI (Extra Low Interstitital) ferritic stainless steels (types 25Cr-4Ni-4Mo) and a commercial superaustenitic stainless steel (type 20Cr-18Ni-6Mo-N) have been investigated. Differences in the photoelectrochemical behaviour have been attributed to the different nature of the passive films grown on ferritic or superaustenitic stainless steels. An interpretation is provided to explain the complex dependence of the photocurrent transients on the applied potential. Manuscript received 27 February 1986; in amended form 19 June 1986.

PhotocurrentMaterials scienceGeneral Chemical EngineeringMetallurgyGeneral Materials ScienceGeneral ChemistryApplied potentialCharacterization (materials science)CorrosionCorrosion Science
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