Search results for "Passivation"

showing 10 items of 91 documents

Comparison of the effect of non-polluted and underwater-volcano-polluted seawater on the corrosion resistance of different stainless steels

2015

This work compares the effect of non‐polluted and underwater‐volcano‐polluted seawater on the electrochemical behavior of two different alloys, notably an austenitic stainless steel (SS) and a duplex stainless steel. Polarization measurements, potentiostatic passivation tests, electrochemical impedance spectroscopy and capacitance measurements were performed. Results show that the composition of the polluted seawater negatively affects the passivation kinetics of both AISI 316 SS and Alloy 900, decreasing the corrosion resistance of both alloys. Additionally, when both steels are compared, it can be concluded that passive films formed on Alloy 900 presented better protective properties than…

PASSIVE FILMSAEOLIAN ISLANDSDIFFERENT TEMPERATURESFERRITIC-STAINLESSOXIDE-FILMSINGENIERIA QUIMICAElectroquímicaELECTRONIC-STRUCTUREREPASSIVATION KINETICSCHLORIDE SOLUTIONSELECTROCHEMICAL-IMPEDANCE SPECTROSCOPYAcer CorrosióALLOYING ELEMENTS
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Growth of passive layers on nickel during their voltammetric anodic dissolution in a weakly acid medium

2006

Abstract Quartz crystal microbalance in combination with voltammetry has been used for studying the electrochemical oxidation behaviour of a nickel deposit in a weakly acid medium. The instantaneous mass/charge ratio (Fdm/dQ) analysis allows to obtain the fraction of charge consumed in the passivation process, and, that way, the experimental kinetic equation of the passive layer growth. This experimental law has been fitted to the theoretical equation derived from the point defect model theory under voltammetric conditions.

PassivationChemistryGeneral Chemical EngineeringInorganic chemistryAnalytical chemistrychemistry.chemical_elementCharge (physics)Quartz crystal microbalanceElectrochemistryNickelElectrochemistryAnodic dissolutionLayer (electronics)VoltammetryElectrochimica Acta
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Characteristic Excitation Wavelength Dependence of Fluorescence Emissions in Carbon "quantum" Dots

2017

Carbon "quantum" dots (CDots), generally defined as small carbon nanoparticles with various surface passivation schemes, have emerged to represent a rapidly advancing and expanding research field. CDots are known for their bright and colorful fluorescence emissions, where the colorfulness is associated with the emissions being excitation wavelength dependent. In this work, CDots with 2,2′-(ethylenedioxy)bis(ethylamine) (EDA) for surface functionalization were studied systematically by using steady-state and time-resolved fluorescence methods. The observed fluorescence quantum yields are strongly excitation wavelength dependent, and the dependence apparently tracks closely the observed absor…

PassivationField (physics)Carbon Nanoparticleschemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesPhysical and Theoretical ChemistryQuantumExcitation wavelengthbusiness.industryElectronic Optical and Magnetic MaterialSettore FIS/01 - Fisica Sperimentale021001 nanoscience & nanotechnologyFluorescence0104 chemical sciencesElectronic Optical and Magnetic MaterialsSurfaces Coatings and FilmsGeneral EnergyEnergy (all)chemistryCarbon quantum dotsOptoelectronicsAtomic physics0210 nano-technologybusinessCarbon
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Surface passivation of gallium selenide by nitrogen implantation

2002

In this paper we report on the characterization of nitrogen-implanted single-crystal GaSe samples. Nitrogen atoms were implanted at 80 keV, with doses ranging from 4 × 10 13 to 10 15 N + ions cm -2 . Next, samples were aged in open air and characterized by small-area XPS, together with an unimplanted clean surface, in order to quantify the effects of the nitrogen implantation. In general, we found that the oxidation was fully prevented in N + -implanted samples.

PassivationGallium selenideInorganic chemistrychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsNitrogenSurfaces Coatings and FilmsIonIon implantationchemistryX-ray photoelectron spectroscopyMaterials ChemistrySurface structureOpen airSurface and Interface Analysis
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Chloride role in the surface of nickel electrode

1998

The chloride ion participation in the dissolution process on nickel electrodes in acid media as well as in the formation of the passive layer and in the pitting corrosion induction were studied. Composite electrodes containing nickel powder dispersed in a polymeric matrix show similar processes to those observed in polycrystalline nickel. Furthermore, phenformine hydrochloride inhibits the dissolution process due to the adsorption of the organic cation on the metal surface, although it does not protect the metal from pitting corrosion. Electrochemical impedance spectroscopy data allowed us to propose a physical model for the role of chloride ion in the dissolution and passivation processes …

PassivationGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementChlorideDielectric spectroscopyCorrosion inhibitorchemistry.chemical_compoundNickelAdsorptionchemistryElectrochemistrymedicinePitting corrosionDissolutionmedicine.drugElectrochimica Acta
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Zerstörungsfreie Phasenanalyse dünner Oberflächenschichten mittels Konversionselektronen

1987

By use of an appropriate gamma radiation, conversion electrons may be produced by Mossbauer effect also in a depth below the sample surface deeper than the free path for inelastic electron scattering. Because the Mossbauer spectrum of the conversion electrons reflects the local phase composition, the recording of all electrons escaping from the surface allows an integral phase analysis of a layer of some 10–100 nm thickness. If only electrons within a narrow range of energy are recorded, a depth selective phase analysis is possible. The applicability of these two techniques of conversion electron spectroscopy is demonstrated by a few examples concerning oxidation and passivation of steel. C…

PassivationMössbauer effectChemistryClinical BiochemistryAnalytical chemistryGeneral MedicineElectronRadiationElectron spectroscopyAnalytical ChemistryMössbauer spectroscopyInelastic electron scatteringGeneral Materials ScienceAtomic physicsLayer (electronics)Fresenius' Zeitschrift für analytische Chemie
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Determination of time dependence of passive layer on nickel from instantaneous mass/charge function F(dm/dQ) in competitive passivation/dissolution c…

2006

Nickel metal deposited on gold electrodes was studied in the passivity range of potentials under potentiostatic conditions and in a weakly acid sulphate medium. Mass and current variations during electrochemical experiments were analysed with the help of the instantaneous mass/charge ratio (Fdm/dQ). This analysis allows to obtain the intensity current component associated to the formation of a passive layer of Ni(OH)2, and, in this way, the experimental thickness growth. These experimental findings have been fitted to a theoretical model based on the point defect model theory for obtaining the time dependence of the thickness of the passive layer during the first stages of growth of the pas…

PassivationPassivityInorganic chemistryAnalytical chemistrychemistry.chemical_elementlcsh:ChemistryMetalNickellcsh:Industrial electrochemistrylcsh:QD1-999chemistryvisual_artElectrodeElectrochemistryvisual_art.visual_art_mediumSurface layerCyclic voltammetryDissolutionlcsh:TP250-261Electrochemistry Communications
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Photocurrent Spectroscopy Applied to the Characterization of Passive Films on Sputter-Deposited Ti-Zr Alloys

2008

Abstract A photoelectrochemical investigation on thin (⩽13 nm) mixed oxides grown on sputter-deposited Ti–Zr alloys of different composition by air exposure and by anodizing (formation voltage, UF = 4 V/SCE) was carried out. The experimental results showed that the optical band gap, E g opt , increases with increasing Zr content in both air formed and anodic films. Such behaviour is in agreement with the theoretical expectation based on the correlation between the band gap values of oxides and the difference of electronegativity of their constituents. The flat band potential of the mixed oxides was found to be almost independent on the Ti/Zr ratio into the film and more anodic with respect …

PhotocurrentMaterials sciencePassivationAnodizingBand gapGeneral Chemical EngineeringOxideAnalytical chemistryGeneral ChemistryElectronegativitychemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicatachemistrySputteringanodic films photocurrent Spectroscopy band gap tuningGeneral Materials ScienceSpectroscopy
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Photoelectrochemical investigation of passive layers formed on Fe in different electrolytic solutions

2004

Abstract The passive films formed on Fe in different electrolytic solutions, spanning almost the overall pH range, and with different growth procedures were investigated systematically by photocurrent spectroscopy. The potentiodynamic growth curves are compared both in aerated and de-aerated electrolytes and a potentiostatic growth procedure is also employed. For high positive formation potentials, similar anodic spectra are recorded in all solutions giving an optical gap very close to that expected for crystalline Fe2O3. The origin of photocurrent spikes is also investigated and the effect of the formation potential upon the measured absorption threshold is discussed taking into account th…

PhotocurrentMaterials sciencePassivationGeneral Chemical EngineeringIronPhotoelectrochemistryPassive filmAnalytical chemistryBiasingGeneral ChemistryElectrolyteAnodePhotoelectrochemistryGeneral Materials ScienceAbsorption (electromagnetic radiation)Spectroscopy
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Study of passive films on stainless steels by photocurrent measurements

1990

Abstract Passive films formed on three different stainless steels have been studied by means of photocurrent spectroscopy. Differences in the photoelectrochemical behaviour have been attributed to the influence of the nickel content of the alloys and to the formation of different oxide phases.

PhotocurrentMaterials sciencePassivationGeneral Chemical EngineeringMetallurgyOxideGeneral ChemistryCorrosionchemistry.chemical_compoundchemistryGeneral Materials ScienceSurface layerSpectroscopyNickel contentCorrosion Science
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