Search results for "Spectroscopy"

showing 10 items of 10293 documents

Photocatalytic oxidation of phenol on TiO2 powders. A Fourier transform infrared study

1994

Abstract In the present paper a detailed investigation of a well known photoreaction, i.e. phenol photodegradation in the presence of TiO2, has been carried out. The Fourier transform infrared (FT-IR) technique has been used to characterize the catalyst surface and to follow the photoprocess by “in situ” measurements in a gas—solid regime, simulating the aqueous liquid—solid regime in which this photodegradation reaction has been usually carried out. The influence on the photoprocess of the surface hydroxylation of the catalyst has been investigated and the presence of some reaction intermediates has been revealed by FT-IR. The experimental results have demonstrated that the chosen gas—soli…

Aqueous solutionAdsorptionChemistryProcess Chemistry and TechnologyPhotocatalysisInfrared spectroscopyReaction intermediateFourier transform infrared spectroscopyPhotodegradationPhotochemistryCatalysisGeneral Environmental ScienceCatalysisApplied Catalysis B: Environmental
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Interaction between nitroxyl radicals and CdTe quantum dots: Determination of fluorescence-quenching mechanisms in aqueous solution

2019

Abstract The present work characterizes the optical properties of CdTe quantum dots (CdTe QDs) after interaction with nitroxyl radicals based on steady-state and time-resolved fluorescence spectroscopy studies. QDs of different sizes were exposed to 2 different nitroxyl radicals, i.e., TEMPO and 4-amino-TEMPO radicals. A clear dependence of dynamic and static Stern-Volmer constants values, KD and KS, respectively, was observed as a function of the size of QDs used, with a change from a mostly static mechanism (for smaller QD sizes) to a dynamic mechanism predominating as the nanoparticles increase in size. All observed effects are dependent on both the concentration of the radical and the s…

Aqueous solutionAqueous mediumChemistryGeneral Chemical EngineeringRadicalGeneral Physics and AstronomyNanoparticle02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesCadmium telluride photovoltaicsFluorescence spectroscopy0104 chemical sciencesNitroxyl radicalsQuantum dot0210 nano-technologyJournal of Photochemistry and Photobiology A: Chemistry
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Conversion electron Mössbauer study of low carbon steel polarized in aqueous sulfate and sulfite containing sulfate solutions

1993

Abstract The passivation of low carbon steel was studied in aqueous solutions of 0.5 M Na 2 SO 4 (pH = 3.5 and 6.5) and of 0.5 M Na 2 SO 4 + 0.001 M NaHSO 3 (pH 3.5 and 6.5). The used conversion electron Mossbauer spectroscopy (CEMS) with the complementary electrochemical, microscopic and spectrophotometric investigations proved that the presence of sulfite ion induces pitting corrosion. The compositions and thichnesses of the passive films formed during the electrochemical treatments are determined from the conversion electron Mossbauer spectra. γ-FeOOH was found in each case as a major component. At pH = 3.5, the sextet belonging to Fe 3 C appears in the spectra in most cases, and also Fe…

Aqueous solutionCarbon steelGeneral Chemical EngineeringInorganic chemistryengineering.materialElectrochemistrychemistry.chemical_compoundSulfitechemistryConversion electron mössbauer spectroscopyMössbauer spectroscopyElectrochemistryengineeringPitting corrosionSulfateElectrochimica Acta
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Facile synthesis and characterization of functionalized, monocrystalline rutile TiO2 nanorods.

2006

Functionalized, monocrystalline rutile TiO2 nanorods were prepared from TiCl4 in aqueous solution under acidic conditions in the presence of dopamine, followed by aging and hydrothermal treatment at 150 degrees C. The surface-bound organic ligand controls the morphology as well as the crystallinity and the phase selection of TiO2. The presence of monocrystalline rutile TiO2 was confirmed by X-ray powder diffraction and HRTEM investigations. The as-prepared nanorods are soluble in water at pH3. The surface functionalization was analyzed by IR and 1H NMR, confirming the presence of dopamine on the surface. The surface amine groups can be tailored further with functional molecules such as dyes…

Aqueous solutionChemistryAnalytical chemistrySurfaces and InterfacesCondensed Matter PhysicsMonocrystalline siliconCrystallinityChemical engineeringRutileTransmission electron microscopyElectrochemistrySurface modificationGeneral Materials ScienceNanorodHigh-resolution transmission electron microscopySpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Partitioning of macrocyclic compounds in a cationic and an anionic micellar solution: a small-angle neutron scattering study.

2004

Following a previous investigation on partitioning of some macrocycle compounds in sodium dodecyl sulfate (SDS) and dodecyltrimethylammonium bromide (DTAB) aqueous solutions and their effect on the micellar structure, a small-angle neutron scattering (SANS) study has been performed at fixed surfactant content (0.20 mol/L) and varying macrocycle concentrations from 0.20 up to 1.0 mol/L. Conductivity measurements have been also performed in order to evaluate the effect of the presence of macrocycles on the critical micellar concentration (cmc) of the two surfactants. SANS experimental data were fitted successfully by means of a core-plus-shell monodisperse prolate ellipsoid model. It has been…

Aqueous solutionChemistryCationic polymerizationSurfactants Macrocycles SANSSurfaces and InterfacesNeutron scatteringCondensed Matter PhysicsMicelleSmall-angle neutron scatteringCrystallographychemistry.chemical_compoundPulmonary surfactantCritical micelle concentrationElectrochemistryPhysical chemistryGeneral Materials ScienceSodium dodecyl sulfateSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Polyamine Linear Chains Bearing Two Identical Terminal Aromatic Units. Evidence for a Photo Induced Bending Movement

2001

Abstract Several chemosensors bearing a fluorescent unit at both ends of a linear polyamine chain were synthesised. The protonation as well as the association constants with Cu2+ and Zn2+ were determined by potentiometry in 0.15 mol dm−3 NaCl at 298.1 K. In the case of 1,16-bis(1-naphthylmethyl)-1,4,7,10,13,16-hexaazadecane hexahydrochloride (L1), formation of an excimer emission in aqueous acidic solutions was observed. The system was characterized by steady state fluorescence emission and by time resolved fluorescence. In the ground state the molecule is expected to adopt a more or less linear conformation, while in the excited state a bending movement of the chain must occur in order to …

Aqueous solutionChemistryExcited stateMoleculeProtonationGeneral ChemistryTime-resolved spectroscopyExcimerPhotochemistryGround stateFluorescenceSupramolecular Chemistry
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Analysis of an impedance function of zinc anodic dissolution

2004

Zinc anodic dissolution has been studied by means of electrochemical impedance spectroscopy (EIS). The kinetic study of the oxidation mechanism has allowed us to propose a theoretical impedance function for this system in deaerated sulphate medium. Relevant information on the faradaic process is provided by analysis of the theoretical impedance function. Kinetic parameters of this system can be calculated from the fitting of experimental data to the faradaic impedance function deduced theoretically. The physical measurements of this function are analysed by means of the dependence of simulated EIS spectra on kinetic parameters.

Aqueous solutionChemistryGeneral Chemical EngineeringFaradaic impedanceAnalytical chemistrychemistry.chemical_elementZincKinetic energyAnalytical ChemistryDielectric spectroscopyReaction rate constantTransition metalElectrochemistryElectrical impedanceJournal of Electroanalytical Chemistry
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Influence of the dissolution of MnS inclusions under free corrosion and potentiostatic conditions on the composition of passive films and the electro…

2006

Abstract The influence of the dissolution of MnS inclusions at the OCP value and 400 mV versus SCE on the chemical composition of passive films and the electrochemical behaviour of resulfurized austenitic stainless steel was studied in 1 M NaClO 4 , pH 3, solution using SIMS, XPS, electrochemical impedance spectroscopy and the electrochemical microcell technique. The electrochemical dissolution (at 400 mV versus SCE) of inclusions occurred uniformly along the interface and this process was almost complete after 25 min immersion. A small amount of sulfur was detected on the matrix that exhibited a wide passive range. By contrast, the dissolution process under free corrosion was not uniform a…

Aqueous solutionChemistryGeneral Chemical EngineeringMetallurgyengineering.materialElectrochemistryCorrosionDielectric spectroscopyAdsorptionX-ray photoelectron spectroscopyChemical engineeringElectrochemistryengineeringAustenitic stainless steelDissolutionElectrochimica Acta
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Synthesis, Characterization, and Catalysis of β3-[(CoIIO4)W11O31(O2)4],10- the First Keggin-Based True Heteropoly Dioxygen (Peroxo) Anion. Spectrosco…

1999

Reactions of hydrogen peroxide with several lacunary polyoxometalates of the 1:11 series, XW11O39m- (X = Co3+, Ga3+, Fe3+, Si4+, and P5+), are reported. Synthetic pathways to new polyoxotungstates incorporating dioxygen moieties (peroxo and/or superoxo) are developed. The key step involves treating lacunary precursors with H2O2 in strongly buffered aqueous solutions. Upon reaction of H2O2 with α-[Co3+W11O39],9- (a) the central tetrahedral Co3+ is reduced to Co2+ and (b) each of the four unshared oxygens surrounding the vacancy are replaced by a peroxide group, yielding salts of the tetraperoxide anion β3-[(Co2+O4)W11O31(O2)4]10- (1). These results are unequivocally established by a combinat…

Aqueous solutionChemistryGeneral ChemistryCrystal structureBiochemistryPeroxideCatalysisCatalysischemistry.chemical_compoundColloid and Surface ChemistryVacancy defectPolymer chemistrySpectroscopyHydrogen peroxideLacunary functionJournal of the American Chemical Society
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A study of dimethyltin(IV)-L-cysteinate in aqueous solution

1988

The in vivo activity of some R2Sn-L-cysteinate complexes (R = Me, Et, n-Bu) against murine P-388 leukaemia has been tested. Only the Et2Sn(IV) complex showed a marginal positive effect. Trigonal bipyramidal tin environments with two carbon (R) atoms and the sulfur atom in the equatorial plane and oxygen (carboxylate) and nitrogen (NH2) in apical positions have been proposed for the solid compexes (R = Me, Et, n-Bu, Ph) on the basis of experimental Mossbauer parameters and infrared (IR) data. Aqueous solutions of the Me2SnL-cysteinate have been studied by IR, 1H NMR and 119Sn Mossbauer spectroscopy (in frozen solution) at different pH values to identify the Me2Sn(IV) species present. At pH >…

Aqueous solutionChemistryInorganic chemistryInfrared spectroscopychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyInorganic ChemistryNMR spectra databaseCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometryDeprotonationCarboxylateTinApplied Organometallic Chemistry
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