Search results for " Spectroscopy"

showing 10 items of 6851 documents

Adsorbed CO on group 10 metal fragments: A DFT study

2009

DFT calculations on the helicopter and cartwheel rotations of one CO molecule adsorbed at the bridge site on metal-surface fragments, characterized by two (M(8)) or three (M(14)) metal-atom layers (M = Ni, Pd, Pt) were performed by the B3LYP[LANL2DZ+6-31 g(d,p)] method, to rationalize the adsorption energetics and the steric hindrance characteristics of surface CO molecules. Potential Energy Surfaces were obtained, either fixing the C-O bond-length or allowing it to change. The behavior of the three metals, as obtained from the study of the configurational space characterizing the CO adsorption on the fragments was explained on the basis of the interaction energies involved in the different…

ChemistryGeneral Chemical EngineeringDFT Infrared spectroscopy quantum chemistry metal surfaceInfrared spectroscopyGeneral ChemistryLibrary and Information SciencesQuantum chemistryComputer Science ApplicationsMetalCrystallographyAdsorptionGroup (periodic table)Settore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumMolecule
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Li-ion diffusion in Li_{x}Nb_{9}PO_{25}$

2013

Abstract Wadsley–Roth phase Li x Nb 9 PO 25 has been studied as a potential candidate for anode material of Li-ion batteries. Its crystal structure, which consists of ReO 3 -type blocks of NbO 6 octahedra connected with PO 4 tetrahedra, provides a good stability and performance during Li + insertion/removal. Li-ion chemical diffusion coefficient ( D chem ) in Li x Nb 9 PO 25 was determined by means of potentiostatic intermittent titration technique and electrochemical impedance spectroscopy. Different data treatments (classical Warburg equation or the model of an electrode system with ohmic potential drop and/or slow kinetics of the interfacial Li + ion transfer across the electrode/electro…

ChemistryGeneral Chemical EngineeringDiffusionPhysicsDopingAnalytical chemistryCrystal structureElectrolyteAnodeDielectric spectroscopyIonChemistryElectrodeElectrochemistryElectrochimica acta
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Photocatalytic degradation of 4-Nitrophenol by g-C3N4-MCy: Mechanism study and kinetic modeling

2021

Abstract A graphitic carbon nitride (g-C3N4-MCy) photocatalyst was prepared by thermal condensation of melamine and cyanuric acid with equal proportions. The photocatalyst was characterized by Fourier transform infrared spectroscopy (FTIR), Specific surface area (SSA), X-ray diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM), Transmission electron microscope (TEM), and DRS–UV–Vis spectroscopic methods. We studied the photo-degradation kinetics of 4-nitrophenol using a g-C3N4-MCy. Four parameters were applied including initial concentration of 4-nitrophenol, amount of catalyst, dissolved oxygen content, and photon flux. The reaction rate constant was shown to be correlate…

ChemistryGeneral Chemical EngineeringGraphitic carbon nitrideAnalytical chemistryGeneral Physics and Astronomy02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundReaction rate constantSpecific surface areaPhotocatalysisFourier transform infrared spectroscopy0210 nano-technologyCyanuric acidMelamineJournal of Photochemistry and Photobiology A: Chemistry
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The influence of phosphoric acid on steel and on its corrosion products: a Mössbauer spectroscopic approach

1983

Mossbauer spectroscopy was used to study corroded iron after treatment with phosphoric acid or commercial rust transformers. It was found that treatment produced normal iron phosphates from metallic iron, hematite and FeO, and acid ferric phosphate FeH 3 (POI4I)I2I. 2.5H 2 O from alphaand gamma Fe 2 O 3 and alpha, beta, and gammaFeOOH. When these last are present, phosph oric acid treatment does not produce a protective, inhibiting layer. See also AATA 19-702. -- AATA

ChemistryGeneral Chemical EngineeringInorganic chemistryGeneral ChemistryHematitePhosphateCorrosionMetalchemistry.chemical_compoundvisual_artMössbauer spectroscopyvisual_art.visual_art_mediummedicineFerricGeneral Materials ScienceAcid treatmentPhosphoric acidNuclear chemistrymedicine.drugCorrosion Science
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The anodic and cathodic dissolution of Al and Al–Cu–Mg alloy

2010

Abstract Atomic emission spectroelectrochemistry (AESEC) was used to monitor the release of Al from 99.99% aluminum (1199 alloy) and Al, Mg, and Cu from 2024 Al alloy in 30 g/l NaCl electrolyte as a function of pH. The cathodic dissolution of Al was demonstrated and attributed to an increase in the pH at the interface due to the water reduction reaction. The dissolution of Mg was also observed but was a more complex function of current probably depending on the interfacial pH and the Al dissolution rate. The detachment of copper-rich particles was observed as very rapid spectroscopic emission transients (peak width

ChemistryGeneral Chemical EngineeringMetallurgyAlloyInorganic chemistryAtomic emission spectroscopychemistry.chemical_elementElectrolyteengineering.materialMetalAluminiumvisual_artElectrochemistryengineeringAluminium alloyvisual_art.visual_art_mediumMagnesium alloyDissolutionElectrochimica Acta
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A kinetic interpretation of a negative time constant in impedance equivalent circuits for the dissolution/passive transition

2007

Abstract A theoretical impedance function is proposed for the active/passive transition of nickel in an acid sulphate medium. It is considered that passivating species progressively covers the electrode surface. This approximated model predicts the appearance of negative time constants in the impedance spectra when coverage coefficient θ values for passive species are greater than 0.5.

ChemistryGeneral Chemical EngineeringNegative resistanceElectrodeInorganic chemistryElectrochemistryTime constantEquivalent circuitThermodynamicsKinetic energyElectrical impedanceDissolutionDielectric spectroscopyElectrochimica Acta
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Porous materials as delivery and protective agents for Vitamin A

2016

The suitability of porous materials to immobilize and release under control bioactive molecules prompted us to design and study delivery systems of Vitamin A (VitA). This molecule, relevant in several physiological functions, is easily oxidized. Commercial VitA was immobilized in two different clays, montmorillonite K-10 (MMT) and sepiolite (SEP), and in MCM-41, by impregnation. Characterization of the resulting hybrid materials by XRD, FTIR and 13C and 29Si (MAS) NMR spectroscopies revealed its presence. The photo-stability tests showed decreased degradation of VitA in the clays, compared to MCM-41 and the pure VitA, while thermostability is observed until ∼100 °C. The kinetics of the rele…

ChemistryGeneral Chemical EngineeringSepioliteKinetics020101 civil engineering02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnologyControlled release0201 civil engineeringchemistry.chemical_compoundMontmorilloniteOrganic chemistryDegradation (geology)Fourier transform infrared spectroscopy0210 nano-technologyHybrid materialNuclear chemistryThermostabilityRSC Advances
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The equilibrium structure of trans-glyoxal from experimental rotational constants and calculated vibration–rotation interaction constants

2003

A total of six high-resolution FT-IR spectra for trans-glyoxal-d2, trans-glyoxal-d1 and trans-glyoxal-13C2 were recorded with a resolution ranging from 0.003 to 0.004 cm−1. By means of a simultaneous ground state combination difference analysis for each of these isotopologues using the Watson Hamiltonian in A-reduction and Ir-representation the ground state rotational constants are obtained. An empirical equilibrium structure is determined for trans-glyoxal using these experimental ground state rotational constants and vibration–rotation interaction constants calculated at the CCSD(T)/cc-pVTZ level of theory. The least-squares fit yields the following structural parameters for trans-glyoxal…

ChemistryGeneral Physics and AstronomyInfrared spectroscopyThermodynamicsSpectral linesymbols.namesakeComputational chemistryKinetic isotope effectsymbolsMoleculeIsotopologueRotational spectroscopyPhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Ground statePhys. Chem. Chem. Phys.
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Extended Fourier-transform spectroscopy studies and deperturbation analysis of the spin-orbit coupled A1Σ+ and b3Π states in RbCs.

2014

The article presents a study of the strongly spin-orbit coupled singlet A(1)Σ(+) and triplet b(3)Π states of the RbCs molecule, which provide an efficient optical path to transfer ultracold molecules to their rovibrational ground state. Fourier-transform A(1)Σ(+) - b(3)Π → X(1)Σ(+) and (4)(1)Σ(+) → A(1)Σ(+) - b(3)Π laser-induced fluorescence (LIF) spectra were recorded for the natural mixture of the (85)Rb(133)Cs and (87)Rb(133)Cs isotopologues produced in a heat pipe oven. Overall 8730 rovibronic term values of A(1)Σ(+) and b(3)Π states were determined with an uncertainty of 0.01 cm(-1) in the energy range [9012, 14087] cm(-1), covering rotational quantum numbers J ∈ [6, 324]. An energy-ba…

ChemistryGeneral Physics and AstronomyIsotopologueRotational–vibrational spectroscopySinglet statePhysical and Theoretical ChemistryTriplet stateAtomic physicsGround stateSpectroscopyQuantum numberFourier transform spectroscopyThe Journal of chemical physics
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Theoretical spectroscopic parameters of the alkali monofluorides LiF, NaF and KF

1992

Abstract Multireference configuration interaction and second-order perturbation theory are used to determine accurate spectroscopic parameters for the ground state of the alkali monofluorides from LiF to KF. Systematic saturation of the spdf subspaces of the atomic basis sets for the electron affinity of fluorine and the ionization potential of the metals have been shown to be more efficient than for the approximate dissociation energies in the molecule. the calculated rotational and vibrational constants and transitions for the three systems show excellent agreement with the expeirmental data.

ChemistryGeneral Physics and AstronomyMultireference configuration interactionConfiguration interactionAlkali metalMolecular physicsDiatomic moleculeBond lengthComputational chemistryPhysics::Atomic and Molecular ClustersRotational spectroscopyPhysics::Chemical PhysicsPhysical and Theoretical ChemistryIonization energyGround stateChemical Physics Letters
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