Search results for "element"

showing 10 items of 13601 documents

Study of the interaction between [Cu(bipy)]2+ and oxalate in dimethyl sulfoxide. Crystal structure of [Cu2(bipy)2(H2O)2ox]SO4·[Cu(bipy)ox]

1991

Abstract A study of complex formation between [Cu(bipy)]2+ and ox2− (bipy and ox2− being 2,2′-bipyridyl and the dianion of oxalic acid), has been carried out by potentiometry in dimethyl sulfoxide solution. The constants of the equilibria and are log β110 = 11.165(1) and log β210 = 13.185(5) at 25 °C and 0.1 mol dm−3 tetra-n- butylammonium perchlorate. The high values of these constants are consistent with the symmetrical bidentate and bis-bidentate modes of oxalate in [Cu(bipy)ox] and [Cu2(bipy)2ox]2+ units, respectively, as shown by X-ray diffraction studies. Well-formed single crystals of [Cu2(bipy)2(H2O)2ox]SO4· [Cu(bipy)ox] were grown from aqueous solutions and characterized by X-ray d…

Aqueous solutionDenticityChemistryInorganic chemistrychemistry.chemical_elementCrystal structureCopperOxalateInorganic ChemistryPerchloratechemistry.chemical_compoundCrystallographyMaterials ChemistryMoleculePhysical and Theoretical ChemistryMonoclinic crystal systemInorganica Chimica Acta
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Copper(II)-assisted hydrolysis of 2,4,6-tris(2-pyrimidyl)-1,3,5-triazine (tpymt): syntheses, crystal structures and magnetic properties of [Cu(bpcam)…

2005

Abstract The reaction of the 2,4,6-tris(2-pyrimidyl)-1,3,5-triazine (tpymt) ligand with copper(II) perchlorate or sulfate in aqueous solution affords complexes [Cu(bpcam)(H2O)2]ClO4 · 3H2O (1), [Cu(bpcam)(H2O)2][Cu(bpcam)(H2O)(SO4)] · 2H2O (2) and [Cu2(bpcam)2(H2O)2(SO4)] · H2O (3) [bpcam = bis(2-pyrimidylcarbonyl)amidate], whose structures have been determined by single-crystal X-ray diffraction studies. Copper(II) promotes the hydrolysis of tpymt in mild conditions yielding the bpcam group which is present in the structures of 1–3 as a tridentate ligand. The structure of 1 consists of mononuclear [Cu(bpcam)(H2O)2]+ cations, uncoordinated perchlorate anions and water of crystallization. Th…

Aqueous solutionDenticityCoordination sphereChemistrychemistry.chemical_elementCrystal structureCopperSquare pyramidal molecular geometryInorganic ChemistryMetalPerchloratechemistry.chemical_compoundCrystallographyvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryInorganica Chimica Acta
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Influence of Phase Modifiers on the Degradation of Tri-n-octylamine/dodecane Extracting Mixture by an Acidic Solution of Vanadium (V)

2012

The kinetics of degradation of a mixture of tri-n-octylamine (extractant) and various alcoholic phase modifiers in n-dodecane in contact with acidic aqueous sulfate solutions containing vanadium (V) has been investigated. The nature of the modifier influences the kinetics of degradation and an improvement of the resistance against the chemical degradation is obtained when secondary alcohol (2-nonanol) or tertiary alcohols such as 9-octyl-9-heptadecanol are used as phase modifiers instead of 1-tridecanol. For instance, the kinetic constant of degradation is divided by one half when 9-octyl-9-heptadecanol is used as phase modifier instead of 1-tridecanol. On the contrary, the alcohols contain…

Aqueous solutionDodecaneGeneral Chemical EngineeringKineticsInorganic chemistryVanadiumchemistry.chemical_elementAlcoholGeneral ChemistrySolventchemistry.chemical_compoundchemistryPhase (matter)Chemical decompositionSolvent Extraction and Ion Exchange
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Thermodynamic parameters for the formation of glycine complexes with magnesium(II), calcium(II), lead(II), manganese(II), cobalt(II), nickel(II), zin…

1995

Abstract Protonation constants and Mg 2+ , Ca 2+ , Pb 2+ , Mn 2+ -, Co 2+ , Ni 2+ , Cu 2+ , Zn 2+  and Cd 2+ glycine complex formation constants have been determined in different aqueous media at different temperatures. Salt effects are explained by a complex formation model which takes into account the formation of weak species. From the temperature dependence of the formation constants, thermodynamic parameters ΔH θ (and in some cases ΔC θ p ) have been obtained. A rigorous analysis of literature data, together with experimental findings, allows recommended formation parameters, in the ranges 0 ≤ I e ≤ 1 mol l −1 ( I e is the effective ionic strength) and 5°C ≤ T ≤ 45°C, to be obt…

Aqueous solutionEnthalpyInorganic chemistrychemistry.chemical_elementIonic bondingProtonationManganeseCondensed Matter PhysicsNickelchemistryStability constants of complexesIonic strengthPhysical chemistryPhysical and Theoretical ChemistryInstrumentationThermochimica Acta
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Heat Capacity of Transfer of (Ethylene oxide)13-(propylene oxide)30-(ethylene oxide)13 from Water to the Aqueous Anionic Surfactant Solutions at 298 …

2004

Heat capacities of transfer (ACpt) of unimeric (ethylene oxide)(13)-(propylene oxide)(30)-(ethylene oxide)(13) from water to the aqueous surfactant solutions as functions of the surfactant concentrations (m(S)) were determined at 298 K. The surfactants investigated are sodium hexanoate, sodium heptanoate, sodium octanoate, sodium undecanoate, and sodium dodecanoate. For short alkyl chain surfactants, the profiles of the DeltaCp(t) versus ms curves show maxima and minima; for long alkyl chain surfactants, the maximum becomes sharper and moved to lower ms values whereas the minimum tends to disappear. These experimental trends are different from those of the enthalpy in agreement with the fac…

Aqueous solutionEthylene oxideSodiumInorganic chemistryEnthalpychemistry.chemical_elementThermodynamicsSurfaces and InterfacesCondensed Matter PhysicsHeat capacityGibbs free energysymbols.namesakechemistry.chemical_compoundchemistryPulmonary surfactantElectrochemistrysymbolsGeneral Materials SciencePolyethylene oxides Micelles scattering DLSSpectroscopyEquilibrium constant
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Partial molar volumes of cobalt(II) chloride in ethanol + water at 298.15 K

1996

Densities of ethanol + water + cobalt(II) chloride mixtures have been measured with an oscillating-tube densimeter over a large range of concentrations of salt, at 298.15 K. From these densities, apparent molar volumes of the electrolyte in these mixtures have been calculated, and partial molar volumes at infinite dilution have been evaluated, at different concentrations of alcohol in the solvent.

Aqueous solutionGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementGeneral ChemistryElectrolyteChlorideApparent molar propertyDilutionCobalt(II) chloridechemistry.chemical_compoundMolar volumechemistrymedicineCobaltmedicine.drugNuclear chemistry
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A study of thin surface layers by multilayer Mössbauer spectroscopy /MMS/

1990

A stacking Mossbauer technique, MMS has been applied for studying thin surface layers. The surface layers formed on the57Fe film in aqueous solutions of corrosion inhibitors, such as zinc phosphate and barium metaborate, and in distilled water was studied by this method. It has been found that the corrosion is much slower in the presence of zinc phosphate and barium metaborate. XPS analysis suggests the formation of a mixed iron zinc phosphate on the surface of the57Fe film after corrosion in a zinc phosphate solution.

Aqueous solutionHealth Toxicology and MutagenesisInorganic chemistryPublic Health Environmental and Occupational HealthZinc phosphatechemistry.chemical_elementBariumZincPollutionAnalytical ChemistryCorrosionchemistry.chemical_compoundCorrosion inhibitorNuclear Energy and EngineeringchemistryX-ray photoelectron spectroscopyRadiology Nuclear Medicine and imagingThin filmSpectroscopyJournal of Radioanalytical and Nuclear Chemistry Letters
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Viscous Synergy of Pure Monoalcohol Mixtures in Water and Its Relation to Concentration

2004

Pure or aqueous alcohols are the solvents most widely used in industry, including in the manufacture of pharmaceuticals and cosmetic products. However, water–alcohol mixtures generate hydrogen-bonded molecular associations that lead to volume contraction and an increase in viscosity greater than that expected in the absence of any interaction between the components of the mixture. This phenomenon is referred to as viscous synergy. The present study investigates viscous synergy in monoalcohol systems containing up to five carbon atoms, since beyond hexanol all alcohols are practically insoluble in water. In all cases, determinations were made of the proportions of water and alcohol for which…

Aqueous solutionHydrogen bondBiophysicsSolvationThermodynamicschemistry.chemical_elementAlcoholBiochemistrychemistry.chemical_compoundViscositychemistryOrganic chemistryPhysical and Theoretical ChemistryVolume contractionMolecular BiologyCarbonHexanolJournal of Solution Chemistry
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Quantitative XPS analysis of leached layers on optical glasses

1993

The corrosion of optical glasses often reduces the utility of uncoated glasses as well as the adhesion of resistive coatings deposited onto corroded glasses. Photoelectron spectroscopy (XPS) was applied to study glass surfaces with respect to their surface corrosion. In particular, leaching by the influence of polish slurries, pure water, air and even residual gases inside a vacuum device was studied in detail. Pure quartz glass and different sodium and barium silicate glasses were broken in ultrahigh vacuum (4 × 10−10 mbar) for the determination of sensitivity factors of the different XPS signals. It was found that a quantitative determination of the surface composition of corroded and lea…

Aqueous solutionHydrogenAnalytical chemistryAttenuation lengthchemistry.chemical_elementMineralogyBariumSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCorrosionchemistryX-ray photoelectron spectroscopyMaterials ChemistryLeaching (metallurgy)QuartzSurface and Interface Analysis
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Proton Transfer versus Hydrogen Bonding: The Reduction of Ubiquinone Q2Incorporated in a Self-Assembled Monolayer in Unbuffered Aqueous Solution

2014

The electrochemical reduction of ubiquinone Q2 (UQ2) in unbuffered aqueous media was investigated over a pH range of 2 to 11, and the results were compared to those obtained in our previous work in buffered solutions. The short isoprene chains of UQ2 were incorporated in a self-assembled monolayer. Analysis of the mechanism and a study in D2O solutions allowed us to demonstrate the important role of hydrogen bonding in the stabilization of the reduced species, also in water. If the concentration of H+ is low relative to that of the quinone, the electrochemical reaction does not proceed through proton-coupled electron transfer, as it does in buffered medium or at low pH values (pH<4.4). We p…

Aqueous solutionHydrogenHydrogen bondInorganic chemistrychemistry.chemical_elementPhotochemistryElectrochemistryTautomerCatalysischemistry.chemical_compoundElectron transferchemistryMonolayerElectrochemistryIsopreneChemElectroChem
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