Search results for "aqueous solution"

showing 10 items of 1610 documents

The determination of mineral acidity excess in solutions containing Ga(III), Al(III), Bi(III)

2002

Abstract A new procedure is proposed to carry out volumetric determinations of the strong acid content of a solution in the presence of inorganic cations such as Ga 3+ , Al 3+ , Bi 3+ which, showing in aqueous solution an acidic behaviour, introduce non negligible interferences in these determinations. Before the acid–base titration, an equivalent amount of a ligand, such as dihydrogen ethylendiamino tetraacetate is added, in order to strongly complex the cation masking it toward the successive addition of a strong base. Interferences are thus removed, and the volumetric determination of the strong acid excess plus the hydrogen ions set free from the ligand, as a consequence of the complex …

Aqueous solutionMineralHydrogenChemistryLigandInorganic chemistrychemistry.chemical_elementAcid excessIonInorganic ChemistryHydrolysisMaterials ChemistryTitrationPhysical and Theoretical ChemistryPolyhedron
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Crystallization of the CaCO3 mineral in the presence of the protein ovalbumin

2004

Abstract The kinetics of CaCO3 mineralization was studied by SANS in a 0.1 M aqueous CaCl2 solution in the presence of the protein ovalbumin found in chicken eggs. As the scattering from the protein and the mineral was observed within different Q regimes the evolution of the protein and mineral could be followed independently. It is observed that ovalbumin denaturates during the first 3 h and leads to a strong enhancement of mineralization.

Aqueous solutionMineralbiologyChemistryKineticsMineralization (soil science)Condensed Matter PhysicsElectronic Optical and Magnetic Materialslaw.inventionOvalbuminlawbiology.proteinElectrical and Electronic EngineeringCrystallizationBiomineralizationNuclear chemistryPhysica B: Condensed Matter
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Calorimetric study of the solubilization of ethylenediamine, N,N-dimethylaminoethylamine and N,N,N?,N?-tetramethylethylenediamine by reversed AOT mic…

1993

Distribution constants and standard enthalpies of transfer of ethylenediamine (en), N,N-dimethylaminoethylamine (dmen) and N,N,N′,N′-tetramethylethylenediamine (tmen) partitioned between n-heptane and water containing reversed sodium bis(2-ethylhexyl) sulfosuccinate (AOT) micelles as a function of the molar concentration ratio R (R=[water]/[AOT]) were evaluated by a calorimetric method. The results show that en, dmen and tmen molecules, solubilized in the reversed micelles, are distributed between the micellar aqueous core and the micellar palisade layer. An analysis of the thermodynamic parameters of the partition process demonstrates the peculiar solvent properties of the water containing…

Aqueous solutionMolar concentrationBiophysicsEthylenediamineTetramethylethylenediamineBiochemistryMicelleMedicinal chemistrySolventPartition coefficientchemistry.chemical_compoundchemistryDiamineOrganic chemistryPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Membranes Directly Prepared from Solutions of Unsubstituted Cellulose

2005

Summary: Starting from 5 wt.-% solutions of a prehydrolysis kraft pulp ( = 135 kg · mol−1) in the mixed solvent (dimethylacetamide + 7 wt.-% LiCl) we have prepared cellulose membranes on different supports according to the phase inversion process using above all acetone (AC) and 2-propanol as precipitants. In this context we have studied the phase behavior of the quasiternary system (DMAc+LiCl)/AC/cellulose. The obtained membranes are mechanically stable and in their mechanical and separation properties on the whole comparable to membranes consisting of regenerated cellulose. With respect to gas separation the ideal selectivity of CO2 in combination with N2 and O2 turns out to be opposite f…

Aqueous solutionMolar massPolymers and PlasticsChemistryOrganic ChemistryRegenerated celluloseCondensed Matter Physicschemistry.chemical_compoundMembranePolymer chemistryMaterials ChemistrySemipermeable membraneGas separationPhysical and Theoretical ChemistryPhase inversion (chemistry)CelluloseMacromolecular Chemistry and Physics
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Microheterogeneous electrocatalytic chiral recognition at monoclinic vanadium-doped zirconias: enantioselective detection of glucose.

2007

Synthetic tetragonal and monoclinic vanadium-doped zirconias (t- and m-VxZr1-xO2, 0.005x0.150) exert an effective catalytic effect toward the electrochemical oxidation of glucose in aqueous alkaline media. The catalytic effect of monoclinic specimens attached to carbon and fluorine-doped tin oxide electrodes exhibits a remarkable enantioselectivity, so that catalytic currents for the oxidation of L-glucose at +0.92 V vs AgCl/Ag are considerably larger than those obtained for the oxidation of D-glucose. This enantioselectivity can be associated with the existence of a noncentrosymmetric coordination of vanadium centers in the monoclinic crystalline form of zirconia. From the electrochemical …

Aqueous solutionMolecular StructureChemistryInorganic chemistryVanadiumchemistry.chemical_elementElectronsStereoisomerismVanadiumElectrocatalystTin oxideElectrochemistryCatalysisAnalytical ChemistryCatalysisGlucoseMicroscopy Electron TransmissionCalibrationElectrochemistryMicroscopy Electron ScanningCubic zirconiaZirconiumOxidation-ReductionMonoclinic crystal systemAnalytical chemistry
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A simple model for barrier frequencies for enzymatic reactions.

2010

We present a simple model to rationalize the effects of environment on the reaction barrier frequencies derived from free energy profiles. These frequencies are relevant in deviations of a rate constant from its transition state theory value and in determining which environmental dynamics participate in the reaction. In particular, this simple model can be used to understand the changes in the reaction barrier frequencies of an enzymatic catalyzed reaction and the corresponding uncatalyzed process in aqueous solution, a change which has implications for dynamical environmental effects on the enzymatic reaction. Two possible cases are analyzed, in which the polarity (charge separation/locali…

Aqueous solutionMolecular StructureChemistryPolarity (physics)ThermodynamicsInverseAtomic and Molecular Physics and OpticsTransition stateEnzyme catalysisCatalysisEnzymesTransition state theoryReaction rate constantModels ChemicalBiocatalysisPhysical chemistryThermodynamicsPhysical and Theoretical ChemistryNuclear ExperimentChemphyschem : a European journal of chemical physics and physical chemistry
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Selective recognition of fluoride anion in water by a copper(II) center embedded in a hydrophobic cavity

2014

The ability of a water-soluble pentacationic calix[6]arene-based CuII complex to bind anions in water has been explored. Quite remarkably, the complex exhibits strong and selective fluoride binding in the pH range of 6–7. The binding constant at pH 5.9 was evaluated to be 85 000 M−1, which is one of the highest values ever reported for a fluoride probe in water and at this pH. The complex also binds chloride ions, but 1000 times less efficiently. The combination of the calix[6]arene hydrophobic cavity with the CuII complex, presenting its labile site in the endo position, is the reason for the selective recognition process. The single crystal X-ray structure of the organo-soluble parent com…

Aqueous solutionMolecular modelChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryChlorideBinding constantCopperchemistry.chemical_compoundPolymer chemistrymedicineWater clusterSingle crystalFluorideta116medicine.drugChemical Science
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Effect of temperature on the growth of alfa-PbO2 nanostructures

2010

Abstract Ordered arrays of α-PbO 2 nanostructures were grown by galvanostatic anodic deposition into the channels of alumina templates. Electrodepositions were performed in an aqueous solution containing lead acetate and sodium acetate at pH 5.4. Bath temperature and electrodeposition time were varied to check their effect on the growth of nanostructures. It has been found that filling of alumina pores is independent of the time and electrodeposition temperature, whilst height and growth kinetics of nanostructures vary with both parameters. Temperature greatly influences morphology: wires grown at room temperature consisted of clusters of particles, leading to poorly compact structures, whi…

Aqueous solutionNanostructureMaterials scienceLead dioxide Nanostructures Template electrosynthesis Alumina membranes Metal oxideGeneral Chemical EngineeringNanowireLead dioxideNanotechnologyCrystal structureGrain sizechemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicatachemistryChemical engineeringElectrochemistryCrystalliteDeposition (law)
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Entropy of transfer of n-nitroalkanes from n-octane to water at 25�C

1984

Entropy of transfer of nitromethane, nitroethane, 1-nitrobutane, 1-nitropentane, and 1-nitrohexane from n-octane to water at 25°C is calculated using an electrostatic model. The calculations indicate that the electrostatic transfer entropy depends primarily on the dipole moment and the size of the-C−NO2 group, showing a trend which is similar to that previously found for the transfer free energy of the same process.

Aqueous solutionNitromethaneBiophysicsThermodynamicsPhotochemistryBiochemistrychemistry.chemical_compoundDipoleEntropy (classical thermodynamics)chemistryNitroethaneTransfer entropyPhysical and Theoretical ChemistryAliphatic compoundMolecular BiologyOctaneJournal of Solution Chemistry
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Water-Soluble Palladium Nanoparticles: Click Synthesis and Applications as a Recyclable Catalyst in Suzuki Cross-Couplings in Aqueous Media

2010

A new PEG-tagged material, which was prepared by a threefold copper-catalyzed [3+2] cycloaddition (click chemistry), was found to act as an efficient stabilizer for palladium nanoparticles. The newly formed material proved to be active as a recyclable catalyst in Suzuki coupling; the presence of polyether chains allowed for the catalytic runs to be conducted in aqueous media.

Aqueous solutionOrganic ChemistryNanoparticlechemistry.chemical_elementHomogeneous catalysisCycloadditionCatalysisSuzuki reactionchemistryPolymer chemistryClick chemistryOrganic chemistryPhysical and Theoretical ChemistryPalladiumEuropean Journal of Organic Chemistry
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