Search results for "Solution"

showing 10 items of 5638 documents

Application of the small-angle neutron scattering technique to the study of solubilization mechanisms of organic molecules by micellar systems

1996

Abstract We present the possible contribution of the small-angle neutron scattering (SANS) technique to the molecular interpretation of the solubilization phenomena in simple micellar systems. We show for a few ternary micellar systems, that an appropriate analysis of SANS experimental data can provide information on modifications induced on micellar dimension, shape, number of monomer, and charge and on the partition coefficient of the additive and its localization inside the micellar aggregate. The influence of n -alcohols on the thermodynamics and on the structure of sodium dodecyl sulphate (SDS) aqueous solution has been extensively investigated, so the agreement between the results obt…

Aqueous solutionChemistryOrganic ChemistryInorganic chemistryAqueous two-phase systemNeutron scatteringMicelleSmall-angle neutron scatteringAnalytical ChemistryInorganic ChemistryPartition coefficientChemical physicsPhase (matter)Ternary operationSpectroscopyJournal of Molecular Structure
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Hole Localization and Thermochemistry of Oxidative Dehydrogenation of Aqueous Rutile TiO2(110)

2012

Aqueous solutionChemistryOrganic ChemistryOxidative phosphorylationPhotochemistryCatalysisInorganic ChemistryComputational chemistryRutileThermochemistryDensity functional theoryDehydrogenationPhysical and Theoretical ChemistryProton-coupled electron transferChemCatChem
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The photochemical rearrangement of polymeric N-(1-pyridinio) amidates. A novel, aqueous photoresist system

1988

Aqueous solutionChemistryPolymer chemistryRadical polymerizationGeneral EngineeringGeneral Materials ScienceChromophorePhotoresistPhotochemistryJournal of Polymer Science: Polymer Letters Edition
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A novel thermodynamic approach for the complexation study of toxic metal cations by a landfill leachate

2018

Landfill leachates can contaminate nearby aquifers. The hazards deriving from this contamination also depend on the chemical speciation of various contaminants. A novel approach is proposed here to face this problem from a chemical thermodynamics point of view. The complexing ability of the soluble fraction of a landfill leachate (collected from Bellolampo, Palermo, Italy) towards Pb2+, Cd2+ and Cu2+ has been investigated at T = 298.15 K in NaClaq at I = 0.1 mol dm−3. The soluble fraction of the landfill leachate was first characterized by different analytical techniques. Then, its acid–base properties were studied by ISE-H+ potentiometric titrations and modelled by the so-called diprotic-l…

Aqueous solutionChemistryPotentiometric titrationInorganic chemistry02 engineering and technologyGeneral Chemistry010501 environmental sciences021001 nanoscience & nanotechnology01 natural sciencesCatalysisMetalAnodic stripping voltammetryLandfill leachate sequestering ability complexation toxic metalsChemical thermodynamicsSequestrantvisual_artMaterials Chemistryvisual_art.visual_art_mediumTitrationSettore CHIM/01 - Chimica AnaliticaLeachate0210 nano-technology0105 earth and related environmental sciences
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INTERACTIONS OF ORGANOTIN(IV) HALIDES WITH REDUCED GLUTATHIONE IN AQUEOUS-SOLUTION

1993

Abstract Glutathione (GSH) is a compound extremely common among many living organisms in which it plays a fundamental role in the processes of detoxification. Also, organotin(IV) derivatives are more and more commonly used in technological processes or as antitumor drugs. So it seemed interesting to investigate the possible interactions between GSH and organotin compounds in water. Particularly, it has been studied because of its role in the organic radicals linked to the tin center on the stoichiometry and the structure of the adducts. Information was obtained following the reaction between Me n SnCl 4-n (n = 1 to 3) and GSH by Mossbauer and NMR spectroscopies on the assumption that change…

Aqueous solutionChemistryRadicalInorganic chemistrychemistry.chemical_elementQuadrupole splittingBiochemistryMedicinal chemistryInorganic ChemistryTrigonal bipyramidal molecular geometryMössbauer spectroscopyProton NMRTinCoordination geometry
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Determination of organic fluorine in aqueous samples with neutron activation analysis in comparison with the DIN method

1996

Neutron activation analysis (NAA) has been used as detection technique for adsorbable organic fluorine in aqueous samples. The results have been compared with the standardized DIN method which uses a fluoride-ion-selective electrode (ISE).

Aqueous solutionChemistryRadiochemistryElectrodeFluorinechemistry.chemical_elementNeutron activation analysisBiochemistryAnalytical ChemistryNeutron activationAnalytical and Bioanalytical Chemistry
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Rheological study and thermodynamic analysis of the binary system (water/ethanol): Influence of concentration

2004

Water is the most widely used solvent in the chemical and pharmaceutical industry, since it is the most physiological and best tolerated excipient. However, in some cases water cannot be used as a solvent because the active substance or solute is insoluble or only slightly soluble in water. For this and other reasons, nonwater solvents may be used possessing the common characteristic of being soluble or mixable in water; as a result, such solvents can be used to prepare binary or tertiary mixtures, etc., with different purposes such as increasing water solubility, or modifying the viscosity or absorption of the dissolved substance, for example. Ethanol, along with other alcohols either alon…

Aqueous solutionChemistrySolvationExcipientCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsSolventViscosityMaterials ChemistrymedicineOrganic chemistryBinary systemPhysical and Theoretical ChemistryAbsorption (chemistry)Volume contractionmedicine.drugPhysics and Chemistry of Liquids
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Prospects of Ion Chemical Reactions with Heavy Elements in the Gas Phase

2001

Heavy element chemistry is related to the fundamental interest that lies in exploring the upper limits of the periodic table. Chemical properties of the heaviest elements have already been studied at single atoms in aqueous solutions and in the gas phase up to an atomic number Z = 107. These techniques allow to study nuclides with half lives as short as about 1 s. Next generation chemistry experiments could be envisaged with an ion trap technique already developed for stable isotopes. At very low production rates in the order of 1 per 100 s and/or half lives as short as about 10 ms, the ion-molecule reactions can be studied in a buffer gas cell, in which the heavy elements are stopped and t…

Aqueous solutionChemistryStable isotope ratioBuffer gasNuclideAtomic numberIon trapAtomic physicsChemical reactionIon
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Enthalpic and entropic contributions of water molecules to the functional T → R transition of human hemoglobin in solution

1992

Generalized solvent-mediated forces contribute to free energy at the functional T → R transition of human hemoglobin A (HbA). Their contribution is here sorted out quantitatively in both its enthalpic and entropic parts, along with the average number of water molecules involved. The latter (about 75 waters in average) must be considered together with HbA as one statistically defined functional unit for oxygen transport. Their configurations are expected to undergo frequent structural rearrangements. Lifetimes of statistically relevant configurations do not need to (although, of course, they may) exceed by more than a factor 5 the normal H-bond lifetimes of the pure solvent. Compared to the …

Aqueous solutionChemistryStereochemistryEnthalpyOxygen transportThermodynamicsCondensed Matter PhysicsAtomic and Molecular Physics and OpticsGeneralized forcesPhase spaceMoleculePhysical and Theoretical ChemistrySolvent effectsCurse of dimensionalityInternational Journal of Quantum Chemistry
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Enhanced ion transfer rate due to the presence of zwitterionic phospholipid monolayers at the ITIES

2000

Abstract The transfer of cations across phospholipid monolayers at ITIES is studied both experimentally and theoretically. Further evidence of the enhanced rate for cation transfer due to the presence of the monolayer is presented, and a theoretical model that can explain these observations is worked out. The system considered experimentally is Li + ion transfer across a hemispherical water ∣ 1,2-dichloroethane interface covered by distearoyl phosphatidylcholine. The theoretical description is based on the electrical double layer correction to the Butler–Volmer equation, coupled with a solution of the Poisson–Boltzmann equation across the interfacial region. The phospholipid monolayer is mo…

Aqueous solutionChemistryStereochemistryGeneral Chemical EngineeringAqueous two-phase systemPhospholipidCharge (physics)Poisson–Boltzmann equationAnalytical ChemistryCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundChemical physicsPhosphatidylcholineMonolayerElectrochemistryITIESPhysics::Chemical PhysicsJournal of Electroanalytical Chemistry
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