Search results for "aqueous solution"

showing 10 items of 1610 documents

Binding between (Ethylene Oxide)13−(Propylene Oxide)30−(Ethylene Oxide)13 and Sodium Decanoate. Volume, Enthalpy, and Heat Capacity Studies

2002

Volume, enthalpy, and heat capacity of transfer (ΔYt) of (ethylene oxide)13−(propylene oxide)30−(ethylene oxide)13 (L64), at some concentrations, from water to the aqueous sodium decanoate (NaDec) solutions as functions of the surfactant concentration (mS) were determined at 298 K. The copolymer was studied in both the unassociated and associated forms. For a given L64 concentration (mC), the ΔYt vs mS profiles for the volume and the enthalpy are equal but different from that of the heat capacity because the latter contains also the relaxation terms. The experimental data were analyzed by assuming the distribution of L64 between the aqueous and the micellar phases and the shift of micelliza…

Aqueous solutionEthylene oxideInorganic chemistryEnthalpyFlory–Huggins solution theoryMicelleHeat capacityBinding constantSurfaces Coatings and Filmschemistry.chemical_compoundchemistryMaterials ChemistryPropylene oxidePhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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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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Aqueous nonionic copolymer-functionalized laponite clay. A thermodynamic and spectrophotometric study to characterize its behavior toward an organic …

2006

The affinity of functionalized Laponite clay toward an organic material in the aqueous phase was explored. Functionalization was performed by using triblock copolymers based on ethylene oxide (EO) and propylene oxide (PO) units that are EO(11)PO(16)EO(11) (L35) and PO(8)EO(23)PO(8) (10R5). Phenol (PhOH) was chosen as organic compound, which represents a contaminant prototype. To this purpose, densities and enthalpies of mixing as well as PhOH UV-absorption spectra were determined. The enthalpy and the spectrophotometry revealed PhOH-Laponite interactions whereas the volume did not. It emerged that the area occupied by PhOH on the Laponite surface is equal to that computed from the partial m…

Aqueous solutionEthylene oxideSuspensions (fluids)Aqueous two-phase systemPartial molar propertySurfaces and InterfacesCondensed Matter Physicsyield stresschemistry.chemical_compoundAdsorptionchemistryChemical engineeringPolymer chemistryBentoniteElectrochemistryCopolymerSurface modificationGeneral Materials SciencePropylene oxideSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Aqueous block copolymer-surfactant mixtures and their ability in solubilizing chlorinated organic compounds. A thermodynamic and SANS study.

2006

Within the topic of surfactant enhanced solubilization of additives sparingly soluble in water, volumetric, solubility, conductivity, and small-angle neutron scattering (SANS) experiments on mixtures composed of alpha,omega-dichloroalkane, surfactant, copolymer, and water were carried out at 298 K. The triblock copolymers (ethylene oxide)132(propylene oxide)50(ethylene oxide)132 (F108) and (ethylene oxide)76(propylene oxide)29(ethylene oxide)76 (F68) were chosen to investigate the role of the molecular weight keeping constant the hydrophilic/hydrophobic ratio. The selected surfactants are sodium decanoate (NaDec) and decyltrimethylammonium bromide (DeTAB) with comparable hydrophobicity and …

Aqueous solutionEthylene oxidescattering DLSConductivitySurfaces Coatings and Films| Micelleschemistry.chemical_compoundMonomerchemistryPulmonary surfactantChemical engineeringPolymer chemistryMaterials ChemistryCopolymerPropylene oxidePolyethylene oxidePhysical and Theoretical ChemistrySolubilityThe journal of physical chemistry. B
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Interaction of quinine with negatively charged lipid vesicles studied by fluorescence spectroscopy Influence of the pH

1997

Abstract The interaction of quinine with dimyristoylphosphatidic acid (DMPA) and dimyristoylphosphatidyl glycerol (DMPG) small unilamellar vesicles in the gel phase was studied by steady-state fluorescence spectroscopy at pHs 7, 6, 5 and 4 and 20°C. In aqueous solution, with excitation at 335 nm, the emission fluorescence spectrum of quinine varied with pH reflecting the occurrence of different charged species of the drug. In all cases, the emission maximum centered at 383 or 443 nm shifted to lower wavelength in the presence of vesicles. This indicates that the membrane-bound state quinine is in an environment of low polarity. Drug monocationic species were deeply buried in DMPG relative t…

Aqueous solutionFluorophoreChemistryVesicleAnalytical chemistryFluorescenceAtomic and Molecular Physics and OpticsFluorescence spectroscopyAnalytical ChemistryPartition coefficientchemistry.chemical_compoundMembranePhase (matter)InstrumentationSpectroscopySpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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Kinetics of the permanganate oxidation of formic acid in aqueous solution

1987

The kinetics of the permanganate oxidation of formic acid in aqueous perchloric acid at 30°C were examined by the spectrophotometric method. The chemical reaction 2MnO + 3HCOOH + 2H+ 2MnO2 + 3CO2 + 4H2O, appears to proceed via several parallel reactions. The overall rate equation has been obtained by using statistical multilinear regression analysis of the 660 cases studied, and the presence in the rate equation of two new terms in relation to previous studies shows that both permanganate autocatalytic effects and acid media inhibition must be taken into account when the reaction proceeds at constant ionic strength.

Aqueous solutionFormic acidOrganic ChemistryPermanganateInorganic chemistryRate equationBiochemistryChemical reactionInorganic ChemistryAutocatalysischemistry.chemical_compoundchemistryIonic strengthPerchloric acidPhysical and Theoretical ChemistryInternational Journal of Chemical Kinetics
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Reactor model for fast reactions in the micro-bubble column and validation

2007

A simple reactor model for predicting conversions in a micro-bubble column is described. It assumes fast reactions so that the gaseous component is readily consumed at the gas-liquid interface. Then, gas-liquid mass transfer becomes determining. As input parameters for the model, the hydrodynamics, specific interfacial area, and mass transport need to be described. Two fast model reactions, the catalytic oxidation of butyraldehyde and the absorption of CO2 in aqueous NaOH, show the applicability of the model but also its limits. The model was used for predicting reaction performance in dependence of operating conditions, in particular to get maximum conversion with the antagonistic paramete…

Aqueous solutionGeneral Chemical EngineeringAnalytical chemistryThermodynamicsGeneral ChemistryResidence time (fluid dynamics)TolueneIndustrial and Manufacturing EngineeringVolumetric flow ratechemistry.chemical_compoundchemistryCatalytic oxidationMass transferPhysics::Chemical PhysicsAbsorption (electromagnetic radiation)ButyraldehydeIndustrial and Engineering Chemistry Research
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Photocatalytic oxidation of toluene on irradiated TiO2: comparison of degradation performance in humidified air, in water and in water containing a z…

2003

Photocatalytic degradation of toluene was carried out both in gas–solid and in liquid–solid regime by using polycrystalline samples of TiO2 Merck and TiO2 Degussa P25. For the gas–solid regime two types of continuous photoreactor were used, a fixed bed one of cylindrical shape and a Carberry type photoreactor, both irradiated by near-UV light. The inlet reacting mixture consisted of air containing toluene and water vapours. The influence of the gas flow rate and the presence of water vapour on the photocatalytic process was investigated. CO2 and benzaldehyde were the toluene degradation products detected in the gas phase by using TiO2 Merck. In the presence of water vapour this catalyst exh…

Aqueous solutionGeneral Chemical EngineeringGeneral Physics and AstronomyGeneral ChemistryPhotochemistryTolueneReaction rateBenzaldehydechemistry.chemical_compoundchemistryBenzyl alcoholPhotocatalysisPhotodegradationNuclear chemistryBenzoic acidJournal of Photochemistry and Photobiology A: Chemistry
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Characterization of Zirconium Phosphate/Polycation Thin Films Grown by Sequential Adsorption Reactions

1997

Monolayer and multilayer thin films consisting of anionic α-zirconium phosphate (α-ZrP) sheets and polycations (poly(allylamine hydrochloride) (PAH), cytochrome c) were characterized by transmission electron microscopy (TEM), ellipsometry, UV−visible absorbance spectroscopy, reflectance FT-IR, XPS, and X-ray diffraction. Titration and powder X-ray diffraction experiments confirm that exfoliation of α-ZrP begins to occur when enough tetra(n-butylammonium) hydroxide (TBA+OH-) has been added to exceed single-layer packing of TBA+ ions (x ≈ 0.50) in the intercalation compound Zr(HPO4)2-x(TBA+PO4-)x·nH2O. The identical contrast of many sheets in TEM micrographs suggests that the suspension is un…

Aqueous solutionGeneral Chemical EngineeringInorganic chemistryIntercalation (chemistry)General ChemistryExfoliation jointchemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyZirconium phosphateTransmission electron microscopyMonolayerMaterials ChemistryHydroxideChemistry of Materials
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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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