Search results for "cellar"

showing 10 items of 230 documents

Development and validation of a procedure for estimating the hydrophobicity of structurally unrelated compounds by micellar liquid chromatography

1999

Reversed-phase liquid chromatography has been used most often to estimate values of log P, but despite years of study, there is no universally accepted method of performing these estimations. The main problem has to do with the fact that the hydrophobic parameter, log k w , depends on the hydrogen bond acceptor-donor character of the compounds. The use of micellar mobile phases to perform these estimations is evaluated here, and the influence of the nature of the surfactant (anionic, cationic, and nonionic) on the log k-log P relationships is studied. The use of a nonionic surfactant, such as Brij35, to prepare the mobile phases provided adequate results regardeless of the hydrogen bond acc…

AnthraceneChromatographyHydrogen bondAnalytical chemistryCationic polymerizationGeneral MedicineMicellar electrokinetic chromatographyAnalytical ChemistryPartition coefficientchemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographyPyrene
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Volumes, heat capacities and solubilities of amyl compounds in decyltrimethylammonium bromide aqueous solutions

1989

Apparent molar heat capacities and volumes of amylamine (PentNH2) 0.02m, capronitrile (PentCN) 0.02m and nitropentane (PentNO2) 0.009m in decyltrimethylammonium bromide (DeTAB) micellar solutions, in water and in octane were measured at 25°C. By assuming that their concentration approaches the standard infinite dilution state, heat capacities and volumes were rationalized by means of previously reported equations following which the distribution constant between the aqueous and the micellar phase and heat capacity and volume of the additives in both phases are simultaneously derived. The present results are compared to those we have previously obtained for pentanol (PentOH). The thermodynam…

Aqueous solutionChemistryDistribution constantBiophysicsThermodynamicsBiochemistryHeat capacityDilutionchemistry.chemical_compoundMolar volumeMicellar solutionsOrganic chemistryPhysical and Theoretical ChemistrySolubilityMolecular BiologyOctaneJournal of Solution Chemistry
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Enthalpies of mixing of some nitriles aqueous solutions with dodecylsurfactants micellar solutions

1988

The enthalpies of mixing of some n-nitriles (from acetonitrile to valeronitrile) aqueous solutions with dodecyltzimethylammonium bromide, sodium dodecylsulfate and dodecyltzimethylammonium oxide micellar solutions were determined. The measurements were performed by systematically changing the surfactant concentration at a given solute concentration. The experimental enthalpies were rationalized in terms of the standard enthalpy of transfer of solute from the aqueous to the micellar phase and of the distribution constant between the two phase. Information on the effect of the nature of the surfactant on the standard thermodynamic quantities of transfer(ΔG t o , ΔH t o , TΔS t o ) is reported…

Aqueous solutionChemistryDistribution constantEnthalpyInorganic chemistryBiophysicsEntropy of mixingBiochemistryMicelleStandard enthalpy of formationPhase (matter)Micellar solutionsPhysical chemistryPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Micellar Liquid Chromatography: Fundamentals

2015

The reversed phase liquid chromatography (RPLC) mode with surfactant above the critical micellar concentration (CMC) has been called micellar liquid chromatography (MLC). In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and micellar pseudo-phase. Surfactant adsorption on the porous RPLC packing affects chromatographic retention, owing to the change of diverse surface properties of the stationary phase. In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and mice…

Aqueous solutionColumn chromatographyAqueous normal-phase chromatographyChemistryMicellar liquid chromatographyHydrophilic interaction chromatographytechnology industry and agricultureAnalytical chemistrylipids (amino acids peptides and proteins)macromolecular substancesReversed-phase chromatographyMicelleMicellar electrokinetic chromatography
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Effect of Large Changes in Temperature and Pressure on the Thermodynamic Properties of Micellization and on the Distribution Constant of a Polar Solu…

1996

Density measurements of pentanol (PentOH)−dodecyltrimethylammonium bromide (DTAB)−water mixtures as functions of both alcohol and surfactant (mS) concentrations were carried out at 0.1 MPa from 45 to 75 °C and at 19 MPa from 25 to 130 °C. The standard (infinite dilution) partial molar volumes and expansibilities of DTAB in water and the corresponding properties in the micellar phase were calculated from the experimental data. As far as PentOH in DTAB micellar solutions is concerned, with the exception of the standard partial molar volume (V°R) data at 130 °C and 19 MPa, all the V°R vs mS trends are monotonic curves with mS. The data of V°R as a function of mS were treated by means of an equ…

Aqueous solutionDistribution constantGeneral EngineeringThermodynamicsPartial molar propertyDilutionGibbs free energychemistry.chemical_compoundsymbols.namesakechemistryBromidePhase (matter)Micellar solutionssymbolsPhysical and Theoretical ChemistryThe Journal of Physical Chemistry
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Solubilization of an Organic Solute in Aqueous Solutions of Unimeric Block Copolymers and Their Mixtures with Monomeric Surfactant: Volume, Surface T…

2008

The ability of aqueous systems, formed by unimeric copolymers and their mixtures with a monomeric surfactant, in solubilizing large quantities of 1-nitropropane (PrNO2) was explored. The copolymers are F68 and L64, which differ for the hydrophilicity, and the surfactant is sodium dodecanoate. For a better understanding of the mechanism of solubilization, thermodynamic (volume and differential scanning calorimetry), spectroscopy (steady-state fluorescence), viscosity, and interfacial investigations were carried out. PrNO2 causes the micellization of the unimeric copolymer, and the required amount of PrNO2 depends on the composition, the copolymer nature, and the temperature. Large quantities…

Aqueous solutionISOTHERMAL TITRATION CALORIMETRYChemistryMICELLAR SYSTEMSDYNAMIC LIGHT-SCATTERINGIONIC SURFACTANTSTRIBLOCK COPOLYMERSMicelleFluorescence spectroscopySurfaces Coatings and FilmsSurface tensionViscosityDifferential scanning calorimetryAGGREGATION BEHAVIORPulmonary surfactantChemical engineeringMIXED MICELLESPolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistrySODIUM DODECYL-SULFATEOXIDE)(13)-(PROPYLENE OXIDE)(30)-(ETHYLENE OXIDE)(13)GEMINI SURFACTANTS
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Adsorption of the anionic surfactant sodium dodecyl sulfate on a C18column under micellar and high submicellar conditions in reversed-phase liquid ch…

2015

Micellar liquid chromatography makes use of aqueous solutions or aqueous-organic solutions containing a surfactant, at a concentration above its critical micelle concentration. In the mobile phase, the surfactant monomers aggregate to form micelles, whereas on the surface of the nonpolar alkyl-bonded stationary phases they are significantly adsorbed. If the mobile phase contains a high concentration of organic solvent, micelles break down, and the amount of surfactant adsorbed on the stationary phase is reduced, giving rise to another chromatographic mode named high submicellar liquid chromatography. The presence of a thinner coating of surfactant enhances the selectivity and peak shape, es…

Aqueous solutionInorganic chemistryAnalytical chemistryFiltration and SeparationReversed-phase chromatographyMicelleAnalytical Chemistrychemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographyPhase (matter)Critical micelle concentrationSodium dodecyl sulfateJournal of Separation Science
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Thermodynamics of transfer of some nitroalkanes from aqueous to dodecyltrimethylammonium bromide micellar phases

1988

Abstract The enthalpies of mixing of some aqueous n-nitroalkane solutions with dodecyltrimethylammonium bromide micellar solutions were determined. The experimental data were treated by using a previously reported approach giving the enthalpies of transfer of solute from the aqueous to the micellar phases and the distribution constant of solute between the two phases at the same time. From these, the standard thermodynamic quantities of transfer (ΔtrfG°, ΔtrfH° and ΔtrfS°) are derived. In order to study the effect of the nature of both the solvent and the head group of solute, these properties are compared with those from water to octane and with those of alcohols and nitriles from aqueous …

Aqueous solutionInorganic chemistryDistribution constantMixing (process engineering)Condensed Matter PhysicsSolventchemistry.chemical_compoundchemistryPhase (matter)Micellar solutionsPhysical and Theoretical ChemistryDodecyltrimethylammonium bromideInstrumentationOctaneThermochimica Acta
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Excess enthalpies of solution of primary and secondary alcohols in dodecyldimethylamine oxide micellar solutions

1987

The excess enthalpies of solution with respect to water of some primary and secondary alcohols in dodecyldimethylamine oxide (DDAO) micellar solutions were measured by mixing aqueous solutions of alcohols with surfactant solutions. Standard free energies, enthalpies and entropies were obtained from the distribution of alcohols between aqueous and micellar phases. It is shown that thermodynamics of transfer of secondary alcohols from aqueous to the DDAO micellar phase differ slightly from those of their corresponding primary alcohols, that the additivity rule holds for free energies of transfer and that enthalpy and entropy display convex curves. The present data are compared with those from…

Aqueous solutionInorganic chemistryEnthalpytechnology industry and agricultureBiophysicsmacromolecular substancesPrimary alcoholBiochemistryHydrophobic effectchemistry.chemical_compoundchemistryMicellar solutionslipids (amino acids peptides and proteins)2-PentanolPhysical and Theoretical ChemistryMolecular Biology2-ButanolOctaneJournal of Solution Chemistry
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Double-Shell Vesicles, Strings of Vesicles and Filaments Found in Crosslinked Micellar Solutions of Poly(1,2-butadiene)-block-poly(ethylene oxide) Di…

2001

Micellar structures of amphiphilic poly(1,2-butadiene)-block-poly(ethylene oxide) diblock copolymers have been crosslinked in aqueous solution by γ-irradiation. By transmission electron microscopy (TEM) of neganively stained specimen it is shown that the precominant structures present are sopolymer sesicles (which appear to be double latered. These fived vesules are stable with respect to their share and can be transferred from water into a good solvent for blue filbeks, such as tetrahydrofuran, this demonstrating the effectiveness of the crosslinking. In addition to the resicles a small number of flexible cylindrichl/filimented structures sequentially fused vesicles/strings of vesicles and…

Aqueous solutionMaterials sciencePolymers and PlasticsEthylene oxideVesicleOrganic ChemistryUranyl acetatechemistry.chemical_compoundCrystallographychemistryTransmission electron microscopyMicellar solutionsAmphiphilePolymer chemistryMaterials ChemistryCopolymerMacromolecular Rapid Communications
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