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Aqueous Hexadecyltrimethylammonium Acetate Solutions: pH and Critical Micelle Concentration Evidence for Dependence of the Degree of Micelle Ionic Dissociation on Acetate Ion Concentration
17
Citations
46
References
1997
Year
C16taoac−naoac−acoh SolutionsEngineeringChemical AnalysisChemistryAnalytical UltracentrifugationIon ProcessSolution (Chemistry)Micelle Ionic DissociationChemical EngineeringBioanalysisAnalytical ChemistryAcetate Ion ActivityAnion SensingChromatographyChemical MeasurementIon ExchangeBiochemistryPhysical ChemistryDeep Eutectic SolventElectrochemistryNatural SciencesChemical KineticsAcetate Ion ConcentrationIon StructureDrug Analysis
The counterion binding parameters (β) of aqueous hexadecyltrimethylammonium acetate (C16TAOAc) are estimated from pH data at various C16TAOAc−AcOH concentrations with or without added sodium acetate buffer. In contrast to what is usually reported for ionic amphiphiles associated with less hydrophilic counterions, β varies from ca. 0.4 to ca. 0.7 and depends upon the acetate ion concentration in the aqueous phase. The critical micelle concentrations (cmc) for C16TAOAc, C16TAOAc−NaOAc, C16TAOAc−AcOH, and C16TAOAc−NaOAc−AcOH solutions, measured from extinction data for fluorescence of acridine, are also examined in terms of AcO- concentration dependence. The plot of the logarithm of the amphiphile activity at cmc vs the logarithm of acetate ion activity is markedly curved, as expected for significant variations in β.
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