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  • alcohols  (1)
  • alkyl poly(ethyleneglycol) monoether  (1)
  • aqueous solutions  (1)
  • 1
    ISSN: 1572-8927
    Keywords: Mixed micelles ; surfactants ; alcohols ; thermodynamic transfer functions ; volume ; heat capacity ; hydrophobic solutes ; chemical equilibrium model and distribution constant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In ternary aqueous solutions, hydrophobic solutes such as alcohols tend to aggregate with surfactants to form mixed micelles. These systems can be studied by meas of the functions of transfer of hydrophobic solutes from water to aqueous solutions of surfactant. These thermodynamic functions often go through extrema in the critical micellar concentration (CMC) region of the surfactant. A simple model based on interactions between surfactant and hydrophobic solute monomers, on the distribution of the hydrophobic solute between water and the micelles and on the shift in the CMC induced by the hydrophobic solute, can simulate the magnitude and trends of the transfer functions using parameters which are mostly derived from the binary systems. In order to check the model more quantitatively, volumes and heat capacities of transfer of alcohols from water to aqueous solutions of a nonionic surfactant, octyldimethylamine oxide, were measured. A quantitative agreement was achieved with three adjustable parameters. Good fits are also obtained for the transfers to the ionic surfactants, octylamine hydrobromide and sodium dodecylsulfate. When the equilibrium displacement contribution is small, the distribution constants and the partial molar properties of the alcohols in the micellar phase agree well with the parameters obtained with similar models.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8927
    Keywords: Excess quantities ; reduced and apparent excess quantities ; molar volume ; molar isentropic compressibility ; ultrasonic speed ; alkyl poly(ethyleneglycol) monoether
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The densities and the ultrasonic speeds of the aqueous solutions of 2-(2-hexyloxyethoxy)ethanol (C6E2) were measured over the entire range of mole fractions at 5°C. Excess molar volumes V E were readily calculated from the densities. The densities, in combination with the ultrasonic speeds, furnish estimates of the molar (and excess molar) isentropic compressibilities K S and the deviations u D of the ultrasonic speeds from the values calculated for ideal mixtures. Radical changes in the mole fraction derivatives of the excess molar properties of the (C6E2 + water) system, in the vicinity of an amphiphile mole fraction of 0.003, indicate that C6E2 like C6E3 is capable of micelle formation. Our data have been compared with those reported earlier for (C4E2 +, C2E2 +, and C6E3 + water). We have employed both mass action and pseudophase approaches to data analysis, together with the four-segment model approach.
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  • 3
    ISSN: 1572-8927
    Keywords: Apparent molar heat capacities ; apparent molar volumes ; partial molar properties ; infinite dilution ; aqueous solutions ; organic pollutants ; group contribution method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Well-known Picker flow microcalorimeters for the differential measurements of volumetric heat capacities have been employed in conjunction with vibrating tube densimeters to determine the molar heat capacity, volume, and the apparent properties in dilute aqueous solutions for 17 organic solutes of moderate hydrophobicity. The dependence on concentration of the apparent properties allowed the limiting partial molar quantities at infinite dilution to be extrapolated and the limiting partial molar excess quantities to be evaluated. Comparison with available literature data shows good agreement. The application of group contribution rules to the limiting partial properties has been tested using the original method and parameters proposed by Cabani et al. The predicted values of the partial molar volumes are in fair agreement with the present data except for some less common solutes. With partial molar heat capacities, the agreement is less satisfactory. To improve the performance of the method, missing parameters for some types of monofunctional and bifunctional molecules have been evaluated.
    Type of Medium: Electronic Resource
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