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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 15 (1986), S. 947-956 
    ISSN: 1572-8927
    Keywords: Vapor pressure ; second virial coefficient ; dimerization constant ; hydrophobic interactions ; benzene ; dilute aqueous solutions ; fluorobenzene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An automated vapor pressure apparatus has been used to obtain measurements of the vapor pressure of aqueous solutions of fluorobenzene at temperatures of 15, 25, 35, and 45°C, and in the concentration range 0 to 0.011M. The results have been interpreted to infer the dimerization constant of fluorobenzene in very dilute aqueous solutions, equivalent to the second virial coefficient of interaction between fluorobenzene molecules. The hydrophobic association of fluorobenzene molecules is thermodynamically quite similar to that of benzene at comparable temperatures and concentrations. A dimerization constant of fluorobenzene of 0.56 M−1 at 30°C and an endothermic enthalpy of association equal to 3.9 kcal-mol−1 are calculated from the measurements.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8927
    Keywords: Vapor pressure ; dimerization constant ; hydrophobic association ; benzene ; fluorobenzene ; benzyl alcohol ; phenethyl alcohol ; dilute aqueous solutions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Vapor pressure measurements have been made on dilute aqueous solutions of benzene-benzyl alcohol (BZOH), benzene-phenethyl alcohol (PEOH), and fluorobenzene-BZOH at 15, 25, 35, and 45°C. The benzene results have been interpreted with a mass action model which attributes deviations from ideality to the formation of benzene dimers and heterodimers with BZOH and PEOH. The benzene heterodimers form endothermically at 25°C with large and negative heat capacity changes. The dimerization constant for the benzene-BZOH dimer reaches a maximum of 0.57 M−1 at about 37°C, while the benzene-PEOH dimer reaches a maximum of 0.60 M−1 around 30°C. The fluorobenzene results have been interpreted with a mass action model which, in addition to fluorobenzene dimers and heterodimers, includes the formation of a fluorobenzene-BZOH trimer. Thermodynamic properties for these aggregates are reported and compared with results obtained in previous studies.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 1969-1975 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An automated vapor pressure method is used to obtain solubilization isotherms for trichloroethylene (TCE) in polyelectrolyte/surfactant complexes throughout a wide range of solute activities at 20 and 25°C. The polyelectrolyte chosen is sodium poly (styrenesulfonate), PSS, and the surfactant is cetylpyridinium chloride or N-hexadecylpyridinium chloride, CPC. Data are fitted to the quadratic equation K = K0 (1 - αX + βX2), which correlates the solubilization equilibrium constant (K) with the mole fraction of TCE (X) in the micelles or complexes at each temperature. Activity coefficients are also obtained for TCE in the PSS/CPC complexes as a function of X. The general solubilization behavior of TCE in PSS/CPC complexes resembles that of TCE in CPC micelles, as well as that of benzene or toluene in CPC micelles, suggesting that TCE solubilizes in ionic micelles both within the hydrocarbon micellar interior and near the micellar surface. The presence of the polyelectrolyte causes a small decrease in the ability of the cationic surfactant to solubilize TCE, while greatly reducing the concentration of the surfactant present in monomeric form. PSS/CPC complexes may be useful in colloid-enhanced ultrafiltration processes to purify organic-contaminated water.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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