A comprehensive review is presented of experimental data on the limiting activity coefficients γ1∞, infinite dilution partial molar excess enthalpies H¯1E,∞ and heat capacities C¯p,1E,∞ of lower 1-alkanols (C1–C5) in water. For each alkanol, the compiled data are critically evaluated and correlated with a suitable model equation providing adequate simultaneous description of the equilibrium measurements and the calorimetric information. As a result, recommended thermodynamically consistent temperature dependences of γ1∞, H¯1E,∞, and C¯p,1E,∞ of superior accuracy are established in the range from the melting point to the normal boiling point of water. In addition, by employing literature data on the respective residual properties of the pure 1-alkanols, analogous recommendations are also derived for the temperature dependences of the Henry’s law constants, hydration enthalpies, and hydration heat capacities. Evolution of the various infinite dilution thermodynamic properties of aqueous 1-alkanols with temperature and homologous series is briefly discussed.

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Air-water partitioning for 21 volatile chlorinated or brominated alkanes, alkenes, and aromatics was measured at 20°C by the inert gas stripping method. Results of the measurements are presented in the form of Henry's law constants (H 12 ), air-water partition coefficients (K aw ), and limiting activity coefficients (γ 1 ∞ ), accurate γ 1 ∞ values being obtained only if accurate pure solute vapor pressure data are available.The halocarbons studied in this work are hydrophobic and exhibit enhanced volatilities from their dilute aqueous solutions representing approximately ranges of γ 1 ∞ from 230 to 70 000 and H 12 from 2 to 70MPa. Correct performance of the stripping method for such systems requires special precautions. As confirmed by test measurements on benzene, chlorobenzene, 1,1,1-trichloroethane, and 1,1,2-trichloroethane, the complete equilibration in the stripping cell can be achieved under vigorous mixing of the cell, low stripping gas flow rates (approximately 10 cm 3 ‚min -1 ), and low relative elution rates (0.01 min -1 ). Choosing for each system a cell of a suitable volume made it possible to comply with the latter requirement. The results compare well with recent literature values obtained by various methods for some of the halocarbons. For two selected halocarbons (bromobenzene and 1,1-dichloroethane), detailed measurements of the temperature dependence of air-water partitioning were carried out in the range of (10-50)°C. These measurements corresponding to the range of H 12 from 5 to 72 MPa provide additional support for the validity of the method.

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