Vapor-liquid equilibria in presence of solvents

Figure 13.23. Examples of vapor-liquid equilibria in presence of solvents, (a) Mixture of-octane and toluene in the presence of phenol, (b) Mixtures of chloroform and acetone in the presence of methylisobutylketone. The mole fraction of solvent is indicated, (c) Mixture of ethanol and water (a) without additive (b) with 10gCaCl2 in 100 mL of mix. (d) Mixture of acetone and methanol (a) in 2.3Af CaCl2 ip) salt-free, (e) Effect of solvent concentration on the activity coefficients and relative volatility of an equimolal mixture of acetone and water (Carlson and Stewart, in Weissbergers Technique of Organic Chemistry IV, Distillation, 1965). (f) Relative volatilities in the presence of acetonitrile. Compositions of hydrocarbons in liquid phase on solvent-free basis (1) 0.76 isopentane + 0.24 isoprene (2) 0.24 iC5 + 0.76 IP (3) 0.5 iC5 + 0.5 2-methylbutene-2 (4) 0.25-0.76 2MB2 + 0.75-0.24 IP [Ogorodnikov et al., Zh. Prikl. Kh. 34, 1096-1102 (1961)].

When both components of a binary gas or vapor mixture are separately adsorbed to roughly the same extent, the amount of either one adsorbed from the mixture will be affected by the presence of the other. Since such systems are composed of three components when the adsorbent is included, the equilibrium data are conveniently shown in the maimer used for ternary liquid equilibria in Chap. 10. For this purpose it is convenient to consider the solid adsorbent as being analogous to liquid solvent in extraction operations. However, adsorption is greatly influenced by both temperature and pressure, unlike liquid solubility, which is scarcely affected by pressure under ordinary circumstances. Equilibrium diagrams are consequently best plotted at constant temperature and constant total pressure, and they are therefore simultaneously isotherms and isobars. 

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