for the system reported here. The calculation method used is similar to the one suggested by Prausnitz et al. ( 4 ) .Calculated values of yl based on 712 and ~2~ are given in Table 11 cy1 &d). The maximum percentage deviation between y1 expt~ and y1 calcd = (lOOAy/yl exptl) is less than 3.03%. Plots of log ( y l / y 2 ) us. x1 in accordance with the Redlich and Kister equation ( 5 ) showed the integrated value was 0.417 and the absolute value was 4.075. The small integrated value showed that the data were consistent. NOMENCLATURE g,, = energies of interaction between an i-j pair of molecules P = vapor pressure, mm of Hg x = mole fraction in liquid phase y = mole fraction in vapor phase CY,, = nonrandomness constant for binary i -j interactions AY = (Y1 exptl -y1 calcd) y = activity coefficient T = total pressure, mm of Hg T,, = coefficient defined in Equation 3Subscripts 1 = carbon disulfide 2 = methanol