NOMENCLATURE P, = vapor pressure of pure component i at equilibrium temperax, = mole fraction of component i in the liquid phaae y8 = mole fraction of component i in the vapor phase 7 , = activity coefficient of component i x = total pressure, mm. of Hg Subscripts ture, mm. of Hg 1 = hexamethyldisiloxane 2 = n-propyl alcohol ACKNOWLEDGMENT The services of R. Engineering students, in the experimental phases of this investigation, are gratefully acknowledged.Figure 3. Density at 25" C. vs. weight fraction hexamethyldisiloxane for the system hexamethyldisiloxane-n-propyl alcohol Data were obtained for the solubility of helium at pressures up to 2000 p.s.i.a. in liquid argon at temperatures of -125O, -140°, -160°, and -180°C.; in liquid oxygen at -130°, -145', -160°, -180°, and -195.8"C.; and in liquid carbon monoxide at -145', -160', -180°, and -195.8" C. A static sampling technique was used and samples were analyzed by gas chromatography. The data are presented in temperature-composition and pressure-composition diagrams. A comparison is madebetween the data of this study and previously published data for the helium-argon and helium-oxygen systems.