IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: 2-Propanol with o-Xylene and Water

Components:
   (1) Water; H2O; [7732-18-5]  NIST Chemistry WebBook for detail
   (2) 2-Propanol (isopropanol, isopropyl alcohol); C3H8O; [67-63-0]  NIST Chemistry WebBook for detail
   (3) o-Xylene (1,2-dimethylbenzene, 1,2-xylene); C8H10; [95-47-6]  NIST Chemistry WebBook for detail

Original Measurements:
   Letcher, T.M.; Siswana, P.M., Fluid Phase Equilib. 74, 203 (1992).

Variables:
   Temperature = 298 K

Prepared By:
   A. Skrzecz

Experimental Data:   (Notes on the Nomenclature)
  
Compositions along the saturation curve
t/°CT/KMass Fraction w1 (compiler) Mass Fraction w2 (compiler)Mole Fraction x1Mole Fraction x2
25.0298.20.0000.0000.0000.000
25.0298.20.2490.0050.0910.001
25.0298.20.3460.0130.1390.003
25.0298.20.4310.0430.1950.011
25.0298.20.4930.1040.2600.031
25.0298.20.5010.2140.3190.077
25.0298.20.4770.3170.3560.134
25.0298.20.4330.4340.3860.219
25.0298.20.3670.5510.3860.328
25.0298.20.2870.6680.3510.463
25.0298.20.1960.7820.2740.620
25.0298.20.0990.8930.1580.804
25.0298.20.0500.9470.0840.899
25.0298.20.0000.99980.0000.999
Compositions of coexisting phases
t/°CT/KMass Fraction w1 (compiler) Mass Fraction w2 (compiler)Mole Fraction x1Mole Fraction x2Comment(s)
25.0298.20.0000.99980.0000.999hydrocarbon-rich phase
25.0298.20.0270.9700.0460.938hydrocarbon-rich phase
25.0298.20.0600.9340.0980.867hydrocarbon-rich phase
25.0298.20.2170.7540.2930.577hydrocarbon-rich phase
25.0298.20.3100.6350.3640.422hydrocarbon-rich phase
25.0298.20.4400.4160.3810.204hydrocarbon-rich phase
25.0298.20.0000.0000.0000.000water-rich phase
25.0298.20.2380.0050.0860.001water-rich phase
25.0298.20.3060.0090.1180.002water-rich phase
25.0298.20.4430.0530.2060.014water-rich phase
25.0298.20.4200.1210.2080.034water-rich phase
25.0298.20.5010.2430.3350.092water-rich phase
Method/Apparatus/Procedure:
   The points on the binodal curve were determined by the formation of a cloudy mixture on shaking after the addition of a known mass of one component to a mixture of known masses of the other two components. Precision weighing syringes were used as described by the refractive index method reported in Ref. 2 and a complementary method using the Karl Fischer titrations as reported in Ref. 3.

Source and Purity of Materials:
   (1) Merck, AR grade; distilled, dried by refluxing with Mg and I2; purity better than 99.6 mole % by glc; d=0.781 51, n=1.3752.
   (2) BDH; used as received; purity better than 99.6 mole % by glc; d=0.875 88, n=1.5029.
   (3) Source not specified.

Estimated Errors:
   Solubility: Not reported.
   Temperature: Estimated comp. 0.005 mole fraction on the binodal curve and 0.01 mole fraction for tie lines (estimated by the authors).

References:
   1 T. M. Letcher, S. Wootten, B. Shuttleworth, and C. Heward, J. Chem. Thermodyn. 18, 1037 (1986).
   2 S. W. Briggs and E. W. Comings, Ind. Eng. Chem. 35, 411 (1943).
   3 T. M. Letcher, P. M. Siswana, P. Van der Watt, and S. Radloff, J. Chem. Thermodyn. 21, 1053 (1989).