IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Benzyl alcohol with 1,2,3,4-Tetrahydronaphthalene (tetralin) and Water

Components:
   (1) Water; H2O; [7732-18-5]  NIST Chemistry WebBook for detail
   (2) 1,2,3,4-Tetrahydronapthalene (tetralin); C10H12; [119-64-2]  NIST Chemistry WebBook for detail
   (3) Benzyl alcohol (benzenemethanol); C7H8O; [100-51-6]  NIST Chemistry WebBook for detail

Original Measurements:
   Goto, S.; Matsubara, M.; Washino, K., Kagaku Kogaku 38, 869-73 (1974).

Variables:
   Temperature = 363 K

Prepared By:
   A. Skrzecz

Experimental Data:   (Notes on the Nomenclature)
  
Compositions along the saturation curve
t/°CT/KMass Fraction w1Mass Fraction w2Mole Fraction x1 (compiler)Mole Fraction x2 (compiler)
90363.20.21000.78400.23670.7227
90363.20.41300.57600.43470.4958
90363.20.51550.46450.50760.3741
90363.20.59940.37200.55740.2830
90363.20.69200.27600.62350.2034
90363.20.75960.17690.59090.1126
90363.20.82810.08570.58500.0495
90363.20.87570.00000.54000.0000
Compositions of coexisting phases
t/°CT/KMass Fraction w1Mass Fraction w2Mole Fraction x1 (compiler)Mole Fraction x2 (compiler)Comment(s)
90363.20.03400.95860.03940.9091organic-rich phase
90363.20.07940.91290.09100.8560organic-rich phase
90363.20.17680.81570.19890.7505organic-rich phase
90363.20.38050.60390.39300.5102organic-rich phase
90363.20.58110.38900.53870.2949organic-rich phase
90363.20.65880.28100.52700.1839organic-rich phase
90363.20.83970.04700.53890.0247organic-rich phase
90363.20.01000.00190.00170.0003water-rich phase
90363.20.01680.00160.00280.0002water-rich phase
90363.20.02600.00200.00440.0003water-rich phase
90363.20.04300.00750.00750.0011water-rich phase
90363.20.05600.00200.00980.0003water-rich phase
90363.20.06070.00190.01070.0003water-rich phase
90363.20.06920.00020.01220.0000water-rich phase
Method/Apparatus/Procedure:
   The cloud point method was used to find compositions along the saturation curve. The analytical method was used to describe phases in equilibrium. The ternary samples of about 50 mL were thermostated for 1 h, then the phases were separated and the compositions were determined by glc analysis.

Source and Purity of Materials:
   (1) Source not specified, "high purity" commercial samples; used as received; purity > 99 mass % by glc.
   (2) Source not specified, "high purity" commercial samples; used as received; purity > 99 mass % by glc.
   (3) Distilled.

Estimated Errors:
   Solubility: Not reported.
   Temperature: Not reported.