IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: 1-Butanol with Cyclohexane and Water

Components:
   (1) Water; H2O; [7732-18-5]  NIST Chemistry WebBook for detail
   (2) 1-Butanol (n-butanol, butyl alcohol, n-butyl alcohol); C4H10O; [71-36-3]  NIST Chemistry WebBook for detail
   (3) Cyclohexane; C6H12; [110-82-7]  NIST Chemistry WebBook for detail

Original Measurements:
   Plackov, D.; Stern, I, Fluid. Phase Equilib. 57, 327 (1990).

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
25.00298.150.09250.90490.10280.8853
25.00298.150.17750.81250.18990.7657
25.00298.150.24160.74390.25260.6851
25.00298.150.29500.68510.30080.6153
25.00298.150.35990.61240.35530.5324
25.00298.150.44530.51590.42040.4290
25.00298.150.49660.45660.45520.3686
25.00298.150.55740.38290.48890.2958
25.00298.150.62260.30270.52040.2228
25.00298.150.69210.20810.53810.1425
25.00298.150.74440.12680.53710.0806
25.00298.150.78550.04350.51430.0251
25.00298.150.07270.00000.01870.0000
Compositions of coexisting phases
t/°CT/KMass Fraction w1 (compiler) Mass Fraction w2 (compiler)Mole Fraction x1Mole Fraction x2Comment(s)
25.00298.150.0800.9160.0890.893organic-rich phase
25.00298.150.2510.7330.2610.672organic-rich phase
25.00298.150.4320.5320.4110.446organic-rich phase
25.00298.150.6490.2680.5280.192organic-rich phase
25.00298.150.7320.1400.5300.089organic-rich phase
25.00298.150.7850.0350.5040.020organic-rich phase
25.00298.150.0400.0000.0100.000water-rich phase
25.00298.150.0480.0000.0120.000water-rich phase
25.00298.150.0510.0000.0130.000water-rich phase
25.00298.150.0590.0000.0150.000water-rich phase
25.00298.150.0630.0000.0160.000water-rich phase
25.00298.150.0700.0000.0180.000water-rich phase
Method/Apparatus/Procedure:
   The titration method, as reported in Ref. 1, was used to determine the solubility curve. Mixtures of known composition, mixed by means of a magnetic stirrer and placed in the thermostated double-wall Erlenmeyer flask, we titrated with the less soluble component until the appearance of turbidity. The analytical method was used to determine liquid-liquid equilibra. The mixture was shaken for at least 20 min. Equilibration took place in a  thermostated double-walled separatory funnel of 250 mL over 2 h. The refractive index and density of both phases were measured. The composition was calculated numerically from the calibration data by polynomial regression analysis. The third order polynomials were used. Each experiment was repeated three times.

Source and Purity of Materials:
   (1) Zorka (Sabac), analytical grade; used as received; n=1.3972, p(25°C)=805.9 kg m-3, b.p.=117.4°C.
   (2) Kemika (Zagreb), analytical grade; used as received; n=1.4232, p(25°C)=773.6 kg m-3, b.p.=80.0°C.
   (3) Double distilled in the presence of KMNO4.

Estimated Errors:
   Solubility: Not reported.
   Temperature: Temp. ±0.02°C; composition <±0.05% (by mass) relative error.

References:
   1 E. R. Washburn, C. L. Graham, G. B. Arnold, and L. F. Transuel, J. Am. Chem. Soc. 62, 1454 (1940).