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IUPAC-NIST Solubility Database
NIST Standard Reference Database 106
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/°C
T/K
Mass Fraction w
1
Mass Fraction w
2
Mole Fraction x
1
(compiler)
Mole Fraction x
2
(compiler)
90
363.2
0.2100
0.7840
0.2367
0.7227
90
363.2
0.4130
0.5760
0.4347
0.4958
90
363.2
0.5155
0.4645
0.5076
0.3741
90
363.2
0.5994
0.3720
0.5574
0.2830
90
363.2
0.6920
0.2760
0.6235
0.2034
90
363.2
0.7596
0.1769
0.5909
0.1126
90
363.2
0.8281
0.0857
0.5850
0.0495
90
363.2
0.8757
0.0000
0.5400
0.0000
Compositions of coexisting phases
t/°C
T/K
Mass Fraction w
1
Mass Fraction w
2
Mole Fraction x
1
(compiler)
Mole Fraction x
2
(compiler)
Comment(s)
90
363.2
0.0340
0.9586
0.0394
0.9091
organic-rich phase
90
363.2
0.0794
0.9129
0.0910
0.8560
organic-rich phase
90
363.2
0.1768
0.8157
0.1989
0.7505
organic-rich phase
90
363.2
0.3805
0.6039
0.3930
0.5102
organic-rich phase
90
363.2
0.5811
0.3890
0.5387
0.2949
organic-rich phase
90
363.2
0.6588
0.2810
0.5270
0.1839
organic-rich phase
90
363.2
0.8397
0.0470
0.5389
0.0247
organic-rich phase
90
363.2
0.0100
0.0019
0.0017
0.0003
water-rich phase
90
363.2
0.0168
0.0016
0.0028
0.0002
water-rich phase
90
363.2
0.0260
0.0020
0.0044
0.0003
water-rich phase
90
363.2
0.0430
0.0075
0.0075
0.0011
water-rich phase
90
363.2
0.0560
0.0020
0.0098
0.0003
water-rich phase
90
363.2
0.0607
0.0019
0.0107
0.0003
water-rich phase
90
363.2
0.0692
0.0002
0.0122
0.0000
water-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.