IUPAC-NIST Solubilities Database

IUPAC-NIST Solubility Database
NIST Standard Reference Database 106

Solubility System: Anthracene with 2,2,4-Trimethylpentane and 1-Octanol

Components:
   (1) 2,2,4-Trimethylpentane; C8H18; [540-84-1]  NIST Chemistry WebBook for detail
   (2) 1-Octanol; C8H18O; [111-87-5]  NIST Chemistry WebBook for detail
   (3) Anthracene; C14H10; [120-12-7]  NIST Chemistry WebBook for detail

Original Measurements:
   Acree, W.E., Jr.; Zvaigzne, A.I.; Tucker, S.A., Fluid Phase Equilibr. 1994, 92, 233-253.

Variables:
   Temperature = 298 K
   Concentration = Solvent composition

Prepared By:
   W. E. Acree, Jr.

Experimental Data:   (Notes on the Nomenclature)


t/°C	Mole Fraction x₁	Mole Fraction x₃	x₃s
25.0	0.001074	0.0000	0.0000
25.0	0.001261	0.1234	0.1236
25.0	0.001378	0.2125	0.2128
25.0	0.001608	0.4062	0.4069
25.0	0.001719	0.5083	0.5092
25.0	0.001809	0.6112	0.6123
25.0	0.001987	0.8038	0.8054
25.0	0.002065	0.8973	0.8992
25.0	0.002160	0.9978	1.0000

Notes:
     x₃^(s): initial mole fraction of binary solvent mixture; x₁: mole fraction solubility of the solute; x₃: mole fraction of component 3 in the ternary solution.

Method/Apparatus/Procedure:
   Constant temperature bath, calorimetric thermometer, and an ultraviolet/visible spectrophotometer. Binary solvent mixtures were prepared by weight. Excess solute and solvent placed in amber glass bottles and allowed to equilibrate for several days at constant temperature. Attainment of equilibrium verified by several repetitive measurements and by approaching equilibrium from supersaturation.. Aliquots of saturated solutions transferred through a coarse filter into tared volumetric flasks, weighed and diluted with methanol. Concentrations determined spectrophotometrically at 356 nm.

Source and Purity of Materials:
   (1) Gold Label, 99.9+ %, Aldrich Chemical Company, Milwaukee, Wisconsin, USA, used as received.
   (2) HPLC Grade, 99.7+ %, Aldrich Chemical Company.
   (3) 99+ %, anhydrous, Aldrich Chemical Company.
   Components 2 and 3 were stored over molecular sieves and distilled shortly before use.

Estimated Errors:
   Solubility: x₃^(s): ± 0.0001. x₁: ± 1.5 % (relative error).
   Temperature: T/K: ± 0.05.

References:
   ¹W.E. Acree, Jr.