SDS Volume (1432)

Volume 58. Polycyclic Aromatic Hydrocarbons: Binary Non-aqueous Systems, Part I Solutes A-E, p 96

Original Measurements

Acree Jr., W. E.; Zvaigzne, A. I.; Tucker, S. A.; Fluid Phase Equilib. 1994, 92, 233-253.

Variables:

Room Temp: 298 $\pu{K}$
initial mol 3 (binary solvent): 0.0 - 1.0

Prepared by:

W.E. Acree, Jr.

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, was used as received.
  2. 99+%, anhydrous, Aldrich Chemical Company.
  3. 99+%, anhydrous, Aldrich Chemical Company.
Estimated Errors:

Ambient temperature: T/K: ±0.05.
Mass concentration (m/v) (1): x3(s): ±0.0001. x1: ±1.5% (relative error).

Components:
  1. Anthracene, $\ce{ C14H10 }$; [120-12-7] NIST WebBook
  2. Methylcyclohexane, $\ce{ C7H14 }$; [108-87-2] NIST WebBook
  3. 2-Propanol, $\ce{ C3H8O }$; [67-63-0] NIST WebBook
Experimental Data
$T$ (°C) $x^{\rm{init}}_{3}$ $x_{1}$ $x_{3}$
25.00.0000 1.649 x 10-30.0000
25.00.1518 1.683 x 10-30.1515
25.00.2965 1.536 x 10-30.2960
25.00.5234 1.226 x 10-30.5228
25.00.6234 1.055 x 10-30.6227
25.00.7170 8.87 x 10-40.7164
25.00.8649 6.31 x 10-40.8644
25.00.9375 5.08 x 10-40.9370
25.01.0000 4.11 x 10-40.9996

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.

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