SDS Volume

Volume 58. Polycyclic Aromatic Hydrocarbons: Binary Non-aqueous Systems, Part I Solutes A-E, p 128

Source Publication

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

Conditions:

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

Compiler:

W.E. Acree, Jr.

Methodology:

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.

Sample Information:
  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.
Measurement Errors:

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

System Components:
  1. Anthracene, $\ce{ C14H10 }$; [120-12-7] NIST WebBook
  2. Heptane, $\ce{ C7H16 }$; [142-82-5] NIST WebBook
  3. 1-Octanol, $\ce{ C8H18O }$; [111-87-5] NIST WebBook
Experimental Data
$T$ (°C) $x^{\rm{init}}_{3}$ $x_{1}$ $x_{3}$
25.00.0000 1.571 x 10-30.0000
25.00.1018 1.738 x 10-30.1016
25.00.1925 1.835 x 10-30.1921
25.00.3897 2.002 x 10-30.3889
25.00.4808 2.057 x 10-30.4798
25.00.5865 2.098 x 10-30.5853
25.00.7841 2.135 x 10-30.7824
25.00.8958 2.163 x 10-30.8939
25.01.0000 2.160 x 10-30.9978

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.

Download Data   link to XML output link to JSON output link to JSON-LD output