SDS Volume

Volume 58. Polycyclic Aromatic Hydrocarbons: Binary Non-aqueous Systems, Part I Solutes A-E, p 122

Source Publication

Zvaigzne, A. I.; Acree Jr., W. E.; J. Chem. Eng. Data 1994, 39(4), 708–710.

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. 99+%, anhydrous, 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: ±1.3% (relative error).

System Components:
  1. Anthracene, $\ce{ C14H10 }$; [120-12-7] NIST WebBook
  2. Octane, $\ce{ C8H18 }$; [111-65-9] NIST WebBook
  3. 3-Methyl-1-butanol, $\ce{ C5H12O }$; [123-51-3] NIST WebBook
Experimental Data
$T$ (°C) $x^{\rm{init}}_{3}$ $x_{1}$ $x_{3}$
25.00.0000 1.838 x 10-30.0000
25.00.1537 1.814 x 10-30.1534
25.00.2672 1.728 x 10-30.2667
25.00.4914 1.488 x 10-30.4907
25.00.5939 1.345 x 10-30.5931
25.00.6958 1.199 x 10-30.6950
25.00.8537 9.52 x 10-40.8529
25.00.9265 8.44 x 10-40.9257
25.01.0000 7.27 x 10-40.9993

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