SDS Volume

Volume 59. Polycyclic Aromatic Hydrocarbons: Binary Non-aqueous Systems, Part II Solutes F-Z, p None

Source Publication

Zvaignze, A. I.; Acree Jr., W. E.; J. Chem. Eng. Data 1993, 38, 393-395.

Conditions:

Room Temp: 299 $\pu{K}$

Compilers:

W.E. Acree, Jr., A.I. Zvaigzne

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 was 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 372 nm.

Sample Information:
  1. 99%, Aldrich Chemical Company, Milwaukee, Wisconsin, USA, recrystallized three times from absolute ethanol.
  2. 99.9+%, anhydrous, Aldrich Chemical Company.
  3. 99+%, anhydrous, Aldrich Chemical Company. Components (2) and (3) were stored over molecular sieves and distilled shortly before use.
Measurement Errors:

Ambient temperature: T/K: ±0.05. x3(s): ±0.0001. x1: 1.5% (relative error).

System Components:
  1. Pyrene, $\ce{ C16H10 }$; [129-00-0] 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) $x^{\rm{init}}_{3}$ $x_{1}$ $x_{3}$
26.00.0000 0.012920.0000
26.00.1691 0.013250.1669
26.00.2953 0.012210.2917
26.00.5220 9.60 x 10-30.5170
26.00.6240 8.19 x 10-30.6189
26.00.7238 6.73 x 10-30.7189
26.00.8660 4.69 x 10-30.8619
26.00.9336 3.74 x 10-30.9301
26.01.0000 2.90 x 10-30.9971

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