Components:

(1) Anthracene, C14H10; [120-12-7] NIST WebBook
(2) 2,2,4-Trimethylpentane, C8H18; [540-84-1] NIST WebBook
(3) 1-Propanol, C3H8O; [71-23-8] NIST WebBook

Original Measurements

Zvaigzne, A. I.; Teng, I. L.; Martinez, E.; Trejo, J.; Acree Jr., W. E.; J. Chem. Eng. Data 1993, 38, 389-392.

Variables:

Ambient temperature: 298 K
Solvent composition

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 determinedspectrophotometrically at 356 nm.

Source and Purity of Materials:
  1. Gold Label, 99.9+%, Aldrich Chemical Company, Milwaukee, Wisconsin, USA, was used as received.
  2. HPLC Grade, 99.7%, 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% (relative error).

Experimental Values:
T (°C) xinit3 x1 x3
25.0 0.0 1.074 x 10-3 0.0
25.0 2.141 x 10-1 1.089 x 10-3 2.139 x 10-1
25.0 3.510 x 10-1 1.057 x 10-3 3.506 x 10-1
25.0 5.891 x 10-1 9.29 x 10-4 5.886 x 10-1
25.0 6.884 x 10-1 8.62 x 10-4 6.878 x 10-1
25.0 7.911 x 10-1 7.83 x 10-4 7.905 x 10-1
25.0 8.968 x 10-1 6.93 x 10-4 8.962 x 10-1
25.0 9.454 x 10-1 6.49 x 10-4 9.448 x 10-1
25.0 1.0 5.91 x 10-4 9.994 x 10-1

(None) 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