SDS Volume (1395)

Volume 58. Polycyclic Aromatic Hydrocarbons: Binary Non-aqueous Systems, Part I Solutes A-E, p 72

Original Measurements

Doane, E. P.; Drickamer, H. G.; J. Phys. Chem. 1955, 59, 454-457.

Variables:

Room Temp: 298 $\pu{K}$
Pressure: 1 - 4000 $\pu{atm}$

Prepared by:

W.E. Acree, Jr.

Method/Apparatus/Procedure:

Constant temperature bath, analytical balance and high pressure equipment. Excess solute and solvent allowed to equilibrate in a specially designed high pressure cell at constant temperature for 20-24 hours. Known amount of saturated solution removed, solvent evaporated to dryness, and concentration determined from weight of solid residue.

Source and Purity of Materials:
  1. Purest grade, Eastman Kodak Chemical Company, Rochester, New York, USA, was used as received.
  2. C.P. Grade, J.T. Baker, was dried over phosphorous pentoxide and distilled.
Estimated Errors:

Ambient temperature: T/K: precision ±0.1.
Mole fraction - Liquid (1): x1: ±1-3% at atomospheric pressure, and ±10% at the higher pressures.

Components:
  1. Anthracene, $\ce{ C14H10 }$; [120-12-7] NIST WebBook
  2. Carbon disulfide, $\ce{ CS2 }$; [75-15-0] NIST WebBook
Experimental Data
$P$ ($\pu{atm}$) $x_{1}$ $x_{2}$
1 8.4 x 10-30.9916
240 7.0 x 10-30.9930
500 5.9 x 10-30.9941
1.000 x 103 4.1 x 10-30.9959
2.000 x 103 2.7 x 10-30.9973
4.000 x 103 1.3 x 10-30.9987

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