SDS Volume (2074)

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

Original Measurements

Mayer, M. M.; Howell, W. J.; Tomasko, D. L.; Eckert, C. A.; J. Chem. Eng. Data 1990, 35, 446-449.

Variables:

Room Temp: Temperature $\pu{K}$

Prepared by:

W.E. Acree, Jr.

Method/Apparatus/Procedure:

Samples were equilibrated in an apparatus similar to the one used by Ott and co-workers [1]. Temperature of the sample monitored with an Omega RTD probe inside a stainless steel tube that went down through the center of the pyrex tube. Samples heated above their melting point temperature, and time-temperature cooling curves were measured.

Source and Purity of Materials:
  1. 99.5%, Aldrich Chemical Company, Milwaukee, Wisconsin, USA, was recrystallized before use.
  2. 99.5%, Aldrich Chemical Company, was recrystallized before use.
Estimated Errors:

Ambient temperature: T/K: ±precision 0.5. x1: ±0.005 (compiler).

References

1 Ott, et. al, J. Phys. Chem. 1962, 66, 1387

Components:
  1. Phenanthrene, $\ce{ C14H10 }$; [85-01-8] NIST WebBook
  2. Thianthrene, $\ce{ C12H8S2 }$; [92-85-3] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $x_{1}$ $x_{2}$
429 0.001.00
425 0.050.95
423 0.100.90
420 0.150.85
416 0.200.80
412 0.250.75
409 0.300.70
405 0.350.65
400 0.400.60
397 0.450.55
390 0.500.50
383 0.550.45
377 0.600.40
370 0.650.35
362 0.700.30
356 0.750.25
357 0.800.20
361 0.850.15
365 0.900.10
369 0.950.05
372 1.000.00

Authors state that system exhibits simple eutectic behavior.

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