SDS Volume (2125)

Volume 59. Polycyclic Aromatic Hydrocarbons: Binary Non-aqueous Systems, Part II Solutes F-Z, p 31

Original Measurements

Shinomiya, C.; J. Chem. Soc. Japan 1940, 15, 259-270.

Variables:

Room Temp: Temperature $\pu{K}$

Prepared by:

W.E. Acree, Jr.

Method/Apparatus/Procedure:

No experimental details given in paper.

Source and Purity of Materials:
  1. Purity and chemical source were not specified in paper.
  2. Purity and chemical source were not specified in paper.
Estimated Errors:

Ambient temperature: T/K: ±precision 0.2. (compiler). x1: ±0.002 (compiler).

Components:
  1. Fluoranthene, $\ce{ C16H10 }$; [206-44-0] NIST WebBook
  2. 3-Methyl-2,4,6-trinitrophenol, $\ce{ C7H5N3O7 }$; [602-99-3] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $x_{1}$ $x_{2}$
381.7 0.0001.000
383.2 0.1100.890
412.2 0.3230.677
416.2 0.4310.569
417.2 0.5170.483
416.2 0.5680.432
412.2 0.6360.364
399.7 0.7860.214
385.2 0.8620.138
378.2 0.8830.117
381.0 0.9620.038
382.7 1.0000.000

Authors reports formations of a 1:1 fluoranthene - 3-methyl-2,4,6-trinitrophenol yellow compound having a melting point of 417.2 K. Two eutectic points occur at x1 = 0.082 and T/K = 374.2, and at x1 = 0.890 and T/K = 374.2.

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