SDS Volume

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

Source Publication

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

Conditions:

Room Temp: Temperature $\pu{K}$

Compiler:

W.E. Acree, Jr.

Methodology:

No experimental details given in paper.

Sample Information:
  1. Purity and chemical source were not specified in paper.
  2. Purity and chemical source were not specified in paper.
Measurement Errors:

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

System Components:
  1. Pyrene, $\ce{ C16H10 }$; [129-00-0] NIST WebBook
  2. 2,4,6-Trinitro-1-methylbenzene, $\ce{ C7H5N3O6 }$; [118-96-7] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $x_{1}$ $x_{2}$
354.7 0.0001.000
354.2 0.0560.944
375.2 0.1100.890
400.2 0.1650.835
408.7 0.2100.790
417.2 0.2590.741
426.7 0.3300.670
436.2 0.4500.550
437.7 0.5180.482
436.7 0.5690.431
427.2 0.6850.315
415.7 0.7610.239
405.2 0.8440.156
421.2 0.9710.029
423.2 1.0000.000

Author reports formation of a 1:1 pyrene - 2,4,6-trinitromethylbenzene orange molecular compound having a melting point temperature of 437.7 K. Two eutectic points occur at x1 = 0.048 and T/K = 348.2, and at x1 = 0.812 and T/K = 399.2.

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