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-Trinitromethoxybenzene, $\ce{ C7H5N3O7 }$; [606-35-9] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $x_{1}$ $x_{2}$
341.2 0.0001.000
356.2 0.1330.867
365.2 0.2040.796
365.7 0.2180.782
373.2 0.3400.660
376.2 0.4310.569
377.2 0.4680.532
377.7 0.5290.471
377.7 0.6240.376
385.2 0.6540.346
401.2 0.7780.222
413.7 0.8750.125
423.2 1.0000.000

Author reports formation of a 1:1 pyrene - 2,4,6-trinitromethoxybenzene yellowish-orange molecular compound having a melting point temperature of 377.7 K. Two eutectic points occur at x1 = 0.030 and T/K = 333.7, and at x1 = 0.605 and T/K = 371.7.

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