SDS Volume (2156)

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

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. Pyrene, $\ce{ C16H10 }$; [129-00-0] NIST WebBook
  2. 1,3-Dinitrobenzene, $\ce{ C6H4N2O4 }$; [99-65-0] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $x_{1}$ $x_{2}$
363.2 0.0001.000
358.2 0.0870.913
354.2 0.1460.854
357.2 0.1690.831
359.7 0.2100.790
360.2 0.2380.762
362.2 0.2980.702
362.5 0.3350.665
362.2 0.3790.621
363.7 0.4140.586
364.7 0.4370.563
365.0 0.4460.554
365.7 0.5010.499
366.0 0.5040.496
365.2 0.5240.476
364.2 0.5510.449
376.2 0.5700.430
367.2 0.5710.429
376.2 0.6090.391
384.2 0.6590.341
395.7 0.7230.277
423.2 1.0000.000

Author reports formation of a 1:1 pyrene - 1,3-dinitrobenzene orangish-yellow molecular compound having a melting point temperature of 365.9 K, and a second 1:2 pyrene - 1,3-dinitrobenzene yellow compound with melting point of 362.5 K. Three eutectic points occur at x1 = 0.130 and T/K = 352.2, x1 = 0.366 and T/K = 361.2, and at x1 = 0.565 and T/K = 362.2.

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