SDS Volume (2065)

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. Phenanthrene, $\ce{ C14H10 }$; [85-01-8] NIST WebBook
  2. 1,2,3,5-Tetranitrobenzene, $\ce{ C6H2N4O8 }$; [3698-53-1] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $x_{1}$ $x_{2}$
399.2 0.0001.000
394.2 0.0790.921
394.2 0.1850.815
394.2 0.1900.810
396.5 0.2800.720
396.7 0.3040.696
398.2 0.3770.623
397.7 0.4250.575
396.7 0.4510.549
396.2 0.4630.537
395.7 0.5150.485
393.7 0.5170.483
391.2 0.5870.413
391.2 0.5980.402
384.7 0.6800.320
372.2 0.7620.238
364.2 0.7930.207
360.2 0.8640.136
363.2 0.8860.114
373.7 1.0000.000

Author reports formation of an incongruently melting 1:1 phenanthrene - 1,2,3,5-tetranitrobenzene compound, and a 2:3 phenanthrene - 1,2,3,5-tetranitrobenzene molecular compound having a melting point temperature of 398.2 K. Two eutectic points occur at x1 = 0.120 and T/K = 388.2, and at x1 = 0.822 and T/K = 352.2. A peritectic point occurs at x1 = 0.615 and T/K = 388.2. Compiler: From a thermodynamic viewpoint, phase diagram is more in agreement with formation of a 1:1 molecular compound, with the existence of a peritectic point at x1 = 0.615 and at T/K = 388.2 and a miscibility gap at higher temperature, with a monotectic point close to x1 = 0.12 and T/K = 392, and an eutectic point at x1 = 0.822 and T/K = 352.2.

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