SDS Volume (2006)

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

Original Measurements

Nigam, R. K.; Dhillon, M. S.; Indian J. Chem. 1970, 8, 821-825.

Variables:

Room Temp: Temperature $\pu{K}$

Prepared by:

W.E. Acree, Jr.

Method/Apparatus/Procedure:

Phase diagram was determined using a thaw-melt method (described in detail in [1]).

Source and Purity of Materials:
  1. Purity and chemical source were not specified in paper, was recrystallized before use.
  2. Purity and chemical source were not specified in paper, was recrystallized before use.
Estimated Errors:

Ambient temperature: T/K: precision ±0.1. x1: ±0.0001 (compiler).

References

1 Rastogi and Nigam, Proc. Natl. Inst. Sci. India 1960, 26, 184

Components:
  1. Naphthalene, $\ce{ C10H8 }$; [91-20-3] NIST WebBook
  2. 2,4,6-Trinitrophenol, $\ce{ C6H3N3O7 }$; [88-89-1] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $x_{1}$ $x_{2}$
395.2 0.00001.0000
387.2 0.08650.9135
404.0 0.17540.8246
409.2 0.21450.7855
416.8 0.28650.7135
423.0 0.39400.6060
424.2 0.45250.5475
424.1 0.55330.4467
421.2 0.64120.3588
407.4 0.80190.1981
381.2 0.91810.0819
353.4 1.00000.0000

Compiler: Phase diagram shows formation of a 1:1 naphthalene - 2,4,6-trinitrophenol molecular compound. The two eutectic points occur at about x1 = 0.059 and T/K = 382.6 and at x1 > 0.95 and T/K = 345.6.

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