SDS Volume

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

Source Publication

Cullinane, N. M.; Rees, W. T.; Trans. Faraday Soc. 1940, 36, 506-514.

Conditions:

Room Temp: 412.9 - 457.6 $\pu{K}$

Compiler:

W.E. Acree, Jr.

Methodology:

Mixtures were placed in small capillary tubes. Temperature was slowly varied with ample time given for equilibration. Transition temperatures determined by visual observations. Reported temperatures verified by repetitive measurements.

Sample Information:
  1. Purity and chemical source were not specified in paper, was sublimed and recrystallized from alcohol.
  2. Synthesized by the authors, was purified by sublimation and recrystallized from alcohol.
Measurement Errors:

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

System Components:
  1. Phenothiazine, $\ce{ C12H9NS }$; [92-84-2] NIST WebBook
  2. Phenoxazine, $\ce{ C12H8NO }$; [135-67-1] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $T$ ($\pu{K}$) $x_{1}$ $x_{2}$
429.9429.1 0.0001.000
427.3415.3 0.0590.941
424.3413.0 0.1290.871
416.7413.2 0.2560.744
415.2412.9 0.2650.735
415.8413.1 0.3110.689
430.1413.6 0.5170.483
438.1413.0 0.6400.360
449.5416.9 0.8240.176
452.0421.5 0.8820.118
457.6456.8 1.0000.000

(a) Phase diagram, given in the original paper, shows formation of a partial series of solid solutions having compositions from circa x2 = 0.00 to x2 = 0.22 and from x2 = 0.93 to x2 = 1.00. Tin refers to the temperature at which crystallization begins; Tfin is the temperature at which crystallization of the solid solution concludes.

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