SDS Volume

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

Source Publication

Kravchenko, V. M.; Pastukhova, I. S.; J. Appl. Chem. USSR 1952, 25, 343-350.

Conditions:

Room Temp: 297.2 - 353.2 $\pu{K}$

Compiler:

W.E. Acree, Jr.

Methodology:

Phase diagram was determined using a thermal analysis method [1], supplemented by visual observation.

Sample Information:
  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 distilled before use.
Measurement Errors:

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

Methodology Citation

1 Kravchenko, V. M.; Zh. Fiz. Khim. 1939, 13, 133-145.

System Components:
  1. Naphthalene, $\ce{ C10H8 }$; [91-20-3] NIST WebBook
  2. Isoquinoline, $\ce{ C9H7N }$; [119-65-3] NIST WebBook
Experimental Data
$T$ ($\pu{K}$) $T$ ($\pu{K}$) $x_{1}$ $x_{2}$
297.2297.2 0.0001.000
301.2299.7 0.0470.953
306.2304.2 0.1090.891
314.2311.2 0.2080.792
319.7316.2 0.2970.703
326.7323.2 0.4120.588
331.2327.2 0.5000.500
336.7333.2 0.6020.398
341.2338.2 0.7000.300
345.2343.2 0.8000.200
349.2348.2 0.9040.096
353.2353.2 1.0000.000

(a) Phase Diagram, given in the original paper, shows formation of a complete series of solid solutions. Melting points of binary mixtures lie between those of the two pure components. 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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