SDS Volume (5026)

Volume 78. Acetonitrile Binary Systems, p None

Original Measurements

Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; Microchem. J. 9, 134-144 (1965).

Variables:

Room Temp: 296 - 339 $\pu{K}$

Prepared by:

V.P. Sazonov

Method/Apparatus/Procedure:

The synthetic method was used. A Reichert microscope, type RCH, equipped with a heating stage was used as described elsewhere [1]. The disappearance and reappearance of the interface between (1) and (2) could be observed without difficulty.

Source and Purity of Materials:
  1. Baker Chemical Co.; reagent No. 9011; $n_{D}^{20}$ = 1.3445, $d_{4}^{20}$ = 0.780.
  2. Some alcohols obtained from Aldrich Chemical Co.; all other alcohols prepared by reduction of the corresponding methyl ketones with lithium aluminum hydride; purified by gas-liquid partition chromatography.
Estimated Errors:

Ambient temperature: ±0.5 K.

References

1 Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; J. Am. Oil Chem. Soc. 42, 372 (1965).

Components:
  1. Acetonitrile, $\ce{ C2H3N }$; [75-05-8] NIST WebBook
  2. 2-Alcohols (C11-C19), $\ce{ C11H24O - C19H40O }$;
Experimental Data
Upper critical solution temperatures of the systems acetonitrile (1) + 2-alcohol (2)
$T$ (°C) $T$ ($\pu{K}$)
22.5295.7
29.0302.2
35.0308.2
39.5312.7
45.0318.2
50.0323.2
55.5328.7
66.0339.2

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