SDS Volume (4265)

Volume 71. Nitromethane with Water or Organic Solvents, p 1299

Original Measurements

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

Variables:

Room Temp: 322 - 348 $\pu{K}$

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 in Schmid, et al. [1]. The disappearance and reappearance of the interface between (1) and (2) could be observed without difficulty.

Source and Purity of Materials:
  1. Fisher Scientific Co.; certified, No. N-98;
    $n_{D}^{20}$ = \pu{1.3820}$, $\rho^{20} = \pu{1134 g L-1}$.
  2. Obtained by reduction of the respective α-chloroketones with lithium aluminum hydride; purified by gas-liquid partition and thin-layer adsorption chromatography.
Estimated Errors:

Upper Critical Solution 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. Nitromethane $\ce{ CH3NO2 }$ [75-52-5]; NIST WebBook
  2. 1-Octadecatrienol $\ce{ C18H32O }$ [506-44-5]; NIST WebBook
    1-Octadecadienol $\ce{ C18H34O }$ [506-43-4]; NIST WebBook
    1-Octadecenol $\ce{ C18H36O }$ [143-28-2]; NIST WebBook
Experimental Data

Upper critical solution temperatures of the systems nitromethane (1) with unsaturated 1-alcohols (2)

Unsaturated 1-alcohols (C18 x3) $t$ (°C) $T$ ($\pu{K}$)
1-Octadecatrienol (link to XML output link to JSON output link to JSON-LD output) 48.5 321.7
1-Octadecadienol (link to XML output link to JSON output link to JSON-LD output) 62.0 335.2
1-Octadecenol (link to XML output link to JSON output link to JSON-LD output) 74.5 347.7