SDS Volume (4317)

Volume 71. Nitromethane with Water or Organic Solvents, p None

Original Measurements

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

Variables:

Room Temp: 318 - 341 $\pu{K}$

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; $n_{D}^{20}$ = 1.3820, $\rho^{20} = \pu{1134 g L-1}$.
  2. Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.
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. Nitromethane, $\ce{ CH3NO2 }$; [75-52-5] NIST WebBook
  2. Ethyl dodecanoate, $\ce{ C14H28O2 }$; [106-33-2] NIST WebBook
  3. Undecyl propanoate, $\ce{ C14H28O2 }$; [5458-33-3] NIST WebBook
  4. Decyl butanoate, $\ce{ C14H28O2 }$; [5454-09-1] NIST WebBook
  5. Undecanoic acid, propyl ester, $\ce{ C14H28O2 }$; [487061-22-3] NIST WebBook
  6. Butyl decanoate, $\ce{ C14H28O2 }$; [30673-36-0] NIST WebBook
  7. Octyl hexanoate, $\ce{ C14H28O2 }$; [4887-30-3] NIST WebBook
  8. Hexyl octanoate, $\ce{ C14H28O2 }$; [1117-55-1] NIST WebBook
Experimental Data
Upper critical solution temperatures of the systems nitromethane + ester
$T$ (°C) $T$ ($\pu{K}$)
44.5317.7
47.5320.7
53.5326.7
59.5332.7
60.0333.2
63.0336.2
63.5336.7
65.0338.2
66.5339.7
67.5340.7
68.0341.2
68.0341.2

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