SDS Volume (4287)

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

Original Measurements

Broughton, G.; Jones, D. C.; Trans. Faraday Soc. 32, 685-9 (1936).

Variables:

Room Temp: 366 - 378 $\pu{K}$

Prepared by:

V.P. Sazonov

Method/Apparatus/Procedure:

The synthetic method, as described in Broughton, [1] was used. Liquids were pipetted into glass tubes. Temperatures at which complete miscibility occurred were measured by thermometers standardized against a set of thermometers having NPL certificates.

Source and Purity of Materials:
  1. Prepared from sodium monochloroacetate with sodium nitrite; distilled; $n_{D}^{25}$ = 1.3796, $\rho^{25} = \pu{1130.8 g L-1}$.
  2. Source not specified; purified according to Jones and Betts [2] (recrystallized from petrol ether and ethanol, MP = 62.6°C).
Estimated Errors:

Ambient temperature: ±0.05 K.

References

1 Broughton, G.; Trans. Faraday Soc. 30, 367 (1934).
2 Jones, D. C.; Betts, H. F.; J. Chem. Soc. 1177 (1928).

Components:
  1. Nitromethane, $\ce{ CH3NO2 }$; [75-52-5] NIST WebBook
  2. Hexadecanoic acid, $\ce{ C16H32O2 }$; [57-10-3] NIST WebBook
Experimental Data
Mutual solubility of nitromethane and hexadecanoic acid
$T$ (°C) $T$ ($\pu{K}$) 100w1 $x_{1}$
92.40365.55 27.16 0.6104
92.40365.55 - -
94.05367.20 - -
94.05367.20 87.86 0.9682
100.05373.65 38.20 0.7220
100.05373.65 - -
101.60374.75 - -
101.60374.75 81.55 0.9489
101.65374.80 41.07 0.7454
101.65374.80 - -
102.75375.90 - -
102.75375.90 77.10 0.9340
103.55376.70 46.85 0.7874
103.55376.70 - -
103.95377.10 - -
103.95377.10 71.56 0.9136
104.15377.30 - -
104.15377.30 68.03 0.8994
104.30377.45 - -
104.30377.45 66.64 0.8935
104.30377.45 - -
104.30377.45 65.70 0.8895
104.45377.60 54.23 0.8327
104.45377.60 - -
104.50377.65 61.05 0.8682
104.50377.65 - -
104.55377.70 62.52 0.8751
104.55377.70 - -
104.55377.70 - -
104.55377.70 - -

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