SDS Volume (409)

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 340

Original Measurements

Nelson, H. D.; De Ligny, C. L.; Recl. Trav. Chim. Pays-Bas 1968, 87, 528-44.

Variables:

Room Temp: 4 - 55 °C

Prepared by:

M.C. Haulait-Pirson

Method/Apparatus/Procedure:

The saturation vessel is drawn in the original paper. (2) was saturated with (10 via the vapor phase: a few drops of a tight-fitting flask filled with water. Complete saturation was reached by shaking overnight in an upright position. Samples were taken from the aqueous solution with a microsyringe through the septum and injected into the gas chromatograph equipped with a flame ionization detector. The gas chromatographic conditions are described in the paper.

Source and Purity of Materials:
  1. Fluka purum.
  2. Tap-water was refluxed for eight hours in the presence of $\ce{KMnO4}$ and $\ce{KOH}$ and distilled. The whole process was repeated once more.
Estimated Errors:

Mass concentration (m/v) (1): error given above (90% probability interval)

Components:
  1. Hexane, $\ce{ C6H14 }$; [110-54-3] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
Solubility of hexane in water
$T$ (°C) $x_{1}$ MR1 (g/kg)
4.0 3.42 x 10-6 0.0164
14.0 3.17 x 10-6 0.0152
25.0 3.83 x 10-6 0.0183
35.0 2.69 x 10-6 0.0129
45.0 4.64 x 10-6 0.0222
55.0 4.42 x 10-6 0.0212

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