SDS Volume

Volume 38. Hydrocarbons in Water and Seawater, Part II, p None

Source Publication

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

Conditions:

Room Temp: 5 - 45 °C

Compiler:

M.C. Haulait-Pirson

Methodology:

The saturation vessel is drawn in the original paper. (2) was saturated with (1) via the vapor phase: a few drops of (1) were put on the bottom of a tight-fitting flask containing a small 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.

Sample Information:
  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.
Measurement Errors:

Mass concentration (m/v) (1): error given above (standard deviation)

System Components:
  1. Octane, $\ce{ C8H18 }$; [111-65-9] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
$T$ (°C) $x_{1}$ MR1 (g/kg) a
5.0 2.6 x 10-7 1.65 x 10-3
15.0 1.4 x 10-7 8.9 x 10-4
45.0 2.9 x 10-7 1.84 x 10-3

(a) Calculated by the compiler.

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