SDS Volume (577)

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 54

Original Measurements

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

Variables:

Room Temp: 4 - 30 °C

Prepared by:

M.C. Haulait-Pirson

Method/Apparatus/Procedure:

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 detector. The gas chromatographic conditions are described in the paper.

Source and Purity of Materials:
  1. Phillips pure grade.
  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. Pentane, $\ce{ C5H12 }$; [109-66-0] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
Solubility of pentane in water
$T$ (°C) $x_{1}$ MR1 (g/kg)
4.0 1.02 x 10-5 0.0409
10.0 1.07 x 10-5 0.0429
20.0 9.8 x 10-6 0.0393
25.0 1.01 x 10-5 0.0405
30.0 1.01 x 10-5 0.0405

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