SDS Volume (430)

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 363

Original Measurements

Jonsson, J. A.; Vejrosta, J.; Novak, J.; Fluid Phase Equilib. 1982, 9, 279-86.

Variables:

Room Temp: 15 - 35 °C

Prepared by:

G.T. Hefter

Method/Apparatus/Procedure:

Air-water partition coefficients were measured by saturating a portion of water by a stream of nitrogen containing a known vapour concentration of (1). After equilibration, the dissolved (1) was adsorbed in a porous polymer trap and the entrapped (1) analyzed by gas chromatography. The method and apparatus are described in detail in [1].

Source and Purity of Materials:
  1. Fluka, >99.7%, used as received.
  2. Not specified.
Estimated Errors:

Ambient temperature: Not specified.

References

1 Vejrosta, J.; Novak, J.; Jonsson, J. A.; Fluid Phase Equil. 1982, 8, 25-35.

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) MR1 (mg/kg) $x_{1}$ MR1 (g1/100 g sln)
15 10.72 2.24 x 10-61.07 x 10-3
20 10.32 2.15 x 10-61.03 x 10-3
25 10.09 2.11 x 10-61.01 x 10-3
30 10.02 2.09 x 10-61.00 x 10-3
35 10.10 2.11 x 10-61.01 x 10-3

(a) Solubility values were calculated by the authors from their smoothed air-water partition coefficient (KAM) by assuming KAM values obtained at infinite dilution were valid at the saturation pressure of (1).

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