SDS Volume (489)

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 426

Original Measurements

Brown, R. L.; Wasik, S. P.; J. Res. Natl. Bur. Stan. 1974, 78A, 453-60.

Variables:

Room Temp: 0 - 20 °C
Salinity: 34.42 g salts/kg sln

Prepared by:

G.T. Hefter, D.G. Shaw

Method/Apparatus/Procedure:

Solubilities were calculated from partition coefficient measurements for the hydrocarbon between an aqueous solution and its vapor using headspace chromatography.
The apparatus and the method of obtaining the partition coefficients are described in detail in the paper. The hydrocarbon was introduced as a vapor (to avoid emulsification) into a glass equilibration cell containing about 45 mL of water. The vapor was subsequently analysed by gas chromatography using He as the carrier. Possible sources of error are discussed in detail although the source of vapor pressure data used to calculate solubilities are not given.

Source and Purity of Materials:
  1. 99.99 mole percent purity;source and methods of purification not specified.
  2. Prepared according to [1]. Purity not specified.
Estimated Errors:

Ambient temperature: ±0.01 K
Mass concentration (m/v) (1): see Table above

References

1 Sverdrup, H. U.; Johnson, M. W.; Fleming, R. H.; The Oceans, 1942, Prentice-Hall, englewood Cliffs, New Jersey p186.

Components:
  1. Toluene, $\ce{ C7H8 }$; [108-88-3] NIST WebBook
  2. Seawater, $\ce{ H2O }$; [7732-18-5(C)] NIST WebBook
Experimental Data
Solubility of toluene in artificial seawater
$T$ (°C) MR1 (g1/100 g2) $x_{1}$
0.19 0.0449 9.0 x 10-5
5.32 0.0429 8.60 x 10-5
10.05 0.0416 8.34 x 10-5
14.96 0.0405 8.12 x 10-5
20.04 0.0397 7.96 x 10-5

(a) Numbers in parentheses are standard deviations from 4 observations

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