SDS Volume (414)

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 344

Original Measurements

Leinonen, P. J.; Mackay, D.; Can. J. Chem. Eng. 1973, 51, 230-3.

Variables:

Temperature: 25 °C

Prepared by:

M.C. Haulait-Pirson

Method/Apparatus/Procedure:

A mixture of (1) and (2) was equilibrated for at least 12 hrs in a 200 mL Teflon stoppered vessel with gentle shaking. The solution was allowed to settle for 6 hrs and the aqueous phase was tested (Tyndall effect). Both phases were analyzed by the gas chromatographic technique of internal standardization. The (1) in the aqueous phase was extracted into 5 mL of heptane and the extract analysed by GLC. The instrument was a Hewlett-Packard model equiped with a flame ionization detector.

Source and Purity of Materials:
  1. Phillips Petroleum Co.; research grade; purity 99%+; used without further purification.
  2. doubly distilled.

Hexane with Water

Components:

(1) Hexane, $\ce{ C6H14 }$; [110-54-3] NIST WebBook
(2) Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook

Experimental Values:

The solubility of hexane in water at 25°C was reported to be 12.3 mg(1)dm -3 sln corresponding to a mole fraction, x1, of 2.5 × 10-6.
The corresponding mass percent calculated by the compiler is 0.00123 g(1)/100 g sln.
The compiler's calculation assumes a solution density of 1.00 g/mL.

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