SDS Volume (380)

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 303

Original Measurements

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

Variables:

Room Temp: 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 analysed 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 equipped with a flame ionization detector.

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

Ambient temperature: ±0.1 K
Mass concentration (m/v) (1): ±1 mg(1) dm-3 sln

Components:
  1. 2-Methylpentane, $\ce{ C6H14 }$; [107-83-5] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data

The solubility of 2-methylpentane in water at 25°C was reported to be 14.2 mg(1) dm-3 sln.
With the assumption of a solution density of 1.00 g cm-3, the corresponding mass percent is 0.00142 g(1)/100 g sln and the corresponding mole fraction, x1, is 3.0 × 10-6 (compiler).

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