SDS Volume (449)

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 390

Original Measurements

Morrison, T. J.; Billett, F.; J. Chem. Soc. 1952, 3819-3822.

Variables:

Room Temp: 25 °C

Prepared by:

A. Maczynski

Method/Apparatus/Procedure:

After an excess of (1) had been shaken with about 1 L of (2) for about a week, a known volume of saturated solution was made slightly alkaline, and a stream of pure air passed through a silica tube packed with cupric oxide and heated to redness, the (2) was removed by concentrated sulfuric acid and calcium chloride and the carbon dioxide absorbed and weighed in soda-asbestos. The precautions usual in organic combustions were taken.

Source and Purity of Materials:
  1. source not specified; purest obtainable material; distilled; purity not specified.
  2. Not specified.
Estimated Errors:

Ambient temperature: ±0.1 K
Mass concentration (m/v) (1): ±0.5% (mean of large numbers of determinations)

Components:
  1. Toluene, $\ce{ C7H8 }$; [108-88-3] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data

The solubility of toluene in water at 25°C was reported tobe 0.00582 mol(1)/1000 g (2).
The corresponding mass percent and mole fraction, x1, calculated by compilers are 0.0536 g(1)/100 g sln and x1 = 1.05 × 10-4. The compiler's calculations assume a solution density of 1.00 g/mL.

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