SDS Volume

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 416

Source Publication

Krzyzanowska, T.; Szeliga, J.; Nafta (Katowice) 1978, 12, 413-7.

Conditions:

Room Temp: 25 °C

Compiler:

M.C. Haulait-Pirson

Methodology:

The saturated solutions of (1) in (2) were prepared in two ways. First, 200 µL of (1) was injected into 20 mL of (2) and thermostatted at 25 °C. Second, the mixture of (1) and (2) as above was thermostatted at 70 °C and then cooled to 25 °C. The time required to obtain equilibrium was three weeks. The solubility of (1) in (2) was measured by glc. A Perkin-Elmer model F-11 gas chromatograph equipped with a 100-150 mesh Porasil column (70 °C) and a flame ionization detector was used. Saturated solutions of heptane in (2) were used as saturated solution.

Sample Information:
  1. Not specified.
  2. not specified.
Measurement Errors:

Mass concentration (m/v) (1): 11.0 mg(1)/kg(2) (standard deviation from 7-9 determinations).

System 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 to be 554.0 mg(1)/kg(2).
The corresponding mass percent and mole fraction, x1, calculated by the compilers are 0.0554 g(1)/100 g sln and 1.08 × 10-4.
Editor's Note: Based on the results for this and other hydrocabon-water systems, uncertainty exists about whether the datum compiled here is independent of that of Price ofor the same system.

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