SDS Volume

Volume 37. Hydrocarbons in Water and Seawater, Part I, p 183

Source Publication

Sanemasa, I.; Arakawa, S.; Araki, M.; Deguchi, T.; Bull. Chem. Soc. Jpn. 1984, 57, 1539-44.

Conditions:

Room Temp: 25 °C

Compiler:

G.T. Hefter

Methodology:

The apparatus used is described in detail in [1]. The method involves the introduction of solute vapor (1) into liquid (2) by bubbling air through liquid (1) using a recirculating pump in a closed system. After solubility equilibrium was attained an aliquot of the saturated aqueous solution was withdrawn and analyzed by solvent extraction - UV spectrophotometry.

Sample Information:
  1. Analytical reagent grade source and purity not stated, used without further purification.
  2. Deioized and redistilled; no further details given
Measurement Errors:

Ambient temperature: Not specified.

Methodology Citation

1 Sanemasa, I.; Araki, M.; Deguchi, T.; Nagai, H.; Bull. Chem. Soc. Jpn. 1982, 55, 1054-62.

System Components:
  1. Benzene, $\ce{ C6H6 }$; [71-43-2] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data

The solubility of benzene in water at 25°C was reported to be 2.07 × 10-2 mol (1)/dm 3 sln. Assuming a solution density of 1.00 kg/dm3 this corresponds to a solubility of 0.162 g(1)/100 g sln, x1 = 3.73 × 10-4, calculated by the compiler.

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