SDS Volume

Volume 38. Hydrocarbons in Water and Seawater, Part II, p None

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 After solubility equilibrium was attained an aliquot of the saturated aqueous solution was withdrawn and analyzed by solvent extraction - UV spectrophotometry.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. Deionized 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. Ethylbenzene, $\ce{ C8H10 }$; [100-41-4] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data

The solubility of ethylbenzene in water at 25°C was reported to be 1.62 × 10-3 mol(1)/dm3 mol(1)/dm3 sln. Assuming a solution density of 1.00 kg/dm3 this corresponds to a solubility of 0.0172 g(1)/100 g sln, x1 = 2.92 × 10-5, calculated by the compiler.

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