SDS Volume

Volume 78. Acetonitrile Binary Systems, p 1088

Source Publication

Smagowski, H.; Zesz. Nauk. Wydz. Mat., Fiz. Chem., Univ. Gdanski, Chem. 3, 45-53 (1974).

Conditions:

Room Temp: 273 - 308 $\pu{K}$

Compiler:

V.P. Sazonov

Methodology:

The titration method was used: 25 mL of [1] and an amount of (2) exceeding the solubility were placed in 50 mL volumetric flasks. The flasks were closed by ground glass stoppers and stored at the required temperature in a thermostat for 45 hours, with intensive stirring every several hours. After this, 5 mL samples of the saturated solution were taken by pipette, diluted to 25 mL with water and titrated against 0.07 0.1 N sodium hydroxide solutions by using phenolphthalein indicator.

Sample Information:
  1. Source not specified; purity not specified; dried over anhydrous $\ce{K2CO3}$ and repeatedly distilled over $\ce{P2O5}$.
  2. Source not specified; purity not specified; purified by crystallization from water.
Measurement Errors:

Ambient temperature: Not reported.
Mass concentration (m/v) (1): Not reported.

Methodology Citation

1 Timmermans, J.; Physico-Chemical Constants of Pure Organic Compounds (Elsevier, New York, 1950).

System Components:
  1. Acetonitrile, $\ce{ C2H3N }$; [75-05-8] NIST WebBook
  2. Nonanedioic acid, $\ce{ C9H16O4 }$; [123-99-9] NIST WebBook
Experimental Data
$T$ (°C) $T$ ($\pu{K}$) $C_{1}$ (mol/L) 100w2 $x_{2}$
0.0273.2 8 x 10-3 1.9 x 10-34.2 x 10-4
15.0288.2 0.010 2.4 x 10-35.2 x 10-4
25.0298.2 0.019 4.6 x 10-31.01 x 10-3
35.0308.2 0.069 0.0173.8 x 10-3

(a) For these calculations the compiler assumed that the densities of the solutions were those of acetonitrile1 at the specified temperatures.

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