IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Acetonitrile with Water

Components:
   (1) Water; H2O; [7732-18-5]  NIST Chemistry WebBook for detail
   (2) Acetonitrile; C2H3N; [75-05-8]  NIST Chemistry WebBook for detail

Original Measurements:
   Benter, G.; Schneider, H., Ber. Bunsen-Ges. Phys. Chem. 77, 997 (1973).

Variables:
   Temperature = 264 K to 272 K

Prepared By:
   Valerii P. Sazonov

Experimental Remarks:

   The mutual solubility of acetonitrile (1) and water (2) in mole fractions was reported over the temperature range in graphical form. The data presented here were extracted from the published graphs by the compiler.

Experimental Data:   (Notes on the Nomenclature)
  
Mutual solubility of acetonitrile (1) and water (2)
t/°CT/K102 * Mass Fraction w1 (compiler) Mole Fraction x1Comment(s)
-8.80264.3532.40.174Water-rich phase
-7.50265.6533.60.182Water-rich phase
-5.90267.2536.30.200Water-rich phase
5.80267.35--Water-rich phase
-4.70268.4538.60.216Water-rich phase
-4.20268.95--Water-rich phase
-3.80269.3540.10.227Water-rich phase
-3.30269.8541.60.238Water-rich phase
-2.90270.2542.90.248Water-rich phase
-2.50270.65--Water-rich phase
-2.30270.8545.30.267Water-rich phase
-1.80271.3548.20.290Water-rich phase
-1.50271.65--Water-rich phase
-1.40271.7552.50.327Water-rich phase
-1.35271.8056.20.360Water-rich phase
-8.80264.35--Acetonitrile-rich phase
-7.50265.6578.40.615Acetonitrile-rich phase
-5.90267.25--Acetonitrile-rich phase
5.80267.3576.20.584Acetonitrile-rich phase
-4.70268.45--Acetonitrile-rich phase
-4.20268.9573.30.547Acetonitrile-rich phase
-3.80269.35--Acetonitrile-rich phase
-3.30269.85--Acetonitrile-rich phase
-2.90270.25--Acetonitrile-rich phase
-2.50270.6568.50.488Acetonitrile-rich phase
-2.30270.85--Acetonitrile-rich phase
-1.80271.3563.70.435Acetonitrile-rich phase
-1.50271.6561.30.410Acetonitrile-rich phase
-1.40271.7558.20.379Acetonitrile-rich phase
-1.35271.8056.2 (UCST)0.360Acetonitrile-rich phase
Method/Apparatus/Procedure:
   The turbidimetric titration method was used. A weighed amount of solution was placed in the mixing chamber described in work1 and the temperature was varied until the opalescence showed that a phase separation occurred.

Source and Purity of Materials:
   (1) Merck; synthetic grade; dried using molecular sieves and twice distilled in a fractionating column under a nitrogen atmosphere; concentration of impurities to be less than 0.003 mole % by GLC.
   (2) De-ionized; twice distilled in a quartz apparatus.

Estimated Errors:

   Temperature: ± 0.05 K

References:
   1. M. Moolel and H. Schneider, Zh. Phys. Chem. (Munich) 74, 237 (1971).