IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Nitroethane with 1-Propanol and Water

Components:
   (1) 1-Propanol; C3H8O; [71-23-8]  NIST Chemistry WebBook for detail
   (2) Nitroethane; C2H5NO2; [79-24-3]  NIST Chemistry WebBook for detail
   (3) Water; H2O; [7732-18-5]  NIST Chemistry WebBook for detail

Original Measurements:
   Malone, J.W.; Vining, R.W., J. Chem. Eng. Data 12, 387-9 (1967).

Variables:
   Temperature = 298 K

Prepared By:
   V. P. Sazonov and N. I. Lisov

Experimental Data:   (Notes on the Nomenclature)
  
Table 1. Mutual solubility of nitroethane (1), 1-propanol (2) and water (3)
t/°CT/K102 * Mass Fraction w1102 * Mass Fraction w2Mole Fraction x1 (compiler)Mole Fraction x2 (compiler)
25298 5.05 0.000.01260.0000
25298 4.83 3.920.01240.0126
25298 4.80 7.680.01270.0253
25298 5.2311.700.01430.0399
25298 5.5815.630.01580.0553
25298 7.4819.460.02230.0723
25298 9.9822.930.03140.0900
2529812.5025.840.04140.1070
2529815.6029.390.05540.1304
2529818.6531.960.07060.1510
2529822.2034.580.09040.1760
2529825.9136.470.11350.1996
2529832.6037.500.15980.2296
2529839.4936.830.21450.2498
2529846.3535.060.27660.2613
2529851.9232.660.33080.2599
2529858.1029.700.39790.2541
2529863.4326.610.45910.2406
2529869.3122.940.53210.2200
2529874.7719.250.60430.1943
2529880.2315.450.68270.1642
2529885.3711.550.75800.1281
2529890.40 7.700.83760.0891
2529894.98 3.780.90570.0450
2529899.14 0.000.96510.0000
Table 2. Composition of equilibrium liquid phases
t/°CT/K102 * Mass Fraction w1102 * Mass Fraction w2Mole Fraction x1 (compiler)Mole Fraction x2 (compiler)Comment(s)
2529893.50 4.900.87970.0576nitroethane-rich phase
2529885.8011.300.76610.1260nitroethane-rich phase
2529874.6019.400.60240.1957nitroethane-rich phase
2529859.7028.600.41410.2478nitroethane-rich phase
2529841.6036.300.23240.2533nitroethane-rich phase
2529831.7037.600.15350.2274nitroethane-rich phase
Table 3. Composition of equilibrium liquid phases
t/°CT/K102 * Mass Fraction w1102 * Mass Fraction w2Mole Fraction x1 (compiler)Mole Fraction x2 (compiler)Comment(s)
252984.80 5.000.01240.0161water-rich phase
252985.00 9.800.01340.0329water-rich phase
252985.2012.400.01430.0426water-rich phase
252985.6014.700.01570.0516water-rich phase
252986.9018.100.02020.0661water-rich phase
252989.4022.100.02920.0856water-rich phase
Method/Apparatus/Procedure:
   Two methods were used. The solubility curve was determined by the titration method. A measured amount of (1) was added to a tarred 50-mL Erlenmeyer flack and titrated to the cloud point with (3). To each succeeding sample of (1) a measured quantity of (2) was added and the mixture was titrated with (3). Weight measurements were made using an analytical balance. Titrations were performed using 5-mL certified micro burettes graduated in 0.01 mL divisions. The analytical method was used for determination of equilibrium liquid phases compositions. The mixture of (1), (2) and (3) was then agitated vigorously and allowed to separate into phases. Densities were used to determine compositions of the equilibrium phases. Refractive index readings were used primarily to identify phases and secondarily to check compositions from density measurements (see Tables 1 and 2).

Source and Purity of Materials:
   (1) Commercial Solvents Corp.; purity 93.9 mass % with 2.3 mass % of nitromethane and 3.8 mass % of 2-nitropropane; n(25°C,D) = 1.3890.
   (2) Fisher; certified reagent grade; b. p. = (97.0 to 97.4)°C, n(25°C,D) = 1.3871.
   (3) Distilled.

Estimated Errors:

   Temperature: ±1 K.