IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Nitromethane with 2-Furancarboxoaldehyde, Toluene and Methylcyclohexane

Components:
   (1) Nitromethane; CH3NO2 ; [75-52-5]  NIST Chemistry WebBook for detail
   (2) 2-Furancarboxaldehyde; C5H4O2; [98-01-1]  NIST Chemistry WebBook for detail
   (3) Methylcyclohexane; C7H14; [108-87-2]  NIST Chemistry WebBook for detail
   (4) Toluene; C7H8; [108-88-3]  NIST Chemistry WebBook for detail

Original Measurements:
   Lafyatis, D. S.; Scott, L. S.; Trampe, D. M. and Eckert, C. A.; Ind. Eng. Chem. Res. 28, 585 (1989).

Variables:
   Temperature = 323 K

Prepared By:
   V. P. Sazonov

Experimental Data:   (Notes on the Nomenclature)
  
Compositions of the two liquid phases at equilibrium for the quaternary system
t/°CT/KMass Fraction w1Mass Fraction w2Mass Fraction w3Mole Fraction x1Mole Fraction x2Mole Fraction x3Comment(s)
50.00323.150.4100.4660.0140.5230.3770.012nitromethane-rich phase
50.00323.150.4080.4480.0280.5200.3630.024nitromethane-rich phase
50.00323.150.3880.4280.0530.5000.3500.045nitromethane-rich phase
50.00323.150.3650.4050.0780.4760.3340.067nitromethane-rich phase
50.00323.150.3560.3850.0940.4650.3200.081nitromethane-rich phase
50.00323.150.3410.3660.1080.4480.3060.094nitromethane-rich phase
50.00323.150.6990.2070.0080.7860.1480.006nitromethane-rich phase
50.00323.150.6920.1980.0240.7800.1420.018nitromethane-rich phase
50.00323.150.6590.1960.0420.7530.1420.032nitromethane-rich phase
50.00323.150.6400.1870.0590.7370.1370.045nitromethane-rich phase
50.00323.150.6070.1770.0870.7080.1310.067nitromethane-rich phase
50.00323.150.5470.1670.1230.6540.1270.097nitromethane-rich phase
50.00323.150.4500.1390.1650.5630.1100.137nitromethane-rich phase
50.00323.150.3670.1140.1880.4770.0940.162nitromethane-rich phase
50.00323.150.1900.6530.0230.2700.5900.022nitromethane-rich phase
50.00323.150.1820.6000.0570.2600.5440.054nitromethane-rich phase
50.00323.150.1610.5250.0910.2320.4810.087nitromethane-rich phase
50.00323.150.0460.0600.0230.0710.0600.024hydrocarbon-rich phase
50.00323.150.0470.0610.0450.0740.0600.046hydrocarbon-rich phase
50.00323.150.0630.0770.0780.0970.0750.080hydrocarbon-rich phase
50.00323.150.0780.0960.1100.1180.0930.111hydrocarbon-rich phase
50.00323.150.0870.1090.1300.1320.1050.130hydrocarbon-rich phase
50.00323.150.1080.1260.1440.1610.1200.142hydrocarbon-rich phase
50.00323.150.0530.0210.0160.0820.0210.016hydrocarbon-rich phase
50.00323.150.0620.0260.0430.0960.0250.044hydrocarbon-rich phase
50.00323.150.0790.0300.0720.1210.0290.073hydrocarbon-rich phase
50.00323.150.0920.0340.0970.1390.0330.097hydrocarbon-rich phase
50.00323.150.1230.0420.1350.1820.0400.133hydrocarbon-rich phase
50.00323.150.1720.0580.1710.2480.0530.163hydrocarbon-rich phase
50.00323.150.2740.0860.1920.3730.0740.173hydrocarbon-rich phase
50.00323.150.3670.1140.1880.4770.0940.162hydrocarbon-rich phase
50.00323.150.0290.1070.0350.0450.1070.037hydrocarbon-rich phase
50.00323.150.0440.1530.0800.0680.1510.083hydrocarbon-rich phase
50.00323.150.0610.1320.1290.0860.1980.121hydrocarbon-rich phase
Method/Apparatus/Procedure:
   The analytical method was used. The equilibrium cell consisted of a vertical glass cylinder with a volume of about 80 mL. A magnetic stir bar was used for mixing the sample, and the cell was thermostated. The two partially miscible components were charged to the equilibrium cell in approximately equal volumes, and the mixture was stirred for a minimum of 15 min. Next, the third component, which distributes itself between the two phases was added to the equilibrium cell, stirred, and allowed to equilibrate before sampling. Samples of each phase were taken and analyzed by gas chromatography.


   Composition: discrepancy of 2 determinations always less than 0.005 mole fraction.
Source and Purity of Materials:
   (1) Source not specified; purity greater than 99.9 mole %; not purified.
   (2) Source not specified, purity greater than 99.9 mole %; not purified.
   (3) Source not specified, purity greater than 99.9 mole %; not purified.
   (4) Source not specified, purity greater than 99.9 mole %; not purified.

Estimated Errors:

   Temperature: control to ± 0.01 K.