IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Nitromethane with 1,4-Dichlorobenzene and Heptane

Components:
   (1) Nitromethane; CH3NO2 ; [75-52-5]  NIST Chemistry WebBook for detail
   (2) 1,4-Dichlorobenzene; C6H4Cl2; [106-46-7]  NIST Chemistry WebBook for detail
   (3) Heptane; C7H16; [142-82-5]  NIST Chemistry WebBook for detail

Original Measurements:
   Patel, A. N.; J. Chem. Eng. Data 26, 124-7 (1981).

Variables:
   Temperature = 294 K

Prepared By:
   V. P. Sazonov

Experimental Data:   (Notes on the Nomenclature)
  
Table 1. Mutual solubility of nitromethane, 1,4-dichlorobenzene and heptane
t/°CT/KMass Fraction w1Mass Fraction w2Mole Fraction x1 (compiler)Mole Fraction x2 (compiler)
20.5293.70.0620.0000.0980.000
20.5293.70.0760.0350.1200.023
20.5293.70.0760.1140.1230.077
20.5293.70.0760.2080.1270.144
20.5293.70.0850.2950.1450.209
20.5293.70.1100.3700.1890.265
20.5293.70.2010.4080.3300.278
20.5293.70.3700.3800.5440.232
20.5293.70.5000.3380.6770.190
20.5293.70.5940.2940.7570.156
20.5293.70.7100.2110.8390.104
20.5293.70.8000.1430.8950.066
20.5293.70.8760.0770.9350.034
20.5293.70.9400.0150.9660.006
20.5293.70.9570.0000.9730.000
Table 2. Compositions of equilibrium liquid phases of the ternary system
t/°CT/KMass Fraction w1Mass Fraction w2Mole Fraction x1 (compiler)Mole Fraction x2 (compiler)Comment(s)
20.5293.70.9330.0170.9610.007nitromethane-rich phase
20.5293.70.8740.0700.9330.031nitromethane-rich phase
20.5293.70.8420.1000.9160.045nitromethane-rich phase
20.5293.70.8130.1370.8970.063nitromethane-rich phase
20.5293.70.7800.1550.8820.073nitromethane-rich phase
20.5293.70.7100.2100.8390.103nitromethane-rich phase
20.5293.70.0790.0320.1250.021heptane-rich phase
20.5293.70.0780.1350.1270.091heptane-rich phase
20.5293.70.0760.1950.1260.135heptane-rich phase
20.5293.70.0760.2450.1290.172heptane-rich phase
20.5293.70.0850.2950.1450.209heptane-rich phase
20.5293.70.1100.3700.1890.265heptane-rich phase
Method/Apparatus/Procedure:
   Two methods were used. The binodal solubility curve was determined by the method of appearance and disappearance of turbidity (Othmer et al.1). The analytical method was used to determine equilibrium liquid phase compositions. Various mixtures of known composition within the heterogenous region were prepared and brought to equilibrium. Conjugate phases were analyzed by refractive index measurement in conjunction with calibration curve prepared with mixtures of known composition on the solubility curve. Values of composition determined were checked by material-balance calculation.

Source and Purity of Materials:
   (1) Source not specified; laboratory grade reagent; not purified.
   (2) Source not specified; laboratory grade reagent; not purified.
   (3) Source not specified; laboratory grade reagent; not purified.

Estimated Errors:

   Temperature: control to ± 0.5 K
   Titer: ± 0.05 mL
   Titer: to 0.1 mg.

References:
   1D. F. Othmer, R. E. White, E. Trueger, Ind. Eng. Chem. 33, 1240 (1941).