IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Nitromethane with Cyclohexane and Castor oil methyl esters

Components:
   (1) Castor oil methyl esters; ; []  NIST Chemistry WebBook for detail
   (2) Nitromethane; CH3NO2 ; [75-52-5]  NIST Chemistry WebBook for detail
   (3) Cyclohexane; C6H12; [110-82-7]  NIST Chemistry WebBook for detail

Original Measurements:
   Lakshmanan, C. M. and Laddha, G. S.; J. Madras Univ. 29, 97-102 (1959).

Variables:
   Temperature = 303 K

Prepared By:
   V. P. Sazonov

Experimental Remarks:

   The plait point composition: w1 = 0.648, w2 = 0.102, and w3 = 0.250.

Experimental Data:   (Notes on the Nomenclature)
  
Table 1. Mutual solubility of nitromethane, cyclohexane and castor oil methyl esters
t/°CT/KMass Fraction w1Mass Fraction w2Mass Fraction w3
303030.03920.96080.0000
303030.04310.90670.0502
303030.07040.77890.1508
303030.10310.64000.2569
303030.18720.45960.3532
303030.22110.40340.3755
303030.27360.32410.4023
303030.32850.26380.4076
303030.41710.19820.3847
303030.55430.13170.3139
303030.60440.12010.2755
303030.65390.10050.2456
303030.71080.08220.2070
303030.77780.06620.1560
303030.88570.06470.0496
303030.94570.05430.0000
Table 2. Equilibrium tie line data for the ternary system  
t/°CT/KMass Fraction w3Comment(s)
303030.0298(1)-rich phase (OH value of esters = 198.6)
303030.0447(1)-rich phase (OHV = 188.6)          
303030.0632(1)-rich phase (OHV = 186.3)
303030.0669(1)-rich phase (OHV = 186.3)
303030.0806(1)-rich phase (OHV = 185.0)
303030.0889(1)-rich phase (OHV = 184.7)
303030.1037(1)-rich phase (OHV = 179.9)
303030.1451(1)-rich phase (OHV = 175.1)
303030.0819(2)-rich phase (OHV = 148.3)
303030.1532(2)-rich phase (OHV = 159.2)
303030.2592(2)-rich phase (OHV = 155.1)
303030.3114(2)-rich phase (OHV = 154.6)
303030.3535(2)-rich phase (OHV = 157.4)
303030.3802(2)-rich phase (OHV = 156.6)
303030.3984(2)-rich phase (OHV = 158.5)
303030.3957(2)-rich phase (OHV = 163.7)
Notes:

Method/Apparatus/Procedure:
   The method (Othmer et al.1) was used. Known mixtures of (1) and (3), or of (2) and (3), were held in a water bath and titrated with the third component until turbidity. Known mixtures of (1), (2) and (3) within the heterogeneous region were placed in the bath after agitation, and allowed to attain equilibrium. Two phases were seprated and weighted. The amount of (3) distributed in each phase was determined by taking a weighed quantity of each phase and distilling off the solvents on a water bath. Total weight of the esters thus obtained was checked against the weight of esters taken originally in the mixture.

Source and Purity of Materials:
   (1) Fluka AG; distilled over a rectification column; b. p. = (100.5 to 101.5) °C, n(30 °C, D) = 1.3770, d(30 °C, 4 °C) = 1.1237.
   (2) BDH Ltd.; rectified; b. p. = (80.5 to 81.5) °C, n(30 °C, D) = 1.4206, d(30 °C, 4 °C) = 0.7725.
   (3) Prepared by methylation of castor oil; dried and distilled; n(30 °C, D) = 1.4602, d(30 °C, 4 °C) = 0.9250 .

Estimated Errors:

   Temperature: control to ± 1 K.

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