IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Fluorene with 2,4,6-Trinitrophenol

Components:
   (1) Fluorene; C13H10; [86-73-7]  NIST Chemistry WebBook for detail
   (2) 2,4,6-Trinitrophenol; C6H3N3O7; [88-89-1]  NIST Chemistry WebBook for detail

Original Measurements:
   Kremann, R., Monatsch. Chem. 1911, 32, 609-617.

Variables:
   Temperature = Temperature

Prepared By:
   W.E. Acree, Jr.

Experimental Data:   (Notes on the Nomenclature)
  
T/KMole Fraction x1Mole Fraction x2Comment(s)
395.20.0001.000Solid Phase (2)
384.20.1340.866Solid Phase (2)
376.20.2290.771Solid Phase (2)
369.20.2930.707Solid Phase (2)
357.20.3950.605Solid Phase (2)
355.20.4460.5541:1 Compound
356.70.4780.5221:1 Compound
357.20.5260.4741:1 Compound
357.20.5660.4341:1 Compound
355.20.6060.3941:1 Compound
354.20.6380.362Eutectic (?)
359.20.7030.297Solid Phase (1)
365.70.7660.234Solid Phase (1)
372.20.8320.168Solid Phase (1)
378.70.8970.103Solid Phase (1)
383.20.9590.041Solid Phase (1)
385.71.0000.000Solid Phase (1)
Notes:
     Compiler: Phase diagram shows formation of a 1:1 molecular compound melting at about T/K = 377.5. Two eutectic points at about x1 = 0.42 and T/K = 353.4 and at x1 = 0.64 and T/K = 353.8.

Method/Apparatus/Procedure:
   Binary mixtures prepared by weight. While the experimental details were not given in the paper, compiler speculates (based upon quantity of material used) that the sample was sealed in a glass container, temperature slowly varied, and the phase diagram determined by visually noting the temperature at which the last/first crystal of solid disappeared/appeared.

Source and Purity of Materials:
   (1) Purity and chemical source were not specified in paper.
   (2) Purity and chemical source were not specified in paper.

Estimated Errors:

   Temperature: T/K: precision ± 0.2 (compiler). x1: ± 0.002 (compiler).