IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Pentachlorophenol with Ammonium Chloride and Water

Components:
   (1) Ammonium Chloride; NH4Cl; [12125-02-9]  NIST Chemistry WebBook for detail
   (2) Pentachlorophenol; C6HCl5O; [87-86-5]  NIST Chemistry WebBook for detail
   (3) Water; H2O; [7732-18-5]  NIST Chemistry WebBook for detail

Original Measurements:
   Toyota, H.; Kuwahara, M., Nippon Dojohiryogaku Zasshi 1967, 38(2,3), 93-97.

Variables:
   Temperature = 27 °C   
pH = pH
   Concentration = Concentrations of NH4Cl

Prepared By:
   H. Ohtaki

Experimental Remarks:

   COMMENTS AND/OR ADDITIONAL DATA:

Solubilities of pentachlorophenol in water versus hydrogen ion activity, in the absence of KCl, at 27 °C were measured and calculated. The stoichiometric amounts of dissolved pentachlorophenol were calculated from mass balance based upon incomplete dissociation. The dissociation constant was given as Kp = [C6CL5O -] [H +] / [C6CL5OH] = 3.2 x 10-5 mol/dm3. This value together with the activity of the hydrogen ion, {H +}, as determined from pH measurements was incorporated in an equation for calculating the solubility:

S = [1.796 x 10-6/{H +}0.170] [1 + 3.2 x 10-5/{H +}]

Observed and calculated values reported:

pH

5.0                     6.0                      7.0

105mol(1)/dm3     104mol(1)/dm3     103mol(1)/dm3

Observed value:
4.05                    6.05                    8.85

Calculated value:
5.34                    6.20                    8.90



Experimental Data:   (Notes on the Nomenclature)
  

t/°C102 * g1/V2 [g dm**-3]105 * Concentration c1 [mol dm**-3]Concent. c1 NoteConcentration c2 [mol dm**-3]107 * Mole Fraction x1x1 NoteInitial pHpHpH Note
270.83903.15b1.05.690a,c55.12d
271.3775.17b0.509.335a,c55.20d
273.316112.45b0.0522.472a,c55.41d
273.065711.51b0.020.774a,c55.35d
t/°C102 * g1/V2 [g dm**-3]104 * Concentration c1 [mol dm**-3]Concent. c1 NoteConcentration c2 [mol dm**-3]106 * Mole Fraction x1x1 NoteInitial pHpHpH Note
276.1532.31b0.054.170a,c5.55.73d
t/°C101 * g1/V2 [g dm**-3]104 * Concentration c1 [mol dm**-3]Concent. c1 NoteConcentration c2 [mol dm**-3]105 * Mole Fraction x1x1 NoteInitial pHpHpH Note
271.4895.59b1.01.010a,c66.01d
271.3455.05b0.500.9120a,c66.05d
272.964511.13b0.302.0099a,c66.19d
272.6509.95b0.201.797a,c66.14d
270.59932.25b0.00.4061a,c65.70d
t/°C101 * g1/V2 [g dm**-3]103 * Concentration c1 [mol dm**-3]Concent. c1 NoteConcentration c2 [mol dm**-3]105 * Mole Fraction x1x1 NoteInitial pHpHpH Note
272.3520.883b1.01.595a,c6.56.46d
273.98191.495b0.502.7005a,c6.56.50d
275.9662.24b0.104.045a,c6.56.40d
276.2332.34b0.04.226a,c6.56.52d
t/°C101 * g1/V2 [g dm**-3]103 * Concentration c1 [mol dm**-3]Concent. c1 NoteConcentration c2 [mol dm**-3]105 * Mole Fraction x1x1 NoteInitial pHpHpH Note
272.94321.105b1.01.9967a,c7.06.97d
275.1141.92b0.503.469a,c7.06.98d
277.7772.92b0.305.275a,c7.07.03d
278.7363.28b0.205.926a,c7.07.10d
2711.134.18b0.107.553a,c7.06.86d
2714.765.54b0.0510.01a,c7.06.92d
2720.407.66b0.013.85a,c7.06.92d
t/°Cg1/V2 [g dm**-3]103 * Concentration c1 [mol dm**-3]Concent. c1 NoteConcentration c2 [mol dm**-3]104 * Mole Fraction x1x1 NoteInitial pHpHpH Note
271.6756.29b.101.137a,c7.57.50d
t/°Cg1/V2 [g dm**-3]103 * Concentration c1 [mol dm**-3]Concent. c1 NoteConcentration c2 [mol dm**-3]105 * Mole Fraction x1x1 NoteInitial pHpHpH Note
270.32761.23b1.02.223a,c88.02d
270.57802.17b0.503.920a,c88.00d
270.63392.38b0.304.299a,c88.05d
271.2474.68b0.208.458a,c88.01d
271.8516.95b0.1012.57a,c88.01d
272.90310.9b0.0519.73a,c87.95d
2719.3972.8b0.0133.8a,c87.80d
Notes:
   a  Calculated by F. W. Getzen.
   b  Reported.
   c  Calculated mole fraction based upon complete dissociation of NH4Cl.
   d  pH value of solution equilibriated with precipitate.

Method/Apparatus/Procedure:
   Pentachlorophenol and various amounts of NaOH and NH4Cl were dissolved in water at 27°C and the solutions were left for 3 days with occasional stirring (once a day for 1 hour). Then, the undissolved pentachlorophenol was filtered off and the pH values of the filterates were measured with a glass electrode. To each aliquot of the solutions was added hydrochloric acid to maintain their pH less than 3. The precipitates which resulted were aged and weighed.

Source and Purity of Materials:
   (1) Nothing specified.

Estimated Errors:
   Solubility: No estimation was given for errors in the solubility measurements. However, the reported values of S/S° (S the solubility of pentachlorophenol in KCI solutions and S° its solubility in pure water) do not fall on a single smooth curve, but rather spread. T