SDS Volume (4795)

Volume 73. Metal and Ammonium Formate Systems, p None

Original Measurements

Hampshire, C. H.; Pratt, W. R.; Pharm. J. (London) 91, 138 (1913).

Variables:

Room Temp: 17 - 33.5 °C

Prepared by:

St. Trendafilova, St. Tepavitcharova

Method/Apparatus/Procedure:

Water and an excess of the crystallized salt were stirred in the apparatus described by Lumsden [1]. The formic acid content was determined by the method of Jones [2]. Iron was determined by direct ignition and weighed as the oxide.

Source and Purity of Materials:
  1. The salt was prepared by dissolving ferric hydroxide in 50% $\ce{CH2O2}$ (d = 1.124) on a water bath, evaporating down, and cooling [3].
Estimated Errors:

Ambient temperature: No information is given.
Mass concentration (m/v) (1): No information is given.

References

1 Lumsden, J. C.; J. Chem. Soc. 81, 355 (1902).
2 Jones, H. C.; Amer. Chem. Journ. 17, 539 (1895).
3 Bellini; Arch. Pharm. 247, 423 (1909).

Components:
  1. Ferric hydroxide formate, $\ce{ Fe3(CHO2)7(OH)2.4H2O }$; [111195-22-5] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
Solubility of ferric formate in water.
$T$ (°C) 100w1 g1/100 g H2O m1 (mol/kg) Phase (s) ()
17 5.055.32 0.11A
20 5.245.53 0.12A
22 5.325.62 0.12A
24 5.405.71 0.12A
25.5 5.816.17 0.13A
27 6.096.49 0.14A
29 6.336.76 0.14A
33.5 6.717.19 0.15A

(a) These values were calculated by the compilers.

(b) The solid phase is: A = Fe3(CHO2)7(OH)2ยท4H2O.

Download Data   link to XML output link to JSON output link to JSON-LD output