SDS Volume

Volume 73. Metal and Ammonium Formate Systems, p None

Source Publication

Ashton, F. W.; Houston, D. F.; Saylor, C. P.; J. Res. Natl. Bur. Stan. 11, 233-53 (1933).

Conditions:

Room Temp: 0 - 100 °C

Compilers:

St. Trendafilova, Chr. Balarew

Methodology:

The isothermal method was used. Samples were taken at 6 and 18 h, filtered into weighing bottles and weighed. They were then evaporated to dryness in an oven at 125 °C, cooled in a desiccator and weighed. From the weight of anhydrous salt thus obtained, the solubility in g/100 g $\ce{H2O}$ was calculated. The barium content was determined by dissolving a sample in sulfuric acid, concentrating it by evaporation, and the acid driven off. The residue was then ignited, cooled, and weighed as sulfate.

Sample Information:
  1. Commercial barium formate was recrystallized twice from aqueous solutions, dried at 125°C and stored in a desiccator. The calcium and strontium content is 0.05%.
Measurement Errors:

Mass concentration (m/v) (1): The solubility is ±0.1 g/100 g H2O.

System Components:
  1. Barium formate, $\ce{ Ba(CHO2)2 }$; [541-43-5] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
$T$ (°C) 100w1 g1/100 g H2O m1 (mol/kg) a Phase (s) () b
0 20.8a26.2 1.15A
10 21.9a28.0 1.23A
20 23.0a29.9 1.32A
30 24.2a31.9 1.40A
40 25.4a34.0 1.50A
50 26.6a36.3 1.60A
60 27.9a38.6 1.70A
70 29.2a41.3 1.82A
80 30.7a44.2 1.94A
90 32.3a47.6 2.09A
100 33.9a51.3 2.26A

(a) These values and the molality values were calculated by the compilers.

(b) The solid phase is: A = Ba(CHO2)2.

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