SDS Volume (4627)

Volume 73. Metal and Ammonium Formate Systems, p None

Original Measurements

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

Variables:

Room Temp: -5.05 - 100 °C

Prepared by:

St. Trendafilova, Chr. Balarew

Method/Apparatus/Procedure:

The isothermal method was used. Samples were taken at 6 and 18 hours, filtered into weighing bottles and weighed. They were then evaporated to dryness and the residue ignited to MgO.The lower portion of the solubility curve and the eutectic were determined by freezing point measurements. These determinations were made in a Beckmann type apparatus with a thermometer graduated in 0.1 °C.

Source and Purity of Materials:
  1. Magnesium formate was prepared by adding basic magnesium carbonate to excess formic acid. It was recrystallized from an aqueous solution containing a small amount of formic acid to prevent formation of basic salts.
Estimated Errors:

Mass concentration (m/v) (1): ±0.25 g/100 g H2O.

Components:
  1. Magnesium formate, $\ce{ Mg(CHO2)2 }$; [557-39-1] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
Solubility of magnesium formate in water.
$T$ (°C) 100w1 g1/100 g H2O m1 (mol/kg) Phase (s) ()
-5.05 12.314.0 1.22A + B
0 12.314.0 1.22A
10 12.414.1 1.23A
20 12.614.4 1.26A
30 13.015.0 1.31A
40 13.715.9 1.39A
50 14.416.8 1.47A
60 15.318.0 1.57A
70 16.119.2 1.68A
80 17.120.6 1.80A
90 18.222.2 1.94A
100 19.424.0 2.10A

(b) The solid phases are: A = Mg(CHO2)2·2H2O; B = ice.

(a) The molality values were calculated by the compilers.

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