SDS Volume

Volume 73. Metal and Ammonium Formate Systems, p None

Source Publication

Stoilova, D.; Balarew, C.; Vassileva, V.; Comm. Dept. Chem. Bulg. Acad. Sci. 18, 3 (1985).

Conditions:

Room Temp: 10 - 70 °C

Compilers:

St. Trendafilova, Chr. Balarew

Methodology:

The method used was the isothermal decrease of supersaturation, under stirring, for 15-20 hrs. The $\ce{Cu^{2+}}$ content of the liquid and solid phases was determined complexometrically using Complexon III at pH 5.5-6.0 and Xylenol Orange as indicators.

Sample Information:
  1. Analytical Reagent grade substances were used. The copper formate was obtained by neutralizing formic acid solutions with basic copper carbonate.
Measurement Errors:

Mass concentration (m/v) (1): The solubility of the salt is determined in a slight excess of formic acid (about 2%) to suppress salt hydrolysis.

System Components:
  1. Copper (II) formate, $\ce{ Cu(CHO2)2 }$; [544-19-4] NIST WebBook
  2. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
$T$ (°C) 100w1 m1 (mol/kg) a Phase (s) () b
10 5.58 0.385A
15 6.49 0.452A
20 7.03 0.492A
25 8.80 0.628A
30 11.06 0.810A
35 14.23 1.080A
40 18.52 1.480A
45 21.71 1.806B
50 25.17 2.190B
55 27.34 2.450B
60 27.48 2.467C
65 28.05 2.539C
70 28.50 2.595C

(a) These values were calculated by the compilers.

(b) The solid phases are: A = Cu(CHO2)2·4H2O, B = Cu(CHO2)2·2H2O, C = Cu(CHO2)2.

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