SDS Volume (4641)

Volume 73. Metal and Ammonium Formate Systems, p None

Original Measurements

Balarew, C. C.; Vassileva, V. Z.; Compt. Rend. Acad. Bulg. Sci. 43, 51-4 (1990).

Variables:

Room Temp: Composition at 25 °C

Prepared by:

St. Trendafilova, Chr. Balarew

Method/Apparatus/Procedure:

The method used was the isothermal decrease of supersaturation, for 15-20 hrs. The $\ce{Ni^{2+}}$ content of the liquid and solid phases was determined gravimetrically with dimethylglyoxime. The sum of $\ce{Ni^{2+}}$ and $\ce{Zn^{2+}}$ was determined complexometrically by back titration in excess of Complexon III with $\ce{ZnSO4}$ at pH 5.5-6 using Xylenol Orange as indicator. The composition of the suction-dried mixed crystals was determined by the algebraic indirect identification of the solid phase composition method [1].

Source and Purity of Materials:
  1. The reagents used were of p.a. grade. Nickel and zinc formates were prepared by the action of dilute formic acid with nickel and zinc carbonates, respectively.
Estimated Errors:

Ambient temperature: Not given.
Mass concentration (m/v) (1): The solubility of the salts was determined in a slight excess of formic acid (about 2%) to suppress salt hydrolysis.

References

1 Trendafelov, D.; Balarew, Chr.; Comm. Dept. Chem. Bulg. Acad. Sci. 1 , 73 (1968).

Components:
  1. Nickel formate, $\ce{ Ni(CHO2)2 }$; [3349-06-2] NIST WebBook
  2. Zinc formate, $\ce{ Zn(CHO2)2 }$; [557-41-5] NIST WebBook
  3. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data
Solubility values in the Ni(CHO2)2-Zn(CHO2)2-H2O system at 25°C.
100w1 100w2 D2|1 D1|2 m1 (mol/kg) m2 (mol/kg) Phase (s) ()
2.14--- 0.146-A
1.750.750.591.68 0.1210.049B
1.181.450.581.73 0.0810.096B
1.061.800.551.80 0.0730.119B
0.762.500.392.59 0.0530.166B
0.423.280.204.89 0.0290.219B
0.193.600.128.37 0.0130.241B
0.064.420.118.86 4 x 10-30.298B
-5.38-- -0.366C

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

(b) The solid phases are: A = Ni(CHO2)2·2H2O; B = (Ni,Zn)(CHO2)2·2H2O; C = Zn(CHO2)2·2H2O.

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