SDS Volume (4707)

Volume 73. Metal and Ammonium Formate Systems, p None

Original Measurements

Bianco, P.; Haladjian, J.; Lanza, E.; Asso, M.; Bull. Soc. Chim. Fr. 1253 (1971).

Variables:

Room Temp: Composition at 25 °C

Prepared by:

T.A. Ageyeva

Method/Apparatus/Procedure:

The isothermal method was used. Equilibrium was reached within 24 hours. The sodium formate content was determined by potentiometric titration. Acetone and water were determined spectrophotometrically using $\lambda = \pu{275 nm}$ and $\lambda = \pu{1920 nm}$, respectively. The solid phase was identified with thermogravimetry.

Source and Purity of Materials:
  1. Commercial $\ce{NaCHO2}$ was dehydrated and dried at 413.2 K for 48 hrs. Commercial acetone was purified by drying with anhydrous $\ce{CaSO4}$ [1]. It contained 0.03% ±0.01% water. Freshly distilled water was used.
Estimated Errors:

Ambient temperature: The temperature was controlled to within ±0.05 K.

References

1 Weissberger; A.; Proskauer, E. S.; Techniques of Organic Chemistry, VII Organic Solvents, Interscience, New York, p. 293 (1955).

Components:
  1. Sodium formate, $\ce{ NaCHO2 }$; [141-53-7] NIST WebBook
  2. Acetone, $\ce{ C3H6O }$; [67-64-1] NIST WebBook
  3. Water, $\ce{ H2O }$; [7732-18-5] NIST WebBook
Experimental Data

Two immiscible solutions were observed: L1, water saturated with acetone, and, L2, acetone saturated with water.

Table 2. Solubility values in the NaCHO2-C3H6O-H2O system.
100w1 100w2 100w3 $100 x_{1}$ $100 x_{2}$ $100 x_{3}$ Phase (s) () Phase (l) ()
48.80.051.220.20.079.8 A + BL2
48.92.9848.120.21.4977.6 A + BL2
35.55.5059.113.42.4381.2 L1 + L2 + BL2
27.210.862.09.934.6285.5 L1 + L2L2
24.013.262.88.685.5985.7 L1 + L2L2
19.616.763.77.017.0087.0 L1 + L2L2
17.419.563.16.258.1785.9 L1 + L2L2
11.529.559.14.2712.882.9 L1 + L2L2
10.034.056.03.8315.280.9 AL2

(a) These values were calculated by the compilers.

(b) The phases are: A = liquid; B = NaCHO2.

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