Thermodynamics Research Center / ThermoML | Journal of Chemical and Engineering Data

Solid-Liquid Phase Equilibria in the Aqueous Systems (CaCl2 + SrCl2 + H2O) and (NaCl + CaCl2 + SrCl2 + H2O) at 288.15 K

Li, D.[Dongchan], Zhang, Z.[Ziyi], Fan, R.[Rong], Yang, S.[Sennan]
J. Chem. Eng. Data 2019, 64, 6, 2767-2773
ABSTRACT
The solubilities of ternary system (CaCl2 + SrCl2 + H2O) and quaternary system (NaCl + CaCl2 + SrCl2 + H2O) at T =288.15 K and p = 0.1 MPa were investigated experimentally with the method of isothermal dissolution equilibrium, and the corresponding phase diagrams were plotted. Compared with the phase diagram of the ternary system (CaCl2 + SrCl2 + H2O) at 291.15 K which only includes one crystallization region of a completely miscible solid solution (Ca,Sr)Cl2*6H2O, there were also found the pure single salts CaCl2*6H2O and SrCl2*6H2O in the ternary system at 288.15 K besides the crystallization of solid solution (Ca,Sr)Cl2*6H2O. The solid solution of (Ca,Sr)Cl2*6H2O was also formed in the quaternary system (NaCl + CaCl2 + SrCl2 + H2O) at 288.15 K, and there were four crystalline fields in the quaternary system, which correspond to single salts NaCl, SrCl2*6H2O, CaCl2*6H2O and the solid solution (Ca,Sr)Cl2*6H2O, respectively. On the basis of the analyses of the phase diagrams of (CaCl2 + SrCl2 + H2O) and (NaCl + CaCl2 + SrCl2 + H2O) at 288.15 K, CaCl2*6H2O and SrCl2*6H2O can be separated from each other through avoiding crystallizing in the solid solution crystallization region in the systems, and SrCl2*6H2O and NaCl can be produced using CaCl2 as salting-out agent directly.
Compounds
# Formula Name
1 Cl2Sr strontium chloride
2 CaCl2 calcium chloride
3 ClNa sodium chloride
4 H2O water
Datasets
The table above is generated from the ThermoML associated json file (link above). POMD and RXND refer to PureOrMixture and Reaction Datasets. The compound numbers are included in properties, variables, and phases, if specificied; the numbers refer to the table of compounds on the left.
Type Compound-# Property Variable Constraint Phase Method #Points
  • POMD
  • 2
  • 1
  • 4
  • Mass fraction - 1 ; Liquid
  • Mass fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal of intercomponent compound 1
  • titration and spectrometry
  • 7
  • POMD
  • 2
  • 1
  • 4
  • Mass fraction - 1 ; Liquid
  • Mass fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal
  • titration and spectrometry
  • 11
  • POMD
  • 2
  • 1
  • 4
  • Mass fraction - 1 ; Liquid
  • Mass fraction - 2; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal of intercomponent compound 2
  • titration and spectrometry
  • 5
  • POMD
  • 3
  • 1
  • 4
  • Mass fraction - 1 ; Liquid
  • Mass fraction - 3; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal of intercomponent compound 1
  • titration and spectrometry
  • 1
  • POMD
  • 3
  • 1
  • 4
  • Mass fraction - 1 ; Liquid
  • Mass fraction - 3; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal - 3
  • titration and spectrometry
  • 1
  • POMD
  • 3
  • 2
  • 4
  • Mass fraction - 2 ; Liquid
  • Mass fraction - 3; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal of intercomponent compound 1
  • titration and spectrometry
  • 1
  • POMD
  • 3
  • 2
  • 4
  • Mass fraction - 2 ; Liquid
  • Mass fraction - 3; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal - 3
  • titration and spectrometry
  • 1
  • POMD
  • 1
  • 4
  • Mass fraction - 1 ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal of intercomponent compound 1
  • titration and spectrometry
  • 1
  • POMD
  • 2
  • 4
  • Mass fraction - 2 ; Liquid
  • Pressure, kPa; Liquid
  • Temperature, K; Liquid
  • Liquid
  • Crystal of intercomponent compound 2
  • titration and spectrometry
  • 1