Solid–liquid
equilibria on the reciprocal quaternary system
(Na+, K+//Cl–, SO4
2––H2O) and its ternary system
(Na+, K+// SO4
2––H2O) at 313.15 K are studied with the method of
isothermal solution saturation. The solubilities and physical properties
(n
D, η, ρ) of saturated solutions in the two systems are determined. The phase
diagram of the ternary system at 313.15 K includes two invariant points,
three invariant curves, and three fields of crystallization of single
salts corresponding to K2SO4, Na2SO4·3K2SO4, Na2SO4. The two invariant points are cosaturated with two salts,
that is (K2SO4 + Na2SO4·3K2SO4) and (Na2SO4 + Na2SO4·3K2SO4), respectively. The reciprocal quaternary system at 313.15 K is
divided into seven univariant curves, three invariant points cosaturated
with three-salts and five crystallization fields. A double salt Na2SO4·3K2SO4 can be proven
to exist in the reciprocal quaternary system (Na+, K+//Cl–, SO4
2––H2O) and the ternary system (Na+, K+// SO4
2––H2O) under phase equilibrium conditions at 313.15 K. On the basis of
the phase diagram, the crystallization field of GLa and K2SO4 is bigger than that of the other three salts, whereas
the KCl crystallization field is the smallest. Therefore, K2SO4 can crystallize out more easily from this mixing equilibrium
solution except for Na2SO4·3K2SO4. The experimental results showed that both systems
are a complex eutectic type, and no solid solutions are found at the
investigated temperature. All the physical properties (n
D, η, ρ) of the equilibrium
quaternary system and ternary system change regularly with concentration
change of the liquid phase. The measured data and phase equilibrium
diagrams can be used for a new technology to design and optimize the
separation process of K2SO4 (KH2PO4), and provide fundamental data support for chemical industry
development.
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