-
Date submitted2018-12-28
-
Date accepted2019-03-24
-
Date published2019-06-25
Modern physicochemical equilibrium description in Na2O–Al2O3–H2O system and its analogues
Equilibrium and non-equilibrium states of systems Na 2 O–Al 2 O 3 –H 2 O and K 2 O–Al 2 O 3 –H 2 O are crucial for establishing key technological parameters in alumina production and their optimization. Due to a noticeable discrepancy between experimental results and thermodynamic calculations based on materials of individual researchers the necessity of systematization and statistical processing of equilibrium data in these systems to create a reliable base of their physicochemical state, analysis and mathematical modeling of phase equilibria is substantiated. The tendency to a decrease of the hydration degree of solid sodium aluminates with increasing temperature and the transition of systems from the steady state of gibbsite to equilibrium with boehmite is revealed. The paper contains approximating functions that provide high-precision description of equilibrium isotherms in technologically significant area of Na 2 O–Al 2 O 3 –H 2 O and K 2 O–Al 2 O 3 –H 2 O concentrations. Approximating function can be simplified by dividing the isotherm into two sections with the intervals of alkaline content 0-0.25 and 0.25-0.4 mole/100 g of solution. The differences in solubility isotherms for Na 2 O–Al 2 O 3 –H 2 O and K 2 O–Al 2 O 3 –H 2 O systems provide are associated with changes in the ionic composition solutions that depends on concentration and temperature, as well as differences connecting with alkali cation hydration, which is crucially important for thermodynamic modeling of equilibria under consideration.
-
Date submitted2015-07-25
-
Date accepted2015-09-01
-
Date published2016-02-24
The phenomenon of isothermal transition of metastable aluminate solutions into the labile area and prospects of its industrial use
- Authors:
- V. N. Brichkin
- A. Kraslawski
The paper presents theoretically based requirements for the activation of synthetic gibbsite for maximum solubility of the activated product. The article describes the methodological foundations of gibbsite thermal activation and its effectiveness evaluation in terms of aluminate solutions decomposition. It is shown that to obtain high-saturation aluminate solutions, activation should provide generation of the reagent with highly-developed surface area, which is not identical to the structure of the deposited gibbsite. As a result of high-gradient thermal activation of synthetic gibbsite, it has been found that the targeted product develops predominantly an amorphous structure with a specific surface area up to 256 m2/ g, preserving its primary particle size. Activation products were investigated using modern methods of physical and chemical analysis. The experimental results confirmed the possibility of the activated product dissolution in the aluminate solution with a metastable compound and their spontaneous decomposition with aluminum hydroxide formation, characterized by high dispersion ability. It is shown, that a significant difference in kinetics and decomposition rates of solutions is connected with the use of a seed material with different particle size composition, which leads to the development of competing mechanisms, resulting in seed recrystallization, homogeneous and heterogeneous nucleation.