Mechanism, Thermodynamics and Kinetics of Rutile Leaching Process by Sulfuric Acid Reactions

Abstract

Rutile decomposition by sulfuric acid, including the formation of two salts, Ti(SO₄)₂/TiOSO₄, is thermodynamically modelled. It is shown that TiO₂ can spontaneously dissolve in H₂SO₄ solutions. However, titania is considered as an inert (ballast) phase component of titanium-containing raw materials due to the decelerated separate nature of such chemical transformations. It is concluded that the hampered related kinetics of dissolution can be attributed to the lability of Ti(IV) cations/the specific engineered features of the hierarchical crystalline structure. It is suggested that the breaking of Ti–O–Ti bonds without additional mechanical strains in crystal lattice geometry becomes more advantageous when smaller negative anions/fluoride ions can be used. The analysis of sulfate-fluoride extraction leaching of titanium confirmed that a decrease in the Gibbs energy in the presence of F occurs. It is indicated by kinetic research studies that the addition of corrosive sodium reagent (NaF) reduces the activation by 45 kJ/mol, which results in intensification. A mechanism is proposed for the interactions involving the Ti–O–Ti cleavage on the surface/the H₂SO₄-induced Ti dioxide degradation on the sites of defects. Moreover, F acts as a homogeneous/heterogeneous bifunctional catalyst.