Insight into leaching of rare earth and aluminum from ion adsorption type rare earth ore: Adsorption and desorption

Clay minerals are inferred to be the primary host materials for ion-exchangeable rare earth in ion adsorption type rare earth ore (IAREO). During the rare earth leaching process, the adsorption and desorption reactions of the cations controlling the leaching process continue to occur at the clay minerals-leaching agent solution interface. In order to understand the leaching mechanism and behavior of rare earth and co-leached aluminum, adsorption, competitive adsorption, and desorption experiments were carried out using kaolin as a typical clay mineral. The powerful electrostatic attraction and concentration driving forces facilitate the adsorption of cations. The adsorption ability and competitive adsorption ability of cations depend on their charge, hydration radius, and hydrolysis properties, and decrease in the order of La3+, Y3+, Al3+, Mg2+, and NH4+. The desorption of rare earth and aluminum is positively affected by the concentration-driving force exerted by high concentrations of Mg2+ and NH4+, with the order of the desorption ability being opposite to the adsorption ability. However, unspecified interactions between clay mineral particles enhanced by high-concentration desorbents, especially by Mg2+ than NH4+, will adversely affect desorption reactions, which result in lower desorption efficiencies of rare earth and aluminum obtained with magnesium sulfate compared to those obtained with ammonium sulfate at high concentrations. Solid-phase Al(OH)3 generated at a high peak aluminum concentration leads to a considerably delayed aluminum efflux, thereby partially separating the rare earth from aluminum during the actual column leaching process. To advance the mining technology of IAREO by selectively improving the rare earth leaching efficiency with minimal leaching agent consumption, higher charged cations with concentrations limited to suitable levels should be preferred as leaching agents.