Abstract:The purpose of present work was to provide mineralogical insight into the rare earth element (REE) phases in bauxite residue to improve REE recovering technologies. Experimental work was performed by electron probe microanalysis with energy dispersive as well as wavelength dispersive spectroscopy and transmission electron microscopy. REEs are found as discrete mineral particles in bauxite residue. Their sizes range from <1 µm to about 40 µm. In bauxite residue, the most abundant REE bearing phases are light REE (LREE) ferrotitanates that form a solid solution between the phases with major compositions (REE,Ca,Na)(Ti,Fe)O 3 and (Ca,Na)(Ti,Fe)O 3 . These are secondary phases formed during the Bayer process by an in-situ transformation of the precursor bauxite LREE phases. Compared to natural systems, the indicated solid solution resembles loparite-perovskite series. LREE particles often have a calcium ferrotitanate shell surrounding them that probably hinders their solubility. Minor amount of LREE carbonate and phosphate minerals as well as manganese-associated LREE phases are also present in bauxite residue. Heavy REEs occur in the same form as in bauxites, namely as yttrium phosphates. These results show that the Bayer process has an impact on the initial REE mineralogy contained in bauxite. Bauxite residue as well as selected bauxites are potentially good sources of REEs.

No abstract

Abstract:The aim of this work was to achieve an understanding of the distribution of selected bauxite trace elements (gallium (Ga), vanadium (V), arsenic (As), chromium (Cr), rare earth elements (REEs), scandium (Sc)) in the Bayer process. The assessment was designed as a case study in an alumina plant in operation to provide an overview of the trace elements behaviour in an actual industrial setup. A combination of analytical techniques was used, mainly inductively coupled plasma mass spectrometry and optical emission spectroscopy as well as instrumental neutron activation analysis. It was found that Ga, V and As as well as, to a minor extent, Cr are principally accumulated in Bayer process liquors. In addition, Ga is also fractionated to alumina at the end of the Bayer processing cycle. The rest of these elements pass to bauxite residue. REEs and Sc have the tendency to remain practically unaffected in the solid phases of the Bayer process and, therefore, at least 98% of their mass is transferred to bauxite residue. The interest in such a study originates from the fact that many of these trace constituents of bauxite ore could potentially become valuable by-products of the Bayer process; therefore, the understanding of their behaviour needs to be expanded. In fact, Ga and V are already by-products of the Bayer process, but their distribution patterns have not been provided in the existing open literature.

No abstract

Bauxite residue is treated for the recovery of aluminum and sodium by sintering with the addition of soda, metallurgical coke and other reagents such as CaO, MgO and BaO. A thorough thermodynamic analysis using Factsage 7.0™ software was completed together with XRD mineralogy of sinters with different fluxes and reagents additions. Through both thermodynamic interpretation and mineralogical confirmations, it was observed that the type of desilication product in bauxite residue influences the total aluminum recovery through the sintering process and formation of sodium aluminum silicate exists in equilibrium with sodium aluminate, unless silica is consumed by additives (such as CaO, MgO, BaO etc.) forming other more thermodynamically favorable species and liberating alumina. Addition of barium oxide improves the aluminum and sodium recovery to 75% and 94% respectively. Complex sinter product formation that are triggered due to high calcium content in the Greek bauxite residue reduces aluminum recovery efficiency. Optimised and feasible recovery of aluminum and sodium for Greek bauxite residue was proved to be 70% and 85% respectively, when sintered with 50% excess stoichiometric soda. It was observed that stoichiometric carbon addition in inert atmosphere only assisted recovery up to 75% of aluminum and 83% of sodium, though there are benefits gained from pre-reducing iron from hematite for downstream recovery.