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Suspension calcination and alkali leaching of low-grade high-sulfur bauxite: Desulfurization, mineralogical evolution and desilication

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Abstract

To enable the utilization of low-grade and high-sulfur bauxite, the suspension calcination was used to remove the sulfur and the activate silica minerals, and the calcinated bauxite was subjected to a desilication process in NaOH solution under atmospheric pressure. The desulfurization and desilication properties and mineralogical evolution were studied by X-ray diffraction, thermogravimetry-differential thermal analysis, scanning electron microscopy, and FactSage methods. The results demonstrate that the suspension calcination method is efficient for sulfur removal: 84.21% of S was removed after calcination at 1000°C for 2 min. During the calcination process, diaspore and pyrite were transferred to α-Al2O3, magnetite, and hematite. The phase transformation of pyrite follows the order FeS2 → Fe3O4 → Fe2O3, and the iron oxides and silica were converted into iron silicate. In the alkali-soluble desilication process, the optimum condition was an alkali solution concentration of 110 g/L, a reaction time of 20 min, and a reaction temperature of 95°C. The corresponding desilication ratio and alumina loss ratio were 44.9% and 2.4%, respectively, and the alumina-to-silica mass ratio of the concentrate was 7.9. The Al2O3·2SiO2, SiO2, and Al2O3 formed during the calcination process could react with NaOH solution, and their activity decreased in the order of Al2O3·2SiO2, SiO2, and Al2O3.

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Acknowledgements

This work was financially supported by the National Natural Science Foundation of China (Nos. U1812402, 51664005, and 51774102) and Talents of Guizhou Science and Technology Cooperation Platform (Talent Team Giant [2015] 4005, Platform Talent [2017] 5788, [2017] 5626, and KY (2015) 334).

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Correspondence to Jun-qi Li.

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Wu, Hf., Li, Jq., Chen, Cy. et al. Suspension calcination and alkali leaching of low-grade high-sulfur bauxite: Desulfurization, mineralogical evolution and desilication. Int J Miner Metall Mater 27, 602–610 (2020). https://doi.org/10.1007/s12613-019-1941-3

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