Abstract

The abundance of limonitic laterite ores in tropical and sub-tropical areas represents a large, and mostly unexploited, cobalt resource. Bioprocessing oxidised ores, and also waste materials such as tailings and processing residues, using acidophilic microorganisms to catalyse the reductive dissolution of iron and manganese minerals, is an environmentally benign alternative approach of extracting valuable base metals associated with these deposits. This work describes results from laboratory-scale experiments in which five cobalt-bearing materials, three primary limonitic laterite ores and two processing residues (filter dust and slag), all sourced from mines and a processing plant in Greece, were bioleached under reducing conditions by a consortium of acidophilic bacteria (using elemental sulfur as electron donor) in stirred tank bioreactors at pH 1.5 and 35 °C. Whilst the target metal, cobalt, was successfully bioleached from all five materials (40–50% within 30 days) the extraction of some other metals was more variable (e.g. between 2 and 48% of iron). Concentrations of soluble cobalt were highly correlated, in most cases, with those of manganese, in agreement with the finding that cobalt was primarily deported in manganese (IV) minerals. Acid consumption also differed greatly between mineral samples, ranging between 3 and 67 moles H2SO4 g−1 cobalt extracted. Comprehensive mineralogical analysis of the three limonitic samples before and after bioprocessing revealed significant variations between the ores, and demonstrated that elemental and mineralogical variabilities can greatly impact their amenability for reductive bioleaching.

Highlights

  • The global demand for cobalt has greatly accelerated over the past 30 years, reflecting its increased use as an essential constituent of high technology materials, such as rechargeable batteries, superalloys and catalysts

  • Mineralogical analysis showed that the filter dust (L1) was dominated by quartz and a spinel, and contained silicates, phyllosilicates and clay minerals, while calcite (CaCO3) was identified as a minor phase

  • In sample L5, hydrated hematite was identified as the main iron (III)

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Summary

Introduction

The global demand for cobalt has greatly accelerated over the past 30 years, reflecting its increased use as an essential constituent of high technology materials, such as rechargeable batteries, superalloys and catalysts. The Democratic Republic of Congo is the world’s leading source of mined cobalt, accounting for approximately 70% of global cobalt production, and China is the world’s leading consumer, with over 80% being used to produce rechargeable batteries (US Geological Survey, 2020). Laterites are iron-rich deposits mostly found in tropical and subtropical areas. They are formed during the pervasive weathering of surface-located ultramafic rock leading to oxidation and precipitation of iron and enrichment of residual elements such as nickel and cobalt. The limonite layer of a laterite deposit typically contains 40 - 60% goethite (FeO·OH) along with

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