Abstract

According to the literature, pyrite (FeS2) oxidation has been previously determined to involve thiosulfate as the first aqueous intermediate sulfur product, which is further oxidized to sulfate. In the present study, pyrite oxidation by Acidithiobacillus ferrooxidans was studied using electrochemical and metabolic approaches in an effort to extend existing knowledge on the oxidation mechanism. Due to the small surface area, the reaction rate of a compact pyrite electrode in the form of polycrystalline pyrite aggregate in A. ferrooxidans suspension was very slow at a spontaneously formed high redox potential. The slow rate made it possible to investigate the oxidation process in detail over a term of 100 days. Using electrochemical parameters from polarization curves and levels of released iron, the number of exchanged electrons per pyrite molecule was estimated. The values close to 14 and 2 electrons were determined for the oxidation with and without bacteria, respectively. These results indicated that sulfate was the dominant first aqueous sulfur species formed in the presence of bacteria and elemental sulfur was predominantly formed without bacteria. The stoichiometric calculations are consistent with high iron-oxidizing activities of bacteria that continually keep the released iron in the ferric form, resulting in a high redox potential. The sulfur entity of pyrite was oxidized to sulfate by Fe3+ without intermediate thiosulfate under these conditions. Cell attachment on the corroded pyrite electrode surface was documented although pyrite surface corrosion by Fe3+ was evident without bacterial participation. Attached cells may be important in initiating the oxidation of the pyrite surface to release iron from the mineral. During the active phase of oxidation of a pyrite concentrate sample, the ATP levels in attached and planktonic bacteria were consistent with previously established ATP content of iron-oxidizing cells. No significant upregulation of three essential genes involved in energy metabolism of sulfur compounds was observed in the planktonic cells, which represented the dominant biomass in the pyrite culture. The study demonstrated the formation of sulfate as the first dissolved sulfur species with iron-oxidizing bacteria under high redox potential conditions. Minor aqueous sulfur intermediates may be formed but as a result of side reactions.

Highlights

  • The oxidation of pyrite by bacteria contributes to microbial sulfur cycling in the environment

  • The results of the present study indicated that sulfate is the first aqueous sulfur species formed in the bacterial oxidation of the pyrite electrode under suitable redox conditions, because about 14 electrons per pyrite molecule were exchanged in the oxidation

  • The mechanism of pyrite oxidation by ferric iron to sulfate includes formation of various sulfur intermediates based on experimental conditions

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Summary

Introduction

The oxidation of pyrite by bacteria contributes to microbial sulfur cycling in the environment. As pyrite is the most common and widely spread metal sulfide in the environment, knowledge of the mechanism of its oxidation and related pathways is fundamentally significant in the biochemistry and physiology of acidophilic iron- and sulfur-oxidizing bacteria and in pyrite biogeochemistry. Pyrite is virtually ubiquitous in sulfide mineralizations and often plays a fundamental role in sulfur biogeochemistry in natural and bioleaching impacted environments. Its bacterial oxidation results in the formation of ferric iron and sulfuric acid as ultimate end products. In addition to the toxic effects of sulfuric acid and heavy metals, non-specific pH-dependent phytotoxic effects of ferric iron in the form of Fe(III)-precipitates can interfere with plant physiological processes (Bartakova et al, 2001)

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