Solid-phase controls on lead partitioning in laboratory bioleaching solutions

The purpose of the work was to examine the co-precipitation of Fe(III) and Pb(II) in Acidithiobacillus ferrooxidans cultures under ambient temperature conditions. The competitive formation of plumbojarosite (PbFe6(SO4)4(OH)12) and anglesite (PbSO4) was of particular interest with respect to defining...

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Bibliographic Details
Published in:Hydrometallurgy Vol. 136; pp. 27 - 30
Main Authors: Bigham, Jerry M., Algur, Ömer Faruk, Jones, F. Sandy, Tuovinen, Olli H.
Format: Journal Article
Language:English
Published: Elsevier B.V 01-04-2013
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Summary:The purpose of the work was to examine the co-precipitation of Fe(III) and Pb(II) in Acidithiobacillus ferrooxidans cultures under ambient temperature conditions. The competitive formation of plumbojarosite (PbFe6(SO4)4(OH)12) and anglesite (PbSO4) was of particular interest with respect to defining the phase(s) controlling Pb solubility. The medium contained no K+ and a low level of 6.06mM NH4+. Precipitates were prepared in two phases. In the first phase (8days), A. ferrooxidans cultures oxidized ferrous iron to ferric iron (pH2.4), which partially precipitated as schwertmannite (Fe8O8(OH)5.5(SO4)1.25). In the second phase, lead nitrate (up to 100mmol Pb/l) was added to the schwertmannite-containing culture solutions, and the suspensions were held for an additional 22days. X-ray diffraction analysis indicated that lead precipitated as anglesite, and ferric iron was associated with schwertmannite and hydronium jarosite. No characteristic X-ray diffraction peaks for plumbojarosite were evident. •The co-precipitation of Fe and Pb was examined in simulated bioleaching solutions.•Fe2+ was oxidized by bacteria to Fe3+ in K+-free media before addition of Pb-nitrate.•When added, dissolved Pb precipitated exclusively as anglesite, not as Pb-jarosite.•Dissolved Fe3+ partially precipitated as schwertmannite and hydronium jarosite.•There was no XRD evidence for partitioning of Pb into the jarosite phase.
ISSN:0304-386X
1879-1158
DOI:10.1016/j.hydromet.2013.03.002