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Selective recovery of nickel over iron from a nickel-iron solution using microbial sulfate reduction in a gas-lift bioreactor.
- Source :
-
Water research [Water Res] 2009 Feb; Vol. 43 (3), pp. 853-61. Date of Electronic Publication: 2008 Nov 30. - Publication Year :
- 2009
-
Abstract
- Process streams with high concentrations of metals and sulfate are characteristic for the mining and metallurgical industries. This study aims to selectively recover nickel from a nickel-iron-containing solution at pH 5.0 using a single stage bioreactor that simultaneously combines low pH sulfate reduction and metal-sulfide formation. The results show that nickel was selectively precipitated in the bioreactor at pH 5.0 and the precipitates consisted of >or=83% of the nickel content. The nickel-iron precipitates were partly crystalline and had a metal/sulfur ratio of 1, suggesting these precipitates were NiS and FeS. Experiments focusing on nickel recovery at pH 5.0 and 5.5 reached a recovery of >99.9%, resulting in a nickel effluent concentration<0.05 microM. The mixed microbial population included known sulfate reducers and acetogens. This study shows that selective metal precipitation in a single stage sulfate reducing bioreactor operated at low pH has the potential to produce metal-sulfides that can be used by the metallurgical industry as a resource for metal production.
- Subjects :
- Bacteria genetics
Biomass
Chemical Precipitation
Cloning, Molecular
Electrophoresis, Agar Gel
Hydrogen-Ion Concentration
Iron analysis
Nickel analysis
Oxidation-Reduction
Phylogeny
RNA, Ribosomal, 16S genetics
Solutions
Sulfates analysis
Sulfides analysis
Bacteria metabolism
Bioreactors microbiology
Gases metabolism
Iron isolation & purification
Nickel isolation & purification
Sulfates metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0043-1354
- Volume :
- 43
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Water research
- Publication Type :
- Academic Journal
- Accession number :
- 19059621
- Full Text :
- https://doi.org/10.1016/j.watres.2008.11.023