Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32
Jarosites are produced during metallurgical processing, on oxidized sulfide deposits, and in acid mine drainage environments. Despite the environmental relevance of jarosites, few studies have examined their biogeochemical stability. This study demonstrates the simultaneous reduction of structural F...
| Main Authors: | , , , , , , , , |
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| Format: | Journal Article |
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American Chemical Society
2012
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| Online Access: | http://hdl.handle.net/20.500.11937/48298 |
| _version_ | 1848758070851665920 |
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| author | Smeaton, C. Walshe, G. Smith, A. Hudson-Edwards, K. Dubbin, W. Wright, Kathleen Beale, A. Fryer, B. Weisener, C. |
| author_facet | Smeaton, C. Walshe, G. Smith, A. Hudson-Edwards, K. Dubbin, W. Wright, Kathleen Beale, A. Fryer, B. Weisener, C. |
| author_sort | Smeaton, C. |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | Jarosites are produced during metallurgical processing, on oxidized sulfide deposits, and in acid mine drainage environments. Despite the environmental relevance of jarosites, few studies have examined their biogeochemical stability. This study demonstrates the simultaneous reduction of structural Fe(III) and aqueous As(V) during the dissolution of synthetic Pb–As jarosite (PbFe3(SO4,AsO4)2(OH)6) by Shewanella putrefaciens using batch experiments under anaerobic circumneutral conditions. Fe(III) reduction occurred immediately in inoculated samples while As(V) reduction was observed after 72 h. XANES spectra showed As(III) (14.7%) in the solid phase at 168 h coincident with decreased aqueous As(V). At 336 h, XANES spectra and aqueous speciation analysis demonstrated 20.2% and 3.0% of total As was present as As(III) in the solid and aqueous phase, respectively. In contrast, 12.4% of total Fe was present as aqueous Fe(II) and was below the detection limits of XANES in the solid phase. TEM-EDS analysis at 336 h showed secondary precipitates enriched in Fe and O with minor amounts of As and Pb. Based on experimental data and thermodynamic modeling, we suggest that structural Fe(III) reduction was thermodynamically driven while aqueous As(V) reduction was triggered by detoxification induced to offset the high As(V) (328 μM) concentrations released during dissolution. |
| first_indexed | 2025-11-14T09:38:09Z |
| format | Journal Article |
| id | curtin-20.500.11937-48298 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T09:38:09Z |
| publishDate | 2012 |
| publisher | American Chemical Society |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-482982017-09-13T15:58:11Z Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32 Smeaton, C. Walshe, G. Smith, A. Hudson-Edwards, K. Dubbin, W. Wright, Kathleen Beale, A. Fryer, B. Weisener, C. Jarosites are produced during metallurgical processing, on oxidized sulfide deposits, and in acid mine drainage environments. Despite the environmental relevance of jarosites, few studies have examined their biogeochemical stability. This study demonstrates the simultaneous reduction of structural Fe(III) and aqueous As(V) during the dissolution of synthetic Pb–As jarosite (PbFe3(SO4,AsO4)2(OH)6) by Shewanella putrefaciens using batch experiments under anaerobic circumneutral conditions. Fe(III) reduction occurred immediately in inoculated samples while As(V) reduction was observed after 72 h. XANES spectra showed As(III) (14.7%) in the solid phase at 168 h coincident with decreased aqueous As(V). At 336 h, XANES spectra and aqueous speciation analysis demonstrated 20.2% and 3.0% of total As was present as As(III) in the solid and aqueous phase, respectively. In contrast, 12.4% of total Fe was present as aqueous Fe(II) and was below the detection limits of XANES in the solid phase. TEM-EDS analysis at 336 h showed secondary precipitates enriched in Fe and O with minor amounts of As and Pb. Based on experimental data and thermodynamic modeling, we suggest that structural Fe(III) reduction was thermodynamically driven while aqueous As(V) reduction was triggered by detoxification induced to offset the high As(V) (328 μM) concentrations released during dissolution. 2012 Journal Article http://hdl.handle.net/20.500.11937/48298 10.1021/es3021809 American Chemical Society restricted |
| spellingShingle | Smeaton, C. Walshe, G. Smith, A. Hudson-Edwards, K. Dubbin, W. Wright, Kathleen Beale, A. Fryer, B. Weisener, C. Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32 |
| title | Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32 |
| title_full | Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32 |
| title_fullStr | Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32 |
| title_full_unstemmed | Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32 |
| title_short | Simultaneous Release of Fe and As during the Reductive Dissolution of Pb-As Jarosite by Shewanella putrefaciens CN32 |
| title_sort | simultaneous release of fe and as during the reductive dissolution of pb-as jarosite by shewanella putrefaciens cn32 |
| url | http://hdl.handle.net/20.500.11937/48298 |