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Spontaneous electrochemical removal of aqueous sulfide
Most of the existing sulfide removal processes from wastewaters and waste gases require substantial amounts of energy inputs. Here we present an electrochemical method by means of a fuel cell that removes sulfide while producing energy. A lab scale fuel cell was operated at ambient temperature and n...
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Published in: | Water research (Oxford) 2008-12, Vol.42 (20), p.4965-4975 |
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container_end_page | 4975 |
container_issue | 20 |
container_start_page | 4965 |
container_title | Water research (Oxford) |
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creator | Dutta, Paritam K. Rabaey, Korneel Yuan, Zhiguo Keller, Jürg |
description | Most of the existing sulfide removal processes from wastewaters and waste gases require substantial amounts of energy inputs. Here we present an electrochemical method by means of a fuel cell that removes sulfide while producing energy. A lab scale fuel cell was operated at ambient temperature and neutral pH, which was capable of removing aqueous sulfide continuously for 2 months at a rate of 0.62
±
0.1
kg
S
m
−3
d
−1 of net anodic compartment (NAC) (0.28
±
0.05
kg
S
m
−3
d
−1 of total anodic compartment, TAC). During continuous operation, on average, the power generated was 12
±
2
W
m
−3 NAC (5
±
1
W
m
−3 TAC), with a maximum capacity of the cell of 166
W
m
−3 NAC (74
W
m
−3 TAC). Potassium ferricyanide was used as cathodic electron acceptor. Elemental sulfur was identified as the predominant final oxidation product that was deposited on the anode. In this abiotic fuel cell, the sulfide oxidation rate was not diminished by the presence of an organic electron donor (acetate) during batch experiments while the acetate concentration remained unchanged. This is particularly important for selective sulfide removal from wastewater where organics are essential for downstream nutrient removal. Elemental sulfur deposited on the anode appeared to limit the operation of the fuel cell after 3 months of operation, necessitating periodic removal of the accumulated sulfur from the electrode. |
doi_str_mv | 10.1016/j.watres.2008.09.007 |
format | article |
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±
0.1
kg
S
m
−3
d
−1 of net anodic compartment (NAC) (0.28
±
0.05
kg
S
m
−3
d
−1 of total anodic compartment, TAC). During continuous operation, on average, the power generated was 12
±
2
W
m
−3 NAC (5
±
1
W
m
−3 TAC), with a maximum capacity of the cell of 166
W
m
−3 NAC (74
W
m
−3 TAC). Potassium ferricyanide was used as cathodic electron acceptor. Elemental sulfur was identified as the predominant final oxidation product that was deposited on the anode. In this abiotic fuel cell, the sulfide oxidation rate was not diminished by the presence of an organic electron donor (acetate) during batch experiments while the acetate concentration remained unchanged. This is particularly important for selective sulfide removal from wastewater where organics are essential for downstream nutrient removal. Elemental sulfur deposited on the anode appeared to limit the operation of the fuel cell after 3 months of operation, necessitating periodic removal of the accumulated sulfur from the electrode.</description><identifier>ISSN: 0043-1354</identifier><identifier>EISSN: 1879-2448</identifier><identifier>DOI: 10.1016/j.watres.2008.09.007</identifier><identifier>PMID: 18954888</identifier><identifier>CODEN: WATRAG</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Acetates ; Applied sciences ; Electricity ; electrochemistry ; Electrochemistry - methods ; electrodes ; Elemental sulfur ; Equipment Design ; equipment performance ; Exact sciences and technology ; Ferricyanides ; Fuel cell ; fuel cells ; Gases - isolation & purification ; Graphite - analysis ; Indicators and Reagents ; Kinetics ; Microscopy, Electron, Scanning ; Other industrial wastes. Sewage sludge ; oxidation ; Oxidation-Reduction ; Pollution ; Removal ; renewable energy sources ; Sulfide ; sulfides ; Sulfides - chemistry ; Sulfides - isolation & purification ; sulfur ; Sulfur - analysis ; temperature ; Waste Disposal, Fluid - instrumentation ; Waste Disposal, Fluid - methods ; Wastes ; Wastewater ; wastewater treatment ; Water - analysis ; Water treatment and pollution</subject><ispartof>Water research (Oxford), 2008-12, Vol.42 (20), p.4965-4975</ispartof><rights>2008 Elsevier Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-8be551b1bdf65eb6db430e235704ba513373523c5cd9eda22d38a76044fd50d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20977067$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18954888$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dutta, Paritam K.</creatorcontrib><creatorcontrib>Rabaey, Korneel</creatorcontrib><creatorcontrib>Yuan, Zhiguo</creatorcontrib><creatorcontrib>Keller, Jürg</creatorcontrib><title>Spontaneous electrochemical removal of aqueous sulfide</title><title>Water research (Oxford)</title><addtitle>Water Res</addtitle><description>Most of the existing sulfide removal processes from wastewaters and waste gases require substantial amounts of energy inputs. Here we present an electrochemical method by means of a fuel cell that removes sulfide while producing energy. A lab scale fuel cell was operated at ambient temperature and neutral pH, which was capable of removing aqueous sulfide continuously for 2 months at a rate of 0.62
±
0.1
kg
S
m
−3
d
−1 of net anodic compartment (NAC) (0.28
±
0.05
kg
S
m
−3
d
−1 of total anodic compartment, TAC). During continuous operation, on average, the power generated was 12
±
2
W
m
−3 NAC (5
±
1
W
m
−3 TAC), with a maximum capacity of the cell of 166
W
m
−3 NAC (74
W
m
−3 TAC). Potassium ferricyanide was used as cathodic electron acceptor. Elemental sulfur was identified as the predominant final oxidation product that was deposited on the anode. In this abiotic fuel cell, the sulfide oxidation rate was not diminished by the presence of an organic electron donor (acetate) during batch experiments while the acetate concentration remained unchanged. This is particularly important for selective sulfide removal from wastewater where organics are essential for downstream nutrient removal. Elemental sulfur deposited on the anode appeared to limit the operation of the fuel cell after 3 months of operation, necessitating periodic removal of the accumulated sulfur from the electrode.</description><subject>Acetates</subject><subject>Applied sciences</subject><subject>Electricity</subject><subject>electrochemistry</subject><subject>Electrochemistry - methods</subject><subject>electrodes</subject><subject>Elemental sulfur</subject><subject>Equipment Design</subject><subject>equipment performance</subject><subject>Exact sciences and technology</subject><subject>Ferricyanides</subject><subject>Fuel cell</subject><subject>fuel cells</subject><subject>Gases - isolation & purification</subject><subject>Graphite - analysis</subject><subject>Indicators and Reagents</subject><subject>Kinetics</subject><subject>Microscopy, Electron, Scanning</subject><subject>Other industrial wastes. Sewage sludge</subject><subject>oxidation</subject><subject>Oxidation-Reduction</subject><subject>Pollution</subject><subject>Removal</subject><subject>renewable energy sources</subject><subject>Sulfide</subject><subject>sulfides</subject><subject>Sulfides - chemistry</subject><subject>Sulfides - isolation & purification</subject><subject>sulfur</subject><subject>Sulfur - analysis</subject><subject>temperature</subject><subject>Waste Disposal, Fluid - instrumentation</subject><subject>Waste Disposal, Fluid - methods</subject><subject>Wastes</subject><subject>Wastewater</subject><subject>wastewater treatment</subject><subject>Water - analysis</subject><subject>Water treatment and pollution</subject><issn>0043-1354</issn><issn>1879-2448</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqF0U2LFDEQBuAgijuu_gPRueit28p3chFk8QsWPOx6DumkWjN0T8akZ8V_b8Ye9Oae6vLUS1EvIc8p9BSoerPrf_qlYO0ZgOnB9gD6AdlQo23HhDAPyQZA8I5yKS7Ik1p3AMAYt4_JBTVWCmPMhqibQ94vfo_5WLc4YVhKDt9xTsFP24Jzvmszj1v_4_iH1OM0pohPyaPRTxWfnecluf3w_vbqU3f95ePnq3fXXRBaLZ0ZUEo60CGOSuKg4iA4IONSgxi8pJxrLhkPMkSL0TMWufFagRBjlBD5JXm9xh5KbgfUxc2pBpym9WCnrNFSWHovpFYpCWDvhwIYSMMaFCsMJddacHSHkmZffjkK7lSA27m1AHcqwIF1rYC29uKcfxxmjP-Wzh9v4NUZ-Np-PBa_D6n-dQys1qBOQS9XN_rs_LfSzNcbBpQDlUZaI5p4uwpsBdwlLK6GhPuAMZXWo4s5_f_W36NVrno</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Dutta, Paritam K.</creator><creator>Rabaey, Korneel</creator><creator>Yuan, Zhiguo</creator><creator>Keller, Jürg</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7QH</scope><scope>7UA</scope><scope>F1W</scope><scope>H96</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>20081201</creationdate><title>Spontaneous electrochemical removal of aqueous sulfide</title><author>Dutta, Paritam K. ; Rabaey, Korneel ; Yuan, Zhiguo ; Keller, Jürg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-8be551b1bdf65eb6db430e235704ba513373523c5cd9eda22d38a76044fd50d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acetates</topic><topic>Applied sciences</topic><topic>Electricity</topic><topic>electrochemistry</topic><topic>Electrochemistry - methods</topic><topic>electrodes</topic><topic>Elemental sulfur</topic><topic>Equipment Design</topic><topic>equipment performance</topic><topic>Exact sciences and technology</topic><topic>Ferricyanides</topic><topic>Fuel cell</topic><topic>fuel cells</topic><topic>Gases - isolation & purification</topic><topic>Graphite - analysis</topic><topic>Indicators and Reagents</topic><topic>Kinetics</topic><topic>Microscopy, Electron, Scanning</topic><topic>Other industrial wastes. Sewage sludge</topic><topic>oxidation</topic><topic>Oxidation-Reduction</topic><topic>Pollution</topic><topic>Removal</topic><topic>renewable energy sources</topic><topic>Sulfide</topic><topic>sulfides</topic><topic>Sulfides - chemistry</topic><topic>Sulfides - isolation & purification</topic><topic>sulfur</topic><topic>Sulfur - analysis</topic><topic>temperature</topic><topic>Waste Disposal, Fluid - instrumentation</topic><topic>Waste Disposal, Fluid - methods</topic><topic>Wastes</topic><topic>Wastewater</topic><topic>wastewater treatment</topic><topic>Water - analysis</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dutta, Paritam K.</creatorcontrib><creatorcontrib>Rabaey, Korneel</creatorcontrib><creatorcontrib>Yuan, Zhiguo</creatorcontrib><creatorcontrib>Keller, Jürg</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Aqualine</collection><collection>Water Resources Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Water research (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dutta, Paritam K.</au><au>Rabaey, Korneel</au><au>Yuan, Zhiguo</au><au>Keller, Jürg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous electrochemical removal of aqueous sulfide</atitle><jtitle>Water research (Oxford)</jtitle><addtitle>Water Res</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>42</volume><issue>20</issue><spage>4965</spage><epage>4975</epage><pages>4965-4975</pages><issn>0043-1354</issn><eissn>1879-2448</eissn><coden>WATRAG</coden><abstract>Most of the existing sulfide removal processes from wastewaters and waste gases require substantial amounts of energy inputs. Here we present an electrochemical method by means of a fuel cell that removes sulfide while producing energy. A lab scale fuel cell was operated at ambient temperature and neutral pH, which was capable of removing aqueous sulfide continuously for 2 months at a rate of 0.62
±
0.1
kg
S
m
−3
d
−1 of net anodic compartment (NAC) (0.28
±
0.05
kg
S
m
−3
d
−1 of total anodic compartment, TAC). During continuous operation, on average, the power generated was 12
±
2
W
m
−3 NAC (5
±
1
W
m
−3 TAC), with a maximum capacity of the cell of 166
W
m
−3 NAC (74
W
m
−3 TAC). Potassium ferricyanide was used as cathodic electron acceptor. Elemental sulfur was identified as the predominant final oxidation product that was deposited on the anode. In this abiotic fuel cell, the sulfide oxidation rate was not diminished by the presence of an organic electron donor (acetate) during batch experiments while the acetate concentration remained unchanged. This is particularly important for selective sulfide removal from wastewater where organics are essential for downstream nutrient removal. Elemental sulfur deposited on the anode appeared to limit the operation of the fuel cell after 3 months of operation, necessitating periodic removal of the accumulated sulfur from the electrode.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>18954888</pmid><doi>10.1016/j.watres.2008.09.007</doi><tpages>11</tpages></addata></record> |
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ispartof | Water research (Oxford), 2008-12, Vol.42 (20), p.4965-4975 |
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language | eng |
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source | Elsevier |
subjects | Acetates Applied sciences Electricity electrochemistry Electrochemistry - methods electrodes Elemental sulfur Equipment Design equipment performance Exact sciences and technology Ferricyanides Fuel cell fuel cells Gases - isolation & purification Graphite - analysis Indicators and Reagents Kinetics Microscopy, Electron, Scanning Other industrial wastes. Sewage sludge oxidation Oxidation-Reduction Pollution Removal renewable energy sources Sulfide sulfides Sulfides - chemistry Sulfides - isolation & purification sulfur Sulfur - analysis temperature Waste Disposal, Fluid - instrumentation Waste Disposal, Fluid - methods Wastes Wastewater wastewater treatment Water - analysis Water treatment and pollution |
title | Spontaneous electrochemical removal of aqueous sulfide |
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