Electron Transfer Budgets and Kinetics of Abiotic Oxidation and Incorporation of Aqueous Sulfide by Dissolved Organic Matter
The reactivity of natural dissolved organic matter toward sulfide and has not been well studied with regard to electron transfer, product formation, and kinetics. We thus investigated the abiotic transformation of sulfide upon reaction with reduced and nonreduced Sigma-Aldrich humic acid (HA), at pH...
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Veröffentlicht in: | Environmental science & technology 2015-05, Vol.49 (9), p.5441-5449 |
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description | The reactivity of natural dissolved organic matter toward sulfide and has not been well studied with regard to electron transfer, product formation, and kinetics. We thus investigated the abiotic transformation of sulfide upon reaction with reduced and nonreduced Sigma-Aldrich humic acid (HA), at pH 6 under anoxic conditions. Sulfide reacted with nonreduced HA at conditional rate constants of 0.227–0.325 h–1. The main transformation products were elemental S (S0) and thiosulfate (S2O3 2–), yielding electron accepting capacities of 2.82–1.75 μmol e– (mg C)−1. Native iron contents in the HA could account for only 6–9% of this electron transfer. About 22–37% of S reacted with the HA to form organic S (Sorg). Formation of Sorg was observed and no inorganic transformation products occurred for reduced HA. X-ray absorption near edge structure spectroscopy supported Sorg to be mainly zerovalent, such as thiols, organic di- and polysulfides, or heterocycles. In conclusion, our results demonstrate that HA can abiotically reoxidize sulfide in anoxic environments at rates competitive to sulfide oxidation by molecular oxygen or iron oxides. |
doi_str_mv | 10.1021/es505531u |
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We thus investigated the abiotic transformation of sulfide upon reaction with reduced and nonreduced Sigma-Aldrich humic acid (HA), at pH 6 under anoxic conditions. Sulfide reacted with nonreduced HA at conditional rate constants of 0.227–0.325 h–1. The main transformation products were elemental S (S0) and thiosulfate (S2O3 2–), yielding electron accepting capacities of 2.82–1.75 μmol e– (mg C)−1. Native iron contents in the HA could account for only 6–9% of this electron transfer. About 22–37% of S reacted with the HA to form organic S (Sorg). Formation of Sorg was observed and no inorganic transformation products occurred for reduced HA. X-ray absorption near edge structure spectroscopy supported Sorg to be mainly zerovalent, such as thiols, organic di- and polysulfides, or heterocycles. In conclusion, our results demonstrate that HA can abiotically reoxidize sulfide in anoxic environments at rates competitive to sulfide oxidation by molecular oxygen or iron oxides.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/es505531u</identifier><identifier>PMID: 25850807</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Aqueous solutions ; Chemical reactions ; Electron transfer ; Electron Transport ; Ferric Compounds - chemistry ; Humic Substances ; Iron - chemistry ; Kinetics ; Oxidation ; Oxidation-Reduction ; Spectrum analysis ; Sulfhydryl Compounds - chemistry ; Sulfides - chemistry ; Thiosulfates - chemistry ; Water - chemistry ; X-Ray Absorption Spectroscopy</subject><ispartof>Environmental science & technology, 2015-05, Vol.49 (9), p.5441-5449</ispartof><rights>Copyright © 2015 American Chemical Society</rights><rights>Copyright American Chemical Society May 5, 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a413t-961ab96aac808c7c847febcd44e10ee6814d2426e72bb56da3b32d29fe04d7f53</citedby><cites>FETCH-LOGICAL-a413t-961ab96aac808c7c847febcd44e10ee6814d2426e72bb56da3b32d29fe04d7f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/es505531u$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/es505531u$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25850807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Zhi-Guo</creatorcontrib><creatorcontrib>Peiffer, Stefan</creatorcontrib><creatorcontrib>Göttlicher, Jörg</creatorcontrib><creatorcontrib>Knorr, Klaus-Holger</creatorcontrib><title>Electron Transfer Budgets and Kinetics of Abiotic Oxidation and Incorporation of Aqueous Sulfide by Dissolved Organic Matter</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>The reactivity of natural dissolved organic matter toward sulfide and has not been well studied with regard to electron transfer, product formation, and kinetics. We thus investigated the abiotic transformation of sulfide upon reaction with reduced and nonreduced Sigma-Aldrich humic acid (HA), at pH 6 under anoxic conditions. Sulfide reacted with nonreduced HA at conditional rate constants of 0.227–0.325 h–1. The main transformation products were elemental S (S0) and thiosulfate (S2O3 2–), yielding electron accepting capacities of 2.82–1.75 μmol e– (mg C)−1. Native iron contents in the HA could account for only 6–9% of this electron transfer. About 22–37% of S reacted with the HA to form organic S (Sorg). Formation of Sorg was observed and no inorganic transformation products occurred for reduced HA. X-ray absorption near edge structure spectroscopy supported Sorg to be mainly zerovalent, such as thiols, organic di- and polysulfides, or heterocycles. In conclusion, our results demonstrate that HA can abiotically reoxidize sulfide in anoxic environments at rates competitive to sulfide oxidation by molecular oxygen or iron oxides.</description><subject>Aqueous solutions</subject><subject>Chemical reactions</subject><subject>Electron transfer</subject><subject>Electron Transport</subject><subject>Ferric Compounds - chemistry</subject><subject>Humic Substances</subject><subject>Iron - chemistry</subject><subject>Kinetics</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Spectrum analysis</subject><subject>Sulfhydryl Compounds - chemistry</subject><subject>Sulfides - chemistry</subject><subject>Thiosulfates - chemistry</subject><subject>Water - chemistry</subject><subject>X-Ray Absorption Spectroscopy</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0cFKHTEUBuAgFb3VLvoCJVAKuhh7kswkmaVVa0XLXWjB3ZBJzkhk7uSazJQKffhmuFbEbrpKCF_-nPAT8p7BEQPOPmOqoKoEm7bIglUcikpX7A1ZADBR1ELe7pK3Kd0DABegd8guzwA0qAX5fdajHWMY6E00Q-ow0i-Tu8MxUTM4eukHHL1NNHT0uPUh7-nyl3dm9PnKLC4GG-I6xM3JzB4mDFOi11PfeYe0faSnPqXQ_0RHl_HODDnjuxlHjPtkuzN9wndP6x758fXs5uRbcbU8vzg5vipMycRY1JKZtpbGWA3aKqtL1WFrXVkiA0SpWel4ySUq3raVdEa0gjtedwilU10l9sjBJncdQ54ujc3KJ4t9b4Z51IZJrWQthIT_ocA010Jl-vEVvQ9THPJHZsVqwZUSWR1ulI0hpYhds45-ZeJjw6CZ22ue28v2w1Pi1K7QPcu_dWXwaQOMTS9e-yfoD0CIoTk</recordid><startdate>20150505</startdate><enddate>20150505</enddate><creator>Yu, Zhi-Guo</creator><creator>Peiffer, Stefan</creator><creator>Göttlicher, Jörg</creator><creator>Knorr, Klaus-Holger</creator><general>American Chemical Society</general><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>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>20150505</creationdate><title>Electron Transfer Budgets and Kinetics of Abiotic Oxidation and Incorporation of Aqueous Sulfide by Dissolved Organic Matter</title><author>Yu, Zhi-Guo ; Peiffer, Stefan ; Göttlicher, Jörg ; Knorr, Klaus-Holger</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a413t-961ab96aac808c7c847febcd44e10ee6814d2426e72bb56da3b32d29fe04d7f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aqueous solutions</topic><topic>Chemical reactions</topic><topic>Electron transfer</topic><topic>Electron Transport</topic><topic>Ferric Compounds - chemistry</topic><topic>Humic Substances</topic><topic>Iron - chemistry</topic><topic>Kinetics</topic><topic>Oxidation</topic><topic>Oxidation-Reduction</topic><topic>Spectrum analysis</topic><topic>Sulfhydryl Compounds - chemistry</topic><topic>Sulfides - chemistry</topic><topic>Thiosulfates - chemistry</topic><topic>Water - chemistry</topic><topic>X-Ray Absorption Spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Zhi-Guo</creatorcontrib><creatorcontrib>Peiffer, Stefan</creatorcontrib><creatorcontrib>Göttlicher, Jörg</creatorcontrib><creatorcontrib>Knorr, Klaus-Holger</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Zhi-Guo</au><au>Peiffer, Stefan</au><au>Göttlicher, Jörg</au><au>Knorr, Klaus-Holger</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electron Transfer Budgets and Kinetics of Abiotic Oxidation and Incorporation of Aqueous Sulfide by Dissolved Organic Matter</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2015-05-05</date><risdate>2015</risdate><volume>49</volume><issue>9</issue><spage>5441</spage><epage>5449</epage><pages>5441-5449</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>The reactivity of natural dissolved organic matter toward sulfide and has not been well studied with regard to electron transfer, product formation, and kinetics. We thus investigated the abiotic transformation of sulfide upon reaction with reduced and nonreduced Sigma-Aldrich humic acid (HA), at pH 6 under anoxic conditions. Sulfide reacted with nonreduced HA at conditional rate constants of 0.227–0.325 h–1. The main transformation products were elemental S (S0) and thiosulfate (S2O3 2–), yielding electron accepting capacities of 2.82–1.75 μmol e– (mg C)−1. Native iron contents in the HA could account for only 6–9% of this electron transfer. About 22–37% of S reacted with the HA to form organic S (Sorg). Formation of Sorg was observed and no inorganic transformation products occurred for reduced HA. X-ray absorption near edge structure spectroscopy supported Sorg to be mainly zerovalent, such as thiols, organic di- and polysulfides, or heterocycles. In conclusion, our results demonstrate that HA can abiotically reoxidize sulfide in anoxic environments at rates competitive to sulfide oxidation by molecular oxygen or iron oxides.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25850807</pmid><doi>10.1021/es505531u</doi><tpages>9</tpages></addata></record> |
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subjects | Aqueous solutions Chemical reactions Electron transfer Electron Transport Ferric Compounds - chemistry Humic Substances Iron - chemistry Kinetics Oxidation Oxidation-Reduction Spectrum analysis Sulfhydryl Compounds - chemistry Sulfides - chemistry Thiosulfates - chemistry Water - chemistry X-Ray Absorption Spectroscopy |
title | Electron Transfer Budgets and Kinetics of Abiotic Oxidation and Incorporation of Aqueous Sulfide by Dissolved Organic Matter |
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