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The Fenton Reaction in Water Assisted by Picolinic Acid: Accelerated Iron Cycling and Co-generation of a Selective Fe-Based Oxidant
The Fenton reaction is limited by a narrow acidic pH range, the slow reduction of Fe(III), and susceptibility of the nonselective hydroxyl radical (HO•) to scavenging by water constituents. Here, we employed the biodegradable chelating agent picolinic acid (PICA) to address these concerns. Compared...
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Published in: | Environmental science & technology 2021-06, Vol.55 (12), p.8299-8308 |
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description | The Fenton reaction is limited by a narrow acidic pH range, the slow reduction of Fe(III), and susceptibility of the nonselective hydroxyl radical (HO•) to scavenging by water constituents. Here, we employed the biodegradable chelating agent picolinic acid (PICA) to address these concerns. Compared to the classical Fenton reaction at pH 3.0, PICA greatly accelerated the degradation of atrazine, sulfamethazine, and various substituted phenols at pH 5.0 in a reaction with autocatalytic characteristics. Although HO• served as the principal oxidant, a high-spin, end-on hydroperoxo intermediate, tentatively identified as PICA–FeIII–OOH, also exhibited reactivity toward several test compounds. Chloride release from the oxidation of 2,4,6-trichlorophenol and the positive slope of the Hammett correlation for a series of halogenated phenols were consistent with PICA–FeIII–OOH reacting as a nucleophilic oxidant. Compared to HO•, PICA–FeIII–OOH is less sensitive to potential scavengers in environmental water samples. Kinetic analysis reveals that PICA facilitates Fe(III)/Fe(II) transformation by accelerating Fe(III) reduction by H2O2. Autocatalysis is ascribed to the buildup of Fe(II) from the reduction of Fe(III) by H2O2 as well as PICA oxidation products. PICA assistance in the Fenton reaction may be beneficial to wastewater treatment because it favors iron cycling, extends the pH range, and balances oxidation universality with selectivity. |
doi_str_mv | 10.1021/acs.est.1c00230 |
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Here, we employed the biodegradable chelating agent picolinic acid (PICA) to address these concerns. Compared to the classical Fenton reaction at pH 3.0, PICA greatly accelerated the degradation of atrazine, sulfamethazine, and various substituted phenols at pH 5.0 in a reaction with autocatalytic characteristics. Although HO• served as the principal oxidant, a high-spin, end-on hydroperoxo intermediate, tentatively identified as PICA–FeIII–OOH, also exhibited reactivity toward several test compounds. Chloride release from the oxidation of 2,4,6-trichlorophenol and the positive slope of the Hammett correlation for a series of halogenated phenols were consistent with PICA–FeIII–OOH reacting as a nucleophilic oxidant. Compared to HO•, PICA–FeIII–OOH is less sensitive to potential scavengers in environmental water samples. Kinetic analysis reveals that PICA facilitates Fe(III)/Fe(II) transformation by accelerating Fe(III) reduction by H2O2. Autocatalysis is ascribed to the buildup of Fe(II) from the reduction of Fe(III) by H2O2 as well as PICA oxidation products. PICA assistance in the Fenton reaction may be beneficial to wastewater treatment because it favors iron cycling, extends the pH range, and balances oxidation universality with selectivity.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/acs.est.1c00230</identifier><language>eng</language><publisher>Easton: American Chemical Society</publisher><subject>2,4,6-Trichlorophenol ; Acidic oxides ; Atrazine ; Autocatalysis ; Biodegradability ; Biodegradation ; Chelating agents ; Chelation ; Cogeneration ; Cycles ; Herbicides ; Hydrogen peroxide ; Hydroxyl radicals ; Iron ; Iron constituents ; Oxidants ; Oxidation ; Oxidizing agents ; pH effects ; Phenols ; Picolinic acid ; Reduction ; Scavenging ; Selectivity ; Sulfamethazine ; Treatment and Resource Recovery ; Trichlorophenol ; Trichlorophenols ; Wastewater treatment ; Water analysis ; Water sampling</subject><ispartof>Environmental science & technology, 2021-06, Vol.55 (12), p.8299-8308</ispartof><rights>2021 American Chemical Society</rights><rights>Copyright American Chemical Society Jun 15, 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a334t-60d4d97a0bd96ed23156fcdf21220e1881c7a245e66520bc04c6537e5d87952f3</citedby><cites>FETCH-LOGICAL-a334t-60d4d97a0bd96ed23156fcdf21220e1881c7a245e66520bc04c6537e5d87952f3</cites><orcidid>0000-0002-2772-5250 ; 0000-0003-4732-1015 ; 0000-0003-3626-1539</orcidid></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></links><search><creatorcontrib>Yang, Zhichao</creatorcontrib><creatorcontrib>Shan, Chao</creatorcontrib><creatorcontrib>Pan, Bingcai</creatorcontrib><creatorcontrib>Pignatello, Joseph J</creatorcontrib><title>The Fenton Reaction in Water Assisted by Picolinic Acid: Accelerated Iron Cycling and Co-generation of a Selective Fe-Based Oxidant</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>The Fenton reaction is limited by a narrow acidic pH range, the slow reduction of Fe(III), and susceptibility of the nonselective hydroxyl radical (HO•) to scavenging by water constituents. Here, we employed the biodegradable chelating agent picolinic acid (PICA) to address these concerns. Compared to the classical Fenton reaction at pH 3.0, PICA greatly accelerated the degradation of atrazine, sulfamethazine, and various substituted phenols at pH 5.0 in a reaction with autocatalytic characteristics. Although HO• served as the principal oxidant, a high-spin, end-on hydroperoxo intermediate, tentatively identified as PICA–FeIII–OOH, also exhibited reactivity toward several test compounds. Chloride release from the oxidation of 2,4,6-trichlorophenol and the positive slope of the Hammett correlation for a series of halogenated phenols were consistent with PICA–FeIII–OOH reacting as a nucleophilic oxidant. Compared to HO•, PICA–FeIII–OOH is less sensitive to potential scavengers in environmental water samples. Kinetic analysis reveals that PICA facilitates Fe(III)/Fe(II) transformation by accelerating Fe(III) reduction by H2O2. Autocatalysis is ascribed to the buildup of Fe(II) from the reduction of Fe(III) by H2O2 as well as PICA oxidation products. PICA assistance in the Fenton reaction may be beneficial to wastewater treatment because it favors iron cycling, extends the pH range, and balances oxidation universality with selectivity.</description><subject>2,4,6-Trichlorophenol</subject><subject>Acidic oxides</subject><subject>Atrazine</subject><subject>Autocatalysis</subject><subject>Biodegradability</subject><subject>Biodegradation</subject><subject>Chelating agents</subject><subject>Chelation</subject><subject>Cogeneration</subject><subject>Cycles</subject><subject>Herbicides</subject><subject>Hydrogen peroxide</subject><subject>Hydroxyl radicals</subject><subject>Iron</subject><subject>Iron constituents</subject><subject>Oxidants</subject><subject>Oxidation</subject><subject>Oxidizing agents</subject><subject>pH effects</subject><subject>Phenols</subject><subject>Picolinic acid</subject><subject>Reduction</subject><subject>Scavenging</subject><subject>Selectivity</subject><subject>Sulfamethazine</subject><subject>Treatment and Resource Recovery</subject><subject>Trichlorophenol</subject><subject>Trichlorophenols</subject><subject>Wastewater treatment</subject><subject>Water analysis</subject><subject>Water sampling</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kM1LAzEQxYMoWKtnrwGPsm0-Ntldb3WxWihUtKK3JU1ma0rN1mQr9uw_btaKNy-Tgfd-b8hD6JySASWMDpUOAwjtgGpCGCcHqEcFI4nIBT1EPUIoTwouX47RSQgr8uPJe-hr_gp4DK5tHH4ApVsbF-vws2rB41EINrRg8GKH761u1tZZjUfamqs4NazBq06e-EiVOx31JVbO4LJJluA6tctraqzwY3TH-I_uXHKtQsRmn9Yo156io1qtA5z9vn30NL6Zl3fJdHY7KUfTRHGetokkJjVFpsjCFBIM41TIWpuaUcYI0DynOlMsFSBl_PhCk1RLwTMQJs8KwWreRxf73I1v3rexq2rVbL2LJysmUp5zmWVpdA33Lu2bEDzU1cbbN-V3FSVV13QVm646-rfpSFzuiU74i_zP_Q2jIYBk</recordid><startdate>20210615</startdate><enddate>20210615</enddate><creator>Yang, Zhichao</creator><creator>Shan, Chao</creator><creator>Pan, Bingcai</creator><creator>Pignatello, Joseph J</creator><general>American Chemical Society</general><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><orcidid>https://orcid.org/0000-0002-2772-5250</orcidid><orcidid>https://orcid.org/0000-0003-4732-1015</orcidid><orcidid>https://orcid.org/0000-0003-3626-1539</orcidid></search><sort><creationdate>20210615</creationdate><title>The Fenton Reaction in Water Assisted by Picolinic Acid: Accelerated Iron Cycling and Co-generation of a Selective Fe-Based Oxidant</title><author>Yang, Zhichao ; Shan, Chao ; Pan, Bingcai ; Pignatello, Joseph J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a334t-60d4d97a0bd96ed23156fcdf21220e1881c7a245e66520bc04c6537e5d87952f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>2,4,6-Trichlorophenol</topic><topic>Acidic oxides</topic><topic>Atrazine</topic><topic>Autocatalysis</topic><topic>Biodegradability</topic><topic>Biodegradation</topic><topic>Chelating agents</topic><topic>Chelation</topic><topic>Cogeneration</topic><topic>Cycles</topic><topic>Herbicides</topic><topic>Hydrogen peroxide</topic><topic>Hydroxyl radicals</topic><topic>Iron</topic><topic>Iron constituents</topic><topic>Oxidants</topic><topic>Oxidation</topic><topic>Oxidizing agents</topic><topic>pH effects</topic><topic>Phenols</topic><topic>Picolinic acid</topic><topic>Reduction</topic><topic>Scavenging</topic><topic>Selectivity</topic><topic>Sulfamethazine</topic><topic>Treatment and Resource Recovery</topic><topic>Trichlorophenol</topic><topic>Trichlorophenols</topic><topic>Wastewater treatment</topic><topic>Water analysis</topic><topic>Water sampling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Zhichao</creatorcontrib><creatorcontrib>Shan, Chao</creatorcontrib><creatorcontrib>Pan, Bingcai</creatorcontrib><creatorcontrib>Pignatello, Joseph J</creatorcontrib><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><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Zhichao</au><au>Shan, Chao</au><au>Pan, Bingcai</au><au>Pignatello, Joseph J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Fenton Reaction in Water Assisted by Picolinic Acid: Accelerated Iron Cycling and Co-generation of a Selective Fe-Based Oxidant</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2021-06-15</date><risdate>2021</risdate><volume>55</volume><issue>12</issue><spage>8299</spage><epage>8308</epage><pages>8299-8308</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><abstract>The Fenton reaction is limited by a narrow acidic pH range, the slow reduction of Fe(III), and susceptibility of the nonselective hydroxyl radical (HO•) to scavenging by water constituents. Here, we employed the biodegradable chelating agent picolinic acid (PICA) to address these concerns. Compared to the classical Fenton reaction at pH 3.0, PICA greatly accelerated the degradation of atrazine, sulfamethazine, and various substituted phenols at pH 5.0 in a reaction with autocatalytic characteristics. Although HO• served as the principal oxidant, a high-spin, end-on hydroperoxo intermediate, tentatively identified as PICA–FeIII–OOH, also exhibited reactivity toward several test compounds. Chloride release from the oxidation of 2,4,6-trichlorophenol and the positive slope of the Hammett correlation for a series of halogenated phenols were consistent with PICA–FeIII–OOH reacting as a nucleophilic oxidant. Compared to HO•, PICA–FeIII–OOH is less sensitive to potential scavengers in environmental water samples. Kinetic analysis reveals that PICA facilitates Fe(III)/Fe(II) transformation by accelerating Fe(III) reduction by H2O2. Autocatalysis is ascribed to the buildup of Fe(II) from the reduction of Fe(III) by H2O2 as well as PICA oxidation products. PICA assistance in the Fenton reaction may be beneficial to wastewater treatment because it favors iron cycling, extends the pH range, and balances oxidation universality with selectivity.</abstract><cop>Easton</cop><pub>American Chemical Society</pub><doi>10.1021/acs.est.1c00230</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2772-5250</orcidid><orcidid>https://orcid.org/0000-0003-4732-1015</orcidid><orcidid>https://orcid.org/0000-0003-3626-1539</orcidid></addata></record> |
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subjects | 2,4,6-Trichlorophenol Acidic oxides Atrazine Autocatalysis Biodegradability Biodegradation Chelating agents Chelation Cogeneration Cycles Herbicides Hydrogen peroxide Hydroxyl radicals Iron Iron constituents Oxidants Oxidation Oxidizing agents pH effects Phenols Picolinic acid Reduction Scavenging Selectivity Sulfamethazine Treatment and Resource Recovery Trichlorophenol Trichlorophenols Wastewater treatment Water analysis Water sampling |
title | The Fenton Reaction in Water Assisted by Picolinic Acid: Accelerated Iron Cycling and Co-generation of a Selective Fe-Based Oxidant |
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