Cobalt/Peracetic Acid: Advanced Oxidation of Aromatic Organic Compounds by Acetylperoxyl Radicals
Peracetic acid (PAA) is increasingly used as an alternative disinfectant and its advanced oxidation processes (AOPs) could be useful for pollutant degradation. Co(II) or Co(III) can activate PAA to produce acetyloxyl (CH3C(O)O•) and acetylperoxyl (CH3C(O)OO•) radicals with little •OH radical f...
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Veröffentlicht in: | Environmental science & technology 2020-04, Vol.54 (8), p.5268-5278 |
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description | Peracetic acid (PAA) is increasingly used as an alternative disinfectant and its advanced oxidation processes (AOPs) could be useful for pollutant degradation. Co(II) or Co(III) can activate PAA to produce acetyloxyl (CH3C(O)O•) and acetylperoxyl (CH3C(O)OO•) radicals with little •OH radical formation, and Co(II)/Co(III) is cycled. For the first time, this study determined the reaction rates of PAA with Co(II) (k PAA,Co(II) = 1.70 × 101 to 6.67 × 102 M–1·s–1) and Co(III) (k PAA,Co(III) = 3.91 × 100 to 4.57 × 102 M–1·s–1) ions over the initial pH 3.0–8.2 and evaluated 30 different aromatic organic compounds for degradation by Co/PAA. In-depth investigation confirmed that CH3C(O)OO• is the key reactive species under Co/PAA for compound degradation. Assessing the structure–activity relationship between compounds’ molecular descriptors and pseudo-first-order degradation rate constants (k′PAA• in s–1) by Co/PAA showed the number of ring atoms, E HOMO, softness, and ionization potential to be the most influential, strongly suggesting the electron transfer mechanism from aromatic compounds to the acetylperoxyl radical. The radical production and compound degradation in Co/PAA are most efficient in the intermediate pH range and can be influenced by water matrix constituents of bicarbonate, phosphate, and humic acids. These results significantly improve the knowledge regarding the acetylperoxyl radical from PAA and will be useful for further development and applications of PAA-based AOPs. |
doi_str_mv | 10.1021/acs.est.0c00356 |
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Co(II) or Co(III) can activate PAA to produce acetyloxyl (CH3C(O)O•) and acetylperoxyl (CH3C(O)OO•) radicals with little •OH radical formation, and Co(II)/Co(III) is cycled. For the first time, this study determined the reaction rates of PAA with Co(II) (k PAA,Co(II) = 1.70 × 101 to 6.67 × 102 M–1·s–1) and Co(III) (k PAA,Co(III) = 3.91 × 100 to 4.57 × 102 M–1·s–1) ions over the initial pH 3.0–8.2 and evaluated 30 different aromatic organic compounds for degradation by Co/PAA. In-depth investigation confirmed that CH3C(O)OO• is the key reactive species under Co/PAA for compound degradation. Assessing the structure–activity relationship between compounds’ molecular descriptors and pseudo-first-order degradation rate constants (k′PAA• in s–1) by Co/PAA showed the number of ring atoms, E HOMO, softness, and ionization potential to be the most influential, strongly suggesting the electron transfer mechanism from aromatic compounds to the acetylperoxyl radical. The radical production and compound degradation in Co/PAA are most efficient in the intermediate pH range and can be influenced by water matrix constituents of bicarbonate, phosphate, and humic acids. These results significantly improve the knowledge regarding the acetylperoxyl radical from PAA and will be useful for further development and applications of PAA-based AOPs.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/acs.est.0c00356</identifier><identifier>PMID: 32186188</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Aromatic compounds ; Atomic properties ; Bicarbonates ; Cobalt ; Disinfectants ; Electron transfer ; Environmental degradation ; Free radicals ; Humic acids ; Ionization ; Ionization potentials ; Molecular structure ; Organic compounds ; Oxidation ; Peracetic acid ; pH effects ; Pollutants ; Radicals ; Rate constants ; Softness</subject><ispartof>Environmental science & technology, 2020-04, Vol.54 (8), p.5268-5278</ispartof><rights>Copyright American Chemical Society Apr 21, 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a361t-bb15c9aed2323a7beaa5be2abd66aa438b39811f3647b9982f56eaeb1d2bf76a3</citedby><cites>FETCH-LOGICAL-a361t-bb15c9aed2323a7beaa5be2abd66aa438b39811f3647b9982f56eaeb1d2bf76a3</cites><orcidid>0000-0002-6787-2431 ; 0000-0002-3786-094X ; 0000-0002-0162-7388</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.est.0c00356$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.est.0c00356$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32186188$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Juhee</creatorcontrib><creatorcontrib>Du, Penghui</creatorcontrib><creatorcontrib>Liu, Wen</creatorcontrib><creatorcontrib>Luo, Cong</creatorcontrib><creatorcontrib>Zhao, He</creatorcontrib><creatorcontrib>Huang, Ching-Hua</creatorcontrib><title>Cobalt/Peracetic Acid: Advanced Oxidation of Aromatic Organic Compounds by Acetylperoxyl Radicals</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>Peracetic acid (PAA) is increasingly used as an alternative disinfectant and its advanced oxidation processes (AOPs) could be useful for pollutant degradation. Co(II) or Co(III) can activate PAA to produce acetyloxyl (CH3C(O)O•) and acetylperoxyl (CH3C(O)OO•) radicals with little •OH radical formation, and Co(II)/Co(III) is cycled. For the first time, this study determined the reaction rates of PAA with Co(II) (k PAA,Co(II) = 1.70 × 101 to 6.67 × 102 M–1·s–1) and Co(III) (k PAA,Co(III) = 3.91 × 100 to 4.57 × 102 M–1·s–1) ions over the initial pH 3.0–8.2 and evaluated 30 different aromatic organic compounds for degradation by Co/PAA. In-depth investigation confirmed that CH3C(O)OO• is the key reactive species under Co/PAA for compound degradation. Assessing the structure–activity relationship between compounds’ molecular descriptors and pseudo-first-order degradation rate constants (k′PAA• in s–1) by Co/PAA showed the number of ring atoms, E HOMO, softness, and ionization potential to be the most influential, strongly suggesting the electron transfer mechanism from aromatic compounds to the acetylperoxyl radical. The radical production and compound degradation in Co/PAA are most efficient in the intermediate pH range and can be influenced by water matrix constituents of bicarbonate, phosphate, and humic acids. These results significantly improve the knowledge regarding the acetylperoxyl radical from PAA and will be useful for further development and applications of PAA-based AOPs.</description><subject>Aromatic compounds</subject><subject>Atomic properties</subject><subject>Bicarbonates</subject><subject>Cobalt</subject><subject>Disinfectants</subject><subject>Electron transfer</subject><subject>Environmental degradation</subject><subject>Free radicals</subject><subject>Humic acids</subject><subject>Ionization</subject><subject>Ionization potentials</subject><subject>Molecular structure</subject><subject>Organic compounds</subject><subject>Oxidation</subject><subject>Peracetic acid</subject><subject>pH effects</subject><subject>Pollutants</subject><subject>Radicals</subject><subject>Rate constants</subject><subject>Softness</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLw0AYRQdRbK2u3UnApaSdRzNN3IXgCwoVUXAXvnlEUpJMnEmk-fdOaO3O1d2cey8chK4JnhNMyQKkm2vXzbHEmEX8BE1JRHEYxRE5RVOMCQsTxj8n6MK5LcaYMhyfowmjJOYkjqcIMiOg6hav2oLUXSmDVJbqPkjVDzRSq2CzKxV0pWkCUwSpNTWM0MZ-QeMzM3Vr-ka5QAy-qbuharU1u6EK3kCVEip3ic4KH_rqkDP08fjwnj2H683TS5auQ2CcdKEQJJIJaEUZZbASGiASmoJQnAMsWSxYEhNSML5ciSSJaRFxDVoQRUWx4sBm6Ha_21rz3Xsp-db0tvGXOWXJkvKIcuKpxZ6S1jhndZG3tqzBDjnB-ag090rzsX1Q6hs3h91e1Fod-T-HHrjbA2Pz-Pnf3C9wIIKo</recordid><startdate>20200421</startdate><enddate>20200421</enddate><creator>Kim, Juhee</creator><creator>Du, Penghui</creator><creator>Liu, Wen</creator><creator>Luo, Cong</creator><creator>Zhao, He</creator><creator>Huang, Ching-Hua</creator><general>American Chemical Society</general><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><orcidid>https://orcid.org/0000-0002-6787-2431</orcidid><orcidid>https://orcid.org/0000-0002-3786-094X</orcidid><orcidid>https://orcid.org/0000-0002-0162-7388</orcidid></search><sort><creationdate>20200421</creationdate><title>Cobalt/Peracetic Acid: Advanced Oxidation of Aromatic Organic Compounds by Acetylperoxyl Radicals</title><author>Kim, Juhee ; Du, Penghui ; Liu, Wen ; Luo, Cong ; Zhao, He ; Huang, Ching-Hua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a361t-bb15c9aed2323a7beaa5be2abd66aa438b39811f3647b9982f56eaeb1d2bf76a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aromatic compounds</topic><topic>Atomic properties</topic><topic>Bicarbonates</topic><topic>Cobalt</topic><topic>Disinfectants</topic><topic>Electron transfer</topic><topic>Environmental degradation</topic><topic>Free radicals</topic><topic>Humic acids</topic><topic>Ionization</topic><topic>Ionization potentials</topic><topic>Molecular structure</topic><topic>Organic compounds</topic><topic>Oxidation</topic><topic>Peracetic acid</topic><topic>pH effects</topic><topic>Pollutants</topic><topic>Radicals</topic><topic>Rate constants</topic><topic>Softness</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Juhee</creatorcontrib><creatorcontrib>Du, Penghui</creatorcontrib><creatorcontrib>Liu, Wen</creatorcontrib><creatorcontrib>Luo, Cong</creatorcontrib><creatorcontrib>Zhao, He</creatorcontrib><creatorcontrib>Huang, Ching-Hua</creatorcontrib><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><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Juhee</au><au>Du, Penghui</au><au>Liu, Wen</au><au>Luo, Cong</au><au>Zhao, He</au><au>Huang, Ching-Hua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cobalt/Peracetic Acid: Advanced Oxidation of Aromatic Organic Compounds by Acetylperoxyl Radicals</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2020-04-21</date><risdate>2020</risdate><volume>54</volume><issue>8</issue><spage>5268</spage><epage>5278</epage><pages>5268-5278</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><abstract>Peracetic acid (PAA) is increasingly used as an alternative disinfectant and its advanced oxidation processes (AOPs) could be useful for pollutant degradation. Co(II) or Co(III) can activate PAA to produce acetyloxyl (CH3C(O)O•) and acetylperoxyl (CH3C(O)OO•) radicals with little •OH radical formation, and Co(II)/Co(III) is cycled. For the first time, this study determined the reaction rates of PAA with Co(II) (k PAA,Co(II) = 1.70 × 101 to 6.67 × 102 M–1·s–1) and Co(III) (k PAA,Co(III) = 3.91 × 100 to 4.57 × 102 M–1·s–1) ions over the initial pH 3.0–8.2 and evaluated 30 different aromatic organic compounds for degradation by Co/PAA. In-depth investigation confirmed that CH3C(O)OO• is the key reactive species under Co/PAA for compound degradation. Assessing the structure–activity relationship between compounds’ molecular descriptors and pseudo-first-order degradation rate constants (k′PAA• in s–1) by Co/PAA showed the number of ring atoms, E HOMO, softness, and ionization potential to be the most influential, strongly suggesting the electron transfer mechanism from aromatic compounds to the acetylperoxyl radical. The radical production and compound degradation in Co/PAA are most efficient in the intermediate pH range and can be influenced by water matrix constituents of bicarbonate, phosphate, and humic acids. These results significantly improve the knowledge regarding the acetylperoxyl radical from PAA and will be useful for further development and applications of PAA-based AOPs.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>32186188</pmid><doi>10.1021/acs.est.0c00356</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6787-2431</orcidid><orcidid>https://orcid.org/0000-0002-3786-094X</orcidid><orcidid>https://orcid.org/0000-0002-0162-7388</orcidid></addata></record> |
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subjects | Aromatic compounds Atomic properties Bicarbonates Cobalt Disinfectants Electron transfer Environmental degradation Free radicals Humic acids Ionization Ionization potentials Molecular structure Organic compounds Oxidation Peracetic acid pH effects Pollutants Radicals Rate constants Softness |
title | Cobalt/Peracetic Acid: Advanced Oxidation of Aromatic Organic Compounds by Acetylperoxyl Radicals |
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