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
Hauptverfasser: Kim, Juhee, Du, Penghui, Liu, Wen, Luo, Cong, Zhao, He, Huang, Ching-Hua
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container_issue 8
container_start_page 5268
container_title Environmental science & technology
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creator Kim, Juhee
Du, Penghui
Liu, Wen
Luo, Cong
Zhao, He
Huang, Ching-Hua
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. 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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 &amp; 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 &amp; 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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source American Chemical Society Journals
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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