Boosting the degradation of antibiotics via peroxymonosulfate activation with a Cu-based metal-organic framework
Highly efficient degradation of antibiotics is a huge challenge due to the extremely stable molecules and the potential for biological resistance. However, conventional degradation methods are limited to lower degradation rate, higher energy consumption and secondary pollution. Herein, we report a n...
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Veröffentlicht in: | Chemical science (Cambridge) 2024-06, Vol.15 (25), p.9733-9741 |
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creator | Wu, Ying Liang, Gang Li, Wen-Bin Zhong, Xiao-Feng Zhang, Yang-Yang Ye, Jia-Wen Yang, Tao Mo, Zong-Wen Chen, Xiao-Ming |
description | Highly efficient degradation of antibiotics is a huge challenge due to the extremely stable molecules and the potential for biological resistance. However, conventional degradation methods are limited to lower degradation rate, higher energy consumption and secondary pollution. Herein, we report a new Cu-based metal-organic framework (MOF), featuring classical planar trinuclear [Cu
(µ
-O)]
clusters within the pores. The presence of the rich open metal sites and the large pore ratio, as well as the high catalytic activity of Cu
ions, are conducive to boosting the degradation of various antibiotics (>95%) under the activation of peroxymonosulfate. Remarkably, this is the first MOF to achieve such exceptional catalytic performance under neutral and even alkaline conditions, which exceeds those of most reported materials. Mechanism investigation demonstrates that multiple active species were produced and promoted the degradation synergistically during the advanced oxidation processes. |
doi_str_mv | 10.1039/d4sc02850c |
format | Article |
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(µ
-O)]
clusters within the pores. The presence of the rich open metal sites and the large pore ratio, as well as the high catalytic activity of Cu
ions, are conducive to boosting the degradation of various antibiotics (>95%) under the activation of peroxymonosulfate. Remarkably, this is the first MOF to achieve such exceptional catalytic performance under neutral and even alkaline conditions, which exceeds those of most reported materials. Mechanism investigation demonstrates that multiple active species were produced and promoted the degradation synergistically during the advanced oxidation processes.</description><identifier>ISSN: 2041-6520</identifier><identifier>EISSN: 2041-6539</identifier><identifier>DOI: 10.1039/d4sc02850c</identifier><identifier>PMID: 38939145</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Antibiotics ; Catalytic activity ; Chemistry ; Copper ; Degradation ; Energy consumption ; Metal-organic frameworks ; Oxidation</subject><ispartof>Chemical science (Cambridge), 2024-06, Vol.15 (25), p.9733-9741</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2024</rights><rights>This journal is © The Royal Society of Chemistry 2024 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c366t-e1fa4bf2e02bfe0d14a4395d8fc016ec6c1bd38230d864b26d928c023478a3c83</cites><orcidid>0000-0002-3353-7918 ; 0000-0003-4198-2998 ; 0000-0001-6925-9772</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11206226/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11206226/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38939145$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Ying</creatorcontrib><creatorcontrib>Liang, Gang</creatorcontrib><creatorcontrib>Li, Wen-Bin</creatorcontrib><creatorcontrib>Zhong, Xiao-Feng</creatorcontrib><creatorcontrib>Zhang, Yang-Yang</creatorcontrib><creatorcontrib>Ye, Jia-Wen</creatorcontrib><creatorcontrib>Yang, Tao</creatorcontrib><creatorcontrib>Mo, Zong-Wen</creatorcontrib><creatorcontrib>Chen, Xiao-Ming</creatorcontrib><title>Boosting the degradation of antibiotics via peroxymonosulfate activation with a Cu-based metal-organic framework</title><title>Chemical science (Cambridge)</title><addtitle>Chem Sci</addtitle><description>Highly efficient degradation of antibiotics is a huge challenge due to the extremely stable molecules and the potential for biological resistance. However, conventional degradation methods are limited to lower degradation rate, higher energy consumption and secondary pollution. Herein, we report a new Cu-based metal-organic framework (MOF), featuring classical planar trinuclear [Cu
(µ
-O)]
clusters within the pores. The presence of the rich open metal sites and the large pore ratio, as well as the high catalytic activity of Cu
ions, are conducive to boosting the degradation of various antibiotics (>95%) under the activation of peroxymonosulfate. Remarkably, this is the first MOF to achieve such exceptional catalytic performance under neutral and even alkaline conditions, which exceeds those of most reported materials. Mechanism investigation demonstrates that multiple active species were produced and promoted the degradation synergistically during the advanced oxidation processes.</description><subject>Antibiotics</subject><subject>Catalytic activity</subject><subject>Chemistry</subject><subject>Copper</subject><subject>Degradation</subject><subject>Energy consumption</subject><subject>Metal-organic frameworks</subject><subject>Oxidation</subject><issn>2041-6520</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkU1v1DAQhiNERau2F34AssQFIQX8Fa9zQhBailSJA3C2Jv7YdUnsxXa27b_HZcsKmMuMNI9ezbxv0zwn-A3BrH9reNaYyg7rJ80JxZy0omP908NM8XFznvMNrsUY6ejqWXPMZM96wruTZvshxlx8WKOyscjYdQIDxceAokMQih99LF5ntPOAtjbFu_s5hpiXyUGxCHTxuz1_68sGARqWdoRsDZptgamNaQ3Ba-QSzPY2ph9nzZGDKdvzx37afL-8-DZctddfPn0e3l-3mglRWksc8NFRi-noLDaEA2d9Z6TTmAirhSajYZIybKTgIxWmp7IawfhKAtOSnTbv9rrbZZyt0TaUBJPaJj9DulcRvPp3E_xGreNOEUKxoFRUhVePCin-XGwuavZZ22mCYOOSFcMrRqulklX05X_oTVxSqP89UFR0FcKVer2ndIo5J-sO1xCsHsJUH_nX4XeYQ4Vf_H3_Af0THfsFDq6cMA</recordid><startdate>20240626</startdate><enddate>20240626</enddate><creator>Wu, Ying</creator><creator>Liang, Gang</creator><creator>Li, Wen-Bin</creator><creator>Zhong, Xiao-Feng</creator><creator>Zhang, Yang-Yang</creator><creator>Ye, Jia-Wen</creator><creator>Yang, Tao</creator><creator>Mo, Zong-Wen</creator><creator>Chen, Xiao-Ming</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3353-7918</orcidid><orcidid>https://orcid.org/0000-0003-4198-2998</orcidid><orcidid>https://orcid.org/0000-0001-6925-9772</orcidid></search><sort><creationdate>20240626</creationdate><title>Boosting the degradation of antibiotics via peroxymonosulfate activation with a Cu-based metal-organic framework</title><author>Wu, Ying ; Liang, Gang ; Li, Wen-Bin ; Zhong, Xiao-Feng ; Zhang, Yang-Yang ; Ye, Jia-Wen ; Yang, Tao ; Mo, Zong-Wen ; Chen, Xiao-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-e1fa4bf2e02bfe0d14a4395d8fc016ec6c1bd38230d864b26d928c023478a3c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antibiotics</topic><topic>Catalytic activity</topic><topic>Chemistry</topic><topic>Copper</topic><topic>Degradation</topic><topic>Energy consumption</topic><topic>Metal-organic frameworks</topic><topic>Oxidation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Ying</creatorcontrib><creatorcontrib>Liang, Gang</creatorcontrib><creatorcontrib>Li, Wen-Bin</creatorcontrib><creatorcontrib>Zhong, Xiao-Feng</creatorcontrib><creatorcontrib>Zhang, Yang-Yang</creatorcontrib><creatorcontrib>Ye, Jia-Wen</creatorcontrib><creatorcontrib>Yang, Tao</creatorcontrib><creatorcontrib>Mo, Zong-Wen</creatorcontrib><creatorcontrib>Chen, Xiao-Ming</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemical science (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Ying</au><au>Liang, Gang</au><au>Li, Wen-Bin</au><au>Zhong, Xiao-Feng</au><au>Zhang, Yang-Yang</au><au>Ye, Jia-Wen</au><au>Yang, Tao</au><au>Mo, Zong-Wen</au><au>Chen, Xiao-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Boosting the degradation of antibiotics via peroxymonosulfate activation with a Cu-based metal-organic framework</atitle><jtitle>Chemical science (Cambridge)</jtitle><addtitle>Chem Sci</addtitle><date>2024-06-26</date><risdate>2024</risdate><volume>15</volume><issue>25</issue><spage>9733</spage><epage>9741</epage><pages>9733-9741</pages><issn>2041-6520</issn><eissn>2041-6539</eissn><abstract>Highly efficient degradation of antibiotics is a huge challenge due to the extremely stable molecules and the potential for biological resistance. However, conventional degradation methods are limited to lower degradation rate, higher energy consumption and secondary pollution. Herein, we report a new Cu-based metal-organic framework (MOF), featuring classical planar trinuclear [Cu
(µ
-O)]
clusters within the pores. The presence of the rich open metal sites and the large pore ratio, as well as the high catalytic activity of Cu
ions, are conducive to boosting the degradation of various antibiotics (>95%) under the activation of peroxymonosulfate. Remarkably, this is the first MOF to achieve such exceptional catalytic performance under neutral and even alkaline conditions, which exceeds those of most reported materials. Mechanism investigation demonstrates that multiple active species were produced and promoted the degradation synergistically during the advanced oxidation processes.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38939145</pmid><doi>10.1039/d4sc02850c</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-3353-7918</orcidid><orcidid>https://orcid.org/0000-0003-4198-2998</orcidid><orcidid>https://orcid.org/0000-0001-6925-9772</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibiotics Catalytic activity Chemistry Copper Degradation Energy consumption Metal-organic frameworks Oxidation |
title | Boosting the degradation of antibiotics via peroxymonosulfate activation with a Cu-based metal-organic framework |
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