Photografting Graphene Oxide to Inert Membrane Materials to Impart Antibacterial Activity

Surface modification with bactericides is a promising approach to imparting membrane materials with biofouling resistance. However, chemical modification of membranes made from inert materials, such as polyvinylidene fluoride (PVDF) and polysulfone, is challenging because of the absence of reactive...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Environmental science & technology letters 2019-03, Vol.6 (3), p.141-147
Hauptverfasser: Kaneda, Masashi, Lu, Xinglin, Cheng, Wei, Zhou, Xuechen, Bernstein, Roy, Zhang, Wei, Kimura, Katsuki, Elimelech, Menachem
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 147
container_issue 3
container_start_page 141
container_title Environmental science & technology letters
container_volume 6
creator Kaneda, Masashi
Lu, Xinglin
Cheng, Wei
Zhou, Xuechen
Bernstein, Roy
Zhang, Wei
Kimura, Katsuki
Elimelech, Menachem
description Surface modification with bactericides is a promising approach to imparting membrane materials with biofouling resistance. However, chemical modification of membranes made from inert materials, such as polyvinylidene fluoride (PVDF) and polysulfone, is challenging because of the absence of reactive functional groups on these materials. In this study, we develop a facile procedure using benzophenone as an anchor to graft biocidal graphene oxide (GO) to chemically inactive membrane materials. GO nanosheets are first functionalized with benzophenone through an amide coupling reaction. Then, benzophenone-functionalized GO nanosheets are irreversibly grafted to the inert membrane surfaces via benzophenone-initiated cross-linking under ultraviolet irradiation. The binding of GO to the membrane surface is confirmed by scanning electron microscopy and Raman spectroscopy. When exposed to a model bacterium (Escherichia coli), GO-functionalized PVDF and polysulfone membranes exhibit strong antibacterial activity, reducing the number of viable cells by 90% and 75%, respectively, compared to the number with the pristine membranes. Notably, this bactericidal effect is imparted to the membranes without compromising membrane permeability or solute retention properties. Our results highlight the potential application of benzophenone chemistry in membrane surface modification as well as its promise in developing antimicrobial surfaces for a variety of environmental applications.
doi_str_mv 10.1021/acs.estlett.9b00012
format Article
fullrecord <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_acs_estlett_9b00012</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>h5456076</sourcerecordid><originalsourceid>FETCH-LOGICAL-a289t-f5e59b239e3c326858fe20bf0ab54767a47556dca9830bd70301d0e2ba14b80a3</originalsourceid><addsrcrecordid>eNp9kM9OAjEQhxujiQR5Ai_7AgvTdv-0R0IUSSB40IOnzXR3Fkpgl7TVyNtbhIMnTzOZb36TycfYI4cxB8EnWPsx-bCnEMbaAAAXN2wgpFCp0hJu__T3bOT9Lq6ALiEDOWAfr9s-9BuHbbDdJpk7PG6po2T9bRtKQp8sOnIhWdHBOIzzFQZyFvf-lx2OGOG0C9ZgfQHJtA72y4bTA7tr4x6NrnXI3p-f3mYv6XI9X8ymyxSF0iFtc8q1EVKTrKUoVK5aEmBaQJNnZVFiVuZ50dSolQTTlCCBN0DCIM-MApRDJi93a9d776itjs4e0J0qDtVZUBUFVVdB1VVQTE0uqTPc9Z-uiz_-m_gBZNptWg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Photografting Graphene Oxide to Inert Membrane Materials to Impart Antibacterial Activity</title><source>American Chemical Society Journals</source><creator>Kaneda, Masashi ; Lu, Xinglin ; Cheng, Wei ; Zhou, Xuechen ; Bernstein, Roy ; Zhang, Wei ; Kimura, Katsuki ; Elimelech, Menachem</creator><creatorcontrib>Kaneda, Masashi ; Lu, Xinglin ; Cheng, Wei ; Zhou, Xuechen ; Bernstein, Roy ; Zhang, Wei ; Kimura, Katsuki ; Elimelech, Menachem</creatorcontrib><description>Surface modification with bactericides is a promising approach to imparting membrane materials with biofouling resistance. However, chemical modification of membranes made from inert materials, such as polyvinylidene fluoride (PVDF) and polysulfone, is challenging because of the absence of reactive functional groups on these materials. In this study, we develop a facile procedure using benzophenone as an anchor to graft biocidal graphene oxide (GO) to chemically inactive membrane materials. GO nanosheets are first functionalized with benzophenone through an amide coupling reaction. Then, benzophenone-functionalized GO nanosheets are irreversibly grafted to the inert membrane surfaces via benzophenone-initiated cross-linking under ultraviolet irradiation. The binding of GO to the membrane surface is confirmed by scanning electron microscopy and Raman spectroscopy. When exposed to a model bacterium (Escherichia coli), GO-functionalized PVDF and polysulfone membranes exhibit strong antibacterial activity, reducing the number of viable cells by 90% and 75%, respectively, compared to the number with the pristine membranes. Notably, this bactericidal effect is imparted to the membranes without compromising membrane permeability or solute retention properties. Our results highlight the potential application of benzophenone chemistry in membrane surface modification as well as its promise in developing antimicrobial surfaces for a variety of environmental applications.</description><identifier>ISSN: 2328-8930</identifier><identifier>EISSN: 2328-8930</identifier><identifier>DOI: 10.1021/acs.estlett.9b00012</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Environmental science &amp; technology letters, 2019-03, Vol.6 (3), p.141-147</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a289t-f5e59b239e3c326858fe20bf0ab54767a47556dca9830bd70301d0e2ba14b80a3</citedby><cites>FETCH-LOGICAL-a289t-f5e59b239e3c326858fe20bf0ab54767a47556dca9830bd70301d0e2ba14b80a3</cites><orcidid>0000-0003-4186-1563 ; 0000-0002-0229-7712</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.estlett.9b00012$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.estlett.9b00012$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27074,27922,27923,56736,56786</link.rule.ids></links><search><creatorcontrib>Kaneda, Masashi</creatorcontrib><creatorcontrib>Lu, Xinglin</creatorcontrib><creatorcontrib>Cheng, Wei</creatorcontrib><creatorcontrib>Zhou, Xuechen</creatorcontrib><creatorcontrib>Bernstein, Roy</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Kimura, Katsuki</creatorcontrib><creatorcontrib>Elimelech, Menachem</creatorcontrib><title>Photografting Graphene Oxide to Inert Membrane Materials to Impart Antibacterial Activity</title><title>Environmental science &amp; technology letters</title><addtitle>Environ. Sci. Technol. Lett</addtitle><description>Surface modification with bactericides is a promising approach to imparting membrane materials with biofouling resistance. However, chemical modification of membranes made from inert materials, such as polyvinylidene fluoride (PVDF) and polysulfone, is challenging because of the absence of reactive functional groups on these materials. In this study, we develop a facile procedure using benzophenone as an anchor to graft biocidal graphene oxide (GO) to chemically inactive membrane materials. GO nanosheets are first functionalized with benzophenone through an amide coupling reaction. Then, benzophenone-functionalized GO nanosheets are irreversibly grafted to the inert membrane surfaces via benzophenone-initiated cross-linking under ultraviolet irradiation. The binding of GO to the membrane surface is confirmed by scanning electron microscopy and Raman spectroscopy. When exposed to a model bacterium (Escherichia coli), GO-functionalized PVDF and polysulfone membranes exhibit strong antibacterial activity, reducing the number of viable cells by 90% and 75%, respectively, compared to the number with the pristine membranes. Notably, this bactericidal effect is imparted to the membranes without compromising membrane permeability or solute retention properties. Our results highlight the potential application of benzophenone chemistry in membrane surface modification as well as its promise in developing antimicrobial surfaces for a variety of environmental applications.</description><issn>2328-8930</issn><issn>2328-8930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kM9OAjEQhxujiQR5Ai_7AgvTdv-0R0IUSSB40IOnzXR3Fkpgl7TVyNtbhIMnTzOZb36TycfYI4cxB8EnWPsx-bCnEMbaAAAXN2wgpFCp0hJu__T3bOT9Lq6ALiEDOWAfr9s-9BuHbbDdJpk7PG6po2T9bRtKQp8sOnIhWdHBOIzzFQZyFvf-lx2OGOG0C9ZgfQHJtA72y4bTA7tr4x6NrnXI3p-f3mYv6XI9X8ymyxSF0iFtc8q1EVKTrKUoVK5aEmBaQJNnZVFiVuZ50dSolQTTlCCBN0DCIM-MApRDJi93a9d776itjs4e0J0qDtVZUBUFVVdB1VVQTE0uqTPc9Z-uiz_-m_gBZNptWg</recordid><startdate>20190312</startdate><enddate>20190312</enddate><creator>Kaneda, Masashi</creator><creator>Lu, Xinglin</creator><creator>Cheng, Wei</creator><creator>Zhou, Xuechen</creator><creator>Bernstein, Roy</creator><creator>Zhang, Wei</creator><creator>Kimura, Katsuki</creator><creator>Elimelech, Menachem</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-4186-1563</orcidid><orcidid>https://orcid.org/0000-0002-0229-7712</orcidid></search><sort><creationdate>20190312</creationdate><title>Photografting Graphene Oxide to Inert Membrane Materials to Impart Antibacterial Activity</title><author>Kaneda, Masashi ; Lu, Xinglin ; Cheng, Wei ; Zhou, Xuechen ; Bernstein, Roy ; Zhang, Wei ; Kimura, Katsuki ; Elimelech, Menachem</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a289t-f5e59b239e3c326858fe20bf0ab54767a47556dca9830bd70301d0e2ba14b80a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaneda, Masashi</creatorcontrib><creatorcontrib>Lu, Xinglin</creatorcontrib><creatorcontrib>Cheng, Wei</creatorcontrib><creatorcontrib>Zhou, Xuechen</creatorcontrib><creatorcontrib>Bernstein, Roy</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Kimura, Katsuki</creatorcontrib><creatorcontrib>Elimelech, Menachem</creatorcontrib><collection>CrossRef</collection><jtitle>Environmental science &amp; technology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaneda, Masashi</au><au>Lu, Xinglin</au><au>Cheng, Wei</au><au>Zhou, Xuechen</au><au>Bernstein, Roy</au><au>Zhang, Wei</au><au>Kimura, Katsuki</au><au>Elimelech, Menachem</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photografting Graphene Oxide to Inert Membrane Materials to Impart Antibacterial Activity</atitle><jtitle>Environmental science &amp; technology letters</jtitle><addtitle>Environ. Sci. Technol. Lett</addtitle><date>2019-03-12</date><risdate>2019</risdate><volume>6</volume><issue>3</issue><spage>141</spage><epage>147</epage><pages>141-147</pages><issn>2328-8930</issn><eissn>2328-8930</eissn><abstract>Surface modification with bactericides is a promising approach to imparting membrane materials with biofouling resistance. However, chemical modification of membranes made from inert materials, such as polyvinylidene fluoride (PVDF) and polysulfone, is challenging because of the absence of reactive functional groups on these materials. In this study, we develop a facile procedure using benzophenone as an anchor to graft biocidal graphene oxide (GO) to chemically inactive membrane materials. GO nanosheets are first functionalized with benzophenone through an amide coupling reaction. Then, benzophenone-functionalized GO nanosheets are irreversibly grafted to the inert membrane surfaces via benzophenone-initiated cross-linking under ultraviolet irradiation. The binding of GO to the membrane surface is confirmed by scanning electron microscopy and Raman spectroscopy. When exposed to a model bacterium (Escherichia coli), GO-functionalized PVDF and polysulfone membranes exhibit strong antibacterial activity, reducing the number of viable cells by 90% and 75%, respectively, compared to the number with the pristine membranes. Notably, this bactericidal effect is imparted to the membranes without compromising membrane permeability or solute retention properties. Our results highlight the potential application of benzophenone chemistry in membrane surface modification as well as its promise in developing antimicrobial surfaces for a variety of environmental applications.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.estlett.9b00012</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4186-1563</orcidid><orcidid>https://orcid.org/0000-0002-0229-7712</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 2328-8930
ispartof Environmental science & technology letters, 2019-03, Vol.6 (3), p.141-147
issn 2328-8930
2328-8930
language eng
recordid cdi_crossref_primary_10_1021_acs_estlett_9b00012
source American Chemical Society Journals
title Photografting Graphene Oxide to Inert Membrane Materials to Impart Antibacterial Activity
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T13%3A46%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Photografting%20Graphene%20Oxide%20to%20Inert%20Membrane%20Materials%20to%20Impart%20Antibacterial%20Activity&rft.jtitle=Environmental%20science%20&%20technology%20letters&rft.au=Kaneda,%20Masashi&rft.date=2019-03-12&rft.volume=6&rft.issue=3&rft.spage=141&rft.epage=147&rft.pages=141-147&rft.issn=2328-8930&rft.eissn=2328-8930&rft_id=info:doi/10.1021/acs.estlett.9b00012&rft_dat=%3Cacs_cross%3Eh5456076%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true