File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: In situ reduction of silver by polydopamine: A novel antimicrobial modification of a thin-film composite polyamide membrane

TitleIn situ reduction of silver by polydopamine: A novel antimicrobial modification of a thin-film composite polyamide membrane
Authors
Issue Date2016
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journal/esthag
Citation
Environmental Science & Technology, 2016, v. 50 n. 17, p. 9543-9550 How to Cite?
AbstractWe report a facile method for the antimicrobial modification of a thin-film composite polyamide reverse osmosis (RO) membrane. The membrane surface was first coated with polydopamine (PDA), whose reducing catechol groups subsequently immobilized silver ions in situ to form uniformly dispersed silver nanoparticles (AgNPs) inside the coating layer. Agglomeration of AgNPs was not observed despite a high silver loading of 13.3 ± 0.3 μg/cm2 (corresponding to a surface coverage of 18.5% by the nanoparticles). Both diffusion inhibition zone tests and colony formation unit tests showed clear antimicrobial effects of the silver loaded membranes on model bacteria Bacillus subtilis and Escherichia coli. Furthermore, the silver immobilized membrane had significantly enhanced salt rejection compared to the control PDA coated membrane, which is attributed to the preferential formation of AgNPs at defect sides within the PDA layer. This self-healing mechanism can be used to prepare antimicrobial RO membranes with improved salt rejection without scarifying the membrane permeability, which provides a new dimension for membrane surface modification.
Persistent Identifierhttp://hdl.handle.net/10722/247301
ISSN
2021 Impact Factor: 11.357
2020 SCImago Journal Rankings: 2.851
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYang, Z-
dc.contributor.authorWu, Y-
dc.contributor.authorWang, J-
dc.contributor.authorCao, B-
dc.contributor.authorTang, C-
dc.date.accessioned2017-10-18T08:25:14Z-
dc.date.available2017-10-18T08:25:14Z-
dc.date.issued2016-
dc.identifier.citationEnvironmental Science & Technology, 2016, v. 50 n. 17, p. 9543-9550-
dc.identifier.issn0013-936X-
dc.identifier.urihttp://hdl.handle.net/10722/247301-
dc.description.abstractWe report a facile method for the antimicrobial modification of a thin-film composite polyamide reverse osmosis (RO) membrane. The membrane surface was first coated with polydopamine (PDA), whose reducing catechol groups subsequently immobilized silver ions in situ to form uniformly dispersed silver nanoparticles (AgNPs) inside the coating layer. Agglomeration of AgNPs was not observed despite a high silver loading of 13.3 ± 0.3 μg/cm2 (corresponding to a surface coverage of 18.5% by the nanoparticles). Both diffusion inhibition zone tests and colony formation unit tests showed clear antimicrobial effects of the silver loaded membranes on model bacteria Bacillus subtilis and Escherichia coli. Furthermore, the silver immobilized membrane had significantly enhanced salt rejection compared to the control PDA coated membrane, which is attributed to the preferential formation of AgNPs at defect sides within the PDA layer. This self-healing mechanism can be used to prepare antimicrobial RO membranes with improved salt rejection without scarifying the membrane permeability, which provides a new dimension for membrane surface modification.-
dc.languageeng-
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journal/esthag-
dc.relation.ispartofEnvironmental Science & Technology-
dc.titleIn situ reduction of silver by polydopamine: A novel antimicrobial modification of a thin-film composite polyamide membrane-
dc.typeArticle-
dc.identifier.emailTang, C: tangc@hku.hk-
dc.identifier.authorityTang, C=rp01765-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acs.est.6b01867-
dc.identifier.pmid27479138-
dc.identifier.scopuseid_2-s2.0-84985918630-
dc.identifier.hkuros281274-
dc.identifier.volume50-
dc.identifier.issue17-
dc.identifier.spage9543-
dc.identifier.epage9550-
dc.identifier.isiWOS:000382805800070-
dc.identifier.issnl0013-936X-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats