Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/115748
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDuan, X.-
dc.contributor.authorAo, Z.-
dc.contributor.authorSun, H.-
dc.contributor.authorZhou, L.-
dc.contributor.authorWang, G.-
dc.contributor.authorWang, S.-
dc.date.issued2015-
dc.identifier.citationChemical Communications, 2015; 51(83):15249-15252-
dc.identifier.issn1359-7345-
dc.identifier.issn1364-548X-
dc.identifier.urihttp://hdl.handle.net/2440/115748-
dc.descriptionPublished on 10 August 2015-
dc.description.abstractEmerging characteristics upon nitrogen-doping were differentiated in the activation of superoxides over single-walled carbon nanotubes. Both experimental and theoretical studies revealed that enhanced peroxymonosulfate (PMS) activation is ascribed to a nonradical process while persulfate (PS) activation is accelerated via directly oxidizing water, yet hydrogen peroxide (H2O2) activation is inert to N-doping. This study details the first insights into versatile N-doping in carbocatalysis for organic oxidation in sustainable remediation.-
dc.description.statementofresponsibilityXiaoguang Duan, Zhimin Ao, Hongqi Sun, Li Zhou, Guoxiu Wang and Shaobin Wang-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsThis journal is © The Royal Society of Chemistry 2015. Open Access Article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.-
dc.titleInsights into N-doping in single-walled carbon nanotubes for enhanced activation of superoxides: a mechanistic study-
dc.typeJournal article-
dc.identifier.doi10.1039/c5cc05101k-
dc.relation.granthttp://purl.org/au-research/grants/arc/DP130101319-
pubs.publication-statusPublished-
dc.identifier.orcidDuan, X. [0000-0001-9635-5807]-
dc.identifier.orcidWang, S. [0000-0002-1751-9162]-
Appears in Collections:Aurora harvest 8
Chemical Engineering publications

Files in This Item:
File Description SizeFormat 
hdl_115748.pdfPublished version2.72 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.