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dc.contributor.authorDuan, X.
dc.contributor.authorSun, Hongqi
dc.contributor.authorWang, Yuxian
dc.contributor.authorKang, J.
dc.contributor.authorWang, Shaobin
dc.date.accessioned2017-01-30T11:06:11Z
dc.date.available2017-01-30T11:06:11Z
dc.date.created2015-07-16T06:22:00Z
dc.date.issued2015
dc.identifier.citationDuan, X. and Sun, H. and Wang, Y. and Kang, J. and Wang, S. 2015. N-doping-induced nonradical reaction on single-walled carbon nanotubes for catalytic phenol oxidation. ACS Catalysis. 5 (2): pp. 553-559.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/8346
dc.identifier.doi10.1021/cs5017613
dc.description.abstract

Metal-free materials have been demonstrated to be promising alternatives to conventional metal-based catalysts. Catalysis on nanocarbons comparable to that of cobalt- or manganese-based catalysts in peroxymonosulfate (PMS) activation has been achieved, yet the catalyst stability has to be addressed and the mechanism also needs to be elucidated. In this study, N-doped carbon nanotubes (NoCNTs) were employed as metal-free catalysts for phenol catalytic oxidation with sulfate radicals and, more importantly, a detailed mechanism of PMS activation and the roles of nitrogen heteroatoms were comprehensively investigated. For the first time, a nonradical pathway accompanied by radical generation (•OH and SO4•–) in phenol oxidation with PMS was discovered upon nitrogen heteroatom doping. The NoCNTs presented excellent stability due to the emerging nonradical processes. The findings can be used for the design of efficient and robust metal-free catalysts with both superior catalytic performance and high stability for various heterogeneous catalytic processes.

dc.publisherAmerican Chemical Society
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/DP130101319
dc.titleN-doping-induced nonradical reaction on single-walled carbon nanotubes for catalytic phenol oxidation
dc.typeJournal Article
dcterms.source.volume5
dcterms.source.startPage553
dcterms.source.endPage559
dcterms.source.issn2155-5435
dcterms.source.titleACS Catalysis
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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