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dc.contributor.authorLiang, Hanwen
dc.contributor.authorSun, Hongqi
dc.contributor.authorPatel, A.
dc.contributor.authorShukla, P.
dc.contributor.authorZhu, Z.
dc.contributor.authorWang, Shaobin
dc.date.accessioned2017-01-30T10:50:33Z
dc.date.available2017-01-30T10:50:33Z
dc.date.created2015-03-03T20:16:34Z
dc.date.issued2012
dc.identifier.citationLiang, H. and Sun, H. and Patel, A. and Shukla, P. and Zhu, Z. and Wang, S. 2012. Excellent performance of mesoporous Co3O4/MnO2 nanoparticles in heterogeneous activation of peroxymonosulfate for phenol degradation in aqueous solutions. Applied Catalysis B: Environmental. 127: pp. 330-335.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/6087
dc.identifier.doi10.1016/j.apcatb.2012.09.001
dc.description.abstract

Mesoporous α-MnO2 and its supported Co3O4 nanoparticles were synthesized, characterized and tested in heterogeneous activation of peroxymonosulfate (PMS) for phenol degradation in aqueous solution. α-MnO2 supported Co3O4 presented as nanorod particles and showed H2 redox reduction at low temperature. Bulk α-MnO2 and Co3O4 could activate peroxymonosulfate to generate sulfate radicals for phenol degradation but at low activity. Co3O4/MnO2 nanoparticles exhibited much high activity in peroxymonosulfate activation for phenol degradation with 100% conversion in 20 min and 3 wt% is the optimum Co loading. Phenol degradation followed a first order kinetics. Stability tests also showed that Co3O4/MnO2 presented stable performance in phenol degradation in several runs.

dc.publisherelsevier
dc.subjectWater treatment
dc.subjectAdvanced oxidation
dc.subjectSupported Co oxide
dc.subjectMesoporous MnO2
dc.subjectNanorod particles
dc.titleExcellent performance of mesoporous Co3O4/MnO2 nanoparticles in heterogeneous activation of peroxymonosulfate for phenol degradation in aqueous solutions
dc.typeJournal Article
dcterms.source.volume127
dcterms.source.startPage330
dcterms.source.endPage335
dcterms.source.issn09263373
dcterms.source.titleApplied Catalysis B: Environmental
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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