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dc.contributor.authorMuhammad, Syaifullah
dc.contributor.authorSaputra, Edy
dc.contributor.authorSun, Hongqi
dc.contributor.authorAng, Ming
dc.contributor.authorTade, Moses
dc.contributor.authorWang, Shaobin
dc.date.accessioned2017-01-30T14:27:49Z
dc.date.available2017-01-30T14:27:49Z
dc.date.created2015-03-03T20:16:34Z
dc.date.issued2012
dc.identifier.citationMuhammad, S. and Saputra, E. and Sun, H. and Ang, M. and Tade, M. and Wang, S. 2012. Heterogeneous Catalytic Oxidation of Aqueous Phenol on Red Mud-Supported Cobalt Catalysts. Industrial and Engineering Chemistry Research. 51 (47): pp. 15351-15359.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/38908
dc.identifier.doi10.1021/ie301639t
dc.description.abstract

Red mud (RM), an industrial waste from the alumina refinery industry, was used as a support for preparation of Co-oxide-based catalysts (Co/RM). The samples were characterized by N2 adsorption, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and UV-vis diffusive reflectance spectroscopy. The heterogeneous catalytic activity was evaluated in aqueous phenol degradation using peroxymonosulphate (PMS) as an oxidizing agent. It was found that Co3O4 particles were highly dispersed on the RM surface and that pretreatment of the red mud (RM-T) would significantly influence catalytic activity. Co/RM-T catalysts exhibited high effectiveness in heterogeneous activation of PMS to produce sulfate radicals for phenol degradation compared with Co/RM-NT. Phenol degradation followed first-order kinetics, and activation energies on Co/RM-T and Co/RM-NT are 46.2 and 47.0 kJ/mol, respectively.

dc.publisherAmerican Chemical Society
dc.titleHeterogeneous Catalytic Oxidation of Aqueous Phenol on Red Mud-Supported Cobalt Catalysts
dc.typeJournal Article
dcterms.source.volume51
dcterms.source.number47
dcterms.source.startPage15351
dcterms.source.endPage15359
dcterms.source.issn08885885
dcterms.source.titleIndustrial and Engineering Chemistry Research
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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