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dc.contributor.authorMistri, Rajib
dc.contributor.authorMaiti, Sayantani
dc.contributor.authorLlorca Piqué, Jordi
dc.contributor.authorDomínguez Escalante, Montserrat
dc.contributor.authorMandal, Tapas Kumar
dc.contributor.authorMohanty, Paritosh
dc.contributor.authorRay, Bidhan Chandra
dc.contributor.authorGayen, Arup
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament d'Enginyeria Elèctrica
dc.date.accessioned2015-01-12T16:46:00Z
dc.date.created2014-09-05
dc.date.issued2014-09-05
dc.identifier.citationMistri, R. [et al.]. Copper ion substituted hercynite (Cu0.03Fe0.97Al2O4): A highly active catalyst for liquid phase oxidation of cyclohexane. "Applied catalysis A. General", 05 Setembre 2014, vol. 485, p. 40-50.
dc.identifier.issn0926-860X
dc.identifier.urihttp://hdl.handle.net/2117/25230
dc.description.abstractCopper ion substituted MAl2O4 (M = Mg, Mn, Fe, Ni and Zn) spinels, CuxM1-xAl2O4 (x = 0.03 and 0.05), have been synthesized by a single step solution combustion method. Of the various compositions studied the 3 at.% copper ion substituted hercynite, Cu0.03Fe0.97Al2O4, reported here for the first time, is shown to be much more active (similar to 92% conversion with similar to 99% selectivity) than other spinet analogues towards liquid phase oxidation of cyclohexane in acetonitrile with H2O2 as oxidant in air. Powder XRD analyses have revealed formation of pure hercynite phases. The least-square refined lattice parameters obtained from XRD data together with microstructural data by HRTEM have indicated copper ion substitution in the spinel lattice. The oxidation state of copper has been established as +2 from XPS analysis and it seem to be primarily substituted in the Fe-site of hercynite. Incorporation of the copper in the spinel structure of FeAl2O4 leading to an ionic interaction is explained to be responsible for the higher oxidation activity observed over the combustion synthesized catalyst than the corresponding impregnated catalyst which contains finely dispersed CuO crystallites. Effect of recycling (repeated thrice) has shown almost no degradation of activity of the copper ion substituted hercynite. In contrast, the analogous impregnated catalyst has shown appreciable loss of activity in the consecutive cycles due to the presence of dispersed CuO crystallites which can agglomerate with ease and subsequently leach out. (C) 2014 Elsevier B.V. All rights reserved.
dc.format.extent11 p.
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Enginyeria química::Química orgànica::Compostos orgànics
dc.subject.lcshCopper catalysts
dc.subject.lcshAluminum
dc.subject.otherSpinel
dc.subject.otherCopper substitution
dc.subject.otherSolution combustion
dc.subject.otherCyclohexane oxidation
dc.subject.otherIonic interaction
dc.titleCopper ion substituted hercynite (Cu0.03Fe0.97Al2O4): A highly active catalyst for liquid phase oxidation of cyclohexane
dc.typeArticle
dc.subject.lemacCatalitzadors de coure
dc.subject.lemacAlumini
dc.contributor.groupUniversitat Politècnica de Catalunya. GREENER - Grup de recerca d'estudis energètics i de les radiacions
dc.identifier.doi10.1016/j.apcata.2014.07.027
dc.rights.accessRestricted access - publisher's policy
drac.iddocument15315291
dc.description.versionPostprint (published version)
dc.date.lift10000-01-01
upcommons.citation.authorMistri, R.; Maiti, S.; Llorca, J.; Dominguez, M.; Mandal, T.; Mohanty, P.; Ray, B.C.; Gayen, A.
upcommons.citation.publishedtrue
upcommons.citation.publicationNameApplied catalysis A. General
upcommons.citation.volume485
upcommons.citation.startingPage40
upcommons.citation.endingPage50


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Except where otherwise noted, content on this work is licensed under a Creative Commons license: Attribution-NonCommercial-NoDerivs 3.0 Spain