Synthesis and acidic catalytic properties of ordered mesoporous alumina-tungstophosphoric acid composites

dc.contributor.authorArmatas, G. S.en
dc.contributor.authorKatsoulidis, A. P.en
dc.contributor.authorPetrakis, D. E.en
dc.contributor.authorPomonis, P. J.en
dc.date.accessioned2015-11-24T16:48:51Z
dc.date.available2015-11-24T16:48:51Z
dc.identifier.issn0959-9428-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9380
dc.rightsDefault Licence-
dc.subjectheteropoly aciden
dc.subjectselective oxidationen
dc.subjectdifferent supportsen
dc.subjectthermal-stabilityen
dc.subjectsilicaen
dc.subjectdehydrationen
dc.subjectsba-15en
dc.subjectperformanceen
dc.subjectsurfaceen
dc.subjectmcm-41en
dc.titleSynthesis and acidic catalytic properties of ordered mesoporous alumina-tungstophosphoric acid compositesen
heal.abstractA series of well-ordered mesoporous alumina-tungstophosphoric (HPW) acid composite frameworks has been prepared by a sol-gel copolymerization route in the presence of non-ionic surfactants. The resulting materials feature a high loading of HPW acids (up to similar to 53 wt%) in composite framework and possess hexagonal p6mm pore structure with uniform large pores. The mesoscopic order of these structures was evidenced by SAXS analysis, TEM images and N(2) physisorption measurements. The composite materials exhibited BET surface areas in the range of 54-71 m(2) g(-1), total pore volumes in the range of 0.11-0.14 cm(3) g(-1) and quite narrow pore size distributions with peak maxima in the 7.1-8.3 nm range. The Keggin clusters were incorporated in mesoporous alumina walls by strong chemical bonds according to the FT-IR and UV/vis spectroscopy analysis. This chemical linkage of HPW to the alumina matrix is responsible for the outstanding stability of these materials against water-leaching. The mesoporous surfaces exhibited exceptional acidity that arises from the unique alumina-HPW composite structure. As the loading of HPW increases, the surface acidic character of the composites enhanced, and this is reflected in the higher catalytic activity towards isopropanol conversion.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1039/C0jm01283a-
heal.identifier.secondary<Go to ISI>://000282223700028-
heal.identifier.secondaryhttp://pubs.rsc.org/en/content/articlepdf/2010/jm/c0jm01283a-
heal.journalNameJournal of Materials Chemistryen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2010-
heal.publisherThe Royal Society of Chemistryen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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