Highly loaded and thermally stable Cu-containing mesoporous silica-active catalyst for the NO plus CO reaction

dc.contributor.authorPantazis, C. C.en
dc.contributor.authorTrikalitis, P. N.en
dc.contributor.authorPomonis, P. J.en
dc.date.accessioned2015-11-24T16:38:56Z
dc.date.available2015-11-24T16:38:56Z
dc.identifier.issn1520-6106-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8104
dc.rightsDefault Licence-
dc.subjectliquid-phase oxidationen
dc.subjectmolecular-sievesen
dc.subjectpolyacrylic-aciden
dc.subjectnitric-oxideen
dc.subjectredox propertiesen
dc.subjectcarbon-monoxideen
dc.subjectno+co reactionen
dc.subjectcopperen
dc.subjectreductionen
dc.subjectsurfactanten
dc.titleHighly loaded and thermally stable Cu-containing mesoporous silica-active catalyst for the NO plus CO reactionen
heal.abstractWe report the synthesis of a highly loaded and thermally stable Cu-containing mesoporous silica, which was developed by making use of poly(acrylic acid) (Pac) assembled with surfactant (C(16)TAB), as template. On this backbone, TEOS and Cu(II) hydrolysis takes place leading to the development of the final mesostructure. Poly(acrylic acid) is used not only as a micelle structural component but also as a complexation agent for Cu(II) species resulting in high metal loading and increased thermal stability of the mesoporous network. The original uncalcined material possesses hexagonal ordering, while upon calcination it is transformed into a wormlike mesoporous network with metal loading > 14 wt % Cu. An evaluation of its performance as heterogeneous catalyst in NO reduction by CO shows catalytic activity comparable with that of noble metal catalysts. Complete NO conversion, with > 90 % selectivity to N(2), was achieved between 190 and 200 degrees C. The material retained its structure and catalytic activity after 24-h testing at the maximum catalytic conversion of NO and CO.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondary<Go to ISI>://000230122900048-
heal.identifier.secondaryhttp://pubs.acs.org/doi/pdfplus/10.1021/jp0516689-
heal.journalNameJournal of Physical Chemistry Ben
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2005-
heal.publisherAmerican Chemical Societyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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