Comparative-Study of the Solid-State and Catalytic Properties of La2-Xsrxnio4-Lambda Perovskites (X = 0.00-1.50) Prepared by the Nitrate and Citrate Methods

dc.contributor.authorLadavos, A. K.en
dc.contributor.authorPomonis, P. J.en
dc.date.accessioned2015-11-24T16:54:07Z
dc.date.available2015-11-24T16:54:07Z
dc.identifier.issn0956-5000-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10117
dc.rightsDefault Licence-
dc.subjectn2o decompositionen
dc.subjectoxide lacoo3en
dc.subjectadsorptionen
dc.subjectoxidationen
dc.subjectkineticsen
dc.subjectla2nio4en
dc.subjectsurfaceen
dc.subjectaluminaen
dc.subjectionsen
dc.subjectcoen
dc.titleComparative-Study of the Solid-State and Catalytic Properties of La2-Xsrxnio4-Lambda Perovskites (X = 0.00-1.50) Prepared by the Nitrate and Citrate Methodsen
heal.abstractPerovskites of the form La2-xSrxNiO4-lambda (x = 0.00, 0.25, 0.50, 0.75, 1.00, 1.25 and 1.50) have been prepared using both the nitrate and citrate methods. The solids obtained were examined by X-ray diffraction at various temperatures to examine the development of their crystal structure. Surface area determinations showed that the citrate method yields solids with surface areas that are on average three times as high as those of the nitrate species, a result that is due to the lower temperature required for the formation of the perovskite phase in the former case. Iodometric determination of the nickel oxidation state showed that this is similar for the two sets of samples in the range 0.00 < x < 0.75 but appreciably higher for nitrate solids for x > 0.75. These results are corroborated by magnetic measurements. The catalytic activity for both sets of solids, probed by N2O decomposition, increases from x = 0.00 up to x = 0.75 - 1.00 if measured per unit mass, but up to 1.25 if measured per unit area of the solids. A comparison of the catalytic activity per unit mass for the two series indicates that citrate solids are about three times more active than the nitrate ones. This effect can be attributed to the higher surface area of the citrate solids. Nevertheless, the comparison per unit surface area shows that the citrate solids are still twice as active as the nitrates. Both series show a unique dependence of activity on oxygen deficiencies. Kinetic analysis of the catalytic results showed that this last factor alters the kinetics of the surface reaction and the apparent activation energies, a fact which is reflected in the reaction rates.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1039/FT9918703291-
heal.identifier.secondary<Go to ISI>://A1991GK45600031-
heal.identifier.secondaryhttp://pubs.rsc.org/en/Content/ArticleLanding/1991/FT/ft9918703291-
heal.journalNameJournal of the Chemical Society-Faraday Transactionsen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate1991-
heal.publisherRoyal 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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