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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/10043
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dc.contributor.authorGodelitsas, A.en
dc.contributor.authorCharistos, D.en
dc.contributor.authorTsipis, A.en
dc.contributor.authorTsipis, C.en
dc.contributor.authorFilippidis, A.en
dc.contributor.authorTriantafyllidis, C.en
dc.contributor.authorManos, G.en
dc.contributor.authorSiapkas, D.en
dc.date.accessioned2015-11-24T16:53:37Z-
dc.date.available2015-11-24T16:53:37Z-
dc.identifier.issn0947-6539-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10043-
dc.rightsDefault Licence-
dc.subjectaluminosilicatesen
dc.subjectdensity functional calculationsen
dc.subjectmicroporous materialsen
dc.subjectnickelen
dc.subjectzeolitesen
dc.subjectdensity-functional theoryen
dc.subjectray photoelectron-spectroscopyen
dc.subjectx-rayen
dc.subjectexchanged heulanditeen
dc.subjectclinoptilolite structureen
dc.subjectcation distributionen
dc.subjectnmr-spectroscopyen
dc.subjectcomplexesen
dc.subjectenergiesen
dc.subjectionsen
dc.titleCharacterisation of zeolitic materials with a HEU-type structure modified by transition metal elements: Definition of acid sites in nickel-loaded crystals in the light of experimental and quantum-chemical resultsen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondary<Go to ISI>://000170914500008-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/1521-3765(20010903)7:17<3705::AID-CHEM3705>3.0.CO;2-5/asset/3705_ftp.pdf?v=1&t=h0f8zszm&s=a9dfd594e416f3e90ed7f1f8906cf4a6ace61511-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2001-
heal.abstractNickel-loaded HEU-type zeolite crystals have been obtained by well-known synthetic procedures and characterised by X-ray fluorescence (XRF), scanning-electron microscopy/energy-dispersive spectroscopy (SEM-EDS), FT-IR, diffuse reflectance UV/Vis spectroscopy (DR(UV/Vis)S) and X-ray photoelectron spectroscopy (XPS) measurements as non-homoionic and non-stoichiometric substances containing exchangeable hydrated Ni(2+) ions in the micropores and nickel hydroxide phases supported on the surface. Thermogravimetric analysis/ differential gravimetry (TGA/DTG) and differential thermal analysis (DTA) demonstrated that full dehydration below approximately 400 degreesC follows a clearly endothermic process, whereas at higher temperatures the zeolite is amorphised and finally partially recrystallised to Ni(Al,Si) oxides, detected by powder X-ray powder diffraction (XRD). The solid acidity of NiHEU, initially determined by temperature-programmed desorption (TPD) of ammonia to be 8.93 mg g(-1) NH(3), is attributed to the weak acid sites (fundamentally Lewis sites) resolved at approximately 183 degreesC, and to the strong acid sites (essentially Bronsted sites) resolved at approximately 461 degreesC in the TPD pattern. A more sophisticated study based on in situ/ex situ FT-IR with in situ/ex situ (27)Al MAS NMR and pyridine (Py) as a probe molecule, revealed that the Lewis acid sites can be attributed primarily to Ni(2+) ions, whereas the Bronsted ones can probably be associated with the surface-supported nickel hydroxide phases. The spectroscopic measurements in conjunction with powder XRD and (29)Si MAS NMR data strongly suggest that distorted Al tetrahedra are formed during the dehydration process and Py chemisorption/complexation (NiHEU-Py), whereas the crystal structure is remarkably well preserved in the rehydrated material (NiHEU-Py/R). The structural, electronic, energetic and spectroscopic properties of all possible nickel(II) aqua and dihydroxy complexes absorbed in the zeolite micropores or supported on the zeolite surface were studied theoretically by density functional theory (DFT). The computed proton affinity, found to be in the range 182.0-210.0 kcal mol(-1), increases with increasing coordination number of the aqua and dihydroxy nickel(II) complexes.en
heal.journalNameChemistry-a European Journalen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
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