Tg/dta,Xrd and NH3-TPD Characterization of Layered VOPO4·2H2O and its Fe3+-Substituted Compound |
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Authors: | Bagnasco G Beneš L Galli P Massucci M A Patrono P Turco M Zima V |
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Institution: | (1) Dipartimento di Ingegneria Chimica, Università ‘Federico II’, P. le Tecchio 80, 80125- Naples, Italy;(2) Joint Laboratory of Solid State Chemistry, Academy of Sciences of Czech Republic and University of Pardubice, Studenska 84, 530 09 Pardubice, Czech Republic;(3) Dipartimento di Chimica, Università ‘La sapienza’, P. le Aldo Moro, 5-00185- Rome, Italy;(4) IMAI-CNR, Area della Ricerca, Via Salaria Km 29, 6-00016- Monterotondo Scalo, Rome, Italy |
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Abstract: | Iron(III)-substituted vanadyl phosphate, Fe(H2O)]0.20VO0.80PO4·2.25H2O (FeVOP), has been prepared and characterized by XRD
and TG/DTA analyses. The new compound is isomorphous with layered tetragonal VOPO4·2H2O (VOP), but it possesses a lower interlayer
distance. Information on the reactivity and surface acidity of both VOP and FeVOP has been obtained by NH3-TPD experiments.
The hydrated materials adsorb high amounts of NH3 (up to 2 mmol g-1). Different ammonia-containing phases are formed, characterized
by lower interlayer distances in comparison with the NH3-free parent compounds. NH3 is intercalated between the layers without
displacement of water. The materials dehydrated by heat treatment at 450°C retain the layered structure but adsorb NH3 only
on the external surface. A wide variety of acid sites, from weak to strong, was observed. A mechanism is proposed for the
NH3- acid sites interaction. SEM micrographs of VOP and FeVOP are shown.
This revised version was published online in July 2006 with corrections to the Cover Date. |
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Keywords: | Fe3+-vanadyl phosphate NH3-TPD surface acidity TG/DTA vanadyl phosphate XRD |
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