TG/DTA, XRD and NH3-TPD characterization of layered VOPO4•2H2O and its Fe3+-substituted compound

被引:18
作者
Bagnasco, G
Benes, L
Galli, P
Massucci, MA
Patrono, P
Turco, M
Zima, V
机构
[1] Univ Naples Federico II, Dipartimento Ingn Chim, I-80125 Naples, Italy
[2] Univ Pardubice, Pardubice 53009, Czech Republic
[3] Acad Sci Czech Republ, Joint Lab Solid State Chem, Pardubice 53009, Czech Republic
[4] Univ Rome La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
[5] CNR, IMAI, Area Ric, I-00016 Monterotondo, Italy
来源
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY | 1998年 / 52卷 / 02期
关键词
Fe3+-vanadyl phosphate; NH3-TPD; surface acidity; TG/DTA; vanadyl phosphate; XRD;
D O I
10.1023/A:1010136126445
中图分类号
O414.1 [热力学];
学科分类号
摘要
Iron(III)-substituted vanadyl phosphate, [Fe(H2O)](0.20)VO0.80PO4. 2.25H(2)O (FeVOP), has been prepared and characterized by XRD and TG/DTA analyses. The new compound is isomorphous with layered tetragonal VOPO4. 2H(2)O (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 degrees 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.
引用
收藏
页码:615 / 630
页数:16
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