Evolution of Fe species during the synthesis of over-exchanged Fe/ZSM5 obtained by chemical vapor deposition of FeCl3

被引:161
作者
Battiston, AA
Bitter, JH
de Groot, FMF
Overweg, AR
Stephan, O
van Bokhoven, JA
Kooyman, PJ
van der Spek, C
Vankó, G
Koningsberger, DC
机构
[1] Univ Utrecht, Debye Inst, Dept Inorgan Chem & Catalysis, NL-3584 CA Utrecht, Netherlands
[2] Delft Univ Technol, Interfac Reactor Inst, NL-2629 JB Delft, Netherlands
[3] CNRS, UMR 8502, Phys Solides Lab, F-91405 Orsay, France
[4] Natl Ctr High Resolut Electron Microscopy, NL-2628 AL Delft, Netherlands
[5] European Synchrotron Radiat Facil, F-38043 Grenoble, France
关键词
Fe/ZSM5; binuclear; iron; synthesis; evolution; calcination;
D O I
10.1016/S0021-9517(02)00051-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The evolution of iron in over-exchanged Fe/ZSM5 prepared via chemical vapor deposition of FeCl3 was studied at each stage of the synthesis. Different characterization techniques (EXAFS, HR-XANES, Fe-57 Mossbauer spectroscopy, Al-27 NMR, EELS, HR-TEM, XRD, N-2 physisorption, and FTIR spectroscopy) were applied in order to correlate the changes occurring in the local environment of the Fe atoms with migration and aggregation phenomena of iron at micro- and macroscopic scale. Mononuclear isolated Fe-species are formed upon FeCl3 sublimation, which are transformed into binuclear Fe-complexes during washing. During calcination, iron detached from the Bronsted sites migrates to the external surface of the zeolite, finally leading to significant agglomeration. Nevertheless, agglomeration of Fe can be strongly suppressed by adequately tuning the conditions of the calcination. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:251 / 271
页数:21
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