Evolution of extraframework iron species in Fe silicalite 1. Effect of Fe content, activation temperature, and interaction with redox agents

被引:166
作者
Berlier, G
Spoto, G
Bordiga, S
Ricchiardi, G
Fisicaro, P
Zecchina, A
Rossetti, I
Selli, E
Forni, L
Giamello, E
Lamberti, C
机构
[1] Univ Turin, Dipartimento Chim Inorgan Fis & Mat, I-10125 Turin, Italy
[2] Univ Milan, Dipartimento Chim Fis & Elettrochim, I-20133 Milan, Italy
[3] Univ Turin, INFM UdR, I-10125 Turin, Italy
关键词
Fe silicalite; extraframework iron; benzene hydroxylation;
D O I
10.1006/jcat.2002.3535
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
A study was made of the iron species dislodged from the tetrahedral lattice position by thermal treatments in four Fe silicalite samples with Si/Fe ratios of 25, 50, 90. and 150. The last two samples have a sufficiently low iron concentration to be considered true catalysts (i.e., having Fe dilutions as low as that used in the industrial conversion of benzene to phenol (Si/Fe > 80)) in partial oxidation reactions. A systematic spectroscopic study is presented in order to obtain a global picture of a system whose complexity can be understood by assuming the formation of a wide variety of transient coordinatively unsaturated iron species, with different oxidation states, which ultimately lead to grafted or anchored isolated and/or clustered species by interaction with residual tetrahedral Si(OH)Fe, defective SiOH groups, or strained SiOSi bridges of the hosting matrix. The structure characterization was obtained by means of the parallel use of IR, X-ray absorption near-edge spectroscopy, and electron paramagnetic resonance techniques, before, during, and after interaction with CO, N2O, and NO probe molecules. This approach was applied to samples characterized by different iron content, activation temperature, and redox treatments. This allowed us to throw light onto structure, oxidation state, and mutual interconversion of a very complex family of extraftamework iron species. Oxidation with O-2 or N2O led to the formation of strongly bonded oxygen. species. The relation between these species and the so-called alpha-oxygen species, claimed as the active sites for the hydroxylation of benzene to phenol by N2O, is discussed. (C) 2002 Elsevier Science (USA).
引用
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页码:64 / 82
页数:19
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