| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 43982 | Applied Catalysis A: General | 2007 | 9 Pages |
Fe-Beta catalysts with iron content of 0.045–2.0 wt.% were studied in the benzene to phenol transformation with N2O and compared to similar Fe-ZSM-5 catalysts to understand the influence of zeolite structure on the Fe-sites activity. The Fe-containing zeolites were prepared either by a direct hydrothermal synthesis or by a post-synthesis Fe deposition followed by activation (steaming or high temperature treatment in He). Total amount of Fe(II) active sites able to form atomic oxygen (O)Fe, from N2O, was quantified by the transient response method at 523 K measuring the released N2. The fraction of the (O)Fe active in CO oxidation was determined via the amount of CO2 released. The catalyst activity in the benzene to phenol transformation over the activated isomorphously substituted Fe-Beta and Fe-ZSM-5 zeolites was directly proportional to the amount of the (O)Fe active in CO oxidation. The turnover frequency (TOF) over Fe-Beta and Fe-ZSM-5 catalysts was found to be close indicating a similarity in the structures of Fe active sites. The observed ∼2-fold difference can be attributed to the influence of the zeolite host lattices. The difference between Fe-Beta and Fe-ZSM-5 was also observed in DRIFT spectra of NO adsorbed on iron sites at room temperature. The bands of NO adsorbed on Fe-Beta and Fe-ZSM-5 were at 1873 and 1878/1891 cm−1, respectively. The areas of these bands correlate with the amount of (O)Fe active in CO oxidation. Comparison of the DRIFT spectra of adsorbed NO on the zeolites with the spectra on some iron containing compounds allowed to attribute the adsorption sites to Fe(II) sites and not to Fe(III) sites.
Graphical abstractFe-Beta and Fe-ZSM-5 were studied in the benzene to phenol transformation with N2O. The activity of isomorphously substituted Fe-ZSM-5 catalysts calculated per a Fe(II) site active in CO oxidation (TOF) was ∼2-fold higher as compared to the TOF of Fe-Beta catalysts. This was attributed to the geometry of Fe(II) active sites which may vary depending on the zeolite host.Figure optionsDownload full-size imageDownload as PowerPoint slide
