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  The nature of the iron oxide-based catalyst for dehydrogenation of ethylbenzene to styrene: I. Solid-state chemistry and bulk characterization

Muhler, M., Schütze, J., Wesemann, M., Rayment, T., Dent, A., Schlögl, R., et al. (1990). The nature of the iron oxide-based catalyst for dehydrogenation of ethylbenzene to styrene: I. Solid-state chemistry and bulk characterization. Journal of Catalysis, 126(2), 339-360. doi:10.1016/0021-9517(90)90003-3.

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 Urheber:
Muhler, Martin1, Autor           
Schütze, Joachim2, Autor           
Wesemann, Michael1, Autor           
Rayment, T.3, Autor
Dent, A.4, Autor
Schlögl, Robert1, Autor           
Ertl, Gerhard1, Autor           
Affiliations:
1Physical Chemistry, Fritz Haber Institute, Max Planck Society, ou_634546              
2Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              
3Department of Physical Chemistry, University of Cambridge, Cambridge, England, ou_persistent22              
4Daresbury Laboratory, USA, ou_persistent22              

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 Zusammenfassung: The active catalyst for the dehydrogenation of ethylbenzene is generated from a precursor material consisting of hematite and potassium hydroxide (with additional promotors) during the initial phase of catalyst operation at 873 K in a steam atmosphere. The active phase is a thin layer of KFeO2 supported on a solid solution of K2Fe22O34 in Fe3O4. The ternary K2Fe22O34 phase acts as storage medium from which the active surface is continuously supplied with a near-monolayer coverage of potassium ions in an environment of Fe3+ ions. The catalyst undergoes a continuous solid-state transformation caused by the migration of potassium ions. This requires a certain degree of imperfection in the matrix lattice which originates from the catalyst preparation and from the addition of promotors which act on the iron oxide lattice rather than on the surface chemistry. The identity of the active phase with KFeO2 was confirmed by independent synthesis of this phase and comparison of its catalytic activity with that of the technical catalyst.

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Sprache(n): eng - English
 Datum: 1990-01-111990-12
 Publikationsstatus: Erschienen
 Seiten: 22
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1016/0021-9517(90)90003-3
 Art des Abschluß: -

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Titel: Journal of Catalysis
  Kurztitel : J. Catal.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Amsterdam : Elsevier
Seiten: 22 Band / Heft: 126 (2) Artikelnummer: - Start- / Endseite: 339 - 360 Identifikator: ISSN: 0021-9517
CoNE: https://pure.mpg.de/cone/journals/resource/954922645027