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  Structure-reactivity relationships in supported VOx catalysts for the oxyhydrative scission (OHS) of 1-butene and n-butane to acetic acid: A comprehensive catalytic and in situ study

Brückner, A., Bentrup, U., Fait, M., & Kubias, B. (2005). Structure-reactivity relationships in supported VOx catalysts for the oxyhydrative scission (OHS) of 1-butene and n-butane to acetic acid: A comprehensive catalytic and in situ study. Catalysis Today, 99(1-2), 123-129. doi:10.1016/j.cattod.2004.09.031.

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BentrupKubiasDGMK04-Manuscript_010904korr27.6.06.pdf (beliebiger Volltext), 161KB
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 Urheber:
Brückner, Angelika, Autor
Bentrup, Ursula, Autor
Fait, Martin, Autor
Kubias, Bernd1, Autor           
Affiliations:
1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Schlagwörter: In situ-FTIR, operando-EPR, in situ-UV/vis-DRS, oxyhydrative scission, 1-butene, n-butane, vanadia-titania catalysts 8: Mixed V-W-Mo oxides for selective oxidation
 Zusammenfassung: A pure and an antimony-modified VOx/TiO2 catalyst have been catalytically tested in a total pressure range of 1-17 bar and studied by in situ-FTIR, in situ-UV/vis and operando-EPR spectroscopy at normal pressure in the oxyhydrative scission (OHS) of 1-butene and n-butane to acetic acid (AA). While 1-butene OHS follows the sequence butene  butoxide  ketone  acetate/AA with a multitude of trace side products also formed, n-butane OHS leads to AA, COx and H2O only. Adding water to the feed improves AA selectivity by favouring the hydrolysis of the ketone intermediate. Doping by Sb was found to improve AA selectivity being due, among other reasons, to deeper V reduction under steady state conditions. Activity in n-butane OHS decreases continuously with rising total pressure while both activity and selectivity in 1-butene OHS pass a maximum at 7 bar.

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Sprache(n): eng - English
 Datum: 2004-11-012005
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: eDoc: 204585
DOI: 10.1016/j.cattod.2004.09.031
 Art des Abschluß: -

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Titel: Catalysis Today
  Alternativer Titel : Catal.Today
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 99 (1-2) Artikelnummer: - Start- / Endseite: 123 - 129 Identifikator: -