Towards Physical Descriptors of Active and Selective Catalysts for the Oxidation of n-Butane to Maleic Anhydride

Based on our newly developed microwave cavity perturbation technique, the microwave conductivity of diverse vanadium(III), (IV), and (V) phosphate catalysts was measured under reaction conditions for the selective oxidation of n‐butane. The conductivity response on the gas phase was identified as a...

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Bibliographic Details
Published inChemCatChem Vol. 5; no. 8; pp. 2318 - 2329
Main Authors Eichelbaum, Maik, Glaum, Robert, Hävecker, Michael, Wittich, Knut, Heine, Christian, Schwarz, Heiner, Dobner, Cornelia-Katharina, Welker-Nieuwoudt, Cathrin, Trunschke, Annette, Schlögl, Robert
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.08.2013
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
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Summary:Based on our newly developed microwave cavity perturbation technique, the microwave conductivity of diverse vanadium(III), (IV), and (V) phosphate catalysts was measured under reaction conditions for the selective oxidation of n‐butane. The conductivity response on the gas phase was identified as a very sensitive measure for the redox kinetics, reversibility, and stability of the samples, which are important prerequisites for highly selective and active catalysts. The sensitivity achieved by our method was comparable to surface‐sensitive methods such as X‐ray photoelectron spectroscopy, whereas more conventional analytic techniques such as X‐ray diffractometry or Raman spectroscopy only indicated the stability of the bulk crystal phase under the same reaction conditions. Charge transport matters: The gas‐phase response of the electrical conductivity, measured contact‐free with the in situ microwave cavity perturbation technique, is studied for vanadium(III), (IV), and (V) phosphorus oxide catalysts under selective n‐butane oxidation conditions. The deduced surface–bulk charge transport properties of the samples provide a fingerprint for the activity and selectivity in the demanding selective oxidation that requires a 14 e− transfer per catalytic cycle.
Bibliography:ark:/67375/WNG-MD7WZJSV-H
ArticleID:CCTC201200953
istex:A620185F1D712B28E83EBF446C2168D681DC7348
German Federal Ministry of Education and Research
BMBF - No. 033R028
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201200953