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  Styrene synthesis: In-situ characterization and reactivity studies of unpromoted and potassium promoted iron oxide model catalysts

Shekhah, O., Ranke, W., & Schlögl, R. (2004). Styrene synthesis: In-situ characterization and reactivity studies of unpromoted and potassium promoted iron oxide model catalysts. Journal of Catalysis, 225, 56-68. Retrieved from http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6WHJ-4C7DCK3-5-4X&_cdi=6852&_user=28741&_orig=browse&_coverDate=07%2F01%2F2004&_sk=997749998&view=c&wchp=dGLbVlz-zSkWb&md5=78aaf4b135dbc30abb6a4d05ecb62f2a&ie=/sdarticle.pdf.

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FHIAC_SRS04_Styrene_synthesis_J_Catal_225_2004_56_68.pdf (Any fulltext), 2MB
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FHIAC_SRS04_Styrene_synthesis_J_Catal_225_2004_56_68.pdf
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 Creators:
Shekhah, Osama1, Author           
Ranke, Wolfgang1, Author           
Schlögl, Robert1, Author           
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1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Free keywords: Carbonaceous deposits, dehydrogenation, deactivation, ethylbenzene, iron oxide, oxygen, potassium, promotor, styrene, water 19: Iron oxide model catalysts: Adsorption and catalysis
 Abstract: Styrene synthesis over iron oxide model catalysts was studied by combining UHV characterization methods with in-situ conversion measurements in a micro-flow reactor under realistic reaction conditions. Both unpromoted Fe2O3 and K-promoted model catalysts show a similar high starting activity while that of Fe3O4 is clearly lower. Water limits and K-promotion slows down deactivation by coking and oxide reduction. The deactivation can be prevented and the high initial yield preserved by adding a small amount of oxygen to the feed. Both the presence of Fe3+ and intermediate adsorption strength for ethylbenzene and styrene are essential for high conversion yields.

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Language(s): eng - English
 Dates: 2004-03-122004-05-01
 Publication Status: Issued
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 Table of Contents: -
 Rev. Type: Peer
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Title: Journal of Catalysis
  Alternative Title : J. Catal.
Source Genre: Journal
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Pages: - Volume / Issue: 225 Sequence Number: - Start / End Page: 56 - 68 Identifier: -