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Title
Cu/Ni loaded CeO2-ZrO2 catalyst for a water gas shift reaction: effects of loaded metals and CeO2 addition
AuthorChamnankid, Busaya ; Föttinger, Karin ; Rupprechter, Günther ; Kongkachuichay, Paisan
Published in
Chemical Engineering & Technology, 2014, Vol. 37, Issue 12, page 2129-2134
PublishedWILEY-VCH Verlag GmbH & Co. KGaA, 2014
Edition
Accepted version
Annotation
This is the peer reviewed version of the following article: Chamnankid, B. , Föttinger, K. , Rupprechter, G. and Kongkachuichay, P. (2014), Cu/NiLoaded CeO2ZrO2 Catalyst for the WaterGas Shift Reaction: Effects of Loaded Metals and CeO2 Addition. Chem. Eng. Technol., 37: 2129-2134. doi:10.1002/ceat.201300869, which has been published in final form at https://doi.org/10.1002/ceat.201300869. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
LanguageEnglish
Document typeJournal Article
Keywords (EN)Ceria / Copper / DRIFTS / Nickel / Water gas shift / Zirconia
Project-/ReportnumberAustrian Science Funds (FWF): F4502-N16
Project-/ReportnumberThailand Research Fund (TRF): PHD/0182/2551
ISSN15214125
URNurn:nbn:at:at-ubtuw:3-4437 Persistent Identifier (URN)
DOI10.1002/ceat.201300869 
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 The work is publicly available
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Cu/Ni loaded CeO2-ZrO2 catalyst for a water gas shift reaction: effects of loaded metals and CeO2 addition [0.79 mb]
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Abstract (English)

Two different types of metals (Cu and Ni) and the effect of CeO2 addition to produce a CeO2ZrO2 cosupporter were investigated through the watergas shift (WGS) reaction. It was found that the WGS activity could be enhanced with CeO2 addition. At relatively high temperature, Niloaded catalysts exhibited higher CO conversion while Culoaded catalysts demonstrated better performance at low temperatures. The stability and yield of the CO2 and H2 products of the Cu catalysts were higher than those of the Ni catalysts. These results may be caused by an irreversible adsorption of CO on Ni and the reverse WGS reaction occurring on the Ni catalysts. In situ diffusereflection infrared Fourier transform spectroscopy data suggests that the WGS mechanism likely proceeded via formate species.

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