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Loss of alkali promoter by desorption from promoted vanadium oxide catalysts

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Abstract

Experiments have been done with molecular beam mass spectrometric methods to characterize the desorption and emission processes of alkali promoter from a commercial vanadium oxide catalyst. It is a potassium and cesium promoted catalyst used for SO3 production, with a K, Cs/V molar ratio of 2.5. An excited state signal is detected, as in our previous studies of other oxide catalysts. Desorption of both K and Cs is also detected. All signals are observed at temperatures above 910 K, which is just above the process temperature range. The values found for atomic desorption are 2.66±0.16 eV for K and 3.89±0.27 eV for Cs, while the excited state emission has a barrier of 0.89±0.08 eV. The difference in desorption energies between Cs and K is larger than expected. This is probably mainly due to different rate limiting steps in the release and diffusion processes. After an approximate compensation for this, Cs still has a larger activation barrier equal to 3.0±0.3 eV towards desorption than K, which indicates a slower loss for Cs from the catalyst.

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Engvall, K., Holmlid, L., Prinz, H. et al. Loss of alkali promoter by desorption from promoted vanadium oxide catalysts. Catal Lett 11, 41–48 (1991). https://doi.org/10.1007/BF00866899

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  • DOI: https://doi.org/10.1007/BF00866899

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