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Performance of Reverse Water Gas Shift on Coprecipitated and C‐Templated BaFe‐Hexaaluminate: The Effect of Fe Loading, Texture, and Promotion with K
Author(s) -
Utsis Natalie,
Landau Miron V.,
Erenburg Alexander,
Nehemya Roxana Vidruk,
Herskowitz Moti
Publication year - 2018
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201800709
Subject(s) - catalysis , water gas shift reaction , texture (cosmology) , redox , materials science , potassium , coprecipitation , x ray photoelectron spectroscopy , selectivity , chemical engineering , chemistry , inorganic chemistry , metallurgy , artificial intelligence , computer science , engineering , image (mathematics) , biochemistry
The effects of chemical composition, texture, and promotion with potassium of coprecipitated and carbon‐templated BaFe‐hexaaluminate catalysts on their performance in reverse water gas shift (RWGS) reaction were studied in a fixed‐bed catalytic reactor at T =350 °C, p =20 bar, H 2 : CO 2 of 3. The methane selectivity at these conditions did not exceed 0.1 %. It was established that the rate of RWGS is strongly affected by the catalysts iron content gradually increasing up to 45 % Fe. Decreasing the catalyst nanocrystals platelets size (diameter/thickness) from 500–800/50–80 nm to 150–250/30–50 nm (SEM) by implementing the CT increased the surface area and the rates of reaction. Modeling of the redox cycle of RWGS by CO 2 ‐TPD, TP reaction and TP reduction indicated that H 2 reduction is needed for regeneration of active sites Fe 2+ ions associated with oxygen vacancies. Potassium displayed a strong promotion effect on the activity of Ba−Fe‐hexaaluminates. At optimal K content of 6 wt %, the RWGS rates increased by a factor of 12–15 without changing the TOF number. This was attributed to increasing concentration of active sites due to the reduction of Fe 3+ ions (XPS).
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