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Promoting role of potassium in the reverse water gas shift reaction on Pt/mullite catalyst

[Display omitted] •Addition of K promotor to Pt/mullite enhances the TOF of RWGS reaction by 7 times.•The interaction between Pt and KOx at the interface alters the chemical state of Pt.•The presence of K promotes the formation and decomposition of formate intermediates.•The presence of K weakens th...

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Bibliographic Details
Published in:Catalysis today 2017-03, Vol.281, p.319-326
Main Authors: Liang, Binglian, Duan, Hongmin, Su, Xiong, Chen, Xiaodong, Huang, Yanqiang, Chen, Xiaowei, Delgado, Juan José, Zhang, Tao
Format: Article
Language:English
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Summary:[Display omitted] •Addition of K promotor to Pt/mullite enhances the TOF of RWGS reaction by 7 times.•The interaction between Pt and KOx at the interface alters the chemical state of Pt.•The presence of K promotes the formation and decomposition of formate intermediates.•The presence of K weakens the strength of CO adsorption on Pt. The promotional effect of potassium in the reverse water gas shift reaction (RWGS) was studied for Pt/mullite catalyst. The addition of potassium on Pt/mullite significantly enhanced the CO2 conversion and hindered the formation of methane as a by-product. The turnover frequency (TOF) at 340°C was enhanced by potassium up to 7 times that of Pt/mullite. TEM observations indicated a slight Pt particle size growth on the K-promoted sample. Characterization results by means of H2-TPR and XPS revealed the strong interaction between KOx and Pt, which stabilized the Pt in a higher oxidation state. DRIFTS observation under the RWGS conditions suggested that the newly created interface between KOx and Pt served as the active site for formate decomposition to produce CO. The presence of potassium also weakened the strength of CO adsorption on Pt, which hindered the further hydrogenation of CO into CH4 through CO bond dissociation.
ISSN:0920-5861
1873-4308
DOI:10.1016/j.cattod.2016.02.051