Article ID Journal Published Year Pages File Type
61608 Journal of Catalysis 2011 13 Pages PDF
Abstract

The transformations and the state of cobalt species during steam reforming of ethanol over Co/CeO2 were investigated using in situ X-ray diffraction, controlled-atmosphere X-ray absorption fine structure, and X-ray photoelectron spectroscopy as well as steady state activity measurements. The catalyst was pretreated under an oxidizing or reducing atmosphere prior to characterization and activity testing to yield a Co3O4-rich or a Co0-rich surface, respectively. While Co3O4 was found to be inactive for ethanol steam reforming, gradual activation of the oxidation-pretreated catalyst with temperature through reduction in Co3O4 took place under reaction conditions, and, over the activated catalyst, a mixture of both CoO and metallic Co were observed. Over the reduction-pretreated catalyst, metallic Co was partially oxidized to CoO during steam reforming of ethanol. The extent of cobalt reduction was observed to be independent of the initial state of the metal on the catalyst surface, and cobalt phase had the same composition under reaction above 450 °C.

Graphical abstractThe transformations and state of cobalt species during steam reforming of ethanol were investigated over Co/CeO2 catalysts pretreated with oxidation (O) and reduction (R) steps. Both catalysts were found to transform in situ to the same active phase under reaction conditions, exhibiting both CoO and Co0 species at steady state. The reforming performance of the two catalysts also converged to the same level, giving similar product yields.Figure optionsDownload full-size imageDownload high-quality image (119 K)Download as PowerPoint slideHighlights► Ethanol steam reforming over Co/CeO2 catalysts was studied. ► Coordination environment of Co was examined using in situ and controlled-atmosphere techniques. ► Catalysts converged to similar oxidation states and performance levels regardless of pretreatment. ► Active catalysts were found to be comprised of both CoO and Co0 species.

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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