Effect of Cu addition as a promoter on Re/SiO2 catalysts in the hydrodeoxygenation of 2-methoxyphenol as a model bio oil compound

[Display omitted] •The presence of Cu decreases the Re-support interaction.•The presence of Cu does not change the type of active sites on Re catalysts.•The addition of Cu improves the reducibility of Re active sites.•A higher catalytic activity was observed in Re/SiO2 catalysts with Cu added. The p...

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Published inFuel (Guildford) Vol. 186; no. C; pp. 112 - 121
Main Authors Martínez, N., García, R., Fierro, J.L.G., Wheeler, C., Austin, R.N., Gallagher, J.R., Miller, J.T., Krause, T.R., Escalona, N., Sepúlveda, C.
Format Journal Article
LanguageEnglish
Published United Kingdom Elsevier Ltd 15.12.2016
Elsevier
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Summary:[Display omitted] •The presence of Cu decreases the Re-support interaction.•The presence of Cu does not change the type of active sites on Re catalysts.•The addition of Cu improves the reducibility of Re active sites.•A higher catalytic activity was observed in Re/SiO2 catalysts with Cu added. The promoting effect of Cu on Re/SiO2 catalysts was studied for guaiacol hydrodeoxygenation. Cu(x)Re/SiO2 catalysts containing from 0 to 1.91wt% Cu and 13wt% of Re were prepared by successive wet impregnation and characterized using X-ray diffraction (XRD), nitrogen sorption, CO chemisorption, X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XAS) and surface acidity techniques. Batch reactions were carried out at 300°C and 5MPa of H2. The Cu(x)Re/SiO2 catalysts displayed higher activities than the Re/SiO2 catalyst with a maximum activity at 1.58wt% Cu. At loadings above 1.5wt%, aggregate formation and a loss of metallic Re active sites lead to a decreased activity. The increase of the activity was attributed not only to Cu increasing the Re reducibility, but also to Cu somehow increasing the metallic Re active sites favoring guaiacol conversion. All catalysts displayed the same product distribution, confirming that the Cu in the Cu(x)Re/SiO2 not change the nature of the active site in the metallic Re nanoparticles.
Bibliography:USDOE Office of Science (SC), Basic Energy Sciences (BES)
FG02-07ER46373; AC02-06CH11357
ISSN:0016-2361
1873-7153
DOI:10.1016/j.fuel.2016.08.065