Please use this identifier to cite or link to this item:
https://scholarhub.balamand.edu.lb/handle/uob/2052
DC Field | Value | Language |
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dc.contributor.author | Dahdah, Eliane | en_US |
dc.contributor.author | Aouad, Samer | en_US |
dc.contributor.author | Gennequin, Cédric | en_US |
dc.contributor.author | Estephane, Jane | en_US |
dc.contributor.author | Nsouli, Bilal | en_US |
dc.contributor.author | AbouKais, Antoine | en_US |
dc.contributor.author | Abi Aad, Edmond | en_US |
dc.date.accessioned | 2020-12-23T09:05:30Z | - |
dc.date.available | 2020-12-23T09:05:30Z | - |
dc.date.issued | 2018 | - |
dc.identifier.uri | https://scholarhub.balamand.edu.lb/handle/uob/2052 | - |
dc.description.abstract | Ru-Mg-Al hydrotalcite-derived mixed oxides were synthesized using two preparation methods. The grafted catalyst was prepared by co-precipitation of the Ru/Mg/Al precursors at a constant pH. The impregnated catalyst was prepared by wet-impregnation of a calcined Mg-Al support with the Ru precursor (Ru(NO) (NO3)3). Both catalysts were calcined at 600 °C and characterized by X-ray diffraction, CO2- temperature programmed desorption and H2-temperature programmed reduction techniques. Catalytic activities were compared in the glycerol steam reforming reaction (400–700 °C, WGFR 9:1, flow rate: 0.075 ml/min) followed by a short-term stability test at 600 °C. The impregnated catalyst demonstrated a superior activity beyond 600 °C. This difference in activity was attributed to the easier accessibility of the active phase resulting from the preparation method. Short-term stability tests revealed deactivation of both catalysts as a result of coke formation. | en_US |
dc.language.iso | eng | en_US |
dc.subject | Ruthenium | en_US |
dc.subject | Hydrotalcite | en_US |
dc.subject | Glycerol | en_US |
dc.subject | Reforming | en_US |
dc.subject.lcsh | Catalysts | en_US |
dc.title | Glycerol steam reforming over Ru-Mg-Al hydrotalcite-derived mixed oxides: role of the preparation method in catalytic activity | en_US |
dc.type | Journal Article | en_US |
dc.contributor.affiliation | Department of Chemistry | en_US |
dc.contributor.affiliation | Department of Chemical Engineering | en_US |
dc.description.volume | 43 | en_US |
dc.description.issue | 43 | en_US |
dc.description.startpage | 19864 | en_US |
dc.description.endpage | 19872 | en_US |
dc.date.catalogued | 2019-06-07 | - |
dc.description.status | Published | en_US |
dc.identifier.OlibID | 192260 | - |
dc.relation.ispartoftext | International journal of hydrogen energy | en_US |
dc.provenance.recordsource | Olib | en_US |
crisitem.author.parentorg | Faculty of Arts and Sciences | - |
crisitem.author.parentorg | Faculty of Engineering | - |
Appears in Collections: | Department of Chemistry Department of Chemical Engineering |
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