کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
43127 | 45956 | 2009 | 7 صفحه PDF | دانلود رایگان |

The liquid phase upgrading of a model bio-oil was studied over a series of supported Pt catalysts. Pt/Al2O3 showed the highest activity for deoxygenation, the oxygen content of the model oil decreasing from an initial value of 41.4 wt% to 2.8 wt% after upgrading. GC–MS analysis of the oil showed it to be highly aromatic, the major components corresponding to alkyl-substituted benzenes and cyclohexanes. CO2 was formed as the major gaseous product, together with lower yields of H2 and C1–C6 hydrocarbons. Based on the product distribution, a reaction scheme is proposed in which light oxygenates predominantly undergo reforming to CO2 and H2, with C–O bond breaking/hydrogenation (to afford alkanes) as a minor pathway. In a parallel process, aromatics undergo C–O cleavage/hydrogenation, affording benzenes and cyclohexanes. The highly alkylated nature of the products appears to be a consequence of the acidic nature of the reaction medium, favoring the occurrence of aromatic electrophilic substitution reactions.
The upgrading of a model bio-oil was studied over a series of supported Pt catalysts. Based on the product distribution, a reaction scheme is proposed in which light oxygenates predominantly undergo reforming to CO2 and H2, with C–O bond breaking/hydrogenation (to afford alkanes) as a minor pathway. In a parallel process, aromatics undergo C–O cleavage/hydrogenation, affording benzenes and cyclohexanes.Figure optionsDownload as PowerPoint slide
Journal: Applied Catalysis A: General - Volume 358, Issue 2, 1 May 2009, Pages 150–156