| Autor: |
Naranov, Evgeny R., Sadovnikov, Alexey A., Arapova, Olga V., Bugaev, Aram L., Usoltsev, Oleg A., Gorbunov, Dmitry N., Russo, Vincenzo, Murzin, Dmitry Yu., Maximov, Anton L. |
| Zdroj: |
Catalysis Science & Technology; 2023, Vol. 13 Issue: 5 p1571-1583, 13p |
| Abstrakt: |
We present the conversion of guaiacol and diphenyl ether (DPhE) with ∼100% selectivity towards hydrocarbons over a ruthenium oxide-containing catalyst on a micro–mesoporous support (ZM). To elucidate the structure–catalytic activity correlation of the ruthenium oxide catalysts and achieve a high hydrocarbon yield viadeoxygenation–hydrogenation, three supports were used: non-acidic mesoporous SBA-15, bulk ZSM-5 (CBV 3024E) and micro–mesoporous ZM. It was demonstrated that the acidity of the support was a key factor in the deoxygenation of guaiacol and DPhE, while a developed catalyst surface played an important role in the case of bulk molecule hydrogenation. The best catalytic performance was obtained over the micro–mesoporous RuO2/ZM catalyst. Complete conversion of guaiacol and DPhE with a high cyclohexane yield of ∼100% was achieved after 1 h at 473–498 K under an initial H2pressure of 50 bar in n-alkane solution. OperandoXAS and in situDRIFT spectroscopy analyses of the RuO2-based catalysts during guaiacol hydrogenation revealed that the reaction initiates simultaneously with the formation of the metallic Ru phase. It was shown that RuO2catalysts demonstrated better catalytic activity compared to reduced catalysts. |
| Databáze: |
Supplemental Index |
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