Robust bimetallic Pt–Ru catalysts for the rapid hydrogenation of toluene and tetralin at ambient temperature and pressure
[Display omitted] ► Alloy nanoparticles of Pt–Ru were synthesised. ► The complete catalyst synthesis was performed in air. ► Toluene was hydrogenated under ambient conditions and with no special precautions. ► The alloy with a molar ratio of 1 Pt to 1.5 Ru was much more active than either of the met...
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| Veröffentlicht in: | Applied catalysis. A, General Jg. 454; S. 46 - 52 |
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| Hauptverfasser: | , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
Kidlington
Elsevier B.V
15.03.2013
Elsevier |
| Schlagworte: | |
| ISSN: | 0926-860X, 1873-3875 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | [Display omitted]
► Alloy nanoparticles of Pt–Ru were synthesised. ► The complete catalyst synthesis was performed in air. ► Toluene was hydrogenated under ambient conditions and with no special precautions. ► The alloy with a molar ratio of 1 Pt to 1.5 Ru was much more active than either of the metals by themselves. ► The synergistic alloy may hold the key to a simple reversible hydrogen storage system, operating under mild conditions.
To facilitate the drive towards ever lower energy, ‘greener’ processing, robust bimetallic aluminosilicate-supported Pt–Ru catalysts that can operate under atmospheric conditions have been developed for the rapid room temperature hydrogenation of aromatics (toluene and tetralin) at 1atm H2. The toluene/methylcyclohexane couple has the added interest of being a promising cyclic hydrocarbon combination for the storage of hydrogen.
The easily handled air-stable catalysts were prepared using the incipient wetness method and characterised by ICP-AES, XRD, TEM as well as nitrogen sorption measurements. Compared to their monometallic counterparts, the bimetallic catalysts displayed significantly higher turn-over-frequencies (TOFs), consistent with a synergistic relationship between platinum and ruthenium. |
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| Bibliographie: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
| ISSN: | 0926-860X 1873-3875 |
| DOI: | 10.1016/j.apcata.2013.01.002 |