Palladium supported on reduced graphene oxide as a high-performance catalyst for the dehydrogenation of dodecahydro-N-ethylcarbazole
Liquid organic hydrogen carrier technology has been considered the most promising scheme of alternative to liquid fossil fuels. However, incomplete dehydrogenation has been a bottleneck in the development, as the dehydrogenation catalysts do not have satisfactory catalytic properties. Here we report...
Gespeichert in:
Veröffentlicht in: | Carbon (New York) 2017-10, Vol.122, p.9-18 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Liquid organic hydrogen carrier technology has been considered the most promising scheme of alternative to liquid fossil fuels. However, incomplete dehydrogenation has been a bottleneck in the development, as the dehydrogenation catalysts do not have satisfactory catalytic properties. Here we report on a catalyst of Pd supported on reduced graphene oxide (rGO) prepared by ethylene glycol with excellent catalytic performance for the dehydrogenation of dodecahydro-N-ethylcarbazole (12H-NECZ). The Pd/rGO-EG catalyst exhibits a dramatically enhanced specific activity (up to 14.4 times) and uses half the amount of noble metals in contrast to the state-of-the-art commercial Pd/Al2O3 dehydrogenation catalyst. At 433, 443 and 453 K, amounts of dehydrogenation of 5.27, 5.49 and 5.78 wt%, respectively, were achieved using a 2.5 wt% Pd/rGO-EG catalyst. The dehydrogenation performance of Pd/rGO reduced by different reducing agents was irregular. The catalyst characterization of Pd/rGO-EG shows that Pd is uniformly distributed on the monolayer rGO, mainly in the form of single crystal, with the highest activity Pd (111) surface. A more accurate kinetic calculation was performed to obtain the rate constant of each elementary reaction of the dehydrogenation reaction.
[Display omitted] |
---|---|
ISSN: | 0008-6223 1873-3891 |
DOI: | 10.1016/j.carbon.2017.06.021 |