کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
67107 | 48465 | 2009 | 10 صفحه PDF | دانلود رایگان |

Small gold particles having sizes of 1.0–2.0 nm were deposited on the surface of the sodium trititanate (Na2Ti3O7) nanotube by the ion exchange method. This nanotube-supported gold catalyst was able to oxidize CO at the sub-ambient temperature. In a pulse reactor, the gold catalyst could achieve a T50% of 218 K using 1.0 vol.% CO/He gas pulses (0.34 μmol CO/pulse). In the Au loadings of 0.39–2.53 wt.%, the activity of the gold catalyst increased with the gold loading. Calcination of nanotube support at higher than 383 K prior to the gold deposition produced a catalyst with a lower activity. Regarding the effect of calcining the gold particles on the activity (with NaTNT support calcined at 673 K), the catalyst with gold particles heated at 383 K only exhibited the best CO oxidation activity. XPS indicated that there are three gold species with different oxidation state, Au0, Au+1 and Auδ−, in the calcined gold catalysts. As calcination temperature increased, the Au0 concentration increased at the consumption of Au+1 species, while the Auδ− concentration remained relatively constant. This fact strongly suggested that Au+1 species must play an important role in the activity in the sub-ambient temperature region.
Small gold particles having sizes of 1.0–2.0 nm were deposited on the sodium trititanate nanotube (Na2Ti3O7) surface by the ion exchange method. The gold catalyst with a loading of 2.53 wt.% Au could achieve a T50% of 218 K in a pulse reactor with a reactant pulse containing 0.34 μmol CO/pulse.Figure optionsDownload as PowerPoint slide
Journal: Journal of Molecular Catalysis A: Chemical - Volume 298, Issues 1–2, 2 February 2009, Pages 115–124