کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
55098 | 47040 | 2013 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Oxidation of CO over Ru/Ceria prepared by self-dispersion of Ru metal powder into nano-sized particle Oxidation of CO over Ru/Ceria prepared by self-dispersion of Ru metal powder into nano-sized particle](/preview/png/55098.png)
The oxidation of CO was performed using physical mixture of Ru metal powder and various metal oxide supports after calcination in air and reduction in H2. Among various supports (CeO2, ZrO2, MgO, Al2O3, TiO2, SnO2, and SiO2), only Ru + CeO2 showed very high catalytic activity for CO oxidation with the light-off temperature below 100 °C, which was comparable to Ru/CeO2 prepared by a conventional impregnation method. The optimum conditions for the preparation were loading amount of 2 wt%, calcination at 700 °C in air followed by reduction at 400 °C in 5%H2. It was revealed that the high catalytic activity for Ru + CeO2 is attributed to the high dispersion of Ru on CeO2. The original Ru metal powder having diameter of 36 nm was dispersed during the calcination leading into small Ru particles having diameter around 2 nm. Raman spectra indicated that the formation of RuOCe bond after the calcination is one of the key for the Ru dispersion. The self-dispersion of Ru was not achieved by the calcination in N2. It was proposed that the self-dispersion of Ru into nano-particles was caused by oxidation of Ru metal into Ru oxide in air, then dispersion of nano-sized Ru oxide by forming RuOCe bond, and finally conversion of Ru oxide particles into nano-sized Ru metal particles in a flow of H2.
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► A physical mixing and calcination of Ru powder and CeO2 results in an active Ru/CeO2 catalyst.
► The activity was comparable to Ru/CeO2 by a conventional impregnation method.
► The high activity is caused by self-dispersion of Ru into nano-particle.
► The RuOCe bond formation was suggested to be a key factor for the self-dispersion.
Journal: Catalysis Today - Volume 201, 1 March 2013, Pages 62–67