کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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61521 | 47586 | 2012 | 8 صفحه PDF | دانلود رایگان |
A high-performance bimetallic catalyst with mesoporous silica nanoparticles as support, PdAu/MSN, was prepared by an organic impregnation–hydrogen reduction approach. A series of investigations were conducted to assess the effects of (i) the porous nanoparticle support on the dispersion of active components and on the catalyst’s performance, (ii) the addition of gold on the dispersion of active components and the catalyst’s activity, and (iii) the preparation parameters, such as solvent, pressure, and temperature, on the catalyst’s activity. The active metallic components were highly dispersed, with particle size 2.5 nm. The addition of gold to the catalyst favorably promoted the hydrogenation of cinnamaldehyde. The activity of PdAu0.2/MSN (with Au/Pd molar ratio 0.2:1) was up to four times higher than that of Pd/MSN (without Au as a promoter) and eight times higher than that of commercial Pd/C catalyst. The enhanced activity of PdAu0.2/MSN can be attributed to the synergistic effect of Pd with the added Au and the highly dispersed active components. The ultrahigh activity, as well as its novel structure with controllable compositions, makes this catalyst very attractive for both fundamental research and practical applications.
A high-performance bimetallic catalyst with mesoporous silica nanoparticles as support, PdAu/MSN, was prepared successfully. For the hydrogenation of cinnamaldehyde, the activity of PdAu0.2/MSN (with a Au/Pd molar ratio of 0.2:1) was up to four times and eight times higher than that of Pd/MSN and commercial Pd/C catalysts, respectively. The enhanced activity of PdAu0.2/MSN is attributable to the synergistic effect of Pd with added Au and the high dispersion of its active components, which may result from the high surface area of MSN nanoparticles, and mostly the addition of gold.Figure optionsDownload high-quality image (243 K)Download as PowerPoint slide
Journal: Journal of Catalysis - Volume 291, July 2012, Pages 36–43