کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
65968 | 48410 | 2013 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Chemoselective hydrogenation of halonitroaromatics over γ-Fe2O3-supported platinum nanoparticles: The role of the support on their catalytic activity and selectivity Chemoselective hydrogenation of halonitroaromatics over γ-Fe2O3-supported platinum nanoparticles: The role of the support on their catalytic activity and selectivity](/preview/png/65968.png)
Solvated platinum atoms, obtained by metal vapour synthesis (MVS), were conveniently used to prepare γ-iron oxide and γ-alumina supported Pt catalysts containing small metal nanoparticles of controlled size, ranging 0.5–3.0 nm in diameter (HR-TEM). The γ-Fe2O3-supported Pt system showed higher catalytic activity and selectivity than those of a similarly prepared γ-Al2O3-supported system in the selective hydrogenation reactions of p- and o-chloronitrobenzene to the corresponding haloanilines, in mild reaction conditions (25 °C, 0.1 MPa hydrogen pressure) (p-chloronitrobenzene: specific activity (SA) = 59.5 min−1, Selectivity (Sel.) = 99.9%; o-chloronitrobenzene: SA = 42.8 min−1, Sel. = 99.2%). The Pt/γ-Fe2O3 system also showed high catalytic efficiency (Sel. > 98%, at 100% of conversion) in the selective hydrogenations of m-chloro-, p- and o-bromo- and p- and o-iodonitrobenzenes. XPS structural studies performed on a pristine Pt/γ-Fe2O3 sample as well as on a sample recovered after the reaction, indicate that the catalytic process did not induce permanent modification in the chemical and/or electronic structure of the catalyst according with the high reusability of the system.
Figure optionsDownload high-quality image (161 K)Download as PowerPoint slideHighlights
► Synthesis of supported Pt catalysts by metal vapour synthesis.
► HRTEM and XPS analysis.
► High efficiency of Pt/γ-Fe2O3 system in halonitroaromatic hydrogenations.
► Easily recover and reuse of Pt/γ-Fe2O3 system.
Journal: Journal of Molecular Catalysis A: Chemical - Volume 366, January 2013, Pages 288–293