| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 50613 | Catalysis Communications | 2012 | 5 Pages |
A series of MgAPO-5-supported Pt or bimetallic Pt–Pb catalysts of various Pt loadings were prepared for the hydrogenation of nitrobenzene (NB) to p-aminophenol (PAP). The structural modification and changes in the electronic properties of the catalysts were analyzed using temperature-programmed desorption of hydrogen, high-resolution transmission electron microscopy, and diffuse reflectance infrared Fourier transformation spectroscopy of the adsorbed carbon monoxide. Results show that Pb doping in Pt/MgAPO-5 catalyst decreases the hydrogenation rate of NB and phenylhydroxylamine simultaneously and increases PAP selectivity greatly. A possible reason for the improvement in the PAP selectivity of the Pb–Pt/MgAPO-5 is the increase in electron density of the Pt sites caused by the interaction of Pb and Pt. The decreased rate of NB hydrogenation over the modified Pb–Pt/MgAPO-5 catalyst can be improved considerably by increasing the reaction temperature or hydrogen pressure while maintaining a high PAP selectivity.
► Bifunctional catalyst was used for hydrogenation of nitrobenzene to p-aminophenol. ► Lead doping in the Pt/MgAPO-5 catalyst results in the increase of PAP selectivity. ► The increase in electron density of Pt is favorable for the production of PAP.
