Utilize este identificador para referenciar este registo: http://hdl.handle.net/10198/1687
Título: Photodeposition of Pt nanoparticles on Ce-Ti-O
Autor: Silva, Adrián
Machado, Bruno
Gomes, Helder
Figueiredo, José
Dražić, Goran
Faria, Joaquim
Data: 2008
Citação: Silva, Adrián; Machado, Bruno; Gomes, Helder; Gomes, Helder; Figueiredo, José; Drazic, Goran; Faria, Joaquim (2008) - Photodeposition of Pt nanoparticles on Ce-Ti-O. In XXI Encontro Nacional da Sociedade Portuguesa de Química. Porto.
Resumo: Hydrogenation reactions are the most common examples where transition and noble metal nanoparticles are applied in colloidal solution as quasihomogeneous catalysts [1]. The main drawback in the use of colloidal nanoparticles for catalysis concerns the recovery and reuse of these particles. This is especially important if environmental issues are considered. Therefore, attention has been drawn to the use of supported nanoparticles. In this work, Ce-Ti-O supports were synthesized by the solvothermal method using methanol and a cationic surfactant (CTAB). Pt nanoparticles were then supported by photochemical deposition using a low-pressure mercury lamp with an emission line at 254 nm (ca.3 W of radiant flux) during 4 h. The catalysts were calcined in N2 (4 h, 100 mL min-1), reduced in H2 (2 h, 20 mL min-1) and flushed again with N2 during 30 min at 773 K. Ultrafine platelet shaped CeO2 particles with sizes ~ 3-8 nm were also produced by the solvothermal method. When Ti was combined with Ce, a nanostructured network was obtained. It was proved that Pt spherical nanoparticles (diameter ~ 2-4 nm) can be efficiently photodeposited on these supports. Fig.1 shows a HRTEM micrograph of the Pt/Ce-Ti-O catalyst, where a Pt nanoparticle (marked by an arrow) can be identified. These catalysts were tested in the selective hydrogenation of cinnamaldehyde to cinnamyl alcohol. Enhancement in the catalytic activity for cinnamaldehyde hydrogenation and higher selectivity for cinnamyl alcohol production was observed with the Pt nanoparticles supported on Ce-Ti-O when compared with the single-oxide supports (CeO2 and TiO2).
URI: http://hdl.handle.net/10198/1687
Aparece nas colecções:CIMO - Resumos em Proceedings Não Indexados à WoS/Scopus

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