Preparation of platinum-iridium nanoparticles on titania nanotubes by MOCVD and their catalytic evaluation

被引:22
作者
Capula Colindres, S. [1 ]
Vargas Garcia, J. R. [1 ]
Toledo Antonio, J. A. [2 ]
Angeles Chavez, C. [2 ]
机构
[1] Natl Polytech Inst, Dept Met Eng, Mexico City 07300, DF, Mexico
[2] Petr Mexican Inst, Mexico City 07730, DF, Mexico
关键词
Nanostructured materials; Vapor deposition; Catalysis; OXIDE NANOTUBES; HYDROGENATION;
D O I
10.1016/j.jallcom.2008.08.097
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pt based catalysts are commonly used in several industrial processes involving hydrogenation and dehydrogenation reactions. New deposition methods as well as support materials are being investigated to generate new catalysts with superior catalytic activity. In this work, platinum-iridium (Pt-Ir) nanoparticles of about 5 nm in size were supported on titania (TiO2) nanotubes by metal organic chemical vapor deposition (MOCVD). The TiO2 nanotubes were prepared by an alkali hydrothermal method using sodium hydroxide solution at 100 degrees C, during 64.8 ks. Pt-Ir nanoparticles were obtained by controlling the MOCVD conditions at 400 degrees C and 66.6 kPa. Textural properties and particle size were investigated by nitrogen physisorption (BET method), X-ray diffraction, Raman spectroscopy and high resolution transmission electron microscopy. Catalytic activity was measured in cyclohexene disproportion as the test molecule for hydrogenation/dehydrogenation reactions. The TiO2 nanotubes exhibit a considerable high surface area of about 425,000 m(2)/kg, however, after calcination at 400 degrees C their nanotubular morphology was partially transformed. In spite of this change, the 5 rum Pt-Ir nanoparticles supported on TiO2 nanotubes were more active in the cyclohexene disproportion reaction than conventional Pt-Ir/alumina catalysts in the whole range of temperatures investigated (50-250 degrees C). Hydrogenation reactions (high selectivity to cyclohexane) predominate at temperatures below 150 degrees C. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:406 / 409
页数:4
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