Abstract

AbstractThe effects of several preparation variables on the dispersion of supported platinum catalysts were examined in this study. Supported catalysts were prepared using two different platinum salts, four high surface area support materials, and two aqueous deposition techniques. The catalysts were characterised by hydrogen chemisorption, oxygen chemisorption, and the hydrogen titration reaction. In addition, X‐ray diffraction measurements were conducted on all catalysts. Results from this study show that one of the platinum salts, chloroplatinic acid, always gave an equally or more highly dispersed catalyst than the other salt, tetraammine platinum (II) nitrate. The incipient wetness preparation technique produced equal or better dispersions than did the excess water method, with the possible exception of the silica‐alumina support. The highest dispersions were attained with alumina, and the lowest with carbon. In some samples, a lack of good agreement existed between X‐ray diffraction and chemisorption measurements of crystallite size which indicated broad or bimodal particle size distributions. However, these X‐ray data were qualitatively helpful in understanding the unusual chemisorption behaviour of Pt/C catalysts, one of which had a dispersion higher than any previous reported Pt/C catalyst prepared by aqueous impregnation techniques. Experiments were also conducted which showed that either a 1 h or a 12 h treatment in hydrogen at 723 K was sufficient to reduce the platinum salt, and 1 h or 12 h evacuations at 698 K gave similar results. Finally, it was found that approximately one‐half of the hydrogen monolayer on supported Pt could be removed by evacuating for 1 h at 300 K.

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