Carbon-Supported Platinum-Ruthenium

Nashner MS, Frenkel Al, Adler DL, Shapley JR, Nuzzo RG. 1997. Structural characterization of carbon supported platinum-ruthenium nanoparticles from the molecular cluster precursor PtRu5(CO)i6. J Am Chem Soc 119 7760. 

Munke et al. [196] reported a technique (Figure 10.31) of in situ electrochemical FTIR and used it to study a real carbon-supported platinum + ruthenium catalyst. Different adsorptions were observed when methanol was electrooxidized at bulk Pt, Pt particles, and carbon-black-supported Pt -I- Ru electrodes, particularly with regard to the nature of the adsorbed CO species (Figure 10.32). 

Goodenough, J.B., Hamnett, A., Kennedy, B.J., Manoharan, R. Weeks, S.A. Methanol oxidation on unsupported and carbon supported platinum+ruthenium anodes. J. Electroanal. CheirL Interfacial Electrochem. 240 (1988), pp. 133 145. 

Park, S., Y.T. Tong, A. Wieckowski, and M.J. Weaver, Infrared spectral comparison of electrochemical carbon monoxide adlayers formed by direct chemisorption and methanol dissociation on carbon-supported platinum nanoparticles. Langmuir, 2002.18(8) pp. 3233-3240 Park, S., Y. Tong, A. Wieckowski, and M.J. Weaver, Infrared reflection-absorption properties of platinum nanoparticle films on metal electrode substrates control of anomalous opticalejfects. Electrochemistry Communications, 2001. 3(9) pp. 509-513 Park, S., P.K. Babu, A. Wieckowski, and M.J. Weaver, Electrochemical infrared characterization of CO domains on ruthenium decorated platinum nanoparticles. Abstracts of Papers of the American Chemical Society, 2003. 225 pp. U619-U619... 

Rauhe BR, Mclamon FR, Cairns EJ (1995) Direct anodic-oxidation of methanol on supported platinum ruthenium catalyst in aqueous cesium carbonate. J Electrochem Soc 142(4) 1073-1084... 

Maillard F, Gloaguen F, Leger JM. Preparation of methanol oxidation electrocatalysts ruthenium deposition on carbon-supported platinum nanoparticles. J Appl Electrochem 2003 33 1-8. 

Lin Z, Ji LW, Krause WE, Zhang XW (2010) Synthesis and electrocatalysis of 1-aminopyrene-functionalized carbon nanofiber-supported platinum-ruthenium nanopaiti-cles. J Power Sources 195(17) 5520-5526... 

Rapoport s findings have been confirmed in the authors laboratory where the actions of carbon-supported catalysts (5% metal) derived from ruthenium, rhodium, palladium, osmium, iridium, and platinum, on pyridine, have been examined. At atmospheric pressure, at the boiling point of pyridine, and at a pyridine-to-catalyst ratio of 8 1, only palladium was active in bringing about the formation of 2,2 -bipyridine. It w as also found that different preparations of palladium-on-carbon varied widely in efficiency (yield 0.05-0.39 gm of 2,2 -bipyridine per gram of catalyst), but the factors responsible for this variation are not knowm. Palladium-on-alumina was found to be inferior to the carbon-supported preparations and gave only traces of bipyridine,... 

Rhodium-on-carbon has also been found to bring about the formation of 2,2 -biquinoline from quinoline, the yield and the percentage conversion being similar to that obtained with palladium-on-carbon. On the other hand, rhodium-on-carbon failed to produce 2,2 -bipyridine from pyridine, and it has not yet been tried with other bases. Experiments with carbon-supported catalysts prepared from ruthenium, osmium, iridium, and platinum have shown that none of these metals is capable of bringing about the formation of 2,2 -biquinoline from quinoline under the conditions used with palladium and rhodium. ... 

It was seen when studying mixed systems Pt-WOj/C and Pt-Ti02/C that with increasing percentage of oxide in the substrate mix the working surface area of the platinum crystallites increases, and the catalytic activity for methanol oxidation increases accordingly. With a support of molybdenum oxide on carbon black, the activity of supported platinum catalyst for methanol oxidation comes close to that of the mixed platinum-ruthenium catalyst. 

Palladium gave the highest activity of all the platinum group metals evaluated platinum, rhodium and ruthenium exhibited very poor activity. The choice of support was also demonstrated to be very important the activated carbon supported Pd catalyst showed a nearly fourfold increase in activity than did Pd supported on alumina. 

The feasibility of carbon-supported nickel-based catalysts as the alternative to the platinum catalyst is studied in this chapter. Carbon-supported nickel (Ni/C, 10 wt-metal% [12]), ruthenium (Ru/C, 10 wt-metal% [12]), and nickel-ruthenium composite (Ni-Ru/C, 10 wt-metal%, mixed molar ratio of Ni/Ru 0.25,1,4, 8, and 16 [12]) catalysts were prepared similarly by the impregnation method. Granular powders of the activated carbon without the base pretreatment were stirred with the NiCl2, RuC13, and NiCl2-RuCl3 aqueous solutions at room temperature for 24 h, respectively. Reduction and washing were carried out in the same way as done for the Pt/C catalyst. Finally, these nickel-based catalysts were evacuated at 70°C for 10 h. 

Cyclohexane dehydrogenates rather rapidly to benzene. Its rearrangement has not been reported over pure metals until now. Cg Ring opening is negligible over platinum and palladium 48, 5i) slight hexane formation was reported over carbon supported rhodium, iridium, and, especially, osmium and ruthenium (702), as well as over nickel on alumina (99). 

The results observed in the hydrogenation of higher dialkylalkynes are in general accord with those observed with but-2-yne. Thus, for example, the selectivity and stereoselectivity observed in the liquid phase hydrogenation of pent-2-yne over carbon-supported palladium, rhodium, ruthenium and platinum and iridium—alumina [145], as shown in Table 22, show a similar pattern to that observed in but-2-yne hydrogenation. Similarly, the... 

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