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Bimetallic catalysts hydrogen chemisorption

The preparation of a successful supported bimetallic catalyst is quite a difficult proposition. The main problem is to ensure that the two components reside in the same particle in the finished catalyst, and to know that it is so. The main physical techniques to characterise bimetallic particles are hydrogen chemisorption, XRD, TEM, EDX, XPS, XAFS,197Au Mossbauer (Section 3.3) and CO chemisorption coupled by IR spectroscopy (Section 5.3). The characterisation of bimetallic catalysts is not always thoroughly done, and there is the further complication of structural changes (particularly of the surface) during use. In situ or post-operative characterisation would reveal them, but it is rarely done. [Pg.105]

The addition of iridium to platinum on ij-AlaOa causes a marked increase in the H/M ratio of hydrogen uptake assuming that H/Ms = 1.69.70 value of two was not taken to be conclusive proof of spillover so the authors turned to the chemisorption of carbon monoxide and compared the ratios H/CO for uptake at saturation on the supported and unsupported bimetallic catalysts. The following results were obtained for the quotient of the two H/CO ratios at various catalyst compositions —... [Pg.154]

We believe that ether formation is likely to occur as a result of nucleophilic attack of a methoxy species on the carbinol carbon as shown above. In Ni-Cu and Ni-Fe catalysts, the surface is known to be enriched by Cu and Fe, which was found to be also true in the present case from the hydrogen chemisorption data. Thus in the bimetallic catalysts, Ni atoms will be preferentially... [Pg.255]

Characterization of Supported Metal Catalysts. - Chemisorption of different probe molecules and Temperature Programmed Reduction (TPR) studies are frequently used to study the metal dispersion, surface composition and oxidation state of metals in mono- and bimetallic supported catalysts. Combined use of CO, hydrogen and oxygen chemisorption as well as oxygen-hydrogen titration can provide information about the dispersion and surface composition of metal nanoclusters. TPR studies of bimetallic catalysts can give information about the type, the reducibility, and the oxidation state of metal components. In addition, the position of TPR peaks can be used to characterize the type of interactions of the metal species in the catalysts. - ... [Pg.5]

A MgO-supported W—Pt catalyst has been prepared from IWsPttCOIotNCPh) (i -C5H5)2l (Fig. 70), reduced under a Hs stream at 400 C, and characterized by IR, EXAFS, TEM and chemisorption of Hs, CO, and O2. Activity in toluene hydrogenation at 1 atm and 60 C was more than an order of magnitude less for the bimetallic cluster-derived catalyst, than for a catalyst prepared from the two monometallic precursors. [Pg.113]

The activity of all catalysts were evaluated for the CO hydrogenation reaction. The histogram shown in Fig. 8 reveals that the bimetallic Co-Mo nitride system has appreciable hydrogenation activity with exception of samples 2 and 4. This apparent anomaly was probably due to the relatively high heat of adsorption for these two catalysts, which offered strong CO chemisorption but with imfavourable product release. [Pg.248]

U is known that methanol can be obtained using only ZnO a a catalyst. The role of copper Can be understood as increasing the CO chemisorption and/or hydrogenation function. A synergcstic bimetallic interaction to activate CO may also be considered. [Pg.92]

The data on the catalyst containing rhenium alone indicate signficant chemisorption of carbon monoxide, but no chemisorption of hydrogen. As expected, the platinum catalyst chemisorbs both carbon monoxide and hydrogen, and the values of CO/M and H/M are nearly equal. The platinum-rhenium catalyst exhibits a value of CO/M about twice as high as the value of H/M. This result approximates what one would expect if hydrogen chemisorbed on only the platinum component of the catalyst. While this chemisorption behavior is consistent with the possibility that the platinum and rhenium are present as two separate entities in the catalyst, they do not rule out the possibility that bimetallic clusters of platinum and rhenium are present. [Pg.122]


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Bimetallic catalysts

Hydrogen chemisorption

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