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Carbon monoxide oxidation, platinum supported catalytic activity

Carbon-supported Pt can also be used as the anode catalyst. However, this requires pure H2. Contaminants such as carbon monoxide (CO) poison the catalyst, because CO can strongly adsorb on Pt, blocking the catalytic sites and reducing platinum s catalytic activity. In H2 produced from the reforming of other fuels, CO is always present. Thus, to improve contaminant tolerance, carbon-supported PtRu was developed and now is always used as the anode catalyst. Ru can facilitate the oxidation of CO, releasing the catalytic sites on Pt through the following reactions ... [Pg.7]

Classical analysis has demonstrated that a given quantity of active material should be deposited over the thinnest layer possible in order to minimize diffusion limitations in the porous support. This conclusion may be invalid for automotive catalysis. Carbon monoxide oxidation over platinum exhibits negative order kinetics so that a drop in CO concentration toward the interior of a porous layer can increase the reaction rate and increase the effectiveness factor to above one. The relative advantage of a thin catalytic layer is further reduced when one considers its greater vulnerability to attrition and to the deposition of poisons. [Pg.122]

The selective production of methanol and of ethanol by carbon monoxide hydrogenation involving pyrolysed rhodium carbonyl clusters supported on basic or amphoteric oxides, respectively, has been discussed. The nature of the support clearly plays the major role in influencing the ratio of oxygenated products to hydrocarbon products, whereas the nuclearity and charge of the starting rhodium cluster compound are of minor importance. Ichikawa has now extended this work to a study of (CO 4- Hj) reactions in the presence of alkenes and to reactions over catalysts derived from platinum and iridium clusters. Rhodium, bimetallic Rh-Co, and cobalt carbonyl clusters supported on zinc oxide and other basic oxides are active catalysts for the hydro-formylation of ethene and propene at one atm and 90-180°C. Various rhodium carbonyl cluster precursors have been used catalytic activities at about 160vary in the order Rh4(CO)i2 > Rh6(CO)ig > [Rh7(CO)i6] >... [Pg.89]

The three-way exhaust catalytic converter is used to complete the combustion of carbon monoxide and unburned fuel elements and to remove the NO and N02 produced during combustion. The primary components of the catalytic converter are the catalyst and its physical support. The catalyst is composed of a high-surface-area support that incorporates the primary catalytically active materials, typically mixtures of one or more of platinum, palladium, or rhodium (precious group metals, PGMs). The catalyst also contains promoters that improve the efficiency and stability of the PGM. Of these, the most important is cerium oxide, a... [Pg.25]

Carbon is generally used as catalyst support material because of its high electric and thermal conductivity, chemical stability, and porous structure [11]. The catalytic activity of the catalyst layer increases with increasing carbon surface area due to better platinum dispersion. High surface area carbon blacks such as Ketjenblack and Vulcan are therefore preferred in PEMFC application. However, carbon is thermodynamically unstable at normal cathode potentials between 0.5 and 1V. As shown in Figure 20.1a, carbon is oxidized to carbon dioxide (CO2) or carbon monoxide (CO) at high electrode potentials whereas it is reduced to methane (CH4) at low electrode potentials. The following reactions are relevant for fuel-cell operation ... [Pg.544]

The presence of thallium(0) led to an increase in activity and selectivity of metallic palladium catalysts supported on silica in aldose oxidation reactions. However, silica-supported thallium(0) had no activity by itself (entry 3). ° Similarly, the bimetallic catalyst platinum-thallium/ZSM-5, prepared by impregnation of thallium sulfate and chloroplatinic acid on Zeolite Socony Mobil-5 (ZSM-5), showed greater selectivity in propane aromatisation and almost the same catalytic activity as monometallic thallium/ZSM-5 (entry 4). Similar comparison of vanadium-caesium-copper and vanadium-caesium-copper-thallium catalysts supported on TiOa.SiC demonstrated that addition of thallium improved the catalytic activity in partial oxidation of p-tert-butyltoluene to p-tert-butyl-benzaldehyde (entry The application of solid-supported thallium-based catalysts in different processes includes (a) iron-thallium catalysts in carbon monoxide hydrogenations to form hydrocarbons and alcohols, and catalytic reforming of... [Pg.227]


See other pages where Carbon monoxide oxidation, platinum supported catalytic activity is mentioned: [Pg.191]    [Pg.374]    [Pg.280]    [Pg.280]    [Pg.156]    [Pg.493]    [Pg.16]    [Pg.477]    [Pg.113]    [Pg.326]    [Pg.116]    [Pg.156]    [Pg.319]    [Pg.85]    [Pg.115]    [Pg.340]    [Pg.790]   
See also in sourсe #XX -- [ Pg.199 , Pg.411 , Pg.415 ]




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Activated carbon oxidized (

Activated oxidation

Activation oxidation

Active oxides

Activity oxidation

Carbon monoxide activation

Carbon monoxide activities

Carbon monoxide catalytic

Carbon monoxide catalytic activity

Carbon monoxide catalytic oxidation

Carbon monoxide oxidation, platinum supported

Carbon monoxide platinum

Carbon monoxide supported

Carbon monoxide, oxidation

Carbon oxidation, supported

Carbon support

Carbon supported

Carbon-Supported Platinum

Carbonate supports

Carbonic catalytic

Carbonization catalytic

Catalytic Supports

Monoxide oxides

Oxidation platinum

Oxidation supports

Oxidative activation

Oxide supports

Oxides activated

Oxidizing activators

Platinum activation

Platinum carbon

Platinum monoxide

Platinum oxide

Platinum support

Supported activation

Supporting activity

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