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Oxygen reactant

Pines and Csicsery (90, 90a) proposed three and/or four-membered cyclic intermediates in the isomerization of various branched alkanes over non-acidic chromia-alumina. A similar, 1,3-methyl shift has recently been reported with an oxygenated reactant (tetramethyloxetane) over supported Pt, Pd, and Rh (90b). Future experiments are necessary to elucidate whether hydrocarbons, too, can form C4 cyclic intermediates over metal catalysts. Some products assumedly formed via ethyl shift could be interpreted by C4 cyclic isomerization. [Pg.298]

It is also interesting that if the goal is to produce H2-CO gas mixtures, for instance in the Fischer-Tropsch synthesis, one needs to suppress the WGSR operating in the vapor phase or to operate at higher concentrations of the oxygenated reactant in water or to use a catalyst on which the rate of the WGSR is slow. [Pg.192]

It was shown how strongly the efficienqf of each process depends on the nature of the oxygenated compound. Furthermore, we stressed the concept that the successful development of one process lies largely in the design of a suitable catalytic material in conjunction with the optimization of the working conditions. In our opinion, the development of an efficient catalyst able to cope with the complex chemical nature of the oxygenated reactant is the real challenge. Moreover, improvements are needed to control and direct the reaction pathway to the desired products. [Pg.223]

A chemical change occurred because reactants were changed into new substances. The magnesium oxide is a gray powder. The magnesium is a shiny metal and the oxygen reactant is a colorless, odorless gas. [Pg.88]

The opponents of fundamental studies with idealized electrocatalysts and reactions cannot deny the unique insight into surface molecular and electronic or energetic interactions that new surface and mechanistic techniques generate. A combination of surface spectrometries, isotopic reactions, and conventional electrode kinetics could help unravel some of the surface mysteries. The application of such methods in electrocatalysis is limited at present to hydrogen and oxygen reactants on simple catalytic surfaces. Extension to a variety of model and complex reactions should be attempted soon. The prospective explorer, however, should strive and attend with care the standardization of analytical methods for meaningful interpretations and comparisons. [Pg.322]

One of the main disadvantages of the Damjanovic s scheme is that it does not consider possible weak adsorptions and the reversible adsorption/desorption of hydrogen peroxide at the interface. The mechanism proposed by Wroblowa et al. [104] considers the adsorption/desorption equilibrium either for the oxygen reactant or the hydrogen peroxide intermediate. They also proposed the chemical decomposition of the intermediate (1(4), besides the electrochemical reduction to water through k3 (Scheme 2.5). [Pg.69]

Table 17.1 DFT calculated binding energies (BE) of oxygenated reactants and intermediates of the ORR to Pt3 and Pt-based alloy clusters. Table 17.1 DFT calculated binding energies (BE) of oxygenated reactants and intermediates of the ORR to Pt3 and Pt-based alloy clusters.
The place on the catalyst surface within the fuel cell electrodes where protons, electrons, and the fuel meet in order to oxidize hydrogen or reduce oxygen reactants. [Pg.434]

The diagram shows two different ways to go from graphite and oxygen (reactants) to carbon monoxide (products).Going by way of reactions 1 and 2 is equivalent to the direct reaction 3. [Pg.244]

Electrodes are usually composed of a gas diffusion layer with thin catalyst coatings at the electrode-electrolyte interfaces. Hydrogen and oxygen reactants are supplied to the anode and cathode electrodes surfaces. The original rod-type electrodes are generally replaced with flat or circular annular surfaces to increase the contact surface area for reactions. The structure of the electrode is... [Pg.15]

Determine the change in enthalpy and entropy for a stoichiometric (balanced) hydrogen air redox reaction, H2 + I O2 — H2O, with the hydrogen and oxygen reactants and products at 1000°C. [Pg.116]

FIGURE 9.22 Performance curves for DMFCs with Nation 117 and (a) Nafion-silica, (b) Nafion-MZP, and (c) Nafion-MTP composited membranes at 70°C using aqueous methanol and oxygen reactants at atmospheric pressure. Anode, 2 M aqueous methanol with a flow rate of 2 seem cathode, oxygen with a flow rate of 200 seem. (From Sahu, A.K. et al., J. Membr. Sci., 345, 305, 2009.)... [Pg.418]


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See also in sourсe #XX -- [ Pg.436 ]




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