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Oxygen importance

The application of these concepts to the electroreduction of oxygen, important for fuel cells, with hydrodynamic electrodes is described in Chapter 8. [Pg.122]

Applications are varied, from catalysis of organic and inorganic reactions to electron transfer to and from molecules of biological interest. For example, it has been shown that ruthenium(IV) immobilized inside PVP catalyses organic oxidations such as that of propan-2-ol to acetone19. The electroreduction of oxygen (important in fuel cells, Section 15.10) is catalysed by metalloporphyrins and metallophthalocyanines20. The... [Pg.317]

To this end, both Texaco and Shell are developing their processes to handle coal slurries). The Texaco process is somewhat more flexible in that it has commercial operating experience with pressures up to 1200 psig. Thus the Texaco process requires no synthesis gas compression. The Shell process operates generally around 600 psig. Typically, today s POX plant would be around 60% thermally efficient (plus oxygen import) and can operate on cheaper feedstocks. [Pg.148]

A. Heiss, K. Sahetchian Reactions of the Ai-butoxy radical in oxygen. Importance of isomerization and formation of pollutants, to be published. [Pg.199]

Remarks Species and strains differ in the sensitivity to oxygen, important probiotics and used in the food industry ... [Pg.239]

Three oxide phases have been chosen as supftons SnOi. M0O3 and Fea (Mo04)3. These phases are very active in the oxidation of isobutene, but not very selective in the formation of methacrolein. These three phases have a very low (if any) chemical affinity for antimony oxide. This last oxide (Sb204) is very active for the dissociation of oxygen. Important synergetic effects have been observed in biphasic catalysts formed by mixtures of the above-mentioned oxides, prepared separately, with Sb204. A remote control operates in these systems (14,16,20,22). [Pg.539]

Manufactured by the liquid-phase oxidation of ethanal at 60 C by oxygen or air under pressure in the presence of manganese(ii) ethanoate, the latter preventing the formation of perelhanoic acid. Another important route is the liquid-phase oxidation of butane by air at 50 atm. and 150-250 C in the presence of a metal ethanoate. Some ethanoic acid is produced by the catalytic oxidation of ethanol. Fermentation processes are used only for the production of vinegar. [Pg.164]

With regards to the overall balance of combustion, the chemical structure of the motor or heating fuel, e.g., the number of carbon atoms in tbe chain and the nature of the bonding, does not play a direct role the only important item is the overall composition, that is, the contents of carbon, hydrogen, and — eventually— oxygen in the case of alcohols or ethers added to the fuel. [Pg.179]

In the standard method, the metal enclosure (called the air chamber) used to hold the hydrocarbon vapors is immersed in water before the test, then drained but not dried. This mode of operation, often designated as the wet bomb" is stipulated for all materials that are exclusively petroleum. But if the fuels contain alcohols or other organic products soluble in water, the apparatus must be dried in order that the vapors are not absorbed by the water on the walls. This technique is called the dry bomb" it results in RVP values higher by about 100 mbar for some oxygenated motor fuels. When examining the numerical results, it is thus important to know the technique employed. In any case, the dry bomb method is preferred. [Pg.189]

The Fischer-Tropsch reaction is essentially that of Eq. XVIII-54 and is of great importance partly by itself and also as part of a coupled set of processes whereby steam or oxygen plus coal or coke is transformed into methane, olefins, alcohols, and gasolines. The first step is to produce a mixture of CO and H2 (called water-gas or synthesis gas ) by the high-temperature treatment of coal or coke with steam. The water-gas shift reaction CO + H2O = CO2 + H2 is then used to adjust the CO/H2 ratio for the feed to the Fischer-Tropsch or synthesis reactor. This last process was disclosed in 1913 and was extensively developed around 1925 by Fischer and Tropsch [268]. [Pg.730]

Classic examples are the spontaneous emission of light or spontaneous radioactive decay. In chemistry, an important class of monomolecular reactions is the predissociation of metastable (excited) species. An example is the fonnation of oxygen atoms in the upper atmosphere by predissociation of electronically excited O2 molecules [12, 13 and 14] ... [Pg.765]

The development of neutron diffraction by C G Shull and coworkers [30] led to the detennination of the existence, previously only a hypothesis, of antiferromagnetism and ferrimagnetism. More recently neutron diffraction, because of its sensitivity to light elements in the presence of heavy ones, played a cmcial role in demonstrating the importance of oxygen content m high-temperature superconductors. [Pg.1382]

Zeolites (section C2.13) are unique because they have regular pores as part of their crystalline stmctures. The pores are so small (about 1 nm in diameter) that zeolites are molecular sieves, allowing small molecules to enter the pores, whereas larger ones are sieved out. The stmctures are built up of linked SiO and AlO tetrahedra that share O ions. The faujasites (zeolite X and zeolite Y) and ZSM-5 are important industrial catalysts. The stmcture of faujasite is represented in figure C2.7.11 and that of ZSM-5 in figure C2.7.12. The points of intersection of the lines represent Si or A1 ions oxygen is present at the centre of each line. This depiction emphasizes the zeolite framework stmcture and shows the presence of the intracrystalline pore stmcture. In the centre of the faujasite stmcture is an open space (supercage) with a diameter of about 1.2 nm. The pore stmcture is three dimensional. [Pg.2710]

Thus, it can basically be predicted under what conditions (pH, concentration of redox species) tire metal dissolution reaction (Fe Fe ) proceeds tliennodynamically. From a practical point of view, tire rate of tire reaction and tlierefore tire fate of tire oxidized species (Fe ) is extremely important tliey can eitlier be solvated, i.e., to fonn Fe (H20) complexes, and tlierefore be efficiently dissolved in tire solution, or tliey can react witli oxygen species of... [Pg.2716]


See other pages where Oxygen importance is mentioned: [Pg.243]    [Pg.58]    [Pg.122]    [Pg.325]    [Pg.194]    [Pg.378]    [Pg.339]    [Pg.764]    [Pg.243]    [Pg.58]    [Pg.122]    [Pg.325]    [Pg.194]    [Pg.378]    [Pg.339]    [Pg.764]    [Pg.30]    [Pg.75]    [Pg.75]    [Pg.104]    [Pg.192]    [Pg.207]    [Pg.209]    [Pg.264]    [Pg.275]    [Pg.276]    [Pg.301]    [Pg.344]    [Pg.360]    [Pg.387]    [Pg.396]    [Pg.419]    [Pg.425]    [Pg.416]    [Pg.477]    [Pg.739]    [Pg.440]    [Pg.1143]    [Pg.2398]    [Pg.2418]    [Pg.2420]    [Pg.2616]    [Pg.2754]   
See also in sourсe #XX -- [ Pg.15 , Pg.78 , Pg.79 , Pg.85 , Pg.86 , Pg.92 ]




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