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Oxygen reference form

Uncertainties in Photochemical Models. The ability of photochemical models to accurately predict HO concentrations is undoubtedly more reliable in clean vs. polluted air, since the number of processes that affect [HO ] and [H02 ] is much greater in the presence of NMHC. Logan et al (58) have obtained simplified equations for [HO ] and [HO2 ] for conditions where NMHC chemistry can be ignored. The equation for HO concentration is given in Equation E6. The first term in the numerator refers to the fraction of excited oxygen atoms formed in R1 that react to form HO J refers to the photodissociation of hydrogen peroxide to form 2 HO molecules other rate constants refer to numbered reactions above. [Pg.92]

The space shuttle uses a fuel cell as a source of energy. This cell depends on the oxidation of hydrogen by oxygen to form water. The fuel cell operates under basic conditions, so it is sometimes referred to as an alkaline fuel cell. Figure 11.31, on the next page, shows the design of the cell. The half-reactions and the overall reaction are as follows. [Pg.550]

Nitrogen reacts with oxygen to form five oxides, as shown in the table on the adjoining page. The two most important with regard to air pollution are NO and NO2, which are sometimes referred to together as NO. In some circumstances, the formula may also include other oxides of nitrogen. [Pg.24]

Fig. 4. Stability of carbon on different sites (A-D) on a pure nickel(l 11) surface (below) and a gold-alloyed nickel(l 11) surface (above). The probability of nucleation of graphite is determined by the stability of the adsorbed carbon atoms. The less stable the adsorbed carbon, the larger the tendency to react with adsorbed oxygen to form CO and the lower the coverage. On the pure nickel) 111) surface, the most stable adsorption configuration of carbon is in the threefold (hep) site (lower curve). The upper graph shows that carbon adsorption in threefold sites next to a gold atom is completely unstable (sites B and C), and even the threefold sites that are next-nearest neighbors (sites A and D) to the gold atoms are led to a substantial destabilization of the carbon. From Reference (79). Fig. 4. Stability of carbon on different sites (A-D) on a pure nickel(l 11) surface (below) and a gold-alloyed nickel(l 11) surface (above). The probability of nucleation of graphite is determined by the stability of the adsorbed carbon atoms. The less stable the adsorbed carbon, the larger the tendency to react with adsorbed oxygen to form CO and the lower the coverage. On the pure nickel) 111) surface, the most stable adsorption configuration of carbon is in the threefold (hep) site (lower curve). The upper graph shows that carbon adsorption in threefold sites next to a gold atom is completely unstable (sites B and C), and even the threefold sites that are next-nearest neighbors (sites A and D) to the gold atoms are led to a substantial destabilization of the carbon. From Reference (79).
The discussion of this section has intentionally excluded any mention of the mechanism by which excited oxygen is formed in the discharge. In particular, no reference has been made as to whether the molecules are excited directly by the discharge, or whether excitation arises in secondary reactions of the discharge products. There is some importance attached to this question, since, for example, the studies of Ogryzlo and Arnold24,29,44 assume that O E,4) is formed mainly outside the discharge by the reaction... [Pg.332]

The photolysis of cyclic ketones, in general, results in homolytic cleavage of the carbon-carbon bond adjacent to the carbonyl function. For details of this process, the reader is referred to the review by Srinivasan.425 Included among the photoproducts are certain oxygen heterocycles, formed by cyclization of reactive intermediates. Thus, cleavage in a cyclic /3-diketone, such as tetramethylcyclobutane-1,3-dione or hexamethylcyclohexane-l,3,5-trione [Eq. (110)] is followed by cyclization on the oxygen atom to form a lactone.426,427 y-Lactone formation is also observed on photolysis of 2,2-diphenylindane-l,3-dione [Eq. (Ill)] in ether, and the process is reversible.428... [Pg.114]

The herbicidal activity of 1,1-dimethyl-4,4 -dimethylbipyridylium dication ( Paraquat ) seems to depend on the formation of the cation radical through reaction with a component of photosystem 1 in the chloroplast, followed by reaction with oxygen to form superoxide ion (Eq, 36) (for a summary of references, see >). The rate constant for the latter reaction has been reported... [Pg.157]

Unfortunately, there is no reference structure free of cations, though perhaps a faujasite-type framework containing only Si02 ultimately will be synthesized. The dehydrated H-faujasite produced by heating ammonium-exchanged faujasite (48) is the closest to a cation-free fauja-site, but even it has protons condensed with framework oxygens to form hydroxyls. [Pg.182]

Since 03 constitutes the vast majority of total 0, a change in the abundance of O is usually just referred to as a change in 03. Two molecules of odd oxygen are formed on photolysis of 02, and two molecules of odd oxygen are consumed in reaction 4. [Pg.146]

In most cases, radical A will react very rapidly (to begin the propagation phase of autoxidation) with molecular oxygen, to form a new radical AOO, commonly referred to as a peroxy radical. In the case of carbon-centered radicals, this step is extremely fast (usually approximating diffusion control). [Pg.222]

When the alcohol in wine changes into vinegar, there are two processes involved. The first one is relatively minor. Ethanol, the alcohol of beverages, reacts with oxygen to form acetic acid, a dilute solution of which we refer to as vinegar. This happens only to a very small extent, because the wine doesn t come into contact with much oxygen. What really causes wine to turn to vinegar is contamination with a bacteria called Acetobacter aceti. [Pg.17]

We need to digress briefly to examine the structures of some of the ions that are formed by the condensation of the nesosilicate ion, SiO/" (the word neso is from the Greek nesogaean meaning island. The nesosilicates are sometimes also referred to as insular silicates). Two SiOA ions can combine by sharing one oxygen to form the sorosUicate ion. This ion is shown below with two tetrahedra joined by one comer. [Pg.108]

Oxygen ligands form very stable complexes with hard Lewis-acid met-alloporphyrins such as Sn(IV), Zr(IV), Mn(III), Mo(V), but also with P(V)-porphyrins. Mixed-metal dimers were synthesized from Al(Me)OEP and phosphorus, arsenic or antimony porphyrins in the form of fi-oxo dimers [73]. hi most cases, polymeric structures are obtained because Sn(IV)-, Mn(III)- and Fe(III)-porphyrins can bind two axial ligands on either side of the porphyrin referred to as trans-binding. This is schematically represented in Fig. 25a. An example includes the linear trinuclear or polymers /r-frans-dioxo-MoTPP [74,75]. [Pg.27]


See other pages where Oxygen reference form is mentioned: [Pg.145]    [Pg.127]    [Pg.72]    [Pg.20]    [Pg.1]    [Pg.104]    [Pg.132]    [Pg.213]    [Pg.65]    [Pg.57]    [Pg.4404]    [Pg.197]    [Pg.26]    [Pg.960]    [Pg.535]    [Pg.215]    [Pg.826]    [Pg.128]    [Pg.282]    [Pg.159]    [Pg.156]    [Pg.135]    [Pg.554]    [Pg.178]    [Pg.440]    [Pg.369]    [Pg.208]    [Pg.367]    [Pg.201]    [Pg.420]    [Pg.166]    [Pg.4403]    [Pg.456]    [Pg.210]    [Pg.82]    [Pg.372]    [Pg.539]   
See also in sourсe #XX -- [ Pg.246 ]




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Oxygen forms

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