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Carbon monoxide discussion

Section 6.13.2 and illustrated in Figure 6.5. The possible inaccuracies of the method were made clear and it was stressed that these are reduced by obtaining term values near to the dissociation limit. Whether this can be done depends very much on the relative dispositions of the various potential curves in a particular molecule and whether electronic transitions between them are allowed. How many ground state vibrational term values can be obtained from an emission spectrum is determined by the Franck-Condon principle. If r c r" then progressions in emission are very short and few term values result but if r is very different from r", as in the A U — system of carbon monoxide discussed in Section 7.2.5.4, long progressions are observed in emission and a more accurate value of Dq can be obtained. [Pg.252]

These two rings are virtually unknown. One German patent report of a 1,2,3-oxadiazetidine was later shown to be a methoxymethyl methylnitrosamine (73TL2671). An ab initio calculation (STO-3G) of the decomposition of nitrosyl cyanide to give nitrogen and carbon monoxide discusses the possibility of a 1,2,3-oxadiazetidine carbene as an intermediate (78AJC2349). [Pg.486]

It should now be clear that diffusional interaction effects cannot occur in binary mixtures or in multicomponent systems where all the cross-coefficients, (/ = 7), vanish. This will be the case in mixtures in which all the binary diffusion coefficients are alike (the system oxygen-nitrogen-carbon monoxide discussed in Example 4.2.1 is a case in point), as well as in mixtures where one component is present in very large excess (see Example 4.2.2). Thus, the first requirement for significant interaction effects is that the cross-coefficients be large compared to the main coefficients That is. [Pg.102]

There has been a general updating of the material in all the chapters the treatment of films at the liquid-air and liquid-solid interfaces has been expanded, particularly in the area of contemporary techniques and that of macromolecular films. The scanning microscopies (tunneling and atomic force) now contribute more prominently. The topic of heterogeneous catalysis has been expanded to include the well-studied case of oxidation of carbon monoxide on metals, and there is now more emphasis on the flexible surface, that is, the restructuring of surfaces when adsorption occurs. New calculational methods are discussed. [Pg.802]

With an atomic number of 28 nickel has the electron conflguration [Ar]4s 3c (ten valence electrons) The 18 electron rule is satisfied by adding to these ten the eight elec Irons from four carbon monoxide ligands A useful point to remember about the 18 electron rule when we discuss some reactions of transition metal complexes is that if the number is less than 18 the metal is considered coordinatively unsaturated and can accept additional ligands... [Pg.608]

Oxo Synthesis. Ad of the synthesis gas reactions discussed to this point are heterogeneous catalytic reactions. The oxo process (qv) is an example of an industriady important class of reactions cataly2ed by homogeneous metal complexes. In the oxo reaction, carbon monoxide and hydrogen add to an olefin to produce an aldehyde with one more carbon atom than the original olefin, eg, for propjiene ... [Pg.166]

The long-term effects of CECs and HCECs leaking into the environment have been discussed. Combustion where aU ceUular plastics can evolve smoke containing carbon monoxide and in certain cases cyanide and other toxic gases from various constituents involved in thein manufacture is also a consideration. [Pg.336]

Butane-Based Fixed-Bed Process Technology. Maleic anhydride is produced by reaction of butane with oxygen using the vanadium phosphoms oxide heterogeneous catalyst discussed earlier. The butane oxidation reaction to produce maleic anhydride is very exothermic. The main reaction by-products are carbon monoxide and carbon dioxide. Stoichiometries and heats of reaction for the three principal reactions are as follows ... [Pg.455]

The solubihty of carbon monoxide in a variety of solvents at 928 K is given in Table 5 (18), and a detailed discussion of the solubiHty of carbon monoxide in water has been provided (19). A compilation of early Hterature values is given (20). [Pg.49]

The U.S. Environmental Protection Agency has established National Ambient Air Quality Standards (NAAQS) for protection of human health and welfare. These standards are defined in terms of concentration and hme span for a specific pollutant for example, the NAAQS for carbon monoxide is 9 ppmV for 8 hr, not to be exceeded more than once per year. For a state or local government to establish compliance with a National Ambient Air Quality Standard, measurements of the actual air quality must be made. To obtain these measurements, state and local governments have established stationary monitoring networks with instrumentation complying with federal specifications, as discussed in Chapter 14. The results of these measurements determine whether a given location is violating the air quality standard. [Pg.216]

Unlike the carbon monoxide measuring instrument discussed above, the Lion Intoximeter 3000 uses an interference filter to produce monochromatic radiation... [Pg.747]

In the following discussion use is made of an equation that has been formulated by the method given earlier in a discussion of the equation for resonance between a single bond and a double bond11 and of the interatomic distances in the carbon monoxide molecule and carbon dioxide molecule.13 The potential function for the bond is assumed to have the form... [Pg.235]

The discussion of electronic energy curves also throws light on such questions as the structure of the carbon monoxide molecule. The empirical study of potential curves obtained from band spectral data has shown18 that for atoms in the first row of the periodic system a double bond leads 18 An account of this work will be published at some future time. [Pg.311]

This chapter is concerned initially with kinetic results and mechanistic interpretations of the CO insertion (Section III) and extrusion (Section IV) reactions. A discussion of the stereochemical data follows (Section V), and a comprehensive survey of these reactions by the triads (Section VI) rounds out the review. Carbon monoxide insertion reactions were discussed in 1967 by Basolo and Pearson (21). Since then they have been mentioned in several reviews (49, 118, 203, inter alios) but have not been treated comprehensively. [Pg.94]

Discuss the range of values that the orders in hydrogen, carbon monoxide and methanol may assume if hydrogen adsorbs more weakly than the other gases. [Pg.417]

In contrast, dissimilation of acetate may take place by reversal of the pathway used by organisms snch as Clostridium thermoaceticum for the synthesis of acetate from COj. In the degradation of acetate, the pathway involves a dismutation in which the methyl group is successively oxidized via methyl THF to COj while the carbonyl group is oxidized via bound carbon monoxide. Snch THF-mediated reactions are of great importance in the anaerobic degradation of pnrines, which is discussed in Chapter 10, Part 1. [Pg.319]

Although knowledge on the biodegradation of these compounds is sparse, a number of them are important in industrial processes. Formation of methylated derivatives may take place in metals and metalloids belonging to groups 15 and 16 of the periodic table, and a few of group 14. These have been discussed in a critical review (Thayer 2002) and in Chapter 3, Part 4, and they have been noted in the context of the bacterial resistance to metals and metalloids. Since carbon monoxide has been considered as an organic compound (Chapter 7, Part 1), it is consistent to make brief comments on metal carbonyls. [Pg.592]

PEMFC)/direct methanol fuel cell (DMFC) cathode limit the available sites for reduction of molecular oxygen. Alternatively, at the anode of a PEMFC or DMFC, the oxidation of water is necessary to produce hydroxyl or oxygen species that participate in oxidation of strongly bound carbon monoxide species. Taylor and co-workers [Taylor et ah, 2007b] have recently reported on a systematic study that examined the potential dependence of water redox reactions over a series of different metal electrode surfaces. For comparison purposes, we will start with a brief discussion of electronic structure studies of water activity with consideration of UHV model systems. [Pg.106]


See other pages where Carbon monoxide discussion is mentioned: [Pg.59]    [Pg.87]    [Pg.348]    [Pg.66]    [Pg.62]    [Pg.441]    [Pg.63]    [Pg.2372]    [Pg.137]    [Pg.277]    [Pg.112]    [Pg.40]    [Pg.132]    [Pg.274]    [Pg.29]    [Pg.38]    [Pg.283]    [Pg.1422]    [Pg.112]    [Pg.579]    [Pg.331]    [Pg.377]    [Pg.686]    [Pg.334]    [Pg.99]    [Pg.118]    [Pg.600]    [Pg.707]    [Pg.35]   
See also in sourсe #XX -- [ Pg.316 ]




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