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Nitric oxide thermodynamic data

The Af-HjO diagrams present the equilibria at various pHs and potentials between the metal, metal ions and solid oxides and hydroxides for systems in which the only reactants are metal, water, and hydrogen and hydroxyl ions a situation that is extremely unlikely to prevail in real solutions that usually contain a variety of electrolytes and non-electrolytes. Thus a solution of pH 1 may be prepared from either hydrochloric, sulphuric, nitric or perchloric acids, and in each case a different anion will be introduced into the solution with the consequent possibility of the formation of species other than those predicted in the Af-HjO system. In general, anions that form soluble complexes will tend to extend the zones of corrosion, whereas anions that form insoluble compounds will tend to extend the zone of passivity. However, provided the relevant thermodynamic data are aveiil-able, the effect of these anions can be incorporated into the diagram, and diagrams of the type Af-HjO-A" are available in Cebelcor reports and in the published literature. [Pg.68]

From the thermodynamic data of Appendix C, show that the product of the reaction of ammonia gas with oxygen would be nitrogen, rather than nitric oxide, under standard conditions and in the absence of kinetic control by, for example, specific catalysis of NO formation by platinum. (Assume the other product to be water vapor.)... [Pg.189]

According to these data the heat of activation for the decomposition of nitric oxide, to which reaction the factor k refers, is A = 82 10 kcal/mole.10 It should be especially noted that there is no systematic divergence between the data on the formation and on the decomposition of nitric oxide this fact justifies the assumption that the rate of decomposition is directly proportional to the square of the nitric oxide concentration.11 The investigation covered the temperature range from 2000°K to 2900°K in which the rate varies by a factor of 300. As appears from Fig. 13, except for the scattering due to the inevitable errors of the experiments and computations, the points actually do fall on a straight line in the coordinates lg kr, 1/Tm, i.e., the Arrhenius temperature dependence of the reaction rate holds. The thermodynamic relation between the rates of the direct and reverse reactions permits determining the heat of activation A for the formation of nitric... [Pg.382]

A combination of UV—vis spectroscopy and electrochemical detection of nitric oxide enabled to determine the overall equifibrium constant for the reversible binding of NO to [Ru (edta)H20] (87). The obtained experimental value for the equifibrium constant (9x10 at 25 °C) is in fine with that calculated on the basis of a Bom—Haber-type cycle using the electrochemical and thermodynamic data for the [Ru (edta)H20] and... [Pg.213]

In a new case in PRO/II, the components involved are selected ammonia, oxygen, nitric oxide, and water. From the Thermodynamic Data in the toolbar, Peng-Robinson EOS is selected from the Most Commonly Used property calculation system. The Conversion Reactor is selected from the palettes in the PFD. A feed... [Pg.129]


See other pages where Nitric oxide thermodynamic data is mentioned: [Pg.73]    [Pg.415]    [Pg.217]    [Pg.128]    [Pg.106]    [Pg.927]    [Pg.927]    [Pg.14]    [Pg.450]    [Pg.7072]   
See also in sourсe #XX -- [ Pg.264 ]




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