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Hydrogen Reactant

TABLE 14.2 Chemical Properties of Hydrogen Reactant Reaction with hydrogen ... [Pg.707]

Fig. 12. Variation with average platinum particle diameter of the initial rate of reaction (isomerization plus dehydrocyclization) of n-hexane (- -) and 2-methylpentane (-O-) over ultrathin film catalysts at 275°C. Hydrogen/reactant hydrocarbon, 10/1 total reactant pressure 100 Torr. Fig. 12. Variation with average platinum particle diameter of the initial rate of reaction (isomerization plus dehydrocyclization) of n-hexane (- -) and 2-methylpentane (-O-) over ultrathin film catalysts at 275°C. Hydrogen/reactant hydrocarbon, 10/1 total reactant pressure 100 Torr.
For every mole of nitrogen reactant, a chemist expects 2 moles of ammonia product. Similarly, for every 3 moles of hydrogen reactant, the chemist expects 2 moles of ammonia product. These expectations are based on the coefficients of the balanced equation and are expressed as mole-mole conversion factors as shown in Figure 9-1. [Pg.130]

What type of nuclear reaction is shown in the following equation How do you know Where might such a reaction take place There s something atypical about the two hydrogen reactants. What is it ... [Pg.278]

This reaction is a fusion reaction. It shows two light nuclei combining to form one heavy nucleus. This reaction fuels the sun. The two hydrogen reactants are atypical because they re rare isotopes of hydrogen, called tritium and deuterium, respectively. [Pg.280]

The individual mass transfer and reaction steps occurring in a gas-liquid-solid reactor may be distinguished as shown in Fig. 4.15. As in the case of gas-liquid reactors, the description will be based on the film theory of mass transfer. For simplicity, the gas phase will be considered to consist of just the pure reactant A, with a second reactant B present in the liquid phase only. The case of hydro-desulphurisation by hydrogen (reactant A) reacting with an involatile sulphur compound (reactant B) can be taken as an illustration, applicable up to the stage where the product H2S starts to build up in the gas phase. (If the gas phase were not pure reactant, an additional gas-film resistance would need to be introduced, but for most three-phase reactors gas-film resistance, if not negligible, is likely to be small compared with the other resistances involved.) The reaction proceeds as follows ... [Pg.230]

In general, for a trickle-bed reactor, a material balance is required for each of the components present, taken over each of the gas and liquid phases. In the example, however, pure hydrogen will be used and the volatility of the other components will be assumed to be sufficiently low that they do not enter the vapour phase. This means that the material balance on the gas phase can be omitted. It also means that there will be no gas-fllm resistance to gas-liquid mass transfer. In the liquid phase, material balances are required for (i) the hydrogen (reactant A), and (ii) the thiophene (reactant B). The amounts of each of the reactants consumed will be linked by the stoichiometric equation ... [Pg.242]

Table 5.1 shows an application of XPS to the study of the promoted iron catalyst used in the Haber synthesis of ammonia. The sizes of the various electron intensity peaks allows a modest level of quantitative analysis. This catalyst is prepared by sintering an iron oxide, such as magnetite (Fe304) with small amounts of potassium nitrate, calcium carbonate, aluminium oxide and other trace elements at about 1900 K. The unreduced solid produced on cooling is a mixture of oxides. On exposure to the nitrogen-hydrogen reactant gas mixture in the Haber process, the catalyst is converted to its operative, reduced form containing metallic iron. As shown in Table 5.1, the elemental components of the catalyst exhibit surface enrichment or depletion, and the extent of this differs between unreduced and reduced forms. [Pg.140]

Recently, it has also been proposed (36) that desorption of the branched carbenium ion can also occur by H species formed by dissociation of the hydrogen reactant on the Pt centers and its diffusion to the acid sites by a hydrogen spillover mechanism ... [Pg.37]

INS spectroscopy has been applied to characterising hydroxo and aquo components of oxide catalysts and adsorbed hydrogenous reactant molecules and intermediates. The INS spectra are complementary to infrared and Raman spectra, which have been used widely in the study of oxide catalysts. In an INS spectrum background scattering from an oxide is weak and can be subtracted from the spectrum the lower energy region (below 600 cm" ) is readily accessible. For an introduction to industrial applications of oxide catalysts see [91]. [Pg.330]

II) This Increases the concentration of hydrogen reactant. Therefore the equilibrium concentration of ethane Increases is unaffected. [Pg.444]

Figure 3.14 Yield of products in the oxidation of propylene at 373 K, propane at 393 K and isobutane at 393 K on 1.20wt% Au/Ti- MCM-41 Ti/Si = 2.8 100) in the presence of oxygen and hydrogen. Reactant gas, C3H6 (or alkane)/02/H2/Ar= 1 1 1 7 space velocity, 4000mL h gcat [122]. Figure 3.14 Yield of products in the oxidation of propylene at 373 K, propane at 393 K and isobutane at 393 K on 1.20wt% Au/Ti- MCM-41 Ti/Si = 2.8 100) in the presence of oxygen and hydrogen. Reactant gas, C3H6 (or alkane)/02/H2/Ar= 1 1 1 7 space velocity, 4000mL h gcat [122].
Aran et al. [5, 21, 30] used porous AI2O3 and stainless steel hollow fiber MMRs for the removal of nitrite (N02 ) from water by the catalytic hydrogenation reaction over Pd catalysts, where the aqueous solution of N02 was pumped into the lumen while the gaseous hydrogen reactant was delivered to the shell side of the reactor. The nitrite... [Pg.243]


See other pages where Hydrogen Reactant is mentioned: [Pg.500]    [Pg.420]    [Pg.53]    [Pg.315]    [Pg.98]    [Pg.53]    [Pg.596]    [Pg.586]    [Pg.3058]    [Pg.3]    [Pg.305]    [Pg.122]    [Pg.127]    [Pg.151]    [Pg.214]    [Pg.283]    [Pg.134]    [Pg.599]   


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