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Ammonia synthesis limiting reactant

A molecular view of a limiting reactant situation for the ammonia synthesis. To make 4 molecules of INH3 and 6 molecules of... [Pg.219]

To solve a quantitative limiting reactant problem, we identify the limiting reactant by working with amounts in moles and the stoichiometric coefficients from the balanced equation. For the ammonia synthesis, if we start with 84.0 g of molecular nitrogen and 24.2 g of molecular hydrogen, what mass of ammonia can be prepared First, convert from... [Pg.219]

We will list the elementary steps and decide which is rate-limiting and which are in quasi-equilibrium. For ammonia synthesis a consensus exists that the dissociation of N2 is the rate-limiting step, and we shall make this assumption here. With quasi-equilibrium steps the differential equation, together with equilibrium condition, leads to an expression for the coverage of species involved in terms of the partial pressures of reactants, equilibrium constants and the coverage of other intermediates. [Pg.291]

A frequent reason for the dependence of catalyst structure on the chemical potential in the gas phase containing all the reactants is the incorporation of molecules or atoms from the reaction mixture into the catalyst phases. Formation of subphases, often only in the near-surface region of the solid, fails to create phases with individual reflections but modifies the reflections of the starting precatalyst phase notably (see previous sections). This complication presents a massive problem in the analysis of working catalysts when significant partial pressures of products are important to the phase formation and when the necessary conversions cannot be reached in the experimental cell. The investigation of ammonia synthesis catalysts when insufficient partial pressures of the product ammonia prevent the formation of the relevant nitride phases is a prominent example of this limitation (Herzog et al., 1996 Walker et al., 1989). [Pg.307]

To further explore the idea of a limiting reactant, consider the ammonia synthesis reaction ... [Pg.72]

Since the ammonia synthesis reaction is limited by equilibrium, another obvious idea is to separate ammonia directly from its reactants - hydrogen and nitrogen for example in a membrane system. Several polymeric materials have been proposed that can separate ammonia from hydrogen and nitrogen (59), however, such polymers are characterised by low selectivity and low permeability for ammonia, and they have poor thermal stability as well. [Pg.35]

Ammonia-synthesis reactions are also frequently limited by the accumulation of inerts in their reactor systems. Argon, arriving with the nitrogen reactant from air, and methane, arriving with the hydrogen, accumulate as inerts within the ammo-... [Pg.137]

An industrial synthesis of urea obtains 87.5 kg of urea upon reaction of 68.2 kg of ammonia with 105 kg of carbon dioxide. Determine the limiting reactant, theo-rehcal yield of urea, and percent yield for the reaction. [Pg.281]

The platinum group metals demonstrate clearly the impact of the key parameters that influence the efficiency of ammonia synthesis catalysts structure sensitivity, the heat of adsorption of reactants and products, and the roles of promoters and supports. The key requirement to minimize the activation energy for nitrogen dissociation limits the active metals to alkali-promoted ruthenium and osmium. Similar activities are then obtained, irrespective of the genesis of the alkali metal promoter (salt or metal), indicating that both convert to a similar... [Pg.348]

The initial alcohol/amine ratio can determine the product distribution. In the synthesis of primary amines a rather high ammonia/alcohol molar ratio (up to 10-25), and usually high pressure, are required to compensate for the low reactivity of ammonia and suppress the formation of secondary amines. Selectivity for primary diamines could be improved in the amination of 1,3-dihydroxy compounds when using supercritical ammonia as solvent and reactant in a continuous fixed-bed reactor [12]. The remarkable changes in selectivity in the near-critical region (100-110 bar) are attributed to the increased concentration of ammonia on the metal surface as a result of elimination of mass-transport limitations in the two-phase system, and to suppression of hydrogenolysis and water elimination reactions which lead to monofunctional by-products. An example is shown in Figure 1. [Pg.249]

There are few reports of successful one-step synthesis of primary diamines, and the examples are limited to amines with a special structure. Amination of 1,4-cy-clohexanediol in supercritical ammonia (135 bar) over a Co-Fe catalyst alforded 67 % 1,4-diaminocyclohexane [21]. Excess ammonia, as both supercritical solvent and reactant, and short contact time in the continuous fixed-bed reactor favored the desired reactions. In the best example the cumulative selectivity for the diamine and the intermediate amino alcohol was 97 % at 76 % conversion. Recycling of the unreacted diol and amino alcohol can provide an alternative to the eurrent process, the hydrogenation of pnra-phenylenediamine. The high seleetivity was because of the rigid structure and the relative positions of OH functionality in the substrate. For comparison, amination of 1,4-butanediol under similar conditions yielded pyiTolidine as the major product 1,4-diaminobutane was barely detectable. When 1,3-cyclohexanediol was aminated with the same catalyst in the continuous system, the yield of 1,3-diaminoeyclohexane dropped below 5%, mainly because elimination of water led to undesired monofunctional products via a,/9-unsaturated alcohol, ketone, and/or amine intermediates [22]. [Pg.253]

Only limited work has been reported on microemulsion-mediated synthesis of aluminum hydroxide [44,45]. In the two publications available [44,45], AOT served as the surfactant. It is possible to form reverse micelles in supercritical fluid media [130], and Matson et al. [44] used such a medium and the microemulsion-plus-reactant technique to synthesize A1(0H)3 particles at 110°C. With supercritical propane as the continuous phase, anhydrous ammonia was injected into the reversed micellar solution containing solubilized Al + [as an aqueous A1(N03)3 solution]. Referring to Fig. 1 and Table 2, the resulting precipitation process followed reaction path AP3 the added ammonia reacted with water molecules in the aqueous pseudophase of the microemulsion to generate hydroxide ions ... [Pg.579]

Since the ammonia reaction is limited by equilibrium with a conversion per pass of reactants of 25 - 35% as mentioned earlier, the synthesis of ammonia takes place in a recycle loop. [Pg.22]

The familiar principle that binary reactions can frequently be used for the detection of either of the reactants is not limited to reactions conducted in liquid media. Recently it has been found that AsgSg or AsgSg are produced when a mixture of elemental arsenic and sulfur is heated at 110° C. The sulfur melts and then reacts. This synthesis of arsenic sulfides followed by treatment with ammonia (formation of ammonium sulfo salts) permits the detection of As or S (see pages 111 and 436). [Pg.21]

The limited carbon dioxide conversion and the huge amounts of the by-product ammonia salt represent major disadvantages with respect to production of pure urea. Thus, once-through urea synthesis processes do not have any significant industrial relevance nowadays. Modified processes have been developed, which allow recycling of the nonconverted reactants, thus increasing overall conversion and yield. [Pg.68]


See other pages where Ammonia synthesis limiting reactant is mentioned: [Pg.118]    [Pg.213]    [Pg.107]    [Pg.284]    [Pg.696]    [Pg.476]    [Pg.55]    [Pg.834]    [Pg.143]    [Pg.153]    [Pg.355]    [Pg.126]    [Pg.1]    [Pg.28]    [Pg.6]    [Pg.364]    [Pg.451]    [Pg.24]    [Pg.594]    [Pg.461]   
See also in sourсe #XX -- [ Pg.74 , Pg.75 ]




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