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Inert component

Assuming that the presence of inert components increases the total number of moles N, and since  [Pg.564]

An increase in, say, the initial number of moles of component A would increase and, consequently, and i.e. the equilibrium conversion. While this is often the case, notice that the increase in will also effect N and, depending on the value of v, it could have an adverse effect on the equilibrium conversion (see Problem 15.19). [Pg.565]

The effect of temperature on the equilibrium conversion has been demonstrated in Example 15.6. In the following Examples, 15.7 and 15.8, we demonstrate the effect of pressure and inerts respectively. [Pg.565]


Dissected Number Mixture Combustible Components Species % Inert Components C02,% N2,% Total, % Ratio of Inert to Combustible Lower Limit % Upper Limit % Source of Limit... [Pg.280]

In cases where the reactants involved are not present in the proper stoichiometric ratios, the limiting reactant will have to be determined and the excess amounts of the other reactants calculated. It is safe to assume that unconsumed reactants and inert components exit with the products in their original forms. Consider the following example. [Pg.372]

Cy = concentration of inert components in a phase, mol/m p = partial pressure of component A in gas phase, kPa Py = partial pressure of inert components in gas phase, kPa... [Pg.475]

If a gas stream contains inert components and the MESG is estimated rising the combination formula in NEPA 497, the result will be selection of an arrester element having larger openings than would be required for the flammable components alone. Eor example, a propane-type rather than an ethylene-type arrester might be... [Pg.101]

As well as phosphorus ligands, heterocyclic carbenes ligands 10 have proven to be interesting donor ligands for stabilization of transition metal complexes (especially palladium) in ionic liquids. The imidazolium cation is usually presumed to be a simple inert component of the solvent system. However, the proton on the carbon atom at position 2 in the imidazolium is acidic and this carbon atom can be depro-tonated by, for example, basic ligands of the metal complex, to form carbenes (Scheme 5.3-2). [Pg.269]

In the present study, we carried out the hydrogenation of CO2. We did not use any inert components in the feed. We changed the value of r by changing the molar ratio of H2 to CO2 in the feed gases, a. The parameter p is defined as the volume ratio of the product gas to the reactant gas when the reaction completely proceeds under a constant pressure. The extent of the gas-volume reduction is affected by the stoichiometric relation of the reaction and the content of the inert components in the feed. As given in Eq.(l), p is the function of only the parameter a and the expression of p is affected by a. When a > 4, the limiting reactant is H2, while it is CO2 in the case of a < 4. [Pg.498]

The gas reacts over the ammonia catalyst in an exothermic process at 450-500 °C, leading to an exit concentration of ammonia of about 15-19%. The ammonia is extracted by condensation and the unreacted gas recycled to the reactor. A fraction is purged to prevent the accumulation of inert components. The ammonia condensation is not complete, meaning that the real inlet gas of the reactor already contains several percent of ammonia. [Pg.330]

Adsorption of other components of the system. This includes components taking part in the electrode reaction as well as inert components not taking part (see Section 10.2 about adsorption processes). [Pg.147]

Many electrochemical phenomena and processes are to a great extent influenced by different adsorption processes. Of prime importance is the adsorption on the electrode s surface of components of the electrolyte solution, as well of those participating in the electrode reaction, as those inert components that do not participate. [Pg.156]

It is usually necessary to bleed off a portion of a recycle stream to prevent the build-up of unwanted material. For example, if a reactor feed contains inert components that are not... [Pg.52]

Conversion is not usually very dependent on the concentration of any inert components. The pseudo fresh feeds of the products formed in the reactor can be calculated from the specified, or estimated, yields for the process. [Pg.185]

Korovin N.V., Kicheev A.G. Luzhin V.K. Influence of the inert component on mass-transfer in the gas phase of porous electrode. Russian Electrochemistry. 1972 .8 146 -49. [Pg.170]

A product of this type will have over 50% of its weight derived from maleic anhydride. This very high content of reactive double bonds will lead to a very brittle solid when it is cross-linked with styrene. Without further modification, this solid material will have very high tensile moduli, probably over 600 kpsi, but a very low tensile elongation, way below 1 %. Such a brittle material obviously has only very limited applications. Thus, for most general-purpose applications, it is necessary to incorporate some chemically inert components to soften the polymer backbone. This will reduce the cross-linking density and improve the physical properties of the cured solid. [Pg.702]

The critical data and values used for inert components were those given by Ambrose (24). The interaction parameters between the water and the inert component were found by performing a dew-point calculation as described above but with the interaction parameter k.. rather than P taken as the iteration variable. [Pg.421]

A peculiarity of the processes described in the patents is that all of them use isobutane-rich conditions, with isobutane-to-dioxygen molar ratios between 2 (for processes that include a relatively low concentration of inert components) and 0.8, and so closer to the stoichiometric value 0.5 (for those processes where a large amount of inert components is present). This is shown in Figure 14.1, which reports in a triangular diagram the feed composition claimed by the various companies, with reference to the flammability area at room temperature. Low isobutane conversions are achieved in all cases, and recirculation of unconverted isobutane becomes a compulsory choice. For this reason, Sumitomo claimed the oxidation of CO to CO2 (contained in the effluents from the oxidation reactor) in... [Pg.268]

Remark 5. Note that the composition of M can be deduced from Eq.(16), so in this case, even with a simple reaction, the presence of inert components gives a mathematical model with six nonlinear differential equations whose numerical analysis and equilibrium points can be difficult to obtain. An analysis of this problem can be found in [16], [17]. [Pg.10]

Figure 22.11. Cellulose is a structural and rather chemically inert component of terrestrial plants. Alginic acid is synthesized by marine algae and has medicinal properties. Some polysaccharides contain nitrogen in the form of amino sugars. The primary example of this is chitin, which composes the exoskeletons of Crustacea. An amino sugar contains an amine in place of a hydroxyl group. In other polysaccharides, sugars combine with lipids and proteins. These form glycoUpids and glycoproteins, respectively. Figure 22.11. Cellulose is a structural and rather chemically inert component of terrestrial plants. Alginic acid is synthesized by marine algae and has medicinal properties. Some polysaccharides contain nitrogen in the form of amino sugars. The primary example of this is chitin, which composes the exoskeletons of Crustacea. An amino sugar contains an amine in place of a hydroxyl group. In other polysaccharides, sugars combine with lipids and proteins. These form glycoUpids and glycoproteins, respectively.
In this case it is assumed that a pure gas A is being absorbed in a solvent eontaining a chemically inert component B. Both the solvent and B are not volatile and the fraction of A in the liquid bulk equals zero. The binary mass transfer coefficient Kij between A and the solvent in eq. (4) is given a typical value of 1 X lO" m/s, whereas the total concentration of the liquid Cr is set to 1 x 10 mol/m, also a typical value. Parameters to be chosen are the solubility of A, x i, the fraction of B in the solvent Xg, the mass transfer coefficient between A and B, K/ g and the mass transfer coefficient between B and the solvent, Kg. The results of the calculations are presented in Table 1. Since both the solvent and component B possess a zero flux. Kgs has no influence on the mass transfer process and has therefore been omitted. The computed absorption rate has been compared with the absorption rate obtained from analytical solutions for the following cases. [Pg.5]

In this case a pure gas is assumed to absorb in a solvent containing a chemically inert component B, where the following chemical reaction takes place in the solvent ... [Pg.9]

One such method can be the separation of the catalyst and products (plus unreacted starting material and inert components of the feed) by extraction. [Pg.132]

The reference snbstance method is based on the addition to the solntion, containing the species for which the transfer rate is going to be investigated, of another inert component for which the rate of extraction is known to be controlled only by diffnsion. By following the simultaneous transfer of the species of interest and of the reference component as function of the hydro-dynamic conditions in the extraction apparatns, a diffusional regime will be indicated by a similar functional dependence, whereas a kinetic regime is indicated by a sharply different one. [Pg.230]

The factor [B] im/[M], the logarithmic mean concentration of the inert component B divided by the total concentration, allows for the fact that the concentration of B may alter significantly. [Pg.38]


See other pages where Inert component is mentioned: [Pg.530]    [Pg.470]    [Pg.232]    [Pg.465]    [Pg.749]    [Pg.290]    [Pg.101]    [Pg.183]    [Pg.380]    [Pg.354]    [Pg.23]    [Pg.608]    [Pg.92]    [Pg.721]    [Pg.162]    [Pg.101]    [Pg.1095]    [Pg.147]    [Pg.641]    [Pg.486]    [Pg.418]    [Pg.421]    [Pg.242]    [Pg.9]    [Pg.10]    [Pg.65]    [Pg.35]   
See also in sourсe #XX -- [ Pg.15 ]

See also in sourсe #XX -- [ Pg.6 ]




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Solvate inert component

Solvation inert component

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