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Equilibrium, chemical characteristics

A change of constant during temperature change is a consequence of enflialpy of process (not equal to zero) and temperature dependence of permittivity. Thus, the change of equilibrium constant with temperature changing depends on both self-chemical equilibrium characteristics (here AH) and solvent characteristics (namely, solvent permittivity influence on equilibrium constant). This is pertinent from Figure 9.23, which shows dependence of equilibrium constant logariflun on reciprocal permittivity (isotherms). Equilibrium constants, obtained experimentally (dotted line a - b) correspond to various values of permittivity. [Pg.558]

In the present work, the technique of XO and MTB immobilization onto silica gel in the form of its complexes with Fe(III) and Bi(III) respectively were found. The acid - base and chemical-analytical characteristics of solid-phase reagents were examined. The optimal conditions of quantitative recovery of Pb(II) and Zn(II) from diluted solutions, such as acidity of aqueous phase, the mass of the sorbents, the volume of solutions and the time of equilibrium reaching, were found. The methods of and F" detenuination were based on a competitive reactions of Zr(IV) with immobilized MTB and or F". Optimal conditions of 0,0 and F" determination in solution using SG, modified ion associates QAS-MTB (pH = 1,5, = 5-10 mol/1). [Pg.334]

Ultrasonic absorption is a so-called stationary method in which a periodic forcing function is used. The forcing function in this case is a sound wave of known frequency. Such a wave propagating through a medium creates a periodically varying pressure difference. (It may also produce a periodic temperature difference.) Now suppose that the system contains a chemical equilibrium that can respond to pressure differences [as a consequence of Eq. (4-28)]. If the sound wave frequency is much lower than I/t, the characteristic frequency of the chemical relaxation (t is the... [Pg.144]

The initial set of experiments and the first few textbook chapters lay down a foundation for the course. The elements of scientific activity are immediately displayed, including the role of uncertainty. The atomic theory, the nature of matter in its various phases, and the mole concept are developed. Then an extended section of the course is devoted to the extraction of important chemical principles from relevant laboratory experience. The principles considered include energy, rate and equilibrium characteristics of chemical reactions, chemical periodicity, and chemical bonding in gases, liquids, and solids. The course concludes with several chapters of descriptive chemistry in which the applicability and worth of the chemical principles developed earlier are seen again and again. [Pg.482]

More concretely, the aim of our investigation is to examine, from a theoretical point of view, the relation between the non-rigidity of pentacoordinate molecules and the characteristics of the temporal evolution of systems of such molecules towards chemical equilibrium. We also want to indicate the type of experimental information needed concerning the time evolution of these systems, in order to sharpen our ideas on the feasibility of the internal movements. We here give an account of the main aspects of our attempt and try to present it in a unified and synthesizing fashion. [Pg.45]

Figure 3.6 shows the equilibrium characteristics for the C-02-H20 reaction system. To favor production of CO and H2 from coal, reactions 3.9 and 3.10 should be carried out at a comparatively low pressure and low temperature. However, during actual production, synthesis of chemicals usually occur at high pressures of CO and H2, and therefore, the gasifier should be operated at high pressure and high temperature to obtain high process efficiency. [Pg.109]

For elementary chemical reactions, it is sometimes possible to assume that all chemical species reach their chemical-equilibrium values much faster than the characteristic time scales of the flow. Thus, in this section, we discuss how the description of a turbulent reacting flow can be greatly simplified in the equilibrium-chemistry limit by reformulating the problem in terms of the mixture-fraction vector. [Pg.196]

The exp-6 potential has also proved successful in modeling chemical equilibrium at the high pressures and temperatures characteristic of detonation. However, to calibrate the parameters for such models, it is necessary to have experimental data for product molecules and mixtures of molecular species at high temperature and pressure. Static compression and sound-speed measurements provide important data for these models. [Pg.165]

Concentration equilibrium among A , A , A , and h is discussed on the assumption that these equations can be treated as chemical equilibrium ones. (Similarly, D", D, (donor levels), and e are regarded as chemical species, see Fig. 1.24(c).) We have a reasonable reason for regarding these species as chemical species. As is well known, the electrical properties of metals and alloys are independent of the concentration of point defects or imperfections existing in their crystals, because the number of electrons or holes in metals or alloys is roughly equal to that of the constituent atoms. For the case of semiconductors or insulators, however, the number of electrons or holes is much lower than that of the constituent atoms and is closely correlated to the concentration of defects. In the latter case, electrons and holes can be considered as kinds of chemical species, for a reason similar to that discussed above for the case of point defects. Let us consider the chemical potential, which is most characteristic of chemical species. Electrochemical potential of electrons is written as... [Pg.44]

Figure 20.5 Physical processes at the air-water interface. For calm (smooth) surfaces the horizontal velocities on both sides of the interface decrease toward the boundary. The turbulent eddies become smaller and disappear completely at the interface (boundary layer characteristics). For rough conditions new surfaces are continuously formed by breaking waves, by air bubbles entrapped in the water, and by water droplets ejected into the air. Generally, these surfaces do not last long enough to reach chemical equilibrium between air and water phase. Figure 20.5 Physical processes at the air-water interface. For calm (smooth) surfaces the horizontal velocities on both sides of the interface decrease toward the boundary. The turbulent eddies become smaller and disappear completely at the interface (boundary layer characteristics). For rough conditions new surfaces are continuously formed by breaking waves, by air bubbles entrapped in the water, and by water droplets ejected into the air. Generally, these surfaces do not last long enough to reach chemical equilibrium between air and water phase.
A most useful characteristic of chemical equilibrium is that all equilibria are satisfied simultaneously. If we know the concentration of I, we can calculate the concentration of Pb2+ by substituting this value into the equilibrium constant expression for Reaction 6-11, regardless of whether there are other reactions involving Pb2+. The concentration of Pb2 that satisfies any one equilibrium must satisfy all equilibria. There can be only one concentration of Pb2 in the solution. [Pg.104]

Since natural waters are generally in a dynamic rather than an equilibrium condition, even the concept of a single oxidation-reduction potential characteristic of the aqueous system cannot be maintained. At best, measurement can reveal an Eh value applicable to a particular system or systems in partial chemical equilibrium and then only if the systems are electrochemically reversible at the electrode surface at a rate that is rapid compared with the electron drain or supply by way of the measuring electrode. Electrochemical reversibility can be characterized... [Pg.285]

The performance of propints is a unique function of the temp of the hot reaction products, their compn and their pressure. The pro-pint bums at constant pressure and forms a set of products which are in thermal and chemical equilibrium with each other. The multiplicity of the reaction products requires that the combustion chamber conditions be calcd from the solution of simultaneous equations of pressure and energy balances. This calcn is best performed by computer, although the manual scheme has been described well by Sutton (Ref 14) and Barr re et al (Ref 10). The chamber conditions determine the condition in the nozzle which in turn characterizes the rocket engine performance in terms of specific impulse and characteristic exhaust velocity... [Pg.687]

The consideration of chemical equilibrium for this mechanism (scheme (6.IX)), has been treated in detail in references [74, 77], where different methods for obtaining the characteristic parameters of the process are proposed. [Pg.460]

When A is positive, the reaction should proceed to the right. When A = 0, chemical equilibrium prevails. Formulated in this way, A suits our perception of chemical affinity perfectly. Another characteristic property is the degree of advancement of reaction , [4]. The chemical reaction velocity and the degree of advancement are related by... [Pg.35]

Application to Simultaneous Phase and Chemical Equilibrium. The single-stage process with simultaneous phase and chemical equilibrium is another application of the inside-out concept where the Newton-Raphson method has been employed in a judicious way in the inside loop. There would appear to be no reaction parameter having characteristics that make it suitable as an outside loop iteration variable in the spirit of the inside-out concept. On the other hand, the chemical equilibrium relationships are simple in form, and do not introduce new thermophysical properties that depend in a complicated way on other variables. Thus it makes sense to include them in the inside loop, and to introduce the reaction extents as a new set of inside loop variables. [Pg.149]

A relevant characteristic of the technology should be the ability to remove the water selectively and continuously in order to shift the chemical equilibrium to full conversion. Because the presence of a liquid water phase will lead to rapid deactivation of the solid catalyst, operating conditions for water-free organic liquid should be found. In addition, the thermodynamic behavior of the reaction mixture is nonideal, particularly with respect to the couple alcohol-water. [Pg.232]

We have mentioned several times that the characteristic of the molecular compounds is that the Van der Waals forces between molecules are small compared to the valence forces holding the atoms together to form a molecule. Thus the substances vaporize at a low temperature, whereas their molecules do not dissociate chemically to any extent except at very high temperatures. For instance, the dissociation H2 = 2H is a typical example of chemical equilibrium, to be handled by the methods... [Pg.413]

A critical characteristic of energetic materials is the Chapman-Jouguet (CJ) state. This describes the chemical equilibrium of the products at the end of the reaction zone of the detonation wave before the isentropic expansion. In the classical ZePdovich-Neumann-Doring (ZND) detonation model, the detonation wave propagates at constant velocity. This velocity is the same as at the CJ point which characterizes the state of reaction products in which the local speed of sound decreases to the detonation velocity as the product gases expand. [Pg.100]

To explore the important characteristics of chemical equilibrium, we will consider the synthesis of ammonia from elemental nitrogen and hydrogen ... [Pg.193]


See other pages where Equilibrium, chemical characteristics is mentioned: [Pg.8]    [Pg.8]    [Pg.1094]    [Pg.78]    [Pg.478]    [Pg.506]    [Pg.257]    [Pg.294]    [Pg.229]    [Pg.112]    [Pg.196]    [Pg.191]    [Pg.241]    [Pg.374]    [Pg.292]    [Pg.307]    [Pg.316]    [Pg.75]    [Pg.490]    [Pg.435]    [Pg.193]    [Pg.218]    [Pg.49]    [Pg.203]   
See also in sourсe #XX -- [ Pg.193 ]




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