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Ternary process

Results. The theory of ternary processes in collision-induced absorption was pioneered by van Kranendonk [402, 400]. He has pointed out the strong cancellations of the contributions arising from the density-dependent part of the pair distribution function (the intermolecular force effect ) and the destructive interference effect of three-body complexes ( cancellation effect ) that leads to a certain feebleness of the theoretical estimates of ternary effects. [Pg.222]

The accumulated mutual neutralization data from the FA experiments together with that available for the ternary recombination process, indicates that binary mutual neutralization is the dominant ionic recombination process above about 30 km in the atmosphere whereas below this altitude the ternary process becomes dominant210. It should be stressed that this generalization is based on dubious ternary recombination data and indeed on mutual neutralization data for moderate-sized clusters only. [Pg.33]

Figure 2.11 shows the ternary process where no B is in the reactor effluent. The size of the reactor and concentrations in the reactor are arbitrary because the consumption of B is independent of these variables, We assume that the separation section consists of a single distillation column. If A is more volatile than C. the overhead product from the column is recycled back to the reactor. If the volatilities are reversed, the bottoms from the column is the recycle stream. Figure 2.11 illustrates the first case. [Pg.38]

Figure 2.11 Ternary process with complete one-pass conversion of reactant B. (a) Ratio control structure with fixed reactant feed (unworkable) (i>) reactant makeup control based on component inventory ( workable). Figure 2.11 Ternary process with complete one-pass conversion of reactant B. (a) Ratio control structure with fixed reactant feed (unworkable) (i>) reactant makeup control based on component inventory ( workable).
Figure 2.12 Ternary process flowsheet with incomplete conversion of both reactants and one recycle stream. Figure 2.12 Ternary process flowsheet with incomplete conversion of both reactants and one recycle stream.
Figure 2.13 Ternary process flowsheet with incomplete conversion and two recycle streams (.heavv-out-first sequence . iai Control structure CS4 reactor composition and level control (workable. (61 control structure CS1 reactant makeup control based on component inventories t workable). Figure 2.13 Ternary process flowsheet with incomplete conversion and two recycle streams (.heavv-out-first sequence . iai Control structure CS4 reactor composition and level control (workable. (61 control structure CS1 reactant makeup control based on component inventories t workable).
Figure 2.15 Dynamic response of ternary process with CS2 for change in fixed reactant feed rate, (a 2 percent increase (b) 5 percent increase o 10 percent increase. Figure 2.15 Dynamic response of ternary process with CS2 for change in fixed reactant feed rate, (a 2 percent increase (b) 5 percent increase o 10 percent increase.
Figure 2.17 Steady-state design for ternary process with incomplete conversion and two recycle streams (heavy-out-first sequence),... Figure 2.17 Steady-state design for ternary process with incomplete conversion and two recycle streams (heavy-out-first sequence),...
Since we are dealing with the product of the two reactant concentrations, making them approximately equal is the best way to minimize reactor holdup. Thus steady-state reactor design favors compositions that are somewhat similar. From a dynamic viewpoint, the system can handle disturbances more easily if the concentrations of the two reactants are very different (very small zA and large zs). We saw an indication of this in the ternary process considered earlier. Control structure CS2 worked when the concentration of the limiting reactant wras very low, but failed when the concentration of the limiting reactant was in the 0.15 mole fraction region. [Pg.51]

In an isolated column environment, w e control reflux drum level and base level with two of the manipulated variables available on the column itself. In a plantwide environment, these levels can aiso be controlled by the flowrates of fresh feed streams being introduced into the plant. This is done when these levels reflect the inventories of the component within the plant. The ternary process illustrated the scheme in Chap. 2 (Fig. 2.136). The fresh feed makeup streams F0A and Foe are used to control the levels in the second column reflux drum and in the first column base. [Pg.232]

Figure 12.2 Ternary process with single recycle. Figure 12.2 Ternary process with single recycle.
Figure 26 Ternary process diagram of solution for S-L equilibrium at 298K from binary data. Figure 26 Ternary process diagram of solution for S-L equilibrium at 298K from binary data.
Fundamental junctive/disjunctive processes involving interactions between two or three fundamental simplexes vide infra) are described as binary and ternary processes, respectively. A given process - be it binary or ternary- is either simple or complex. The junctive process is simple, if only junctive or disjunctive components are present it is complex, if jimctive and disjunctive components are both present vide infra). [Pg.4]

Simplex Combination Binary Process Simplex Combination Ternary Process... [Pg.36]

The FWHM of the gas pulse is 5 ms and, within 20 ms, the number density drops with a fast time constant of 3.5 ms by 2 orders of magnitude. The subsequent decay has a larger time constant of 23 ms however, in most cases the rates of ternary processes involving the buffer gas atoms are negligible after 100 ms. [Pg.147]


See other pages where Ternary process is mentioned: [Pg.244]    [Pg.32]    [Pg.32]    [Pg.71]    [Pg.5]    [Pg.35]    [Pg.35]    [Pg.372]    [Pg.207]    [Pg.19]   
See also in sourсe #XX -- [ Pg.35 ]




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