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Overall Solution

The intersection of the curve and the straight line is the only point at which die reactor energy balance, the design equation, and the F/P exchanger energy balance are satisfied simultaneously. The point of intersection gives the values of xaCZ) and T 2) that result from a specified value of Tin. [Pg.291]


Furthemiore, we must have = 0 since the overall solution is electroneutral. Finally we end up with... [Pg.576]

To prevent the further generation of mixed wastes, decontamination methods should be chosen carefully and implemented to be part of the overall solutions and not part of the cleanup [2]. [Pg.152]

For different regions in the flow field in front of an expanding piston, separate solutions in the form of asymptotic expansions may be developed. An overall solution can be constructed by matching these separate solutions. This mathematical technique was employed by several authors including Guirao et al. (1976), Gorev and Bystrov (1985), Deshaies and Clavin (1979), Cambray and Deshaies (1978), and Cambray et al. (1979). [Pg.101]

Once-through boilers may be either sub- or super-critical. Sub-critical boilers are clearly at some potential risk of on-load corrosion owing to the presence of the evaporator zone. Measures aimed at avoiding on-load corrosion include—keeping the overall solute concentration low, keeping the ionic balance matched, and maintaining the waterside oxide suitably thin. With super-critical plant, there is no chance of on-load corrosion whilst it is operating in the super-critical mode, as there is no phase boundary. The risk is present, however, when the plant is run in the sub-critical mode, as all super-critical plant must be at times. [Pg.849]

The overall solution is based on the method of lines discussed in Chapter 8. The resulting DDEs can then be solved by any convenient method. Appendix 13.2 gives an Excel macro that solves the DDEs using Euler s method. Figure 13.9 shows the behavior of the streamlines. [Pg.501]

The chemistry of [Rh(OEP)h in benzene is dominated by Rh—Rh bond homolysis to give the reactive Rh(Il) radical Rh(OEP)-. This contrasts with the reactivity of fRh(OEP)] in pyridine, which promotes disproportionation via the formation of the thermodynamically favorable Rh(IlI). ct complex [RhjOEPKpy) ] together with the Rh(l) anion, Rh(OEP)J The hydride complex Rh(OEP)H shows NMR chemical shift changes in pyridine consistent with coordination of pyridine, forming Rh(OEP)H(py). Overall, solutions of Rh(OEP)l in pyridine behave as an equimolar mixture of [Rh(OEP)(py ) and (Rh(OEP). For example, reaction... [Pg.306]

For any aqueous strong base, the hydroxide ion concentration can be calculated directly from the overall solution molarity. As is the case for aqueous strong acids, the hydronium and hydroxide ion concentrations are linked through the water equilibrium, as shown by Example. ... [Pg.1212]

Confirm that the overall solute balance is satisfied at steady state. [Pg.550]

Check the steady-state overall solute balances. [Pg.555]

The idea of the new approach is to, first, define only one model that includes all constraints - be it shift models, personnel, batch sizes, maximum perishabilities or soft constraints such as costs and values, characteristic numbers or feasibility and optimum of the plan. The case studies will show that the model follows an intuitive representation of the relevant items. Second, the operator based approach makes the overall solution procedure extensible. If one operator gets stuck in a local optimum another operator may help out and could be added at any time. Third, the whole approach works on understandable objects such that at any time during the solution procedure an easy check can be made what happens. [Pg.62]

The quant-based combinatorial optimization is a new approach. It supports the simultaneous planning and optimization of complex production problems. The solution procedure is built with operators which may be applied in any sequence allowing integrated BOM explosion and scheduling. The overall solution procedure may be extended at any time by simply adding new operators [20, 21],... [Pg.89]

In Heidemann and Khalil (14) additional detail is given about numerical procedures which were found effective in solving these equations. The overall solution strategy, as described above, requires nested one-dimensional searches the critical volume is found by solving (23), but at each volume (16) must be solved for the temperature. The multiplier (T/100) in each term of the matrix Q and the multiplier [(v-b)/2bj 2 in the cubic form were introduced to improve the behavior of the numerical methods. [Pg.383]

The use of dilute polymer solutions for molecular weight measurements requires the macromolecules to be in a true solution, i.e., dispersed on a molecular level. This state may not be realized in certain instances because stable, multimolecular aggregates may persist under the conditions of "solution" preparation. In such cases, a dynamic equilibrium between clustered and isolated polymer molecules is not expected to be approached and the concentration and size of aggregates are little affected by the overall solute concentration. A pronounced effect of the thermal history of the solution is often noted under such conditions. [Pg.273]

The thickness of a partially solidified zone (mushy region) in zone refining under most experimental conditions has been determined. The transfer of solute within this zone is, no doubt, most important in determining the overall solute transfer. All the zone refining theories have failed to take this most important factor into account. [Pg.245]

Monomer—Micelle Equilibria. The distribution of surfactant components between micelles and monomeric state in aqueous solutions depends on surfactant structures as well as on overall solution composition. For example, for a binary system of surfactants A and B in solution, the micelle may contain SO mole % A/SO X B while the monomer may be 90 /. A/10 X B. Since either the monomer or the micelle composition may be crucial to behavior of the system, the ability to predict the relative distribution of surfactant components between monomer and micelle, given the overall solution composition, is an important one. [Pg.5]

NOTE Some original target compounds (see Table I) are not included because of inconsistent or incomplete data. Corrections for losses to adsorption have been factored into these calculations of overall solute recovery. a Sum = Mf + Mads + Mp + Mf. [Pg.446]

Figure 7.4 gives a flow diagram for the overall solution procedure. It starts with solving the reactor initial value differential equation (7.19) for ys, followed by substituting yB into the equations (7.16) and (7.18) to obtain xab and xbb, then solving equation (7.24) to obtain y and then xa and xb from (7.21) and (7.22), and finally obtaining y from equation (7.23). [Pg.434]


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