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Region solution branch

In Fig. 4.3.3b we present a V — I curve with a turning point and a negative differential resistance region with current saturation, computed for the same values of parameters Ni, A, cq as in Fig. 4.3.3a. This V—I curve corresponds to the upper and the middle solution branches. The range of parameters in which the high current solutions exist is again evaluated below, via an asymptotic treatment for /— oo. [Pg.119]

A process model of any chemical process system is given by a system of differential-algebraic equations, which depend on some parameters. The steady state solution branches can be traced out in the parameter space. An exemplary situation is shown in Fig. 10.1 where some norm of the steady states x is plotted above the plane spanned by two selected parameters and py In the triangular shaped region in the parameter space, three steady states can coexist for the same set of para-... [Pg.242]

Some data files that are typically shared, especially in regionalized or multilocation companies, include customer hies, employee hies, and inventory hies. Distributed data access is even more of a concern when the users sharing the data are beyond the reach of a local area network and must share the data via wide area networking solutions. A good starting point for the network analyst might be to ask the question Has anyone done a comparison of the forms that are used in the various regional and branch offices to determine which data needs to be sent across the network ... [Pg.2126]

Further, we will briefly comment other interesting works in this area. Pushpavanam Kienle [16] studied the reaction A- P in a non-isothermal CSTR / Separation / Recycle process. Assuming infinite activation energy and equal eoolant and reactor-inlet temperatures, they reported state multiplicity, isolated solution branches and instability, for both conventional and fixed-recycle control structures. In addition, the conventional structure showed regions of unfeasibility. The authors claimed the superiority of the fixed-recycle control structure over the fixed-fresh flow rate control. [Pg.415]

Dendrimers have distinctive properties, such as the ability to entrap small molecules in their core region and very low intrinsic viscosities in solution. Such properties require molecules to have achieved a particular size, and not all molecules with branches radiating from a core are large enough to develop the characteristic properties of true dendrimers. Branched molecules below this critical size are called dendrons and are the equivalent in dendrimer chemistry of oligomers in polymer chemistry. [Pg.130]

Relationships between dilute solution viscosity and MW have been determined for many hyperbranched systems and the Mark-Houwink constant typically varies between 0.5 and 0.2, depending on the DB. In contrast, the exponent is typically in the region of 0.6-0.8 for linear homopolymers in a good solvent with a random coil conformation. The contraction factors [84], g=< g >branched/ <-Rg >iinear. =[ l]branched/[ l]iinear. are another Way of cxprcssing the compact structure of branched polymers. Experimentally, g is computed from the intrinsic viscosity ratio at constant MW. The contraction factor can be expressed as the averaged value over the MWD or as a continuous fraction of MW. [Pg.15]

Fig. 9. Potentiometric titration curves for branched PAAs obtained by SCVCP of f-BuA with the inimer 1, followed by hydrolysis y=100 (O), 10 (A), 2.5 ( , ) in aqueous solutions. The filled symbols ( ) indicate the region where PAA was insoluble in water. (Reproduced with permission from [31], Copyright 2001 American Chemical Society.)... Fig. 9. Potentiometric titration curves for branched PAAs obtained by SCVCP of f-BuA with the inimer 1, followed by hydrolysis y=100 (O), 10 (A), 2.5 ( , ) in aqueous solutions. The filled symbols ( ) indicate the region where PAA was insoluble in water. (Reproduced with permission from [31], Copyright 2001 American Chemical Society.)...
At node l,y2 is the only fractional variable, and hence any feasible integer solution must satisfy either y2 = 0 ory2 = L We create two new relaxations represented by nodes 2 and 3 by imposing these two integer constraints. The process of creating these two relaxed subproblems is called branching. The feasible regions of these two LPs are... [Pg.355]

Nj,=N/f is the number of beads per branch or arm). For larger chains, however, the solvent can penetrate in outer regions of the star and the situation within these regions is more Hke a concentrated solution or a semi-dilute solution. These portions of the arms constitute a series of blobs, whose sizes increase in the direction of the arm end. The surface of a sphere of radius r from the star center is occupied by f blobs. Then the blob size is proportional to rf. Most internal blobs are placed in conditions similar to concentrated solutions and, consequently, their squared size is proportional to the number of polymer units inside them as in an ideal chain. This permits one to obtain the density of units inside the blob, as a function of r ... [Pg.46]

Figures 4 and 5 compare the exact solutions of the kinetic polynomial (51) (i.e. the quasi-steady-state values of reaction rate) to their approximations. Even the first term of series (65) gives the satisfactory approximation of all four branches of the solution (see Figure 4). Figure 5, in which "brackets" from Appendix 2 are compared to the exact solution, illustrates the existence of the region (in this case, the interval of parameter /2), where hypergeometric series converge for each root. Figures 4 and 5 compare the exact solutions of the kinetic polynomial (51) (i.e. the quasi-steady-state values of reaction rate) to their approximations. Even the first term of series (65) gives the satisfactory approximation of all four branches of the solution (see Figure 4). Figure 5, in which "brackets" from Appendix 2 are compared to the exact solution, illustrates the existence of the region (in this case, the interval of parameter /2), where hypergeometric series converge for each root.
Fig. 10. Linear stability diagram illustrating the branching of a new inhomogeneous steady-state solution. The regions (a), (6), (c) are defined as in Fig. 9. A = 2 D, = 1.6 10-3, D2= 8 10 3. The critical mode /a is the integer that gives to B(n) its minimal value Bc. Fig. 10. Linear stability diagram illustrating the branching of a new inhomogeneous steady-state solution. The regions (a), (6), (c) are defined as in Fig. 9. A = 2 D, = 1.6 10-3, D2= 8 10 3. The critical mode /a is the integer that gives to B(n) its minimal value Bc.
When <0, the bifurcation diagram is as in Fig. 13. There exists a subcritical region in which three stable steady-state solutions may coexist simultaneously the thermodynamic branch and two inhomogeneous solutions. It must be pointed out that the latter are necessarily located at a finite distance from the thermodynamic branch. As a result, their evaluation cannot be performed by the methods described here. The existence of these solutions is, however, ensured by the fact that in the limit B->0, only the thermodynamic solution exists whereas for B Bc it can be shown that the amplitude of all steady-state solutions remains bounded. [Pg.14]

In Fig. 21 we have drawn the bifurcation diagram of the fundamental steady-state solutions for three values of p [ Kxn is plotted versus UK) as the bifurcation parameter]. There is a subcritical region in the upper or lower branch, depending on the relative height of the peaks in Fig. 20c. The asymptotes K and K" of these branches correspond to half-period solutions of infinite length. When p 2 the asymptote K merges with the w-axis therefore situation 2 above can be viewed as a particular case of situation 3 above, in which the bifurcation point moves to infinity. [Pg.25]

A nontrivial feature of a silicon electrode in alkaline aqueous solutions is its ability to pass reversibly, under illumination, from the passive state to the active one, and vice versa. For example, suppose that the initial state is actively dissolved silicon under illumination its potential spontaneously and sharply shifts (at a constant current) to more positive values, i.e., into the passive region, and self-dissolution ceases photopassivation occurs (Fig. 20a). In contrast, once silicon has already been anodically passivated, illumination shifts its potential to less positive values (Fig. 20b). In this case, the point on the dashed line, which characterizes the state of the system, passes from the descending branch to the ascending one, and active selfdissolution starts, i.e., photoactivation takes place. [Pg.294]


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Solute region

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