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Exchangeable components

FIG. 11-36 Heat-exchanger-component nomenclature, (a) Internal-floating-head exchanger (with floating-head hacking device). Type AES. (h) Fixed-tiihe-sheet exchanger. Type BEM. (Standard of Tiihiilar Exchanger Manufacturers Association, 6th ed., 1978. )... [Pg.1066]

This assumes that the gas-solid exchange kinetics at the interface is rapid. When this process affects the exchange kinetics significantly dieii analysis of concentrations layer by layer in die diffused sample is necessaty. This can be done by the use of SIMS (secondary ion mass spectrometry) and the equation used by Kihier, Steele and co-workers for this diffusion study employs a surface exchange component. [Pg.231]

Figure 3-8. Heat exchanger components (continued). (From Tubular Exchanger Manufacturers Association, 1978.)... Figure 3-8. Heat exchanger components (continued). (From Tubular Exchanger Manufacturers Association, 1978.)...
Figure 10-1A. Nomenclature for Heat Exchanger Components. Figures 10-1A-G used by permission Standards of Tubular Exchanger Manufacturers Association, 7 Ed., Fig. N-1.2, 1988. Tubular Exchanger Manufacturers Association, Inc. Figure 10-1A. Nomenclature for Heat Exchanger Components. Figures 10-1A-G used by permission Standards of Tubular Exchanger Manufacturers Association, 7 Ed., Fig. N-1.2, 1988. Tubular Exchanger Manufacturers Association, Inc.
The heat exchanger component of a boiler blowdown, flash steam, and heat recovery system (FSHR). [Pg.735]

The exchange-correlation energy density can be split into two parts exchange component Ex n) and correlation component e Cn). The explicit expression for the exchange component is known from Hartree-Fock theory but the correlation component is known only numerically. Several parametrisations exist for the exchange-correlation energy and potential of a homogeneous gas system which can be used for the LDA calculations within DFT. [Pg.21]

If the basis set is restricted to one pn basis function on each sp2 carbon, if the two-electron integrals ignore all three-center or four-center ones, and if we exclude exchange components, one has the Pariser-Parr-Pople model. If, further, all two-electron integrals are set to zero except for the repulsion between opposite spins on the same site and the one-electron tunneling terms are restricted to nearest neighbors, the result is the Hubbard Hamiltonian... [Pg.10]

Qi is the Coulomb plus exchange component E c is the correlation component of G,... [Pg.127]

The concept of intrinsic barriers provides insight into the poor leaving group ability of alkoxides in other S 2 reactions as well. For instance, the methoxide exchange component of the intrinsic barrier to the reaction X + CH OCH XCH + OCHg is so large that, regardless of the nature of X, the reaction is predicted to be slow unless it is also extremely... [Pg.98]

When heating or cooling is provided, each exchanger component shall be suitable for the process fluid and cooling water to which it is exposed. [Pg.49]

Table 3.5 compares estimates made by the different methods the procedure of Helgeson et al. (1978) effectively leads to the best estimates. According to Robinson and Haas (1983), however, the result of this procedure is path-dependent, because it is conditioned by the selected exchange components different exchange reactions (with different reference components) can lead to appreciably different results for the same component. [Pg.147]

How well an organolithium reagent fares as an exchange component depends on its basicity. Thus, tert-butyllithium outperforms iec-butyllithium, which in turn is superior to butyllithium. MethyUithium is the least reactive alkyllithium but still surpasses phenyl-lithium, at least at low concentrations, i.e. the order is ... [Pg.440]

Now, consider particle motion in a phase (solid, liquid, gas). If the phase is initially inhomogeneous, random motion of atoms tends to homogenize the phase. If several phases are present and there are exchanges between the phases, the interphase reaction or exchange tends to make the chemical potential of all exchangeable components the same in all phases and diffusion again works to homogenize each phase. Hence, at equilibrium, the chemical potential of a component is constant. [Pg.179]

If the difference in concentration is in only two exchangeable components, such as FeO and MgO, the interdiffusion in a multicomponent system may be treated as effective binary. The diffusion of other components in the system may or may not be treated as effective binary diffusion. [Pg.264]

The first-order electrostatic interaction can also play an important role in base-base stacking. The 0) term can, depending on the system and the configuration, stabilize or destabilize stacked nucleic acid complexes. In most cases, the A HL term is positive which indicates that the 0) contribution is canceled out by the exchange component. Similar observations have also been reported recently [25,32]. In the case of guanine-guanine and cytosine-cytosine complexes, the electrostatic term has positive value. The average values of first-order electrostatic component... [Pg.392]

Metathesis (displacement) reactions Two reactants exchange component parts. [Pg.3]

Further optimization rests primarily in further minimizing the cost per transfer unit yx, a well-known criterion first pointed out by Tribus over 25 years ago (1,1A,23). This criterion (often called minimizing the cost of "UA") is thus well-known by manufactures of heat transfer equipment. However, unless the heat exchange component is shown to be thermoeconomically isolated, this criterion has to be viewed with suspicion, and indeed it is currently used more as a "rule of thumb" than as a precise criterion. [Pg.257]

First of all, we will touch a widely believed misunderstanding about impossibility of using the second law of thermodynamics in the analysis of open systems. Surely, the conclusion on inevitable degradation of isolated systems that follows from the second law of thermodynamics cannot be applied to open systems. And particularly unreasonable is the supposition about thermal death of the Universe that is based on the opinion of its isolation. The entropy production caused by irreversible energy dissipation is, however, positive in any system. Here we have a complete analogy with the first law of thermodynamics. Energy is fully conserved only in the isolated systems. For the open systems the balance equalities include exchange components which can lead to the entropy reduction of these systems at its increase due to internal processes as well. [Pg.39]


See other pages where Exchangeable components is mentioned: [Pg.154]    [Pg.530]    [Pg.133]    [Pg.117]    [Pg.247]    [Pg.247]    [Pg.43]    [Pg.31]    [Pg.37]    [Pg.69]    [Pg.507]    [Pg.268]    [Pg.173]    [Pg.272]    [Pg.124]    [Pg.258]    [Pg.267]    [Pg.277]    [Pg.277]    [Pg.293]    [Pg.307]    [Pg.310]    [Pg.307]    [Pg.252]    [Pg.189]   
See also in sourсe #XX -- [ Pg.106 ]




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