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Laterally averaged total

For scenarios 1 and 2 are obtained US 30,905,397 and US 49,746,778 of the average total logistics cost and US 288,393 and US 288,004 of standard deviation, respectively. Considering fair distribution Irom the first time (scenario 1) could save almost 40 % of disaster response operation budget comparing to give the penalty to unfair distribution later (scenario 2. ... [Pg.292]

At = 0.01, and the initial radius vq = 22.21. We use the Lagrange multipher y in order to satisfy the area incompressibility, but a numerical error accumulates during the simulation which violates the fixed local area constraint. In order to suppress the error below a harmless level, we use a penalty functional for local areas [12]. The total area A(t) is nicely conserved ( S(t)/S(0) — 11 < 0.0026) and a maximum deviation of a local area from its initial area in suppressed within 6% of its initial area throughout simulations. Figure 1 shows vesicle shapes (A = 0.5) at a late stage t = 300) for different lateral averages in 0, (a) a critical quench <0> = 0 and off-critical ones (b)... [Pg.286]

Table 4.9 summarizes the results of the 1989 EFC survey, which covered 30 systems developed in 6 countries. A summary of the survey itself indicated that the development effort reported on 22 systems averaged 4.1 person-years (PY), with a median of 2 PY two of the systems reported efforts exceeding 10 PY. The expenditures for development reported for 11 systems averaged 490,000/year, with a median of 127,000/year. Only 4 systems were available at the time of the survey, but some were expected to be put on the market later. A total of 17 different software shells were used by the developers, with each developer tending to stay with a specific shell once a project had started. [Pg.310]

Now encounters between molecules, or between a molecule and the wall are accompanied by momentuin transfer. Thus if the wall acts as a diffuse reflector, molecules colliding wlch it lose all their axial momentum on average, so such encounters directly change the axial momentum of each species. In an intermolecuLar collision there is a lateral transfer of momentum to a different location in the cross-section, but there is also a net change in total momentum for species r if the molecule encountered belongs to a different species. Furthermore, chough the total momentum of a particular species is conserved in collisions between pairs of molecules of this same species, the successive lateral transfers of momentum associated with a sequence of collisions may terminate in momentum transfer to the wall. Thus there are three mechanisms by which a given species may lose momentum in the axial direction ... [Pg.7]

The symbols in the second column represent the electronic state in particular the first number is the total quantum number of the excited electron. We shall see later that in one case at least the symbol is probably incorrect. The third column gives the wave-number of the lowest oscillational-rotational level, the fourth the effective quantum number, the fifth and sixth the oscillational wave-number and the average intemuclear distance for the lowest oscillational-rotational level. The data for H2+ were obtained by extrapolation, except rQ, which is Burrau s theoretical value (Section Via). [Pg.29]

The example demonstrates that the instability and consequent energy dissipation, similar to those in the Tomlinson model, do exist in a real molecule system. Keep in mind, however, that it is observed only in a commensurate system in which the lattice constants of two monolayers are in a ratio of rational value. For incommensurate sliding, the situation is totally different. Results shown in Fig. 21(b) were obtained under the same conditions as those in Fig. 21 (a), but from an incommensurate system. The lateral force and tilt angle in Fig. 21(b) fluctuate randomly and no stick-slip motion is observed. In addition, the average lateral force is found much smaller, about one-fifth of the commensurate one. [Pg.176]

This probability distribution is similar to the probability distribution from (7.28), except that here we average only over configurations that have evolved from configurations in. (/ a time t earlier. By integrating this probability distribution over all order parameter values corresponding to region 23 we obtain the total probability that a system initially in 2 is in 23 at time t later. This is nothing other than the time correlation function C(t) and we can write... [Pg.273]

Red blood cells are amongst the most numerous of the human cell lines an average healthy 70 kg male having a total of approximately 25 x cells in his 51 of blood. A typical red cell contains in excess of 600 million haemoglobin molecules which equates to a total of about 300 g of haemoglobin, an amount that is far greater than for any other protein in the body. The lack of a nucleus clearly indicates that red cells cannot divide and at the end of their life, worn out RBCs are removed by the cells of the reticuloendothelial system. Approximately 2% (5 x 1011) of the red cell number are removed and replaced by new ones each day. Haem synthesis is outlined later in this chapter and its catabolism is discussed in Chapter 6. [Pg.137]


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Laterally averaged total potential

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