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Cycle mechanism space

Heat Pumps. Heat pumps involve the appHcation of external power to pump heat from a lower temperature to a higher temperature. Heat pumps are frequently used for space heating and are simply refrigeration cycles operated in reverse. The heat rejected in the condenser becomes the primary objective of operation. Consequently, refrigerants used for mechanical compression refrigeration have similar appHcation in heat pumps. [Pg.509]

In contrast to dissipative dynamical systems, conservative systems preserve phase-space volumes and hence cannot display any attracting regions in phase space there can be no fixed points, no limit cycles and no strange attractors. There can nonetheless be chaotic motion in the sense that points along particular trajectories may show sensitivity to initial conditions. A familiar example of a conservative system from classical mechanics is that of a Hamiltonian system. [Pg.171]

Fig. 5. Pulse sequence for MR detection of vibration using a radiofrequency field gradient. A binomial 1331 radiofrequency pulse (pulse length D, interpulse delay r) is applied in-phase with the mechanical wave. Thus the vibration period 7V is equal to 4(D + r). The number of cycles can be increased to ensure a better frequency selectivity. The constant RF field gradient generated by a dedicated RF coil allows space encoding without using conventional static field gradients (from Ref. 16 with permission from Elsevier). Fig. 5. Pulse sequence for MR detection of vibration using a radiofrequency field gradient. A binomial 1331 radiofrequency pulse (pulse length D, interpulse delay r) is applied in-phase with the mechanical wave. Thus the vibration period 7V is equal to 4(D + r). The number of cycles can be increased to ensure a better frequency selectivity. The constant RF field gradient generated by a dedicated RF coil allows space encoding without using conventional static field gradients (from Ref. 16 with permission from Elsevier).
Only deterministic models for cellular rhythms have been discussed so far. Do such models remain valid when the numbers of molecules involved are small, as may occur in cellular conditions Barkai and Leibler [127] stressed that in the presence of small amounts of mRNA or protein molecules, the effect of molecular noise on circadian rhythms may become significant and may compromise the emergence of coherent periodic oscillations. The way to assess the influence of molecular noise on circadian rhythms is to resort to stochastic simulations [127-129]. Stochastic simulations of the models schematized in Fig. 3A,B show that the dynamic behavior predicted by the corresponding deterministic equations remains valid as long as the maximum numbers of mRNA and protein molecules involved in the circadian clock mechanism are of the order of a few tens and hundreds, respectively [128]. In the presence of molecular noise, the trajectory in the phase space transforms into a cloud of points surrounding the deterministic limit cycle. [Pg.272]

This observation was not so obvious on coke yields because the coke production is a contribution of mnltiple mechanisms and reactions. Thus, the coke yields are quite similar, probably because the catalytic coke is decreased while the contaminant coke is increased. The coke remarks are also observed on the CPS samples taking into account that the dehydrogenation degree is not strongly affected by the extended ReDox cycles, becanse the lower catalysts decay is limiting the effect of the required mass of catalyst (C/0 ratio). Thus, the small decrement of the coke yield on the CPS samples is possibly related to the descent of the catalyst (less specific area) leaving less available space for coke adsorption and less activity for catalytic coke production. It is clear that prolonging the deactivation procednres is not beneficial as far as the metal effects are concerned. [Pg.138]

Temkin (5,10,11) presented additional studies extending the original ideas of Horiuti to establish the number of routes or mathematically independent mechanisms consistent with a given initial choice of elementary steps. He showed that the algebra of reaction routes was consistent with the specification of the dimension of the space of such routes and that such a basis could include empty routes for which no net reaction occurs. However, instead of using such empty routes or cycles to generate the complete list of direct mechanisms as discussed in Section III,A, he assumed that such cycles could be disregarded in their effect on reaction mechanisms but not on kinetics. This is inconsistent with the treatment in this article since we assume that such cycles would not occur. [Pg.277]

The rows in (12) from mQ+1 through ms are a basis for the space of all cycles, and the coefficients in these rows form a C x S matrix which will be needed in Section IV for the construction of the unique set of all direct steady-state mechanisms. [Pg.286]

Every element of a space is a unique linear combination of its basis elements. Therefore, a general expression for any steady-state mechanism m, including cycles, has the following form ... [Pg.286]

Let us find every direct mechanism for a given overall reaction r. Assume r to be of the general form given in Eq. (14) and of multiplicity R (R = Q - H), which means that an expression for it contains R parameters. Any mechanism for r is of the general form given in Eq. (13) and depends not only on the R parameters in its reaction, but on C additional parameters, where C is the dimension of the space of all cycles (R + C = S — H). Therefore, to determine a unique mechanism for r, we need to determine C parameters, and they can be chosen to make it a direct mechanism by the following reasoning ... [Pg.288]


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Mechanism space

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