Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Small fluctuation

We have derived time-reversible, symplectic, and second-order multiple-time-stepping methods for the finite-dimensional QCMD model. Theoretical results for general symplectic methods imply that the methods conserve energy over exponentially long periods of time up to small fluctuations. Furthermore, in the limit m —> 0, the adiabatic invariants corresponding to the underlying Born-Oppenheimer approximation will be preserved as well. Finally, the phase shift observed for symmetric methods with a single update of the classical momenta p per macro-time-step At should be avoided by... [Pg.418]

Although the temperature can be controlled with a weU-designed air-conditioning system, the small fluctuations which most cycling systems cause may be very harmful. The temperature—time record should be a continuous, flat graph. [Pg.428]

The uncertainty principle necessitates that any extremal trajectory should be spread , and the next step in our calculation is to find the prefactor by incorporating the small fluctuations around... [Pg.44]

At temperatures above there is no instanton, and escape out of the initial well is accounted for by the static solution Q = Q with the action S ff = PVo (where Vq is the adiabatic barrier height here) which does not depend on friction. This follows from the fact that the zero Fourier component of K x) equals zero and hence the dissipative term in (5.38) vanishes if Q = constant. The dissipative effects come about only through the prefactor which arises from small fluctuations around the static solution. Decomposing the trajectory into Fourier series. [Pg.82]

For noiiadditive rulas, can no longer be obtained by merely looking at the evolution of the initial difference state. A fairly typical nonadditive behavior is that of rule R126. We see that, apart from small fluctuations, H t) tends to steadily increase in a ronghly linear fashion. This means that as time increases, the values of particular sites will depend on an over increasing set of initial sites he., space-time patterns arc scnsitivr.ly dependent on the initial conditions. We will pick up this theme in our diseus.sion of chaos in continuous systems in chapter 4. [Pg.80]

Ca2+ sensing receptor, a member of G-protein coupled receptors, is composed of seven transmembrane spanning domains. The extracellular domain contains clusters of negatively charged amino acids sensing even small fluctuations of extracellular calcium. Mutations in this receptor cause inheritable hypo- and hypercalcemic syndromes. [Pg.291]

The next step should clarify why the unstable growth of the variable x occurs through a stable state at the bifurcation point. To determine the stability of the bifurcation point, it is necessary to examine the linear stability of the steady-state solution. For Eq. (1), the steady-state solution at the bifurcation point is given as jc0 = 0. So, let us examine whether the solution is stable for a small fluctuation c(/). Substituting Jt = b + Ax(f) into Eq. (1), and neglecting the higher order of smallness, it follows that... [Pg.221]

For simplicity, it is assumed that the equilibrium value of the macrostate is zero, x = 0. This means that henceforth x measures the departure of the macrostate from its equilibrium value. In the linear regime, (small fluctuations), the first entropy may be expanded about its equilibrium value, and to quadratic order it is... [Pg.11]

Fig. 3a indicates that the bubble-rise velocity measured based on the displacement of the top surface of the bubble ( C/bt) quickly increases and approaches the terminal bubble rise velocity in 0.02 s. The small fluctuation of Ubt is caused by numerical instability. The bubble-rise velocity measured based on the displacement of the bottom surface of the bubble (Ubb) fluctuates significantly with time initially and converges to Ubt after 0.25 s. The overshooting of Ubb can reach 45-50 cm/s in Fig. 3a. The fluctuation of Ubb reflects the unsteady oscillation of the bubble due to the wake flow and shedding at the base of the bubble. Although the relative deviation between the simulation results of the 40 X 40 x 80 mesh and 100 x 100 x 200 mesh is notable, the deviation is insignificant between the results of the 80 x 80 x 160 mesh and those of the 100 X 100 x 200 mesh. The agreement with experiments at all resolutions is generally reasonable, although the simulated terminal bubble rise velocities ( 20 cm/s) are slightly lower than the experimental results (21 25 cm/s). A lower bubble-rise velocity obtained from the simulation is expected due to the no-slip condition imposed at the gas-liquid interface, and the finite thickness for the gas-liquid interface employed in the computational scheme. Fig. 3a indicates that the bubble-rise velocity measured based on the displacement of the top surface of the bubble ( C/bt) quickly increases and approaches the terminal bubble rise velocity in 0.02 s. The small fluctuation of Ubt is caused by numerical instability. The bubble-rise velocity measured based on the displacement of the bottom surface of the bubble (Ubb) fluctuates significantly with time initially and converges to Ubt after 0.25 s. The overshooting of Ubb can reach 45-50 cm/s in Fig. 3a. The fluctuation of Ubb reflects the unsteady oscillation of the bubble due to the wake flow and shedding at the base of the bubble. Although the relative deviation between the simulation results of the 40 X 40 x 80 mesh and 100 x 100 x 200 mesh is notable, the deviation is insignificant between the results of the 80 x 80 x 160 mesh and those of the 100 X 100 x 200 mesh. The agreement with experiments at all resolutions is generally reasonable, although the simulated terminal bubble rise velocities ( 20 cm/s) are slightly lower than the experimental results (21 25 cm/s). A lower bubble-rise velocity obtained from the simulation is expected due to the no-slip condition imposed at the gas-liquid interface, and the finite thickness for the gas-liquid interface employed in the computational scheme.
Complex cyanides are compounds in which the cyanide anion is incorporated into a complex or complexes. These compounds are different in chemical and toxicologic properties from simple cyanides. In solution, the stability of the cyanide complex varies with the type of cation and the complex that it forms. Some of these are dissociable in weak acids to give free cyanide and a cation, while other complexes require much stronger acidic conditions for dissociation. The least-stable complex metallocyanides include Zn(CN)42 , Cd(CN)3 , and Cd(CN)42 moderately stable complexes include Cu(CN)2, Cu(CN)32, Ni(CN)42, and Ag(CN)2 and the most stable complexes include Fe(CN)64, and Co(CN)6. The toxicity of complex cyanides is usually related to their ability to release cyanide ions in solution, which then enter into an equilibrium with HCN relatively small fluctuations in pH significantly affect their biocidal properties. [Pg.910]

The decomposition of a solution with composition outside the spinodal region but within the metastable region can be analyzed in a similar way. Let us assume that a sample with composition in this region is cooled to low temperatures. Small fluctuations in composition now initially lead to an increase in the Gibbs energy and the separation of the original homogeneous solution must occur by nucleation of a new phase. The formation of this phase is thermally activated. Two solutions with different composition appear, but in this case the composition of the nucleated phase is well defined at all times and only the relative amount of the two phases varies with time. [Pg.139]

Control systems may produce small fluctuations of the process variables, as in the sinusoidal cases of problem P4.09.34. When they occur while the system is at an unstable point, the temperature will migrate to that at a neighboring steady condition. In problem P4.10.01, as the unstable condition is approached (T = 280, C = 2.4), the profiles of temperature and... [Pg.267]

For each test case, a non-reacting scalar (e.g., mixture fraction) should be used to determine the spatial distribution of its mean and variance (i.e., (f) and (f/2 . These results can then be compared with those found by solving the RANS transport equations (i.e., (4.70), p. 120 and (4.90), p. 125) with identical values for (U) and Tt. Fike-wise, the particle-weight distribution should be compared with the theoretical value (i.e., (7.74)). While small fluctuations about the theoretical value are to be expected, a systematic deviation almost always is the result of inconsistencies in the particle-convection algorithm. [Pg.380]

To describe such pairing, we consider small fluctuations of up and strange quarks near p. The energy of such fluctuations of up and down quarks is respectively... [Pg.175]

Inner slip, between the solid wall and an adsorbed film, will also influence the surface-liquid boundary conditions and have important effects on stress propagation from the liquid to the solid substrate. Linked to this concept, especially on a biomolecular level, is the concept of stochastic coupling. At the molecular level, small fluctuations about the ensemble average could affect the interfacial dynamics and lead to large shifts in the detectable boundary condition. One of our main interests in this area is to study the relaxation time of interfacial bonds using slip models. Stochastic boundary conditions could also prove to be all but necessary in modeling the behavior and interactions of biomolecules at surfaces, especially with the proliferation of microfluidic chemical devices and the importance of studying small scales. [Pg.82]

From equation (8.1), if both the numerator and denominator terms are very similar, then small fluctuations in either can have a profound influence on Abs, even allowing this to be zero if the error in reading T is appreciable. Such errors are likely to be huge. In effect, below the band edge, absorbances are worthless. [Pg.272]

They were carried out over a 50 day period at different dilution rates and at different input substrate concentrations. In order to do these simulations more realistic, small fluctuations as well as drastic step perturbations were introduced alternately in the input concentrations (see Figures 15 to 18) and in the dilution rate (see Figure 14). The input variables X and were assumed negligible. The measurements of S, S2 and Pco- was calculated directly from the model (see Figures 19, 20 and 21). [Pg.149]

The real input concentrations shown in these figures were only used to validate hypothesis Hlg and to simulate the model (6) from which the measurements S , S2 and Pco2 were taken directly. These measurements are reported in Figures 43 to 45. The variables C j, X and were supposed to be negligible. As in the previous numerical example, small fluctuations as well as drastic step perturbations were alternatively introduced in the dilution rate and in the input concentrations to resemble actual industrial operating conditions. [Pg.152]

The open squares in Fig. 3.30 show the resulting tube diameters. Aside from some small fluctuations they now stay constant, independent of We further... [Pg.65]


See other pages where Small fluctuation is mentioned: [Pg.686]    [Pg.230]    [Pg.412]    [Pg.415]    [Pg.509]    [Pg.703]    [Pg.796]    [Pg.802]    [Pg.1372]    [Pg.60]    [Pg.256]    [Pg.229]    [Pg.85]    [Pg.197]    [Pg.262]    [Pg.141]    [Pg.155]    [Pg.73]    [Pg.95]    [Pg.353]    [Pg.192]    [Pg.250]    [Pg.135]    [Pg.139]    [Pg.312]    [Pg.226]    [Pg.178]    [Pg.244]    [Pg.217]    [Pg.86]    [Pg.157]    [Pg.269]   
See also in sourсe #XX -- [ Pg.7 ]




SEARCH



Nonequilibrium fluctuations, small systems

Other small-scale fluctuations and their effects on the segmental motion

Small amplitude sinusoidal fluctuation

Small systems, nonequilibrium fluctuations temperatures

Small-scale temperature fluctuation

© 2024 chempedia.info