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Non-stationary

It is very important to make classification of dynamic models and choose an appropriate one to provide similarity between model behavior and real characteristics of the material. The following general classification of the models is proposed for consideration deterministic, stochastic or their combination, linear, nonlinear, stationary or non-stationary, ergodic or non-ergodic. [Pg.188]

Fourier transform is widely used for signal analysis purposes and is satisfactory when applied to signals where stationary features are of particular interest. However, it turns out to be very poor when dealing with defect detection, where it is the non stationary characteristics of the signal which has to be highlighted. The main reason is that in the Fourier analysis, the time parameter is discarded. [Pg.360]

Assuming that the system has no pennanent dipole moment, tire existence ofP(t) depends on a non-stationary j induced by an external electric field. For weak fields, we may expand the polarization in orders of the perturbation. [Pg.254]

Figure Al.6.24. Schematic representation of a photon echo in an isolated, multilevel molecule, (a) The initial pulse prepares a superposition of ground- and excited-state amplitude, (b) The subsequent motion on the ground and excited electronic states. The ground-state amplitude is shown as stationary (which in general it will not be for strong pulses), while the excited-state amplitude is non-stationary. (c) The second pulse exchanges ground- and excited-state amplitude, (d) Subsequent evolution of the wavepackets on the ground and excited electronic states. Wlien they overlap, an echo occurs (after [40]). Figure Al.6.24. Schematic representation of a photon echo in an isolated, multilevel molecule, (a) The initial pulse prepares a superposition of ground- and excited-state amplitude, (b) The subsequent motion on the ground and excited electronic states. The ground-state amplitude is shown as stationary (which in general it will not be for strong pulses), while the excited-state amplitude is non-stationary. (c) The second pulse exchanges ground- and excited-state amplitude, (d) Subsequent evolution of the wavepackets on the ground and excited electronic states. Wlien they overlap, an echo occurs (after [40]).
Bala, R, Lesyng, B., McCammon, J.A. Extended Hellmann-Feynman theorem for non-stationary states and its application in quantum-classical molecular dynamics simulations. Chem. Phys. Lett. 219 (1994) 259-266. [Pg.33]

This spatial distribution is not stationary but evolves in time. So in this ease, one has a wavefunetion that is not a pure eigenstate of the Hamiltonian (one says that E is a superposition state or a non-stationary state) whose average energy remains eonstant (E=E2,i ap + El 2 bp) but whose spatial distribution ehanges with time. [Pg.55]

For an initiator concentration which is constant at [l]o, the non-stationary-state radical concentration varies with time according to the following expression ... [Pg.363]

When results are compared for polymerization experiments carried out at different frequencies of blinking, it is found that the rate depends on that frequency. To see how this comes about, we must examine the variation of radical concentration under non-stationary-state conditions. This consideration dictates the choice of photoinitiated polymerization, since in the latter it is almost possible to turn on or off—with the blink of a light—the source of free radicals. The qualifying almost in the previous sentence is actually the focus of our attention, since a short but finite amount of time is required for the radical concentration to reach [M-] and a short but finite amount of time is required for it to drop back to zero after the light goes out. [Pg.374]

The superpositioning of experimental and theoretical curves to evaluate a characteristic time is reminiscent of the time-tefnperature superpositioning described in Sec. 4.10. This parallel is even more apparent if the theoretical curve is drawn on a logarithmic scale, in which case the distance by which the curve has to be shifted measures log r. Note that the limiting values of the ordinate in Fig. 6.6 correspond to the limits described in Eqs. (6.46) and (6.47). Because this method effectively averages over both the buildup and the decay phases of radical concentration, it affords an experimentally less demanding method for the determination of r than alternative methods which utilize either the buildup or the decay portions of the non-stationary-state free-radical concentration. [Pg.379]

The intrinsic drawback of LIBS is a short duration (less than a few hundreds microseconds) and strongly non-stationary conditions of a laser plume. Much higher sensitivity has been realized by transport of the ablated material into secondary atomic reservoirs such as a microwave-induced plasma (MIP) or an inductively coupled plasma (ICP). Owing to the much longer residence time of ablated atoms and ions in a stationary MIP (typically several ms compared with at most a hundred microseconds in a laser plume) and because of additional excitation of the radiating upper levels in the low pressure plasma, the line intensities of atoms and ions are greatly enhanced. Because of these factors the DLs of LA-MIP have been improved by one to two orders of magnitude compared with LIBS. [Pg.234]

It should be noted that the force constant matrix can be calculated at any geometry, but the transformation to nonnal coordinates is only valid at a stationary point, i.e. where the first derivative is zero. At a non-stationary geometry, a set of 3A—7 generalized frequencies may be defined by removing the gradient direction from the force constant matrix (for example by projection techniques, eq. (13.17)) before transformation to normal coordinates. [Pg.314]

The system of quasi-one-dimensional non-stationary equations derived by transformation of the Navier-Stokes equations can be successfully used for studying the dynamics of two-phase flow in a heated capillary with distinct interface. [Pg.462]

The V in the noise term means that the process is non-stationary. [Pg.482]

That is, without some measure of control, the process is unstable and will diverge from the set point. Unlike a stationary process, which will achieve a steady state at some point, a non-stationary process requires some sort of integral control. [Pg.482]

In this section we initiate the design of difference methods for numerical solutions of the simplest problems in gas dynamics. Of our initial concern is the problem about one-dimensional non,stationary gas flow in a plane with the following ingredients velocity v, density p, temperature T, pressure p, internal energy e. [Pg.525]

Because of this, there is a real need for designing the general method, by means of which economical schemes can be created for equations with variable and even discontinuous coefhcients as well as for quasilinear non-stationary equations in complex domains of arbitrary shape and dimension. As a matter of experience, the universal tool in such obstacles is the method of summarized approximation, the framework of which will be explained a little later on the basis of the heat conduction equation in an arbitrary domain G of the dimension p with the boundary F... [Pg.591]

K.I. Schchelkin and Ya.K. Troshin, Non stationary phenomena in the gaseous detonation front. Combust. Flame, 7, 143-151, 1963. [Pg.215]

The possibility that adsorption reactions play an important role in the reduction of telluryl ions has been discussed in several works (Chap. 3 CdTe). By using various electrochemical techniques in stationary and non-stationary diffusion regimes, such as voltammetry, chronopotentiometry, and pulsed current electrolysis, Montiel-Santillan et al. [52] have shown that the electrochemical reduction of HTeOj in acid sulfate medium (pH 2) on solid tellurium electrodes, generated in situ at 25 °C, must be considered as a four-electron process preceded by a slow adsorption step of the telluryl ions the reduction mechanism was observed to depend on the applied potential, so that at high overpotentials the adsorption step was not significant for the overall process. [Pg.73]

A growing number of research groups are active in the field. The activity of reforming catalysts has been improved and a number of test reactors for fuel partial oxidation, reforming, water-gas shift, and selective oxidation reactions were described however, hardly any commercial micro-channel reformers have been reported. Obviously, the developments are still inhibited by a multitude of technical problems, before coming to commercialization. Concerning reformer developments with small-scale, but not micro-channel-based reformers, the first companies have been formed in the meantime (see, e.g., ) and reformers of large capacity for non-stationary household applications are on the market. [Pg.98]

Most electrodes are stationary, such as a mercury pool electrode (SMDE) or the HMDE others are non-stationary, such as the DME, MFE, MTFE, RDE and RRDE. [Pg.24]

In voltammetry as an analytical method based on measurement of the voltage-current curve we can distinguish between techniques with non-stationary and with stationary electrodes. Within the first group the technique at the dropping mercury electrode (dme), the so-called polarography, is by far the most important within the second group it is of particular significance to state whether and when the analyte is stirred. [Pg.128]

A. Stationary (mostly pseudo-stationary) methods -+ static measurement B. Non-stationary methods -> dynamic measurement ... [Pg.151]

At the beginning of Section 3.3 a distinction was made between voltammetric techniques with non-stationary and stationary electrodes the first group consists of voltammetry at the dme or polarography, already treated, and voltammetry at hydrodynamic electrodes, a later subject in this section however, we shall now first consider voltammetry at stationary electrodes, where it is of significance to state whether and when the analyte is stirred. [Pg.178]

Kast, W., 1964, Significance of Nucleating and Non-stationary Heat Transfer in the Heat Exchanger during Bubble Vaporization and Droplet Condensation, Chem. Eng. Tech. 36(9) 933-940. (2) Katto, Y., 1981, General Features of CHF of Forced Convection Boiling in Uniformly Heated Rectangular Channels, Ini. J. Heat Mass Transfer 24.14131419. (5)... [Pg.540]

In Chapters 4 and 5 we made use of the theory of radiationless transitions developed by Robinson and Frosch.(7) In this theory the transition is considered to be due to a time-dependent intramolecular perturbation on non-stationary Bom-Oppenheimer states. Henry and Kasha(8) and Jortner and co-workers(9-12) have pointed out that the Bom-Oppenheimer (BO) approximation is only valid if the energy difference between the BO states is large relative to the vibronic matrix element connecting these states. When there are near-degenerate or degenerate zeroth-order vibronic states belonging to different configurations the BO approximation fails. [Pg.440]

The term three-phase fluidization, in this chapter, is taken as a system consisting of a gas, liquid, and solid phase, wherein the solid phase is in a non-stationary state, and includes three-phase slurry bubble columns, three-phase fluidized beds, and three-phase flotation columns, but excludes three-phase fixed bed systems. The individual phases in three-phase fluidization systems can be reactants, products, catalysts, or inert. For example, in the hydrotreating of light gas oils, the solid phase is catalyst, and the liquid and gas phases are either reactants or products in the bleaching of paper pulp, the solid phase is both reactant and product, and the gas phase is a reactant while the liquid phase is inert in anaerobic fermentation, the gas phase results from the biological activity, the liquid phase is product, and the solid is either a biological carrier or the microorganism itself. [Pg.583]

Besides the resuspension of particles, the perfect sink model also neglects the effect of deposited particles on incoming particles. To overcome these limitations, recent models [72, 97-99] assume that particles accumulate within a thin adsorption layer adjacent to the collector surface, and replace the perfect sink conditions with the boundary condition that particles cannot penetrate the collector. General continuity equations are formulated both for the mobile phase and for the immobilized particles in which the immobilization reaction term is decomposed in an accumulation and a removal term, respectively. Through such equations, one can keep track of the particles which arrive at the primary minimum distance and account for their normal and tangential motion. These equations were solved both approximately, and by numerical integration of the governing non-stationary transport equations. [Pg.211]

In both experimental and theoretical investigations on particle deposition steady-state conditions were assumed. The solution of the non-stationary transport equation is of more recent vintage [102, 103], The calculations of the transient deposition of particles onto a rotating disk under the perfect sink boundary conditions revealed that the relaxation time was of the order of seconds for colloidal sized particles. However, the transition time becomes large (102 104 s) when an energy barrier is present and an external force acts towards the collector. [Pg.212]


See other pages where Non-stationary is mentioned: [Pg.187]    [Pg.189]    [Pg.22]    [Pg.265]    [Pg.2354]    [Pg.80]    [Pg.363]    [Pg.418]    [Pg.7]    [Pg.332]    [Pg.657]    [Pg.317]    [Pg.258]    [Pg.259]    [Pg.362]    [Pg.128]    [Pg.128]    [Pg.168]    [Pg.209]    [Pg.380]    [Pg.583]   
See also in sourсe #XX -- [ Pg.111 ]

See also in sourсe #XX -- [ Pg.484 ]




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