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Normalized impulse response function

Time-resolved emission spectra are reconstructed from the normalized impulse response functions (26) ... [Pg.98]

Impulse Response and the Differential Distribution. Suppose a small amount of tracer is instantaneously injected at time 1 = 0 into the inlet of a reactor. All the tracer molecules enter together but leave at varying times. The tracer concentration at the outlet is measured and integrated with respect to time. The integral will be finite and proportional to the total quantity of tracer that was injected. The concentration measurement at the reactor outlet is normalized by this integral to obtain the impulse response function. ... [Pg.542]

Data are often normalized so that the area under the curve is preserved. This area is given by the dc spectral term, that is, for /t = 0. To preserve the area in the discrete inverse-filtered result, every term should be multiplied by the dc spectral components of the impulse response function (if the impulse response function has not been normalized earlier). We would then have ford... [Pg.286]

From formulas (9) and (10) Figure 6 and Figure 7 were obtained. Them shows normalized impulse response of the Hjfco) and Hfco) corresponding to the absolute and normalized transfer functions G o and G co) (formulas 4 and 5), which shows high accuracy of the transformation. [Pg.139]

Figure 6. Normalized impulse response of the transfer functions HJ cd) and normalized absolute transfer function Gjlpd). Figure 6. Normalized impulse response of the transfer functions HJ cd) and normalized absolute transfer function Gjlpd).
Figure 8. Differences between the normalized impulse response of the power transfer functions HzioS) and H O ) IHjIco) in the frequency domain. Figure 8. Differences between the normalized impulse response of the power transfer functions HzioS) and H O ) IHjIco) in the frequency domain.
Responses obtained from normalized impulse response from the formulas (10) and (11) corresponding to power transfer function from disturbances in the frequency domain are similar. [Pg.140]

With this choice the corresponding impulse response function of V[ ] is symmetric in time domain, and then it violates the causality condition. Even though the causality condition is violated, in the frame of stationary processes, this does not produce any problem since the output of Eq. 51 remains a normal strictly stationary process with PSD Sy(co) that is the target one. [Pg.457]

In electronics, the Fourier transform of the impulse response is defined as the transfer function. Analogously in imaging, S(co)r should be imaging or optical transform function (OFF). However, it is customary to normalize the OTF by its maximum value, so that the normalized OFF varies between unity and zero. Except for the human visual system, S(co)r is maximum when cor=0 and decreases as spatial frequency increases. Fhe magnitude of the optical transform function is called the modulation transfer function (MFF). In other words,... [Pg.162]

Extensions of residence time distributions to systems with multiple inlets and outlets have been described (27-29). If the system contains M inlets and N outlets one can define a conditional density function E. (t) as the normalized tracer impulse response in outlet j to input in inlet i as shown schematically in Figure 2. [Pg.115]

If the tail is truncated, then the tracer impulse response should be normalized based on the area under the curve to obtain a proper density function that approximately describes the distribution of residence times in regions through which there is active flow. [Pg.119]

Cardiac muscle is highly dependent on calcium influx for normal function. Impulse generation in the sinoatrial node and conduction in the atrioventricular node—so-called slow-response, or calcium-dependent, action potentials—may be reduced or blocked by all of the calcium channel blockers. Excitation-contraction coupling in all cardiac cells requires calcium influx, so these drugs reduce cardiac contractility in a dose-dependent fashion. In some cases, cardiac output may also decrease. This reduction in cardiac mechanical function is another mechanism by which the calcium channel blockers can reduce the oxygen requirement in patients with angina. [Pg.262]

Nicotinic acetylcholine (ACh) receptors are responsible for transmission of nerve impulses from motor nerves to muscle fibers (muscle types) and for synaptic transmission in autonomic ganglia (neuronal types). They are also present in the brain, where they are presumed to be responsible for nicotine addiction, although little is known about their normal physiological function there. Nicotinic receptors form cation-selective ion channels. When a pulse of ACh is released at the nerve-muscle synapse, the channels in the postsynaptic membrane of the muscle cell open, and the initial electrochemical driving force is mainly for sodium ions to pass from the extracellular space into the interior of the cell. However, as the membrane depolarizes, the driving force increases for potassium ions to go in the opposite direction. Nicotinic channels (particularly some of the neuronal type) are also permeable to divalent cations, such as calcium. [Pg.358]

Other stimuli that can be used are a random input and a sinusoidal input. The response of a step input is an S-shaped curve see Fig. 11.20 top. The response of a pulse input is a bell-shaped curve see Fig. 11.20 bottom. The ideal pulse input is of infinitely short duration such an input is called a delta function or impulse. The normalized response to a delta function is called the C curve. Thus, the total area under the curve equals unity. [Pg.808]

A linear system that is forced sinusoidally will have a sinusoidal response at the same frequency. One way to approach the analysis is then to assume an input of the form exp(tot) = cos( >i) -I- i sin( )t), where f = -1 the response will also have the form exp(tot). The linearized equations for isothermal, low-speed Newtonian spinning, for example. Equations ll.lOa-c, will then take the form of Equations 11.13a-c, with A replaced by ico the functions 4>, f, and m are complex and are in fact the normalized Fourier transforms of A, v, and a, respectively. The boundary conditions, however, are no longer zero, but reflect the forcing if we wish to determine the sensitivity of the output area to disturbances in the velocity at z = 0, for example, we would set = 1 + Or at f = 0. (The input condition is the Fourier transform of an impulse, or a delta function, not a sinusoid, because the transfer function is the ratio of output to input in Fourier space. There is no loss of generality in setting the imaginary part to zero at f = 0.)... [Pg.184]

Both sodium and potassium are rather abundant in the Earth s surface (Na, 2.6% K, 2.4%), but potassium, due to its greater solubility and subsequent uptake by plant life, is much less prevalent in the seas. Indeed, potassium is so vital to plants that its major use, usually as the chloride or sulfate, is in fertilizers. This is certainly not a newly recognized technology. Even centuries ago, farmers knew that spreading wood ashes on their lands made crops grow better. We now recognize that the potassium in these ashes was primarily responsible for the effect. Both sodium and potassium ions are present in plants and animals and are essential for normal biochemical functions, particularly for the maintenance of the concentrations of ions across various cellular membranes, enzyme functions, and the firing of nerve impulses. [Pg.342]


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See also in sourсe #XX -- [ Pg.94 ]




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Impulse

Impulse function

Impulse response

Impulse-response function

Impulsive

Impulsiveness

Normal function

Normal response

Normalization function

Normalized functions

Response functions

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