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Amplitude distribution measurement

Figure 2.21 Pulse amplitude distributions measured at various diffraction angles from a sample of distilled water using a chromium anode x-ray tube at 50 kV and 10 mA, a scintillation detector, and a LiF(200) crystal. Figure 2.21 Pulse amplitude distributions measured at various diffraction angles from a sample of distilled water using a chromium anode x-ray tube at 50 kV and 10 mA, a scintillation detector, and a LiF(200) crystal.
As the fracture propagates, the elastic energy released due to the micro-fractures occurring within the sample can be measured. This ultrasonic emission due to micro-fracture aftershock relaxation has recently been measured for various laboratory samples. Petri et al (1994) measured the ultrasonic emission amplitude distribution in a large number of stressed solid samples under different experimental conditions. A power law decay for the cumulative energy release distribution n Er) with the released energy amplitude Er was observed in all cases n Er) E (see Fig. 3.21). This is indeed very similar to the Guttenberg-Richter law for the frequency distribution of earthquakes, as discussed briefly in Chapter 1, and will be discussed in detail in the next chapter. [Pg.126]

The lower detection limit is influenced by the noise frequency and amplitude distribution compared with the signal band width and height. The noise level is usually measured over a given time period which is a multiple of the signal width. The noise can be expressed as peak-to-peak (p-t-p) or root-mean-square (rms) values. The latter gives about 70-80% lower noise levels. Figure 15-7 summarizes the detection limits of some selected chromatographic detectors. [Pg.135]

In the computation of amplitude distributions of the EEG, for example, successive EEG amplitudes must be measured and ordered into specific amplitude classes, or bins. The amplitude histogram that results from this process is often a symmetrical, essentially Gaussian distribution. The primary characteristics of the Gaussian distribution are summarized simply by specifying its mean and standard deviation, since the higher control moments of the distribution, such as skewness and kurtosis, are equal to zero. However, in non-Gaussian distributions, the measures of skewness and kurtosis assume nonzero values and can be used to characterize that particular amplitude distribution. The four primary statistical measures used to characterize an EEG amplitude histogram include the mean, standard amplitude, skewness, and kurtosis. [Pg.418]

The central moments of the EEC amphtude histogram, therefore, are capable of (1) characterizing the amplitude distributions of the EEG and (2) quantifying alterations in these electrical processes brought about by pharmacologic manipulations. In addition, use of the centile index for skewness and kurtosis provides a computer-efficient method for obtaining these measures in real time. [Pg.419]

Concerning the variation of AE parameter during the deterioration process, it is found that the amplitude distribution is useful. In Fig. 10.6, amplitude distributions observed in reinforced concrete beams under bending are shown. These beams were deteriorated by cyclic loading of prescribed level. After particular loading cycles, the beam was statically loaded up to the service-load limit, and AE counts were measured. [Pg.217]

In Fig. 10.6 (a), the beam was repeatedly loaded at 85% static load-bearing capacity until final failure. After several cycles of loading, amplitude distributions of AE signals were measured under monotonous loading. With the increase in loading cycles, amplitude distributions shift to the... [Pg.217]

In this formula, there are two variables, A50 and b. If the response from the mean value of the calibration sample is taken as A50, there is only one parameter (b) to be determined by calibration. After a sample with a known particle size distribution is measured using an optical particle counter and its signal amplitude distribution is recorded, a minimization is carried out by comparing the measured data to theoretical data calculated using different values for b. This procedure should be performed a few times to obtain a representative result. Figure 4.22 shows the OPC result of a 500 nm polymer particle sample with and without correction for inhomogeneous illumination [26]. [Pg.204]

The ESEEM amplitude obtained by the procedure described above depends on the local concentration of deuterium atoms. Because it is measured in absolute units (with dimensions of time), it can be used directly for quantitative estimation of the concentration of deuterated molecules in the immediate surroundings of the spin label. To that end, calibration experiments must be performed, in which the ESEEM amplitude is measured for samples with known concentrations of randomly distributed deuterated molecules. [Pg.109]

To confirm the prejunctional action of the enterotoxin, end-plate potentials before and after the treatment of the diaphragm preparation with the enterotoxin. The resting membrane potentials of the muscle fibers were not affected by the enterotoxin measurement. However, the enterotoxin reduced frequency, but not mean amplitude or amplitude distribution, of miniature end-plate potentials (Table 1). The results indicate that the release of transmitter was inhibited by the treatment with the enterotoxin, but that the response of acetylcholine-receptor in the postjunctional membrane to the transmitter was unaffected. [Pg.266]


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