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Decay time constants

The vibrational echo experiments yielded exponential decays at all temperatures. The Fourier-transfonn of the echo decay gives the homogeneous lineshape, in this case Lorentzian. The echo decay time constant is AT, where is... [Pg.3045]

Here K is the kernel matrix determining the linear operator in the inversion, A is the resulting spectrum vector and Es is the input data. The matrix element of K for Laplace inversion is Ky = exp(—ti/xy) where t [ and t,- are the lists of the values for tD and decay time constant t, respectively. The inclusion of the last term a 11 A 2 penalizes extremely large spectral values and thus suppresses undesired spikes in the DDIF spectrum. [Pg.347]

Figure 4. Exponential decay time constant for the absorbance decay of benzoin ethyl ether at 328 nm as a function of BEE concentration. Figure 4. Exponential decay time constant for the absorbance decay of benzoin ethyl ether at 328 nm as a function of BEE concentration.
The degree of activation of the sample is measured by post-irradiation spectroscopy, usually performed with high-purity semiconductors. The time-resolved intensity measurements of one of the several spectral lines enables to get the half-life of the radioactive element and the total number of nuclear reactions occurred. In fact, the intensity of a given spectral line associated with the decay of the radioactive elements decreases with time as Aft) = Aoexp[—t/r], where Aq indicates the initial number of nuclei (at t = 0) and r is the decay time constant related to the element half-life (r = In2/ /2), which can be measured. Integrating this relation from t = 0 to the total acquisition time, and weighting it with the detector efficiency and natural abundance lines, the total number of reactions N can be derived. Then, if one compares this number with the value obtained from the convolution of... [Pg.156]

Triplet-triplet annihilation In concentrated solutions, a collision between two molecules in the Ti state can provide enough energy to allow one of them to return to the Si state. Such a triplet-triplet annihilation thus leads to a delayed fluorescence emission (also called delayed fluorescence of P-type because it was observed for the first time with pyrene). The decay time constant of the delayed fluorescence process is half the lifetime of the triplet state in dilute solution, and the intensity has a characteristic quadratic dependence with excitation light intensity. [Pg.42]

For the highest-temperature explosion (1220 K, 20 MPa), the pressure rise time was about 40 /tsec with a decay-time constant of 3 msec. [Pg.167]

The problem of the electron spin relaxation in the early work from Sharp and co-workers (109 114) (and in some of its more recent continuation (115,116)) was treated only approximately. They basically assume that, for integer spin systems, there is a single decay time constant for the electron spin components, while two such time constants are required for the S = 3/2 with two Kramers doublets (116). We shall return to some new ideas presented in the more recent work from Sharp s group below. [Pg.77]

The decay time constants found ranged from 100 to 300 fs and depended on the potential, interface modification, and the electrolyte used. [Pg.859]

The excellent resolution of the 0-tensor components at W band has been used to measure the relaxation properties of QA in the Zn-substituted bRC of R. sphaeroides.m The experiment showed, in contrast to the respective ubiquinone radical in organic solution, an anisotropic relaxation behavior in the pulse high field ESE experiments. From the analysis of the T2 experiments a motional anisotropy of Q% in the protein pocket was deduced with a preferred libration about the C-O symmetry axis. Recently, similar experiments were also performed on Qb- in ZnbRCs. Compared to QA different echo decay time constants were found. A model was proposed in which the relaxation is related to reorientational fluctuations around the quinones specific H-bonds to the protein.142... [Pg.186]

The decay portion of the rate curve was fitted to an exponential rate decay expression (6), rate = Mi exp (—t/M2), where Mi is the initial rate and M2 is a time constant for rate decay, and values of Mi and M2 were determined. In most cases exponential decay fit the data well as shown in Figure 3. Figures 4 and 5 show the effect of C6 olefin mole ratio on the decay time constant. The maximum possible error in these points is 10 In the propene system at a Ce C3 ratio of 20 the decay constant is 48,000 sec. With HY at 493°K and C6 olefin = 2, the ratio of the time constant for the ethene system to that for the propene system is about 20. Figure 4 shows that the decay time constant is independent of cation form, and for... [Pg.564]

Rate Decay. The decay time constant decreases as the olefin concentration increases. This is consistent with a deactivation mechanism... [Pg.565]

Figure 4 Dependence of rate decay time constant on reactant mole ratio for benzene ethylation over Y zeolites at 573°K... Figure 4 Dependence of rate decay time constant on reactant mole ratio for benzene ethylation over Y zeolites at 573°K...
The rate decay time constant is independent of cation form of the zeolite in the ethene system (Figure 4) although the alkylation activity of the three forms is considerably different (Figure 2). This indicates that the active site within the zeolite (at least for deactivation) is the same for all three cation forms as expected from our current picture of active sites for acid-catalyzed reactions in these zeolites (8, 18, 19). The three catalysts should have different numbers of active sites because of their individual response to activation at 823°K, but these sites should be similar thus M2 should be independent of cation form, Mi should depend on it. [Pg.566]

The activation energy for the rate decay time constant with benzene ethylation over SK-500 at C6. C2 = 8 is 13.6 1 kcal/mole. That for HY in the ethene system at Ce C2 = 2 is 11 kcal/mole. For propene alkylation over HY the activation energy for rate decay is 4 kcal/mole and is independent of C6 0 8 mole ratio. [Pg.566]

GABAA-R-mediated sIPSCs were examined and we found that the marked increase of decay time constant, amplitude, and area caused by this neurosteroid was not different between rats at PI9 and those in estrus. Similarly, the potentiation of sIPSCs recorded in dentate gyrus granule cells induced by the benzodiazepine lorazepam (3 /lM), although slightly reduced in rats at PI9 compared to control, resulted not different among these animals. [Pg.85]


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See also in sourсe #XX -- [ Pg.209 ]




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