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Profile fitting conducting

Depending on the quality of the pattern, profile fitting can be conducted in several different ways. They differ in how peak positions and peak shape parameters are handled, assuming that integrated intensities are always refined independently for each peak, and a single set of parameters describes a background within the processed range ... [Pg.361]

Figure 5. (a) The ( A, SO,) anion symmetric streching mode of polypropylene glycol)- LiCF,SO, for 0 M ratios of 2000 1 and 6 1. Solid symbols represent experimental data after subtraction of the spectrum corre-ponding to the pure polymer. Solid curves represent a three-component fit. Broken curves represent the individual fitted components, (b) Relative Raman intensities of the fitted profiles for the ( Aj, SO,) anion mode for this system, plotted against square root of the salt concentration, solvated ions ion pairs , triple ions, (c) The molar conductivity of the same system at 293 K. Adapted from A. Ferry, P. Jacobsson, L. M. Torell, Electrnchim. Acta 1995, 40, 2369 and F. M. Gray, Solid State Ionics 1990, 40/41, 637. [Pg.509]

The MO concentrations versus time profiles were fitted to second order polynomial equations and the parameters estimated by nonlinear regression analysis. The initial rates of reactions were obtained by taking the derivative at t=0. The reaction is first order with respect to hydrogen pressure changing to zero order dependence above about 3.45 MPa hydrogen pressure. This was attributed to saturation of the catalyst sites. Experiments were conducted in which HPLC grade MIBK was added to the initial reactant mixture, there was no evidence of product inhibition. [Pg.265]

Figure 48. Kenjo s ID macrohomogeneous model for polarization and ohmic losses in a composite electrode, (a) Sketch of the composite microstructure, (b) Description of ionic conduction in the ionic subphase and reaction at the TPB s in terms of interpenetrating thin films following the approach of ref 302. (c) Predicted overpotential profile in the electrode near the electrode/electrolyte interface, (d) Predicted admittance as a function of the electrode thickness as used to fit the data in Figure 47. (Reprinted with permission from refs 300 and 301. Copyright 1991 and 1992 Electrochemical Society, Inc. and Elsevier, reepectively.)... Figure 48. Kenjo s ID macrohomogeneous model for polarization and ohmic losses in a composite electrode, (a) Sketch of the composite microstructure, (b) Description of ionic conduction in the ionic subphase and reaction at the TPB s in terms of interpenetrating thin films following the approach of ref 302. (c) Predicted overpotential profile in the electrode near the electrode/electrolyte interface, (d) Predicted admittance as a function of the electrode thickness as used to fit the data in Figure 47. (Reprinted with permission from refs 300 and 301. Copyright 1991 and 1992 Electrochemical Society, Inc. and Elsevier, reepectively.)...
Initial ion separation. As the lifetime of CC14 is of the order of 200 ps (or smaller) the CCI3-absorption is a very sensitive probe for the very early time profile of the ion kinetics and therefor allows to test various initial ion separations. It is concluded, that from the two possible distributions, compatible with conductivity data, only the exponential distribution with G0 = 5 and width b- 36 A is able to fit the experimental facts. ... [Pg.987]

Figure 6.30. Conductivity profiles obtained from fitting of impedance data for uniform and bilayer cathodes. All electrodes (1 cm2) contained 0.9 mg of Nafion [25]. (Reproduced by permission of ECS—The Electrochemical Society, and the authors, from Li G, Pickup PG. Ionic conductivity of PEMFC electrodes.)... Figure 6.30. Conductivity profiles obtained from fitting of impedance data for uniform and bilayer cathodes. All electrodes (1 cm2) contained 0.9 mg of Nafion [25]. (Reproduced by permission of ECS—The Electrochemical Society, and the authors, from Li G, Pickup PG. Ionic conductivity of PEMFC electrodes.)...
The depletion layer profile contains information about the density of states distribution and the built-in potential. The depletion layer width reduces to zero at a forward bias equal to and increases in reverse bias. The voltage dependence of the jimction capacitance is a common method of measuring W V). Eq. (9.9) applies to a semiconductor with a discrete donor level, and 1 is obtained from the intercept of a plot of 1/C versus voltage. The 1/C plot is not linear for a-Si H because of the continuous distribution of gap states-an example is shown in Fig. 4.16. The alternative expression, Eq. (9.10), is also not an accurate fit, but nevertheless the data can be extrapolated reasonably well to give the built-in potential. The main limitation of the capacitance measurement is that the bulk of the sample must be conducting, so that the measurement is difficult for undoped a-Si H. [Pg.328]

A validation consultancy firm has conducted validation work for several North American and European pharmaceutical manufacturers and has developed a staffing life-cycle model. This firm s experience suggests that this model is rather generic, in that it seems to fit most computer system validation programs. It can be used to assess the total validation workload. Figure 3.8 shows that the staffing profile consists of three phases preparation, implementation, and maintenance. [Pg.64]

Strong binding of specific ions can lead not only to selectivity but also to blockage of synthetic ion channels. In BLMs, blockage by permeant ions is revealed by saturation behavior of the conductance g with increasing activity Aion of the ion of interest (Fig. II.IOD) [33]. Fit of the salt profile to Eq. (11.8) gives the inhibitory concentration fCso (or the apparent dissociation constant Kd) and the maximal conductance gMAX for a permeant ion blocker. [Pg.407]

Accordingly, it is only useful to determine the band structure within the first Brillouin zone. The solution of the Schrodinger equation (see Eqs. 1.11 and 1.12) leads to two energy bands separated by an energy gap, as shown in Fig. 1.4. The energy profile of the conduction band (upper curve) still appears parabolic (at least near the minimum) but it may deviate considerably from a parabolic E k relation. In order to continue to use the relation derived for free electrons (Eq. 1.8), the electron mass is adjusted to provide a good fit. We then have, instead of Eq. (1.8),... [Pg.5]

Twenty-four subjects completed an 8-period balanced crossover study. For each subject, pharmacodynamic responses are taken at the test baseline, test 1 puff, test 4 puffs, reference baseline, reference 1 puff, and reference 4 puffs. A population model fit (Section 16.6.1.2) was conducted to describe the data. Responses at baseline were similar for both formulations, although they appeared to differ somewhat at 1 puff and 4 puffs. Overall, the profiles of the two formulations were judged as similar. [Pg.445]

Combustion tests were conducted with oil and coal as a fuel at firing rates between 300 and 400 kW. The fitting technique described above was used to determine the gas temperature from the collected CARS spectral profiles. A typical comparison between the measured and the theoretical, fitted CARS spectral profiles is shown in Figure 13.16. For these tests about 1,000 individual temperature measurements were made at several points in the near burner region of the flame over a period of about 1.67 min. Using these single shot temperature measurements, the CARS measurement technique can show the frequency distribution of the gas temperature as measured at a point in the... [Pg.301]


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