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Comparison equation technique

The various spectrometric techniques have developed independently, and at different times. They differ as to whether frequency, wavelength or wavenumber is measured, with the result that comparisons between techniques is sometimes difficult - equation (7.2) is a useful aid in this respect. [Pg.271]

It is immediate to see from equation (A2) that whenever elements of P are small, since /2m is a small parameter, equations adiabatically decouple into one-dimensional problems for the effective potentialse (p). In turn, these problems can be analyzed by the Liouville-Green WKB technique, which requires special care whenever e = E (turning points) but this problem is to be considered as effectively solved by the method of comparison equations. It is important to realize that proper coordinate choices may lead to wide regions of p space where this decoupling is very effective in such a case, approximate quantum numbers can be assigned, and it is possible to compute semiclassically bound or resonance states and scattering properties. [Pg.385]

Rigorous calculations of cross sections and rate constants for elementary gas phase chemical reactions are performed for comparison with experiment, to ensure that our picture of the chemical reaction is complete. We focus on the H/D+H2 — H2/DH + H reaction, and use the time independent integral equation technique in quantum reactive scattering theory. [Pg.187]

The rupture force measured in AFM experiments is given, therefore, by the average slope of the energy profile minus a correction related to the effects of thermal fluctuations. Equation (11) demonstrates that the rupture force measured in AFM experiments grows linearly with the activation energy of the system (Chilcotti et ah, 1995). A comparison of (10) and (11) shows that the unbinding induced by stiff springs in SMD simulations, and that induced by AFM differ drastically, and that the forces measured by both techniques cannot be readily related. [Pg.58]

Using different types of time-stepping techniques Zienkiewicz and Wu (1991) showed that equation set (3.5) generates naturally stable schemes for incompressible flows. This resolves the problem of mixed interpolation in the U-V-P formulations and schemes that utilise equal order shape functions for pressure and velocity components can be developed. Steady-state solutions are also obtainable from this scheme using iteration cycles. This may, however, increase computational cost of the solutions in comparison to direct simulation of steady-state problems. [Pg.74]

Comparison with the empirical Equation (1.4) shows that = /re /S/z eg and that n" = 2 for the Balmer series. Similarly n" = 1, 3, 4, and 5 for the Lyman, Paschen, Brackett and Pfimd series, although it is important to realize that there is an infinite number of series. Many series with high n" have been observed, by techniques of radioastronomy, in the interstellar medium, where there is a large amount of atomic hydrogen. For example, the (n = 167) — ( " = 166) transition has been observed with V = 1.425 GFIz (1 = 21.04 cm). [Pg.5]

The economic factors must be considered in every application. It is important to find a technique that will meet both the technical and economical requirements. In short, pollution control costs depend on the system characteristics and the application. Some cost equations that generalize the economics of the managing systems are available in the literature. Most of these equations give rough estimates and have an accuracy of only about 30% to 50%. For a comprehensive cost comparison of different units, a detailed cost analysis based on the equipment tender proposals and the special characteristics of the project is necessary. [Pg.1255]

In the powder diffraction technique, a monochromatic (single-frequency) beam of x-rays is directed at a powdered sample spread on a support, and the diffraction intensity is measured as the detector is moved to different angles (Fig. 1). The pattern obtained is characteristic of the material in the sample, and it can be identified by comparison with a database of patterns. In effect, powder x-ray diffraction takes a fingerprint of the sample. It can also be used to identify the size and shape of the unit cell by measuring the spacing of the lines in the diffraction pattern. The central equation for analyzing the results of a powder diffraction experiment is the Bragg equation... [Pg.334]

The classical scheme for dichroism measurements implies measuring absorbances (optical densities) for light electric vector parallel and perpendicular to the orientation of director of a planarly oriented nematic or smectic sample. This approach requires high quality polarizers and planarly oriented samples. The alternative technique [50, 53] utilizes a comparison of the absorbance in the isotropic phase (Dj) with that of a homeotropically oriented smectic phase (Dh). In this case, the apparent order parameter for each vibrational oscillator of interest S (related to a certain molecular fragment) may be calculated as S = l-(Dh/Di) (l/f), where / is the thermal correction factor. The angles of orientation of vibrational oscillators (0) with respect to the normal to the smectic layers may be determined according to the equation... [Pg.210]

In reality, this term is not small in comparison with the other terms so we should not expect the perturbation technique to give accurate results. With this choice for the perturbation, the Schrodinger equation for the unperturbed Hamiltonian operator may be solved exactly. [Pg.257]

The numerical jet model [9-11] is based on the numerical solution of the time-dependent, compressible flow conservation equations for total mass, energy, momentum, and chemical species number densities, with appropriate in-flow/outfiow open-boundary conditions and an ideal gas equation of state. In the reactive simulations, multispecies temperature-dependent diffusion and thermal conduction processes [11, 12] are calculated explicitly using central difference approximations and coupled to chemical kinetics and convection using timestep-splitting techniques [13]. Global models for hydrogen [14] and propane chemistry [15] have been used in the 3D, time-dependent reactive jet simulations. Extensive comparisons with laboratory experiments have been reported for non-reactive jets [9, 16] validation of the reactive/diffusive models is discussed in [14]. [Pg.211]

In thip appendix, a summary of the error propagation equations and objective functions used for standard characterization techniques are presented. These equations are Important for the evaluation of the errors associated with static measurements on the whole polymers and for the subsequent statistical comparison with the SEC estimates (see references 26 and 2J for a more detailed discussion of the equations). Among the models most widely used to correlate measured variables and polymer properties is the truncated power series model... [Pg.234]

Table 1 gives a comparison of Raman and pmr results for a series of copolymers. In the pmr data of Figure the CHg absorption of the polymer backbone at 6O.8 to 3.0 partially overlaps with the CH doublet centered at S2.h and this reduces the accuracy of the integrated intensity of the ester moiety to no better than 25. On the other hand, the accuracy of the Raman data is on the order of 3%, so the two techniques do agree within experimental error. The error associated with the Raman method could be reduced if calibration curves were employed. The weight percent feed and polymer compositions were converted to mole percent and reactivity ratios for MMA and OM were calculated by the Yezrielev, Erokhina and Riskin (YBR) method (9). The following equation, derived from the copolymer... [Pg.49]


See other pages where Comparison equation technique is mentioned: [Pg.5]    [Pg.8]    [Pg.9]    [Pg.31]    [Pg.46]    [Pg.5]    [Pg.8]    [Pg.9]    [Pg.31]    [Pg.46]    [Pg.157]    [Pg.3010]    [Pg.641]    [Pg.3010]    [Pg.247]    [Pg.155]    [Pg.312]    [Pg.178]    [Pg.514]    [Pg.195]    [Pg.115]    [Pg.47]    [Pg.863]    [Pg.4]    [Pg.268]    [Pg.217]    [Pg.192]    [Pg.112]    [Pg.194]    [Pg.102]    [Pg.414]    [Pg.82]    [Pg.178]    [Pg.273]    [Pg.136]    [Pg.89]    [Pg.232]    [Pg.151]   
See also in sourсe #XX -- [ Pg.46 ]




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