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Invariant calibration

For the time invariant calibration model discussed in Section 41.2, eq. (41.14) reduces to ... [Pg.594]

The measurement model of the time-invariant calibration system (eq. (41.5)) should now be expanded in the following way ... [Pg.598]

The Invariant Calibration of a Radial Coordinate in Terms of Counting Primitive Objects... [Pg.298]

Since the only invariant quantity associated with any given sphere, say S, is the number of material particles contained within it, such as N, then the only way to associate an invariant radial coordinate, say, r with S is to define it according to r = nf N), where ro is a fixed scale constant having units of length and the function / is restricted by the requirements f(Na) > f(Nb) whenever Na > Nb, f(N) > 0 for all N > 0, and /(0) = 0. To summarize, an invariant calibration of a radial coordinate in the model universe is given by r = rof(N) where... [Pg.318]

Once a radial coordinate has been invariantly calibrated, it is a matter of routine to define a rectangular coordinate system based on this radial calibration this is taken as done for the remainder of this chapter. [Pg.319]

Other methods of calibration are discussed by Zimm and by Brice and co-workers.23 Owing to difiSculties of absolute calibration, a reference standard invariably is used. This may consist of a polymer solution of constant properties (i.e., not subject to degradation) or a bulk polymer, such as that used by Debye and Bueche. ... [Pg.287]

A detailed study of the phase relationships in the magnesium oxysulphate cement was carried out by Urwongse Sorrell (1980b). They used X-ray analysis to examine the phases present in the cement, and established the composition of the invariant liquids after equilibration by measuring specific gravity with the aid of a pycnometer. Specific gravities were related to concentration by means of a calibration exercise in which 30 stock solutions of sulphuric acid at concentrations between 0 and 79-5 wt % were prepared with distilled water. [Pg.300]

Time-invariant systems can also be solved by the equations given in Table 41.10. In that case, F in eq. (41.15) is substituted by the identity matrix. The system state, x(j), of time-invariant systems converges to a constant value after a few cycles of the filter, as was observed in the calibration example. The system state. [Pg.595]

A proper calibration constant for any beamline geometry is the invariant Q. Thus, the Lupolen standard or any other semicrystalline polymer that previously has been calibrated in the Kratky camera can be made a secondary standard for a point-focus setup, after its invariant Q has been computed in absolute units - based on a measurement of its SAXS in the Kratky camera. [Pg.106]

Mathematically spoken k is the zero-dimensional projection / 0 of the scattering intensity. After calibration to absolute units 7(s) turns into 7(s) /V - its scattering power is known as Porod s invariant... [Pg.147]

In practice, the invariant can be used for the purpose of calibration to absolute scattering intensity by means of samples for which the absolute invariant can easily be computed. For this purpose colloidal suspensions of noble metals with known volume concentration are suitable [96], All the noble metal particles must be small enough so that they really contribute to the observed particle scattering. They must not agglomerate. [Pg.149]

Once analytical results have been produced, invariably a certain amount of manipulation is necessary to translate the results into information that can be understood by the customer. The reporting analyst may have to sort and process a large and varied amount of information in order to produce a small number of final answers. Data from standards may be used to produce calibration curves or calibrate instrument response. Results from quality control samples will have been plotted on charts to ensure that the system was working satisfactorily at the time the measurements were made. Sample data will be quantified by comparison with the standards and suitable corrections made. Then, checks may be made to confirm the results by examining the answers to look for any obvious wrong data. It is... [Pg.207]

Figure 5-66 shows the relationship between the true and cross-validation predicted qualities. Note the small but significant drop in the correlation compared to pure calibration, as shown in Figure 5-60. Calibration invariably produces a better correlation than prediction. Figure 5-66 shows the relationship between the true and cross-validation predicted qualities. Note the small but significant drop in the correlation compared to pure calibration, as shown in Figure 5-60. Calibration invariably produces a better correlation than prediction.
Almost all contemporary ab initio molecular electronic structure calculations employ basis sets of Gaussian-type functions in a pragmatic approach in which no error bounds are determined but the accuracy of a calculation is assessed by comparison with quantities derived from experiment[l] [2]. In this quasi-empirical[3] approach each basis set is calibrated [4] for the treatment of a particular range of atoms, for a particular range of properties, and for a particular range of methods. Molecular basis sets are almost invariably constructed from atomic basis sets. In 1960, Nesbet[5] pointed out that molecular basis sets containing only basis sets necessary to reach to atomic Hartree-Fock limit, the isotropic basis set, cannot possibly account for polarization in molecular interactions. Two approaches to the problem of constructing molecular basis sets can be identified ... [Pg.158]

Calibration is invariably based on spheres, which means that an instrument can be used with confidence only for such particles. Of course, a response will duly be recorded if a nonspherical particle passes through the scattering volume. But what is the meaning of the equivalent radius corresponding to that response Is it the radius of a sphere of equal cross-sectional area Or equal surface area Or equal volume Or perhaps equal mean chord length Answers to these questions depend on the particular instrument and nonspherical particle comprehensive answers do not come easily because it is difficult to do calculations for nonspherical particles, even those of regular shape. [Pg.404]

The radial parameter about any point is defined by r = rtfiN) since this function is constrained to be monotonic, its inverse exists so that, by definition, N=f l r/rf). Suppose that we now introduce the scale constant mo then Nmo = mo/ 1(r/ro) = M r) can be interpreted as quantifying the total amount of material inside a sphere of radius r centered on the assumed origin. Although r = rof(N) and M r) = Nm ) are equivalent, the development that follows is based on using M r) as a description of the mass distribution given as a function of an invariant radial distance parameter, r, of undefined calibration. [Pg.319]

Finlayson GD and Drew MS 2001 4-sensor camera calibration for image representation invariant to shading, shadows, lighting, and specularities. Proceedings of the 8th IEEE International Conference on Computer Vision, Volume 2, Vancouver, Canada, July 9-12, 2001, pp. 473-480. [Pg.371]

The interpretation and implementation of published methods invariably differ at different laboratories due to diversity of utilized instruments, their incidental elements and supplies, and the differences in method interpretation. Each analytical method must be validated at the laboratory before it is used for sample analysis in order to demonstrate the laboratory s ability to consistently produce data of known accuracy and precision. Method validation includes the construction of a calibration curve that meets the acceptance criteria the determination of the method s accuracy and precision and the MDL study. A method SOPs must be prepared and approved for use. Method validation documentation is kept on file and should be always available to the client upon request. [Pg.261]

Turbidity measurement usually directly relates the forementioned value in a sample to another value in a RM by a controlled comparison of values, or indirectly through an instrument calibration established for values for identical entities in similar RMs. This measurement is characterized, in part, by an observed repeatability and invariably by an estimated uncertainty - the sole indication of the quality for each link. The final link is made to a turbidity unit in an internationally recognized scale. [Pg.56]


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