Reference interpretation

Additionally, the tool enables even less experienced people to imderstand the specified product properties and its consequences. This is because the tool serves as a reference interpreter for the properties. As a consequence, the communication between several people involved in the product lifecycle of the product was significantly improved. 

Repeatability. This refers to two aspects of inspection similarity between objects that are inspected and possibility of maintaining constant inspection conditions (settings) for all the inspections performed. Obviously, interpretation of data in repeatable conditions is significantly simplified. Usually, inspection during or after manufacturing process will be repeatable. Another example of repeatable inspection is inspection of heat exchangers in power nuclear plants, inspection of aircrafts as these are well standardised. However, a large part of the NDT inspection done is not repeatable. 

By determining the depth of the bars using a eovermeter for the near surface bars (to 50 mm) and radar for up to 3 layers of bars (to 200 mm), it is only necessary to make one radiograph at a given loeation. In addition the radar will give usefiil information about the number and spacing of the bars. As described above, the eovermeter is used as a reference in establishing a baseline for radar interpretation. 

Another application of the knowledge of is to employ it for the interpretation of another relaxation measurement in the same system, an approach referred to as the dual spin probe teclmique. A rather old, but... 

In practice, each CSF is a Slater determinant of molecular orbitals, which are divided into three types inactive (doubly occupied), virtual (unoccupied), and active (variable occupancy). The active orbitals are used to build up the various CSFs, and so introduce flexibility into the wave function by including configurations that can describe different situations. Approximate electronic-state wave functions are then provided by the eigenfunctions of the electronic Flamiltonian in the CSF basis. This contrasts to standard FIF theory in which only a single determinant is used, without active orbitals. The use of CSFs, gives the MCSCF wave function a structure that can be interpreted using chemical pictures of electronic configurations [229]. An interpretation in terms of valence bond sti uctures has also been developed, which is very useful for description of a chemical process (see the appendix in [230] and references cited therein). 

How can we apply molecular dynamics simulations practically. This section gives a brief outline of a typical MD scenario. Imagine that you are interested in the response of a protein to changes in the amino add sequence, i.e., to point mutations. In this case, it is appropriate to divide the analysis into a static and a dynamic part. What we need first is a reference system, because it is advisable to base the interpretation of the calculated data on changes compared with other simulations. By taking this relative point of view, one hopes that possible errors introduced due to the assumptions and simplifications within the potential energy function may cancel out. All kinds of simulations, analyses, etc., should always be carried out for the reference and the model systems, applying the same simulation protocols. 

Two different types of dynamic test have been devised to exploit this possibility. The first and more easily interpretable, used by Gibilaro et al [62] and by Dogu and Smith [63], employs a cell geometrically similar to the Wicke-Kallenbach apparatus, with a flow of carrier gas past each face of the porous septum. A sharp pulse of tracer is injected into the carrier stream on one side, and the response of the gas stream composition on the other side is then monitored as a function of time. Interpretation is based on the first two moments of the measured response curve, and Gibilaro et al refer explicitly to a model of the medium with a blmodal pore... 

Many of the molecular modelling force fields in use today for molecular systems can be interpreted in terms of a relatively simple four-component picture of the intra- and inter-molecular forces within the system. Energetic penalties are associated with the deviation of bonds and angles away from their reference or equilibrium values, there is a function... 

The structural unit associated with an electronic transition m UV VIS spectroscopy IS called a chromophore Chemists often refer to model compounds to help interpret UV VIS spectra An appropriate model is a simple compound of known structure that mcor porates the chromophore suspected of being present m the sample Because remote sub stituents do not affect Xmax of the chromophore a strong similarity between the spectrum of the model compound and that of the unknown can serve to identify the kind of rr electron system present m the sample There is a substantial body of data concerning the UV VIS spectra of a great many chromophores as well as empirical correlations of sub stituent effects on k Such data are helpful when using UV VIS spectroscopy as a tool for structure determination... 

Any interpretation of the Type I isotherm must account for the fact that the uptake does not increase continuously as in the Type II isotherm, but comes to a limiting value manifested in the plateau BC (Fig. 4.1). According to the earlier, classical view, this limit exists because the pores are so narrow that they cannot accommodate more than a single molecular layer on their walls the plateau thus corresponds to the completion of the monolayer. The shape of the isotherm was explained in terms of the Langmuir model, even though this had initially been set up for an open surface, i.e. a non-porous solid. The Type I isotherm was therefore assumed to conform to the Langmuir equation already referred to, viz. 

A manual entitled Reporting Physisorption Data for Gas/Solid Systems with Special Reference to the Determination of Surface Area and Porosity has been prepared as a provisional publication by Commission 1.6 of the International Union of Pure and Applied Chemistry (lUPAC). The purpose of the manual is to draw attention to problems involved in reporting physisorption data and to provide guidance on the evaluation and interpretation of isotherm data. The general conclusions and recommendations are very similar to those contained in Chapter 6. 

Although spectroscopy and quantum mechanics are closely interrelated it is nevertheless the case that there is still a tendency to teach the subjects separately while drawing attention to the obvious overlap areas. This is the attitude 1 shall adopt in this book, which is concerned primarily with the techniques of spectroscopy and the interpretation of the data that accme. References to texts on quantum mechanics are given in the bibliography at the end of this chapter. 

It is not the intention that this book should be a primary reference on quantum mechanics such references are given in the bibliography at the end of this chapter. Nevertheless, it is necessary at this stage to take a brief tour through the development of the Schrodinger equation and some of its solutions that are vital to the interpretation of atomic and molecular spectra. 

The simplest interpretation of stm images is in terms of surface topography. However, care must be exercised in this interpretation, since in teahty, tunneling probabiUty is really measured. The many subdeties of stm data interpretation ate beyond the scope of this article. The interested reader is referred to references 14 and 15 for a more detailed discussion of these issues. 

Much more information can be obtained by examining the mechanical properties of a viscoelastic material over an extensive temperature range. A convenient nondestmctive method is the measurement of torsional modulus. A number of instmments are available (13—18). More details on use and interpretation of these measurements may be found in references 8 and 19—25. An increase in modulus value means an increase in polymer hardness or stiffness. The various regions of elastic behavior are shown in Figure 1. Curve A of Figure 1 is that of a soft polymer, curve B of a hard polymer. To a close approximation both are transpositions of each other on the temperature scale. A copolymer curve would fall between those of the homopolymers, with the displacement depending on the amount of hard monomer in the copolymer (26—28). 

Similarity Variables The physical meaning of the term similarity relates to internal similitude, or self-similitude. Thus, similar solutions in boundaiy-layer flow over a horizontal flat plate are those for which the horizontal component of velocity u has the property that two velocity profiles located at different coordinates x differ only by a scale factor. The mathematical interpretation of the term similarity is a transformation of variables carried out so that a reduction in the number of independent variables is achieved. There are essentially two methods for finding similarity variables, separation of variables (not the classical concept) and the use of continuous transformation groups. The basic theoiy is available in Ames (see the references). 

By using these N,ss values, we ean interpret the Nss Graph, and get a picture of the operating window ofthe.se three pumps. To interpret the graph we start on the left eolumn at the flow in gpm. In Figure 6-15, we draw a line from the flow to the Nss value of the pump, and then reference downward for water, or upward for hydroearbons. 

The principle of the measurement is described with the help of Fig. 2-7 [50]. Potential measurement is not appropriate in pipelines due to defective connections or too distant connections and low accuracy. Measurements of potential difference are more effective. Figure 3-24 contains information on the details in the neighborhood of a local anode the positions of the cathodes and reference electrodes (Fig. 3-24a), a schematic representation of the potential variation (Fig. 3-24b), and the derived values (Fig. 3-24c). Figure 2-8 should be referred to in case of possible difficulties in interpreting the potential distribution and sign. The electrical potentials of the pipeline and the reference electrodes are designated by... 

Climatology refers to averaged or analyzed meteorology over a period of record, usually several years. Air pollution climatology involves meteorological variables that are important in air pollution. Alternatively, it is the interpretation of air pollution data from a meteorological perspective. 

The CH COLOC diagram shows correlation signals for the methyl protons which are particularly clear (Table 51.3). Interpretation of these completes the assignments shown in formula D by reference to those CH multiplicities which have already been established (Table 51.1). 

In practice, only the frequencies lu = 0 to+oo are of interest and since in the frequency domain. v = jtu, a simplified Nyquist stability criterion, as shown in Figure 6.18 is A closed-loop system is stable if, and only if, the locus of the G(iLu)H(iuj) function does not enclose the (—l,j0) point as lu is varied from zero to infinity. Enclosing the (—1, jO) point may be interpreted as passing to the left of the point . The G(iLu)H(iLu) locus is referred to as the Nyquist Diagram. 

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