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Point analysis

Sample requirements Solid conductors and coated insulators typically 3 mm in diameter and < 200 nm thick at the analysis point for imaging and EDS, but < 50 nm thick for EELS... [Pg.14]

In order to demonstrate the achievement of quality and the effectiveness of the quality system, records will need to be gathered in from the locations where they were produced. This is more than a convenience because you will be unable to analyze all the data efficiently unless you need it in front of you. If you are lucky enough to operate a computer network and all the data is available on the network, data collection is a simple affair. However, many organizations still rely on paper records and therefore you will need a means of enabling such records to be either submitted to the analysis points or collected from source. To facilitate the collection of records you will need to insert submission or collection instructions in the relevant procedures which specify the records. [Pg.496]

The special single-layered configurations treated in this section are isotropic, specially orthotropic, generally orthotropic, and anisotropic. The generally orthotropic configuration cannot, of course, be distinguished from an anisotropic layer from the analysis point of view, but does have only the four independent material properties of an orthotropic material. [Pg.203]

AlUiougli the terms emergency and accident are discussed from a risk analysis point of view in Parts IV and V, Uiey are now defined in relatively general tenns, to help the reader differentiate between the two and to understand their application to the general subject of process occurrences . [Pg.179]

In process profile analysis, points are awarded to processes in the following categories ... [Pg.20]

Unusual arene-cadmium 7r-complexes have been recently prepared and structurally characterized. For example, the /w /zz-bcn/i porphyrin complex 194, which can be obtained by reaction of the free base with CdCl2, possesses a cadmium atom that is bound to the Mfez-phcnylcnc unit of the ligand in an apparent /-fashion (Figure 32). The resulting Cd-C distance of 2.71 A is shorter than the sum of the van der Waals radii.252 Despite this relatively short contact, DFT calculations and AIM analysis point to the weakness of the interaction. Comparable weak arene-cadmium 7r-interactions are also observed in the /wra-benziporphyrin cadmium chloride complex 195.253... [Pg.465]

For nonisothermal operation, the energy analysis, point (4) above, requires that the energy balance be developed for a complex system. The energy (enthalpy) balance previously developed for a BR, or CSTR, or PFR applies to a simple system (see equations 12.3-16,14.3-9, and 15.2-9). For a complex system, each reaction (i) in a specified network contributes to the energy balance (as (-AHRl)rt), and, thus, each must be accounted for in the equation. We illustrate this in the following example. [Pg.444]

ZSM-5(9), Two types of particles were found a) single crystals and b) polycrystalline aggregates, AB are loci of analysis points across the particles. Reproduced with permission from Ref, 23, Copyright 1983, Elsevier Sequoia. [Pg.322]

Chapter 6 describes the desired improvement of method parameters from the robustness point of view, not from the analyte or the specific analysis point of view. Illustrative examples are provided to help the reader develop methods with the currently available equipment. It is important that the method be described explicitly and unequivocally and that the validation report does not raise expectations that cannot be met in daily use. [Pg.4]

One aspect that has limited the use and introduction of process analyzers, and in particular FTIR analyzers, has been the high cost of the analyzer, and the resultant high cost per analysis point. Many process analyzer installations are financially evaluated in terms of cost per analysis or analysis point, as well as cost of ownership and the rate of payback. Typically, these costs need to be kept as low as possible... [Pg.188]

The use of hber optics and hber-optic multiplexing can increase the number of analysis points, and hence can reduce the overall costs related to a single analyzer. This approach has been used successfully with NIR instrumentation, where typically up to eight points can be handled. As noted earlier, the use of hber optics with IR Fourier transform instruments has in the past been limited. New hber materials with improved optical throughput are available, and also with the considered use of IR lasers, the role of hbers for IR applications is expected to increase. Although in the past commercial multiplexers have been available for mid-lR hber systems, their use has not been widespread. [Pg.188]

The opportunity to reduce the cost per analysis point can be very important for certain applications. One option with FTIR is to use sample stream multiplexing with a manifold system. For gas-based systems this is very straightforward, and does not impose a high cost overhead. Liquid systems are more complex, and are dependent on the nature of the stream involved, and material reactivity, miscibility and viscosity are important factors to consider. As noted previously, with the introduction of new, miniaturized technologies, the hope is that newer, less expensive devices can be produced, and these can provide the needed multiplicity to reduce the cost per analysis point to an acceptable level. [Pg.188]

The cost per analysis point and the projected payback are only two metrics used to evaluate the feasibility of installing a process analyzer. If a spectrometer replaces an existing service intensive analyzer then that is a positive situation. Also, because of the flexibility of infrared analyses, it is feasible that a mid-IR analyzer might replace several existing analyzers it is a case where direct chemical information from IR can be more important than certain inferential methods that only provide indirect information. Also, if the only other... [Pg.188]

S. Wold, J. Cheney, N. Kettaneh and C. McCready, The chemometric analysis point and dynamic data in pharma-centical and biotech prodnction (PAT) - some objectives and approaches, Chemom. Intell. Lab. Syst., 84, 159-163 (2006). [Pg.541]

The primary causes of this event were a direct result of systems, which resulted in a low level of TMAA stability. We had enjoyed freedom from accidents for years because a great many people worked very hard to see that everything was in order however, there were not enough systems with built-in safeguards to ensure that the probability of failure was as low as we really wanted. This analysis pointed out the need for systems studies and subsequent improvements if we were to be satisfied with future performance. Space will not allow detailed discussion of all problems found and their ramifications however, key deficiencies are listed below without comment ... [Pg.400]

Ray s approach was revised by Brown and Cooper (1993) from the system control analysis point of view (see the book of Comish-Bowden and Cardenas, 1990). They stress again that there is no unique rate-limiting step specific for an enzyme, and this step, even if it exists, depends on substrate, product and effector concentrations. They also demonstrated that the control coefficients... [Pg.107]

Keywords Chemical sensors Point contact Exhaled air analysis Point-contact spectroscopy Organic conductors Noninvasive diagnostics Chronic dyspepsia... [Pg.63]

Assuming that/A is 0.01, and we would like to determine this value with the atom-probe to an accuracy of 5% of fA, then the number of ions collected should be at least 39 600. This is already near an impractically large number in the atom-probe analysis. It quickly becomes impractical to determine accurately the concentration of a minority species with the atom-probe at a low counting rate if its concentration is smaller than —0.5%. The following statistical analysis points to a method with which this difficulty can be overcome. [Pg.155]

Williams analysis points the way, but still falls short of being a general method to calculate binding energy when the geometry of a complex is known directly from an X-ray determination, or can be surmised from molecular modelling. The approach suffers from two drawbacks. [Pg.55]

Thallous azide is a yellow, crystalline substance, m.p. 334°C. The crystal structure as determined by X-ray analysis points to the isomorphism of T1N3 with KN3 and RbN3 azides. [Pg.188]

Considering the long-term component of the total ozone monthly series (1926-1998) at Arosa, the analysis points out both the principal solar cycle and the decreasing trend starting from 1970s (Figure 6). [Pg.386]

It is clear that in a certain region of the parameter s = q p Cp, the adiabatic CSTR has three steady states with R(T) = G(T), marked by (1), (2), (3) in Figure 3.2. From a steady-state analysis point of view, the two steady states (1) and (3) are stable, while... [Pg.71]

All these applications have different instrumental configurations and in many cases the laser can be delivered to the analysis point via fibre optics. This provides an implementation challenge as laser exposure and eye safety are paramount concerns particularly in a manufacturing environment. Although mentioned briefly here Raman PAT applications are likely to be an area of significant growth over the coming years. [Pg.226]

Fig. 3.5. The flow of cells within the core of sheath fluid through the analysis point in the illuminating beam. When the sample is injected slowly (left), the core is narrow and the cells flow one at a time through the center of the laser beam. When the sample is injected too rapidly (right), the core is wide (somewhat exaggerated in this drawing) the cells may be illuminated erratically because they can stray from the center of the beam. In addition, more than one cell may be illuminated at the same time. Fig. 3.5. The flow of cells within the core of sheath fluid through the analysis point in the illuminating beam. When the sample is injected slowly (left), the core is narrow and the cells flow one at a time through the center of the laser beam. When the sample is injected too rapidly (right), the core is wide (somewhat exaggerated in this drawing) the cells may be illuminated erratically because they can stray from the center of the beam. In addition, more than one cell may be illuminated at the same time.
Fig. 3.6. Various types of flow chambers. A and B are designs used in sorting cytometers (in A the analysis point is in air after the stream has left the flow cell in B analysis occurs within an optically clear region of the chamber itself). C and D are two designs for nonsorting cytometers (in C the stream flows upward through an optically clear region of the chamber in D the stream is directed at an angle across a glass coverslip). Adapted from Pinkel and Stovel (1985). Fig. 3.6. Various types of flow chambers. A and B are designs used in sorting cytometers (in A the analysis point is in air after the stream has left the flow cell in B analysis occurs within an optically clear region of the chamber itself). C and D are two designs for nonsorting cytometers (in C the stream flows upward through an optically clear region of the chamber in D the stream is directed at an angle across a glass coverslip). Adapted from Pinkel and Stovel (1985).

See other pages where Point analysis is mentioned: [Pg.315]    [Pg.524]    [Pg.311]    [Pg.17]    [Pg.364]    [Pg.162]    [Pg.262]    [Pg.261]    [Pg.312]    [Pg.320]    [Pg.151]    [Pg.17]    [Pg.17]    [Pg.341]    [Pg.156]    [Pg.692]    [Pg.692]    [Pg.8]    [Pg.3]    [Pg.125]    [Pg.23]    [Pg.28]   
See also in sourсe #XX -- [ Pg.21 , Pg.23 , Pg.26 , Pg.237 ]




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Analysis of Intersection Points

Boiling point analysis

Boiling-point determination analysis

Bond critical points, electron density analysis

Cage critical point, electron density analysis

Electron Probe Microanalysis point analysis

End-point analysis

Focal-point analysis

Freezing point depression analysis

Frontal analysis by characteristic point

Fully automatic equipment for standardized boiling point analysis

Function point analysis

Hazard Analysis and Critical Control Points HACCP) system

Hazard Analysis of Critical Control Points

Hazard analysis and critical control point

Hazard analysis and critical control point HACCP)

Hazard analysis and critical control point HACCP) program

Hazard analysis by critical control points

Hazard analysis critical control points

Hazard analysis critical control points HACCP)

Hazard analysis critical control points HACCPs)

Hazard analysis critical control points approach

Heat Pinch point analysis

Inflection-point analysis

Intersection points analysis

Melting point analysis

Melting point thermal analysis

Operating point analysis

Operational functions function-point analysis

Pinch-point analysis

Point Analysis Providing Morphology, Texture and Strata Distribution

Point analysis providing chemical composition of layers and bulk

Point analysis providing molecular and crystalline structure

Point or Spot Analysis

Point-of-care analysis

Process analysis sampling point

Quantitative analysis using single point internal standard

Ring critical point, electron density analysis

Saddle point analysis

Single-point failure analysis

Singular Point Analysis

Systematic classification of transitions by inflection-point analysis

Thermal analysis melting point determination

Wave function analysis critical points

Zero-point analysis

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