Detection Sequential

Normally a FID is acquired using simultaneous quadrature detection, sequential quadrature detection is explained in section 2.3.1. The FID consists of the values of the X- and y-components of the magnetization measured at discrete intervals during the acquisition period T q. The time interval between two successive pairs of data points is called the dwell time For a given (chosen) spectral width SW [Hz], a total number of data points TD and acquisition time T q, the following relation is valid (Nyquist theorem) ... 

In the 4T configuration (Fig. 3c, y), two separate CC and PU electrode couples are used. The CC couple is placed outside the measurement sensitivity zone, while the PU electrodes measure the so called transimpedance . Such a concept is generally referred to as bioimpedance in physiological measurements. On virtue of modem voltage amplifiers, the PU electrodes are ideally non-current carrying, eliminating all Zp contributions to the measurements. Hence, only the properties of the sample are detected. Sequential 4T measurements represent the best method to collect a large matrix of bioimpedance data from several electrode couples to map the impedivity of a sample. 

Multichannel imaging Simultaneous detection, sequential detection Sequential detection... 

Rgure 8.2.4. CEC with a mobile pseudostationary particle phase, (a) Sample containing species A and B injected after the nanoparticle plug has been injected (b) after some time, the sample shows separation and is getting ahead of the particle plug (c) species A and B are ahead of the particle plug and are being detected sequentially. 

Ion detectors can be separated into two classes those that detect the arrival of all ions sequentially at one point (point ion collector) and those that detect the arrival of all ions simultaneously along a plane (array collector). This chapter discusses point collectors (detectors), while Chapter 29 focuses on array collectors (detectors). 

Quadrupole mass spectrometers (mass filters) allow ions at each m/z value to pass through sequentially for example, ions at m/z 100, 101, 102 will pass one after the other through the quadrupole assembly so that first m/z 100 is transmitted, then m/z 101, then m/z 102 (or vice versa), and so on. Therefore, the ion collector (or detector) at the end of the quadrupole unit needs to cover only one point or focus in space (Figure 29.1a), and a complete mass spectrum is recorded over a period of time. The ions arrive at the collector sequentially, and ions are detected in a time domain, not in a spatial domain. 

An array ion collector (detector) consists of a large number of miniature electron multiplier elements arranged side by side along a plane. Point ion collectors gather and detect ions sequentially (all ions are focused at one point one after another), but array collectors gather and detect all ions simultaneously (all ions are focused onto the array elements at the same time). Array detectors are particularly useful for situations in which ionization occurs within a very short space of time, as with some ionization sources, or in which only trace quantities of a substance are available. For these very short time scales, only the array collector can measure a whole spectrum or part of a spectrum satisfactorily in the time available. 

In modem mass spectrometry, ion collectors (detectors) are generally based on the electron multiplier and can be separated into two classes those that detect the arrival of all ions sequentially at a point (a single-point ion collector) and those that detect the arrival of all ions simultaneously (an array or multipoint collector). This chapter compares the uses of single- and multipoint ion collectors. For more detailed discussions of their construction and operation, see Chapter 28, Point Ion Collectors (Detectors), and Chapter 29, Array Collectors (Detectors). In some forms of mass spectrometry, other methods of ion detection can be used, as with ion cyclotron instmments, but these are not considered here. 

Other types of mass spectrometer can use point, array, or both types of ion detection. Ion trap mass spectrometers can detect ions sequentially or simultaneously and in some cases, as with ion cyclotron resonance (ICR), may not use a formal electron multiplier type of ion collector at all the ions can be detected by their different electric field frequencies in flight. 

Recommendation When all measurements were recorded by hand, operators and engineers could use their judgment concerning their validity. Now with most acqmred automatically in enormous numbers, the measurements need to be examined automatically. The goal continues to be to detect correctly the presence or absence of gross errors and isolate which measurements contain those errors. Each of the tests has limitations. The hterature indicates that the measurement test or a composite test where measurements are sequentially added to the measurement set are the most powerful, but their success is limited. If automatic analysis is required, the composite measurement test is the most direct to isolation-specific measurements with gross error. 

In the present work it has been shown that on-line coupling of flowthrough fractionation in RCC with ICP-EAS detection enables not only the fast and efficient fractionation of trace elements (TE) in environmental solids to be achieved but allows real-time studies on the leaching process be made. A novel five-step sequential extraction scheme was tested in on-line mode. The optimal conditions for the fractionation were chosen. Investigating elution curves provides important information on the efficiency of the reagents used, the leaching time needed for the separation of each fraction, and the potential mobility of HM forms. 

Atomic absorption spectroscopy of VPD solutions (VPD-AAS) and instrumental neutron activation analysis (INAA) offer similar detection limits for metallic impurities with silicon substrates. The main advantage of TXRF, compared to VPD-AAS, is its multielement capability AAS is a sequential technique that requires a specific lamp to detect each element. Furthermore, the problem of blank values is of little importance with TXRF because no handling of the analytical solution is involved. On the other hand, adequately sensitive detection of sodium is possible only by using VPD-AAS. INAA is basically a bulk analysis technique, while TXRF is sensitive only to the surface. In addition, TXRF is fast, with an typical analysis time of 1000 s turn-around times for INAA are on the order of weeks. Gallium arsenide surfaces can be analyzed neither by AAS nor by INAA. 

Three different types of grating spectrometer detection sterns are used (Figure 3) sequential (slew-scan) monochromators, simultaneous direct-reading polychroma-... 

In scanning mode the sequential detection of single pixels (picture elements) and voxels (volume elements) results in long measurement times in practice, therefore, only small volumes (10 x 10 x 1 p,m ) can be measured [3.56]. 

Figure 12.11 Coupled SEC-RPLC separation of compound Chemigum mbber stock (a) SEC ti ace (b) RPLC trace of fraction 1, dibutylphthalate (c) RPLC trace of fraction 2, elemental sulfur. Coupled SEC conditions MicroPak TSK 3000H (50 cm) X 2000H (50 cm) X 1000 H (80 cm) columns (8 mm i.d.) eluent, THE at a flow rate of 1 mL/min UV detection at 215 nm (1.0 a.u.f.s.) injection volume, 200 p-L. RPLC conditions MicroPak MCH (25 cm X 2.2 mm i.d.) column flow rate, 0.5 mL/min injection volume, lOpL gradient, acetonitrile-water (20 80 v/v) to 100% acetonitrile at 3% acetonitrile/min UV detection at 254 nm (0.05 a.u.f.s.). Reprinted from Journal of Chromatography, 149, E. L. Jolmson et al., Coupled column cliromatography employing exclusion and a reversed phase. A potential general approach to sequential analysis , pp. 571-585, copyright 1978, with permission from Elsevier Science.

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