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Lines coupling devices

Trace enrichment is the sample preparation procedure which is performed by passing a crude sample through a special collection column, but with a couple of added features. It is often done on-line, one at a time, just prior to the analytical procedure. It usually involves a minicolumn very similar to an off-line device, like a solid-phase extraction tube, but packed into a stainless-steel column and attached to the injection valve. This is called a trace enrichment column in many published procedures. Another name that is often given to this technique is column switching in the title or key words of published articles. This is because this technique involves valves that must be switched from one solvent flow stream to another. The valve, in its initial position, allows the crude sample... [Pg.1651]

The device is readily applicable to multiple installations of different line resistance. For multiple-point recorders and indicators as many resistances BC may be employed as there are couples. These may be inexpensive rheostats having a resistance of approximately 15 ohms each located in each couple line between the couple and the selective switch. These rheostats may be adjusted in the manner described whenever convenient or necessary. The following illustrates a suitable proportioning of resistance for a 300 ohm indicator. [Pg.426]

Flexible electronic devices are increasingly capturing the attention of researchers in radio frequency (RF) technologies and metamaterials physics, and are not limited to electronics applications such as light emitting diodes (7). These devices are driven by the pliable, conformal, and stretchable characteristics of elastomeric substrates [7-13], Examples of RF and terahertz devices demonstrated on flexible device platforms include curved antennas [12], millimeter-wave patch flexible antennas and coupled line filters [13], coplanar waveguide antenna [14], stretchable microfluidic RF antenna [15], frequency selective surfaces and metamaterials [8], microwave frequency switches [16], tunable metamaterials [17, 18], and tunable dielectric and magnetic properties [10]. [Pg.212]

Recently it has been shown that rotating coiled columns (RCC) can be successfully applied to the dynamic (flow-through) fractionation of HM in soils and sediments [1]. Since the flow rate of the extracting reagents in the RCC equipment is very similar to the sampling rate that is used in the pneumatic nebulization in inductively coupled plasma atomic emission spectrometer (ICP-AES), on-line coupling of these devices without any additional system seems to be possible. [Pg.459]

Figure 23.9(b) Typical layout of a line coupling device and carrier equipment (PLCC) showing phase-to-phase coupling... [Pg.738]

Figure 10.4 shows a schematic representation of the multidimensional GC-IRMS System developed by Nitz et al. (27). The performance of this system is demonstrated with an application from the field of flavour analysis. A Siemens SiChromat 2-8 double-oven gas chromatograph equipped with two FIDs, a live-T switching device and two capillary columns was coupled on-line with a triple-collector (masses 44,45 and 46) isotope ratio mass spectrometer via a high efficiency combustion furnace. The column eluate could be directed either to FID3 or to the MS by means of a modified Deans switching system . [Pg.226]

The length of side b is measured with a tape measure and the length of side a is measured with a device such as a dial indicator. Note that this diagram assumes the coupling is centered on the shaft and that its center-line is the same as the shaft s. Angle A in degrees is calculated by ... [Pg.917]

Fig. 8 PossibUities for on-line coupling of thin-layer chromatography with physical measurement and determination methods. CCD = Charge Coupled Device Detection. Fig. 8 PossibUities for on-line coupling of thin-layer chromatography with physical measurement and determination methods. CCD = Charge Coupled Device Detection.
Most of the SFE-SFC devices developed are designed to obtain qualitative results. However, various quantitative analyses of polymer additives have been reported [82,87,91-93], The ability to remove the SCF is particularly important when SFE is coupled on-line... [Pg.440]

The main detectors used in AES today are photomultiplier tubes (PMTs), photodiode arrays (PDAs), charge-coupled devices (CCDs), and vidicons, image dissectors, and charge-injection detectors (CIDs). An innovative CCD detector for AES has been described [147]. New developments are the array detector AES. With modem multichannel echelle spectral analysers it is possible to analyse any luminous event (flash, spark, laser-induced plasma, discharge) instantly. Considering the complexity of emission spectra, the importance of spectral resolution cannot be overemphasised. Table 8.25 shows some typical spectral emission lines of some common elements. Atomic plasma emission sources can act as chromatographic detectors, e.g. GC-AED (see Chapter 4). [Pg.614]

Coupling an electrochemical cell to an analytical device requires that hindering technical problems be overcome. In the last years there has been a considerable improvement in the combined use of electrochemical and analytical methods. So, for instance, it is now possible to analyze on-line electrode products during the simultaneous application of different potential or current programs. A great variety of techniques are based on the use of UH V for which the emersion of the electrode from the electrolytic solution is necessary. Other methods allow the in situ analysis of the electrode surface i.e the electrode reaction may take place almost undisturbed during surface examination. In the present contribution we shall confine ourselves to the application of some of those methods which have been shown to be very valuable for the study of organic electrode reactions. [Pg.128]


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