Measurement wavelength, choice

For a detailed discussion on the choice of the internal standard, the choice of the measuring wavelength, the calculation parameters, the why and the wherefore of this analysis, we refer to our earlier publications (10,12). 

Direct-reading polychromators (Figure 3b) have a number of exit slits and photomultiplier tube detectors, which allows one to view emission from many lines simultaneously. More than 40 elements can be determined in less than one minute. The choice of emission lines in the polychromator must be made before the instrument is purchased. The polychromator can be used to monitor transient signals (if the appropriate electronics and software are available) because unlike slew-scan systems it can be set stably to the peak emission wavelength. Background emission cannot be measured simultaneously at a wavelength close to the line for each element of interest. For maximum speed and flexibility both a direct-reading polychromator and a slew-scan monochromator can be used to view emission from the plasma simultaneously. 

Continuous sources The sources of choice for measurements in the ultraviolet spectral region are hydrogen or deuterium lamps [1]. When the gas pressure is 30 to 60 X10 Pa they yield a continuous emission spectrum. The maxima of their radiation emission occur at different wavelengths (Hi A = 280 nm Di 2 = 220 nm). This means that the deuterium lamp is superior for measurements in the lower UV region (Fig. 15). 

In principle, measurement of the phosphorescence characteristics of samples obtained after extraction of polymers with organic solvents may also yield useful information regarding the nature and concentration of the additives present. Parker and Hatchard [157] have examined the possibilities of phosphorescence measurements for V-phenyl-2-naphthylamine. Although it should be possible to determine various analytes simultaneously by correct choice of ex and em wavelengths and phosphorescence decay, no pertinent reports are available. Phosphorescence finds limited application for the direct determination of additives in polymers (without prior extraction). 

The most basic method for the determination of the methylxanthines is ultraviolet (UV) spectroscopy. In fact, many of the HPLC detectors that will be mentioned use spectroscopic methods of detection. The sample must be totally dissolved and particle-free prior to final analysis. Samples containing more than one component can necessitate the use of extensive clean-up procedures, ajudicious choice of wavelength, the use of derivative spectroscopy, or some other mathematical manipulation to arrive at a final analytical measurement. A recent book by Wilson has a chapter on the analysis of foods using UV spectroscopy and can be used as a suitable reference for those interested in learning more about this topic.1... 

Figure 10. Predicted modulation index (m), as a function of C02 gas concentration (%v/v) in the measurement cell. Reference and measurement cells were of lm length and the reference cell contained 100% C02 gas at lBar/20 °C. A choice of optical filter, having a bandwidth of 100 nm and a centre wavelength of 2.004 pm, was assumed.

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