Monitoring spectrometer

TOMS IWT Total Ozone Monitoring Spectrometer ST, TR, profiles 0, Nimbus 7 (1979-92) ADEOS (1996-97) Earth Probe (1996-) Meteor (1992-94) QuickTOMS (2000)... 

Kim, J.-H., R.D. Hudson and A.M. Thompson (1996) A new method for deriving time averaged tropospheric column ozone over die tropics using total ozone monitoring spectrometer (TOMS) radiances intercomparison and analysis using TRACE A data. Journal of Geophysical Research 101 24317-24330. 

Both the nitroxide decay measuranents of free-radical photoinitiation rates and nitroxide kinetics during HALS stabilization depend on accurate, quantitative measurements of nitroxide concentrations in cross-linked polymers. Quantification of radical concentrations by ESR requires a suitable primary standard, careful sample preparation, a reference standard with which to monitor spectrometer performance, and most important, reproducible positioning of the samples in the resonance cavity of the spectrometer. Most of the experiments described here were carried out with a Bruker-IBM ER 200 D spectrometer equipped with an Aspect 2000 Data System. Because these coatings are cured at temperatures as high as 130°C, the primary nitroxide standard, which was introduced into the coating prior to cure, had to be... 

A refinement of the ENDOR experiment is electron-nnclear-nnclear triple resonance, now commonly denoted TRIPLE. In TRIPLE experiments one monitors the effect of a simnltaneons excitation of two nnclear spm transitions on the level of the EPR absorption. Two versions, known as special TRIPLE (ST) and general TRIPLE (GT), are rontinely perfonned on connnercially available spectrometers. 

Another approach to multielemental analysis is to use a multichannel instrument that allows for the simultaneous monitoring of many analytes. A simple design for a multichannel spectrometer consists of a standard diffraction grating and 48-60 separate exit slits and detectors positioned in a semicircular array around the diffraction grating at positions corresponding to the desired wavelengths (Figure 10.50). 

In the modem scanning mass spectrometer, it is more convenient that ions arrive at a single point for monitoring (collection), so r (or r ) is kept constant. Therefore, B or V must be varied to bring all ions to the same focus viz., one of the relationships in Equation 24.5 must apply ... 

A second use of arrays arises in the detection of trace components of material introduced into a mass spectrometer. For such very small quantities, it may well be that, by the time a scan has been carried out by a mass spectrometer with a point ion collector, the tiny amount of substance may have disappeared before the scan has been completed. An array collector overcomes this problem. Often, the problem of detecting trace amounts of a substance using a point ion collector is overcome by measuring not the whole mass spectrum but only one characteristic m/z value (single ion monitoring or single ion detection). However, unlike array detection, this single-ion detection method does not provide the whole spectrum, and an identification based on only one m/z value may well be open to misinterpretation and error. 

In LC, the most common means for monitoring the eluant is to pass it through a cell connected into an ultraviolet spectrometer. As substances elute from the column, their ultraviolet absorption is measured and recorded. Alternatively, the refractive index of the eluant is monitored since it varies from the value for a pure solvent when it contains organics from the column. 

Selected-ion monitoring (SIM). Describes the operation of a mass spectrometer in which the ion currents at one (or several) selected m/z values are recorded, rather than the entire mass spectrum. The use of the terms multiple-ion detection (MID), multiple-ion (peak) monitoring (MPM), and mass fragmentography are not recommended. 

Chemical Gas Detection. Spectral identification of gases in industrial processing and atmospheric contamination is becoming an important tool for process control and monitoring of air quaUty. The present optical method uses the ftir (Fourier transform infrared) interference spectrometer having high resolution (<1 cm ) capabiUty and excellent sensitivity (few ppb) with the use of cooled MCT (mercury—cadmium—teUuride) (2) detectors. 

Quantitative mass spectrometry, also used for pharmaceutical appHcations, involves the use of isotopicaHy labeled internal standards for method calibration and the calculation of percent recoveries (9). Maximum sensitivity is obtained when the mass spectrometer is set to monitor only a few ions, which are characteristic of the target compounds to be quantified, a procedure known as the selected ion monitoring mode (sim). When chlorinated species are to be detected, then two ions from the isotopic envelope can be monitored, and confirmation of the target compound can be based not only on the gc retention time and the mass, but on the ratio of the two ion abundances being close to the theoretically expected value. The spectrometer cycles through the ions in the shortest possible time. This avoids compromising the chromatographic resolution of the gc, because even after extraction the sample contains many compounds in addition to the analyte. To increase sensitivity, some methods use sample concentration techniques. 

The potential of LA-based techniques for depth profiling of coated and multilayer samples have been exemplified in recent publications. The depth profiling of the zinc-coated steels by LIBS has been demonstrated [4.242]. An XeCl excimer laser with 28 ns pulse duration and variable pulse energy was used for ablation. The emission of the laser plume was monitored by use of a Czerny-Turner grating spectrometer with a CCD two-dimensional detector. The dependence of the intensities of the Zn and Fe lines on the number of laser shots applied to the same spot was measured and the depth profile of Zn coating was constructed by using the estimated ablation rate per laser shot. To obtain the true Zn-Fe profile the measured intensities of both analytes were normalized to the sum of the line intensities. The LIBS profile thus obtained correlated very well with the GD-OES profile of the same sample. Both profiles are shown in Fig. 4.40. The ablation rate of approximately 8 nm shot ... 

Applications The differential optical absorption spectrometer has been used to monitor concentrations of gases or intermediate compounds such as SO, NO, O5, HCHO, HNO, CS, NO, and OH in the atmosphere.In atmospheric measurements with open paths of 100 to 1000 m, a detection limit of about 1 ppb can be achieved. In the emission measurements, the path length across the duct or the plume can range in meters. 

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