Multi-band detectors

Such effects principally cannot be observed in multi band detectors such as a UV diode array detector or a Fourier transform infrared (FTIR) detector because all wavelengths are measured under the same geometry. For all other types of detectors, in principle, it is not possible to totally remove these effects of the laminar flow. Experiments and theoretical calculations show (8) that these disturbances can only be diminished by lowering the concentration gradient per volume unit in the effluent, which means that larger column diameters are essential for multiple detection or that narrow-bore columns are unsuitable for detector combinations. Disregarding these limitations can lead to serious misinterpretations of GPC results of multiple detector measurements. Such effects are a justification for thick columns of 8-10 mm diameter. 

Multi-band fire detector monitors monitor several wavelengths of predominate fire radiation frequencies by photocells. They compare these measurements to normal ambient frequencies through micro processing. Where these are found be above certain levels an alarm is indicated. False alarms may even be "recognized"... 

In order to estimate the stability of triplet carbenes (19) under ambient conditions, laser flash photolysis ( LFP) [26] was carried out on the precursor diazomethanes (18) in solution at room temperature. The transient absorption bands formed upon the flash were recorded by a multi-channel detector. These bands were assigned to the triplet carbenes (19) by comparison with those obtained in matrix at low temperature. The kinetic information was then available by monitoring the decay of the transient absorption with oscillographic tracer. When triplet carbenes decayed unimolecularly, which is often so, lifetime (x) can be determined. However when the decay did not follow a single exponential, which is sometimes the case, x cannot be determined. In this case, a half-life (ti/2) is estimated from the decay curve as a rough measure of the stability. 

Recently, the state-selective detection of reaction products tluough infrared absorption on vibrational transitions has been achieved and applied to the study of HF products from the F + H2 reaction by Nesbitt and co-workers (Chapman et al [7]). The relatively low sensitivity for direct absorption has been circumvented by the use of a multi-pass absorption arrangement with a narrow-band tunable infrared laser and dual beam differential detection of the incident and transmission beams on matched detectors. A particular advantage of probing the products tluough absorption is that the absolute concentration of the product molecules in a given vibration-rotation state can be detenuined. 

Infrared spectrophotometry of ozone based on the principal absorption band near 9.5 pm is relatively free from interference by the bands of other atmospheric constituents. However, a long optical path is necessary for detection of atmospheric ozone. A White cell (multiple reflection cell, 10-1000 m path) combined with a Fourier-transform infrared (FTIR) spectrometer (spectral resolution of lcm or better) with a HgCdTe detector is often used in multi-component air-monitoring and smog chamber experiments. 

A conventional monochromator (either Ebert, Czerny-Turner, Littrow or Echelle) may be used (see AAS sections for details), but some of the more basic instrumentation uses interference filters. These are optical filters that remove large bands of radiation in a nondispersive way. A dispersion element such as a prism or a grating is therefore not required. Only a relatively narrow band of radiation is allowed to pass to the detector. The disadvantage with such devices is that they are not particularly efficient and hence much of the fluoresced light is lost. An alternative development is the multi-reflectance filter. This is shown diagramatically in Figure 3, and has the... 

The easiest hyphenated system consists of an LC instrument with a multi-wavelength (e.g. diode-array) UV detector. Such a system is excellent for characterizing copolymers consisting of two or more types of monomeric units, all of which exhibit (different) UV activity. Unfortunately, this is hardly ever the case. A combination of a UV detector and a refractive-index (RI) detector connected in series does in principle provide sufficient information for copolymers (two different monomeric units). However, the interdetector volumes and band broadening are a complicating factor, as are the different background and blank signals (solvent peaks) provided by the two instruments. 

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