Emission Spectrometry Waves

POSSIBILITY OF USING GRASING EMISSION IN WAVE DISPERSION X-RAY SPECTROMETRIES... 

Modern atomic spectrometry methods can be considered as the most sensitive and specific analytical techniques which are available today for this wide field of application (Schramel et al., 1982). The most commonly used ones are atomic absorption and atomic emission spectrometry. The last mentioned technique is enjoying a renaissance due to the development of the different plasma excitation units, especially ICP, DCP and the different micro-wave induced plasmas (MIP) (Boumans 1978, 1979 Keirs and Vickers, 1977 Skogerboe and Coleman, 1976a, 1976b). 

Hydride generation techniques are superior to direct solution analysis in several ways. However, the attraction offered by enhanced detection limits is offset by the relatively few elements to which the technique can be applied, potential interferences, as well as limitations imposed on the sample preparation procedures in that strict adherence to valence states and chemical form must be maintained. Cold-vapor generation of mercury currently provides the most desirable means of quantitation of this element, although detection limits lower than AAS can be achieved when it is coupled to other means of detection (e.g., nondispersive atomic fluorescence or micro-wave induced plasma atomic emission spectrometry). 

Any of the methods of detection used in liquid chromatography can be used in IC, though some are more useful than others. If the eluent does not affect the detector the need for a suppressor disappears. Common means of detection in IC are ultraviolet (UV) absorption, including indirect absorption electrochemical, especially amperometric and pulsed amperometric and postcolumn derivatization. Detectors atomic absorption spectrometry, chemiluminescence, fluorescence, atomic spectroscopic, refractive index, electrochemical (besides conductivity) including amperometric, coulometric, potentiometric, polaro-graphic, pulsed amperometric, inductively coupled plasma emission spectrometry, ion-selective electrode, inductively coupled plasma mass spectrometry, bulk acoustic wave sensor, and evaporative light-scattering detection. 

To overcome the problem of detection in CE, many workers have used inductively coupled plasma-mass spectrometry (ICP-MS) as the method of detection. Electrochemical detection in CE includes conductivity, amperometry, and potentiometry detection. The detection limit of amperometric detectors has been reported to be up to 10 M. A special design of the conductivity ceU has been described by many workers. The pulsed-amperometric and cyclic voltametry waveforms, as well as multi step wave forms, have been used as detection systems for various pollutants. Potentiometric detection in CE was first introduced in 1991 and was further developed by various workers. 8-Hydroxyquinoline-5-sulfonic acid and lumogallion exhibit fluorescent properties and, hence, have been used for metal ion detection in CE by fluorescence detectors. Overall, fluorescence detectors have not yet received wide acceptance in CE for metal ions analysis, although their gains in sensitivity and selectivity over photometric detectors are significant. Moreover, these detectors are also commercially available. Some other devices, such as chemiluminescence, atomic emission spectrometry (AES), refractive index, radioactivity, and X-ray diffraction, have also been used as detectors in CE for metal ions analysis, but their use is stiU limited. 

Preferred methods in trace determination of the elements include atomic absorption spectrometry (AAS), optical emission spectrometry (OES) with any of a wide variety of excitation sources [e.g., sparks, arcs, high-frequency or microwave plasmas (inductively coupled plasma, ICP microwave induced plasma, MIP capacitively coupled micro-wave plasma, CMP), glow discharges (GD). hollow cathodes, or laser vaporization (laser ablation)], as well as mass spectrometry (again in combination with the various excitation sources listed), together with several types of X-ray fluorescence (XRF) analysis [51]. 

The limitations stemming from the restricted temperatures of flames led to the development of high-temperature plasma sources for atomic emission spectrometry. The development of high-frequency inductively coupled plasmas and micro-wave plasmas has led to the widespread use of these methods for routine analytical work. 

Rodriguez-Pereiro 1, Wasik A, Lobinski R. Trace environmental speciation analysis for organometallic compounds by isothermal multicapillary gas chromatography micro-wave induced plasma atomic emission spectrometry (MC GC MIP AES) 1977. Chem Anal 1997 (42) 799-808. 

Micro-coulometric Atoms-pheric pressure induced helium micro-wave induced plasma emission spectrometry... 

A pattern of emissions from a particle following the application of energy. The emissions may be in the form of electromagnetic waves such as observed in spectroscopy or in the form of a mass such as that observed in mass spectrometry. 

GFAAS), inductively coupled plasma-atomic emission spectroscopy (ICP-AES - also referred to as inductively coupled plasma-optical emission spectroscopy, or ICP-OES) and inductively coupled plasma-mass spectrometry (ICP-MS) are all routinely utilized in pharmaceutical applications. While there are other techniques of note available, such as micro-wave induced plasma (MIP) or direct coupled plasma (DCP), they have not been routinely used in the pharmaceutical industry, and will, therefore, not be discussed here. The theories involved in the use of FAAS, GFAAS, ICP and ICP-MS may be found in other articles of this Encyclopedia. 

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