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Interface liquid chromatography-atomic absorption

Blais, J.-S., Huyghues-Despointes, A., Momplaisir, G.-M. and Marshall, W.D. (1991) High-performance liquid chromatography-atomic absorption spectromety interface for the determination of selenoniocholine and trimethylselenonium cations applications to human urine./. Anal. At. Spectrom., 6, 225-232. [Pg.432]

High, K.A., Azani, R., Fazekas, A.F., Chee, Z.A. and Blais, J.-S. (1992) Thermospray-microatomizer interface for the determination of trace cadmium and cadmium-metallothioneins in biological samples with flow injection- and high-performance liquid chromatography-atomic absorption spectrometry. Anal. Chem., 64, 3197-3201. [Pg.435]

The most important features of liquid membranes are that they olfer highly selective extraction, efficient enrichment of analytes from the matrix in only one step, and the possibility of automated interfacing to different analytical instruments such as liquid chromatography, gas chromatography, capillary zone electrophoresis, UV spectrophotometry, atomic absorption spectrometry, and mass spectrometry [82]. [Pg.578]

D Commercial COTS controlled by external computer Hybrid systems such as automated dissolution workstation with high-performance liquid chromatography (HPLC) or ultraviolet-visible (UV-Vis) interface Liquid chromatographs, gas chromatographs, UV/Vis spectrophotometers, Fourier transform infrared (FTIR) spectrophotometers, near-infrared (NIR) spectrophotometers, mass spectrometers, atomic absorption spectrometers, thermal gravimetric analyzers, COTS automation workstations... [Pg.793]

Diemer, J. and Heumann, K.G. (1997) Bromide/bromate speciation by NTI-IDMS and ICP-MS coupled with ion exchange chromatography. Fresenius J. Anal. Chem., 357,74-79. Duan, YX., Wu, M., Jin, Q.H. and Hieftje, G.M. (1995) Vapour generation of nonmetals coupled to microwave plasma-torch mass-spectrometry. Spectrochim. Acta B, 50,355-368. Ebdon, L., Hill, S. and Jones, R (1987) Interface system for directly coupled high performance liquid chromatography-flame atomic absorption spectrometry for trace metal determination./. Anal. At. Spectrom., 2, 205-210. [Pg.83]

Falter R and Scholer HE (1994) Interfacing high-performance liquid chromatography and cold vapour atomic absorption spectrometry with on-line UV... [Pg.989]

The determination of the different forms (e. g. compounds or complexes) in which an element occurs (often referred to as the speciation of an element and speciation analysis, respectively [28]) is in most cases performed by hyphenated techniques. These are the combination of a high-performance separation technique such as gas or liquid chromatography, or electrophoresis, and an element- or compound-specific detector [29]. While the former provides the separation of the different elemental species prevalent in the sample, the latter brings selective and sensitive detection. In the case of AAS, only the hyphenation with gas and Hquid chromatography, respectively, has gained importance. The combination of atomic absorption spectrometry and electrophoresis has never proven successfiil, obviously due to the incompatibility of the extremely low flow rates of electrophoretic separations with the aspiration volumes of flame atomisers and the difficulties of interfacing the two techniques. [Pg.466]

Silicones have been extracted from environmental samples with solvents such as hexane, diethyl ether, methyl isobutylketone, ethyl acetate, and THF, using either sequential or Soxhlet techniques (690-695). Silicones of a wide range of molecular weights and polarities are soluble in THF. This feature, coupled with its volatility and miscibility with water, makes THF an excellent solvent for the extraction of silicones from wet samples, ie, soils and sediments. Trace levels of silicones extracted from environmental samples have been measured by a number of techniques, including atomic absorption spectroscopy (AA), inductively coupled plasma-atomic emission spectroscopy (ICP-AES), pyrolysis GC-MS, as well as H and Si NMR spectroscopy (674,684,692,696-700). The use of separation techniques, such as gel permeation and high pressure liquid chromatography interfaced with sensitive, silicon-specific AA or ICP detectors, has been particularly advantageous for the analysis of silicones in environmental extracts (685,701-704). [Pg.7624]

Ebdon L, Hill S (1989) Interfaces between liquid chromatography and atomic absorption. In Harrison R, Rapsomanikis S (eds) Environmental Analysis Using Chromatography Interfaced with Atomic Spectroscopy. Ellis Horwood Ltd., Chichester, pp 165-187. [Pg.36]

Fig. 2.6. High pressure liquid chromatography-graphite furnace atomic absorption spectrometer system with well sampler and autosampler as interface [A dead volvime screw B sample well C side duct connected to aspirator for withdrawal of liquid]. Redrawn from the Journal of Chromatographic Science (54] by permission of Preston Publications, a division of Preston Industries, Inc., and the authors. Fig. 2.6. High pressure liquid chromatography-graphite furnace atomic absorption spectrometer system with well sampler and autosampler as interface [A dead volvime screw B sample well C side duct connected to aspirator for withdrawal of liquid]. Redrawn from the Journal of Chromatographic Science (54] by permission of Preston Publications, a division of Preston Industries, Inc., and the authors.

See other pages where Interface liquid chromatography-atomic absorption is mentioned: [Pg.686]    [Pg.437]    [Pg.93]    [Pg.259]    [Pg.251]    [Pg.362]    [Pg.1561]    [Pg.141]    [Pg.662]    [Pg.35]    [Pg.39]    [Pg.42]    [Pg.191]    [Pg.386]   


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