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Coupling, of plasmas

HPLC (in both NP and RP modes) is quite suitable for speciation by coupling to FAAS, ETAAS, ICP-MS and MIP-MS [571,572]. Coupling of plasma source mass spectrometry with chromatographic techniques offers selective detection with excellent sensitivity. For HPLC-ICP-MS detection limits are in the sub-ng to pg range [36]. Metal ion determination and speciation by LC have been reviewed [573,574] with particular regard to ion chromatography [575]. [Pg.243]

Non-Thermal Radiofrequency Discharges Capacitive and Inductive Coupling of Plasma... [Pg.215]

Becker, J. S., Matusch, A., Depboylu, C., Dobrowolska, J., Zoriy, M. (2007) Quantitative imaging of selenium, copper, and zinc in thin sections of biological tissues (slugs-genus arion) measured by laser ablation inductively coupled of plasma mass spectrometry. Anal Chem, 79, 6074-6080. [Pg.80]

Since 02-plasma treatment alone is a rather poor technique for the preparation of a hydroxyl-functionalized PE surface (as was pointed out in Section V.B) the coupling of plasma and wet treatments is a more efficient method of such surface functionalization. For example, the density of surface reactive groups on LDPE and HDPE is greatly increased by aqueous NaBH4 treatment [114]. [Pg.683]

As an example, we look at tire etching of silicon in a CF plasma in more detail. Flat Si wafers are typically etched using quasi-one-dimensional homogeneous capacitively or inductively coupled RF-plasmas. The important process in tire bulk plasma is tire fonnation of fluorine atoms in collisions of CF molecules witli tire plasma electrons... [Pg.2805]

Numerous methods have been pubUshed for the determination of trace amounts of tellurium (33—42). Instmmental analytical methods (qv) used to determine trace amounts of tellurium include atomic absorption spectrometry, flame, graphite furnace, and hydride generation inductively coupled argon plasma optical emission spectrometry inductively coupled plasma mass spectrometry neutron activation analysis and spectrophotometry (see Mass spectrometry Spectroscopy, optical). Other instmmental methods include polarography, potentiometry, emission spectroscopy, x-ray diffraction, and x-ray fluorescence. [Pg.388]

The classical wet-chemical quaUtative identification of chromium is accompHshed by the intense red-violet color that develops when aqueous Cr(VI) reacts with (5)-diphenylcarba2ide under acidic conditions (95). This test is sensitive to 0.003 ppm Cr, and the reagent is also useful for quantitative analysis of trace quantities of Cr (96). Instmmental quaUtative identification is possible using inductively coupled argon plasma—atomic emission spectroscopy... [Pg.140]

Recently it has been shown that rotating coiled columns (RCC) can be successfully applied to the dynamic (flow-through) fractionation of HM in soils and sediments [1]. Since the flow rate of the extracting reagents in the RCC equipment is very similar to the sampling rate that is used in the pneumatic nebulization in inductively coupled plasma atomic emission spectrometer (ICP-AES), on-line coupling of these devices without any additional system seems to be possible. [Pg.459]

Figure 11.4 Chromatograms of plasma samples on a silica-chiralcel OJ coupled column system (a) plasma spiked with oxprenolol (internal standard) (b) plasma spiked with 040 p-g/ml metyrapone and 0.39 p-g/ml metyrapol (racemate) (c) plasma sample obtained after oral administration of 750 mg metaiypone. Peaks are as follows 1, metyrapone 2, metyrapol enantiomers 3, oxprenolol. Reprinted from Journal of Chromatography, 665, J. A. Chiarotto and I. W. Wainer, Determination of metyrapone and the enantiomers of its chfral metabolite metyrapol in human plasma and urine using coupled achfral-chfral liquid cltro-matography, pp. 147-154, copyright 1995, with permission from Elsevier Science. Figure 11.4 Chromatograms of plasma samples on a silica-chiralcel OJ coupled column system (a) plasma spiked with oxprenolol (internal standard) (b) plasma spiked with 040 p-g/ml metyrapone and 0.39 p-g/ml metyrapol (racemate) (c) plasma sample obtained after oral administration of 750 mg metaiypone. Peaks are as follows 1, metyrapone 2, metyrapol enantiomers 3, oxprenolol. Reprinted from Journal of Chromatography, 665, J. A. Chiarotto and I. W. Wainer, Determination of metyrapone and the enantiomers of its chfral metabolite metyrapol in human plasma and urine using coupled achfral-chfral liquid cltro-matography, pp. 147-154, copyright 1995, with permission from Elsevier Science.
Stopher and Gage used size-exclusion chromatography (SEL) coupled to reversed phase HPLC for the direct injection of plasma in the analysis of an antifungal agent, voriconazole (12). Their system consisted of three columns, i.e. first a size-exclusion... [Pg.411]

Alcohol sulfates and alcohol ether sulfates separated by HPLC on a styrene-divinylbenzene copolymer column with 4 1 (v/v) methanol and 0.05 M ammonium acetate aqueous solution as the mobile phase were analyzed by simultaneous inductively coupled argon plasma vacuum emission spectroscopy (IPC), monitoring the 180.7-nm sulfur line as a sulfur-specific detector [294]. This method was applied to the analysis of these surfactants in untreated wastewaters. [Pg.284]

Figure 1. Schematic description of the low-pressure inductively coupled rf plasma CVD system. Adapted with permission from [33], K. Okada et al., J. Mater. Res. 14, 578 (1999). 1999, Materials Research Society. Figure 1. Schematic description of the low-pressure inductively coupled rf plasma CVD system. Adapted with permission from [33], K. Okada et al., J. Mater. Res. 14, 578 (1999). 1999, Materials Research Society.
GC-AAS has found late acceptance because of the relatively low sensitivity of the flame graphite furnaces have also been proposed as detectors. The quartz tube atomiser (QTA) [186], in particular the version heated with a hydrogen-oxygen flame (QF), is particularly effective [187] and is used nowadays almost exclusively for GC-AAS. The major problem associated with coupling of GC with AAS is the limited volume of measurement solution that can be injected on to the column (about 100 xL). Virtually no GC-AAS applications have been reported. As for GC-plasma source techniques for element-selective detection, GC-ICP-MS and GC-MIP-AES dominate for organometallic analysis and are complementary to PDA, FTIR and MS analysis for structural elucidation of unknowns. Only a few industrial laboratories are active in this field for the purpose of polymer/additive analysis. GC-AES is generally the most helpful for the identification of additives on the basis of elemental detection, but applications are limited mainly to tin compounds as PVC stabilisers. [Pg.456]

Microwave plasma detection has been reviewed [351], also in relation to GC [352,353], Coupling of chromatography (GC, SFC, HPLC) and capillary electrophoresis (CE) with ICP-MS and MIP-MS detectors has also been reviewed [181,334,335]. Various specific GC-ICP-MS reviews have appeared [334,337,345,346,354,355]. [Pg.474]

In Figure 8.12, the basic set-up of an ICP-MS instrument is presented as a block diagram, consisting of a sample introduction system, the inductively coupled argon plasma (ICP) and the mass-specific detector. By far the most commonly applied sample introduction technique is a pneumatic nebuliser, in which a stream of argon (typically 1 I.min ), expanding with high... [Pg.652]

The interaction between Ag+ and selenium in the bloodstream has been studied in vitro by means of the HPLC-inductively coupled argon plasma-mass spectrometry (ICPMS) method. The metal ions and selenide form the unit complex (AgSe) and then this unit binds to selenoprotein to form the ternary complex [(AgSe)ra] selenoprotein in the bloodstream.1042... [Pg.965]

Ceccato, A., Boulanger, B., Chiap, P., Hubert, P., Crommen, J. (1998). Simultaneous determination of methylphenobarbital enantiomers and Phenobarbital in human plasma by online coupling of an achiral precolumn to a chiral liquid chromatographic column. J. Chromatogr. A 819, 143-153. [Pg.339]


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See also in sourсe #XX -- [ Pg.118 , Pg.119 ]




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