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Furnace emission spectrometry

Graphite furnace emission spectrometry, with the furnace operated under reduced pressure, has been explored. In FANES, furnace atomic non-thermal excitation spectrometry, an additional discharge is applied for analyte excitation (Falk et al., 1984). Littlejohn et al. (1991) have reviewed recent advances in the field of atomic emission spectrometry, including fundamental processes and instrumentation. [Pg.254]

Furnace Emission Spectrometry. . 701 Glow Discharges with Flat Cathodes 701... [Pg.627]

Highly sensitive iastmmental techniques, such as x-ray fluorescence, atomic absorption spectrometry, and iaductively coupled plasma optical emission spectrometry, have wide appHcation for the analysis of silver ia a multitude of materials. In order to minimize the effects of various matrices ia which silver may exist, samples are treated with perchloric or nitric acid. Direct-aspiration atomic absorption (25) and iaductively coupled plasma (26) have silver detection limits of 10 and 7 l-lg/L, respectively. The use of a graphic furnace ia an atomic absorption spectrograph lowers the silver detection limit to 0.2 l-ig/L. [Pg.91]

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]

ScHiFFER U, Krivan V (i999) A graphite furnace electrothermal vaporization system for inductively coupled plasma atomic emission spectrometry. Anal Chem 70 482-490. [Pg.47]

Principles and Characteristics Flame emission instruments are similar to flame absorption instruments, except that the flame is the excitation source. Many modem instruments are adaptable for either emission or absorption measurements. Graphite furnaces are in use as excitation sources for AES, giving rise to a technique called electrothermal atomisation atomic emission spectrometry (ETA AES) or graphite furnace atomic emission spectrometry (GFAES). In flame emission spectrometry, the same kind of interferences are encountered as in atomic absorption methods. As flame emission spectra are simple, interferences between overlapping lines occur only occasionally. [Pg.615]

ASTM. 1998a. ASTME1613. Standard test method for analysis of digested samples for lead by inductively coupled plasma atomic emission spectrometry (ICP-AES). Flame Atomic Absorption (FAAS), or Graphite Furnace Atomic Absorption (GFAA) Techniques. American Society for Testing and Materials. [Pg.488]

Mykytiuk et al. [184] have described a stable isotope dilution sparksource mass spectrometric method for the determination of cadmium, zinc, copper, nickel, lead, uranium, and iron in seawater, and have compared results with those obtained by graphite furnace atomic absorption spectrometry and inductively coupled plasma emission spectrometry. These workers found that to achieve the required sensitivity it was necessary to preconcentrate elements in the seawater using Chelex 100 [121] followed by evaporation of the desorbed metal concentrate onto a graphite or silver electrode for isotope dilution mass spectrometry. [Pg.287]

Perkin-Elmer ICP 5000 Can be used for flame and graphite furnace ASS and inductively coupled plasma atomic emission spectrometry (sequential) ... [Pg.41]

Chromium metal may be analyzed by various instrumental techniques including flame and furnace AA spectrophotometry (at 357.9 nm) ICP emission spectrometry (at 267.72 or 206.15 nm), x-ray fluorescence and x-ray diffraction techniques, neutron activation analysis, and colorimetry. [Pg.218]

Furnace Atomization Plasma Emission Spectrometry (EAPES)... [Pg.68]

Furnace atomization plasma emission spectrometry (FAPES)... [Pg.220]

Different analytical techniques such as ICP-OES (optical emission spectrometry with inductively coupled plasma source), XRF (X-ray fluorescence analysis), AAS (atomic absorption spectrometry) with graphite furnace and flame GF-AAS and FAAS, NAA (neutron activation analysis) and others, are employed for the trace analysis of environmental samples. The main features of selected atomic spectrometric techniques (ICP-MS, ICP-OES and AAS) are summarized in Table 9.20.1 The detection ranges and LODs of selected analytical techniques for trace analysis on environmental samples are summarized in Figure 9.15.1... [Pg.298]

Furnace atomisation plasma emission spectrometry (FAPES) this consists of an atmospheric pressure source combining a capacitively coupled radiofrequency helium plasma formed inside a graphite tube which contains an axial powered electrode. This miniplasma has rarely been used in analytical atomic spectrometry, probably because of the small number of users and a lack of information about its applications and capabilities [7]. [Pg.16]

Coal contains several elements whose individual concentrations are generally less than 0.01%. These elements are commonly and collectively referred to as trace elements. These elements occur primarily as part of the mineral matter in coal. Hence, there is another standard test method for determination of major and minor elements in coal ash by ICP-atomic emission spectrometry, inductively coupled plasma mass spectrometry, and graphite furnace atomic absorption spectrometry (ASTM D-6357). The test methods pertain to the determination of antimony, arsenic, beryllium, cadmium, chromium, cobalt, copper, lead, manganese, molybdenum, nickel, vanadium, and zinc (as well as other trace elements) in coal ash. [Pg.105]

In the test method, the coal or coke to be analyzed is ashed under controlled conditions, digested by a mixture of aqua regia and hydrofluoric acid, and finally dissolved in 1% nitric acid. The concentration of individual trace elements is determined by either inductively coupled plasma-atomic emission spectrometry (ICPAES) or inductively coupled plasma-mass spectrometry (ICPMS). Selected elements that occur at concentrations below the detection limits of ICPAES can be analyzed quantitatively by graphite furnace atomic absorption spectrometry (GFAA). [Pg.105]

The application of inductively coupled plasma atomic emission spectrometry and graphite furnace atomic absorption spectrometry to the determination of cadmium (and molybdenum) in soils has been discussed by Baucells et al. [53]. Baucells et al. chose the 228.802 nm cadmium line because it is well resolved from the 228.763 nm iron line with the spectrometer used in this work. Background measurements could only be carried out at +0.05 nm. These workers obtained good agreement between cadmium values obtained by direct graphite furnace atomic absorption spectrometry and inductively coupled plasma atomic emission spectrometry. Chelation extraction procedures that require extensive sample handling are avoided. [Pg.35]

Inductively coupled plasma atomic emission spectrometry has proved to be an excellent technique for the direct analysis of soil extracts because it is precise, accurate and not time-consuming, the level of matrix interference being very low. Of course, the graphite furnace technique yields better detection limits than the inductively coupled plasma procedure. [Pg.35]

Baxter DC, Freeh W, Lundberg E. 1985. Determination of aluminum in biological materials by constant-temperature graphite furnace atomic-emission spectrometry. Analyst 110 475-482. [Pg.294]

Figure 6.1 Bar-graph of MeHg in CRM 580. The results correspond to six replicate determinations as performed by different laboratories using various methods. MEANS indicates the mean of laboratory means with 95% confidence interval. Abbreviations-. CVAAS, cold vapour atomic absorption spectrometry CVAFS, cold vapour atomic fluorescence spectrometry ECD, electron capture detection GC, gas chromatography HPLC, high-performance liquid chromatography ICPMS, inductively coupled plasma mass spectrometry MIP, microwave induced plasma atomic emission spectrometry QFAAS, quartz furnace atomic absorption spectrometry SFE, supercritical fluid extraction. Figure 6.1 Bar-graph of MeHg in CRM 580. The results correspond to six replicate determinations as performed by different laboratories using various methods. MEANS indicates the mean of laboratory means with 95% confidence interval. Abbreviations-. CVAAS, cold vapour atomic absorption spectrometry CVAFS, cold vapour atomic fluorescence spectrometry ECD, electron capture detection GC, gas chromatography HPLC, high-performance liquid chromatography ICPMS, inductively coupled plasma mass spectrometry MIP, microwave induced plasma atomic emission spectrometry QFAAS, quartz furnace atomic absorption spectrometry SFE, supercritical fluid extraction.
Grinberg, P., R.C. Campos, Z. Mester, and R.E. Sturgeon. 2003. A comparison of alkyl derivatization methods for speciation of mercury based on solid phase microextraction gas chromatography with furnace atomization plasma emission spectrometry detection. J. Anal. At. Spectrom. 18 902-909. [Pg.137]

Metals contained in samples are determined by a wide variety of analytical methods. Bulk metals, such as copper in brass or iron in steel, can be analyzed readily by chemical methods such as gravimetry or electrochemistry. However, many metal determinations are for smaller, or trace, quantities. These are determined by various spectroscopic or chromatographic methods, such as atomic absorbance spectrometry using flame (FAAS) or graphite furnace (GFAAS) atomization, atomic emission spectrometry (AES), inductively coupled plasma atomic emission spectrometry (ICP-AES), inductively coupled plasma mass spectrometry (ICP-MS), x-ray fluorescence (XRF), and ion chromatography (IC). [Pg.227]

Hui-Ming H, Yao-Han L. 1984. Determination of trace Na, K, Ba, and Li by graphite furnace atomic emission spectrometry. Spectrochim Acta 39B 493- 499. [Pg.117]

Y. Okamoto, T. Fujiwara, T. Kumamaru, Direct determination of trace elements in biological materials by inductively coupled plasma atomic emission spectrometry with a tungsten boat furnace, Anal. Sci., 13 (1997), 25D26. [Pg.48]


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See also in sourсe #XX -- [ Pg.701 ]




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