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Atomic absorption spectrometry, hydride

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]

FLOW INJECTION ELECTROCHEMICAL HYDRIDE GENERATION ATOMIC ABSORPTION SPECTROMETRY EOR THE DETERMINATION OE ARSENIC... [Pg.135]

Lab method using continuous flow or flow injection analysis hydride generation and atomic absorption spectrometry... [Pg.360]

Vol. 130. Hydride Generation Atomic Absorption Spectrometry. By Jiri Dedina and Dimiter L. Tsalev... [Pg.449]

Zhang X, Cornelis R, De Kimpe J, and Mees L (1996) Arsenic speciation in serum of uraemic patients based on liquid chromatography with hydride generation atomic absorption spectrometry and on-line UV photo-oxidation digestion. Anal Chim Acta 319 177-185. [Pg.110]

Munoz O, Velez D, Montoro R (1999) Optimization of the solubilization, extraction and determination of inorganic arsenic [As(III) i- As(V)] in seafood products by acid digestion, solvent extraction and hydride generation atomic absorption spectrometry. Analyst 124 601-607. [Pg.233]

Aroza I, Bonilla M, Madrid Y, et al. 1989. Combination of hydride generation and graphite furnace atomic absorption spectrometry for the determination of lead in biological samples. J Anal Atmos Spectra 4 163-166. [Pg.488]

Samanta G, Chakraborti D. 1996. Flow injection hydride generation atomic absorption spectrometry (FI-HG-AAS) and spectrophotometric methods for determination of lead in environmental samples. Environmental Technology 17(12) 1327-1337. [Pg.571]

Hydride Generation Atomic Absorption Spectrometry High Performance Liquid Chromatography High Performance Thin-Layer Chromatography High Resolution... [Pg.24]

Sturgeon et al. [59] have described a hydride generation atomic absorption spectrometry method for the determination of antimony in seawater. The method uses formation of stibene using sodium borohydride. Stibine gas was trapped on the surface of a pyrolytic graphite coated tube at 250 °C and antimony determined by atomic absorption spectrometry. An absolute detection limit of 0.2 ng was obtained and a concentration detection limit of 0.04 pg/1 obtained for 5 ml sample volumes. [Pg.136]

Howard and Comber [63] converted arsenic in seawater to its hydride prior to determination by atomic absorption spectrometry. [Pg.138]

Soo [96] determined picogram amounts of bismuth in seawater by flameless atomic absorption spectrometry with hydride generation. The bismuth is reduced in solution by sodium borohydride to bismuthine, stripped with helium gas, and collected in situ in a modified carbon rod atomiser. The collected bismuth is subsequently atomised by increasing the atomiser temperature and detected by an atomic absorption spectrophotometer. The absolute detection limit is 3pg of bismuth. The precision of the method is 2.2% for 150 pg and 6.7% for 25 pg of bismuth. Concentrations of bismuth found in the Pacific Ocean ranged from < 0.003-0.085 (dissolved) and 0.13-0.2 ng/1 (total). [Pg.143]

Hydride Generation Furnace Atomic Absorption Spectrometry... [Pg.180]

Amankwah and Fasching [4] have discussed the determination of arsenic (V) and arsenic (III) in estuary water by solvent extraction and atomic absorption spectrometry using the hydride generation technique. [Pg.330]

Willie et al. [17] used the hydride generation graphite furnace atomic absorption spectrometry technique to determine selenium in saline estuary waters and sea waters. A Pyrex cell was used to generate selenium hydride which was carried to a quartz tube and then a preheated furnace operated at 400 °C. Pyrolytic graphite tubes were used. Selenium could be determined down to 20 ng/1. No interference was found due to, iron copper, nickel, or arsenic. [Pg.334]

Total dissolved Fe and Mn were analyzed directly by flame atomic absorption spectrometry (AAS). As was measured by AAS with hydride generation (HG-FIAS). Total dissolved Se concentrations were determined by hydride-generation atomic fluorescence spectrometry (Chen etal., 2005). [Pg.228]

The determination of arsenic by atomic absorption spectrometry with thermal atomization and with hydride generation using sodium borohydride has been described by Thompson and Thomerson [117] and it was evident that this method could be modified for the analysis of soil. [Pg.349]

Cutter [122] used a selective hydride generation procedure as a basis for the differential determination of arsenic and selenium species in sediments. Goulden et al. [123] also discuss the determination of arsenic and selenium in sediments by atomic absorption spectrometry. [Pg.350]

Various workers have discussed the application of atomic absorption spectrometry to the determination of selenium in rocks [159,160] achieving detection limits of 0.06g g-1 [159] and 1.4xl0 10g g-1 [160] respectively. Hydride generation and measurement of hydride fluorescence has been used to determine selenium [120, 161] with a sensitivity of 0.06ug Se mL 1 which is 5-30 times than is achieved by conventional atomic absorption spectrometry. [Pg.363]

The most useful chemical species in the analysis of arsenic is the volatile hydride, namely arsine (AsH3, bp -55°C). Analytical methods based on the formation of volatile arsines are generally referred to as hydride, or arsine, generation techniques. Arsenite is readily reduced to arsine, which is easily separated from complex sample matrices before its detection, usually by atomic absorption spectrometry (33). A solution of sodium borohydride is the most commonly used reductant. Because arsenate does not form a hydride directly, arsenite can be analyzed selectively in its presence (34). Specific analysis of As(III) in the presence of As(V) can also be effected by selective extraction methods (35). [Pg.152]


See other pages where Atomic absorption spectrometry, hydride is mentioned: [Pg.335]    [Pg.335]    [Pg.496]    [Pg.335]    [Pg.335]    [Pg.496]    [Pg.7]    [Pg.249]    [Pg.13]    [Pg.15]    [Pg.129]    [Pg.136]    [Pg.219]    [Pg.227]    [Pg.250]    [Pg.370]    [Pg.190]    [Pg.365]    [Pg.416]    [Pg.423]    [Pg.424]    [Pg.412]    [Pg.152]   


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