Search results for " absorption spectroscopy"
showing 10 items of 293 documents
Chromium speciation using activated alumina microcolumns and sequential injection analysis-flame atomic absorption spectrometry
2001
Abstract A new procedure has been developed for chromium speciation in water by sequential injection analysis and flame atomic absorption spectrometry. The method involves the online retention of Cr(VI) anionic species and Cr(III) cationic species on alumina microcolumns, prepared by packing activated alumina in polytetrafluoroethylene tubes, followed by selective elution of Cr(VI) with 2 mol l −1 NH 4 OH and of Cr(III) with 0.2 mol l −1 HNO 3 . Studies were carried out on the effect of retention and elution conditions for both Cr species. The limit of detection values, established as the concentration corresponding to three times the standard deviation of blank measurements divided by the …
Determination of mercury in dry-fish samples by microwave digestion and flow injection analysis system cold vapor atomic absorption spectrometry
1997
Abstract Flow injection analysis system cold vapor atomic absorption spectrometry (FIAS-CV-AAS) preceded by a wet digestion in a microwave oven, as a method for measuring mercury in fish was studied. The digestion process and conditions of the FIAS (carrier concentration: HCl 3% v v ; reducing agent: SnCl2 2% w v : filling and injection times: 8 and 25 min, respectively; and sample volumes) were optimized. The analytical parameters of the proposed method (detection limit = 7.7 ng/g; precision intraassay = 6.7%; interassay = 14.0%) demonstrates its adequacy and are similar to the ones (detection limit = 19.4 ng/g; precision intraassay = 11.2%; interassay = 15.9%) obtained using a conventiona…
High-frequency electrodeless discharge lamps for atomic absorption analysis
2003
Abstract In this paper we present the results of an investigation of high-frequency electrodeless discharge lamps (HFEDLs), containing Cd, Zn, Hg, As, Te, Se, Pb, Sn, Tl and Bi, developed in our laboratories as light sources for atomic absorption spectrometry (AAS). Important physical processes in the lamps are discussed. Essential characteristics of HFEDLs for AAS, such as intensity, stability and operating life are considered. The intensities and detection limits are compared with the corresponding characteristics of hollow cathode lamps. The temporal behavior of an As HFEDL is compared with that of a commercially available electrodeless discharge lamp. Detection limits in graphite furnac…
Flow injection flame atomic spectrometric determination of iron, calcium, magnesium, sodium and potassium in ceramic materials by using a variable-vo…
1993
A series of different ceramic materials, such as porcelain, feldspar, kaolin, varnish, clay and stoneware have been analyzed. Iron, calcium and magnesium have been determined in these materials by flame atomic absorption and sodium and potassium by flame emission. The use of a variable-volume injector enables one to carry out these analyses in a flow system (after fusion of samples with lithium metaborate) and does not require different dilutions for the determination of each type of sample considered, nor the use of different flow injection manifolds. The developed procedure provides a limit of detection of 100 μg/l for Na, 70 μg/l for Ca, 50 μg/l for both Fe and K and 8 μg/l for Mg. The c…
Atomic-absorption spectrometric determination of calcium, magnesium and potassium in leaf samples after decomposition with molten sodium hydroxide
1991
Abstract The decomposition of standard leaf samples of varied origin and nature by fusion with sodium hydroxide in an open system has been studied. The use of sodium nitrate as an auxiliary agent facilitated the mineralization of most of the samples. The solutions obtained were analysed for calcium, magnesium and potassium by flame atomic-absorption spectrometry. The method is fast and quite precise, with absolute standard deviations of 0.04–0.13, 0.002-0.03 and 0.04–0.12% for calcium, magnesium and potassium contents of O.8-5.0, 0.13–0.48 and 0.36–2.2% respectively. The limits of detection (μg/ml) in the determination step were 0.10 for calcium, 0.011 for magnesium, and 0.09 for potassium.
GFAAS determination of selenium in infant formulas using a microwave digestion method.
1994
A method for determining the selenium content of infant formulas is proposed. It includes wet digestion with nitric acid and hydrogen peroxide in medium pressure teflon bombs in a microwave oven and determination by graphite furnace atomic absorption spectrometry (GFAAS). The absence of interferences is checked. Values obtained for the limit of detection (19.4 ng/g), precision (RSD = 2.2%) and accuracy by analysis of a reference material show that the method is reliable.
Indirect Determination of Cyanide by Atomic Absorption Spectrometry
1995
Abstract Two methods for determination of cyanide by atomic absorption spectrometry (AAS) are developed. Both methods are based on the formation of an ion association compound between a metal complex, (Ag(CN)2 − or Cu(CN)3 2-), and a quaternary ammonium ion (benzyldimethylhexadecylammonium ion). The ion association compound is extracted into isomethylbutylketone (IBMK) and the metal is determined by AAS directly in extract. The method based on the formation of silver cyanide complex provides a reproducibility of 2.5%, a recovery of 99% and a detection limit of 1.7 μg/L while the method based on the formation of copper complex gives a reproducibility of 6%, a recovery of 93% and a detection …
Some observations on the sensitivity of flow-injection techniques for atomic absorption spectrophotometry
1989
Abstract Different strategies for coupling flow-injection manifolds to atomic absorption spectrometers in order to obtain better sensitivity are compared. Using a T-connector interface, different carriers and flow compensation solvents have been assayed in an attempt to improve the sensitivity of flow-injection analysis. Manganese and copper determinations in sewage sludge have been used as a test system and the analytical parameters of both batch and flow-injection methods are compared.
Vapor-phase introduction of alkyltin compounds in atomic absorption spectrophotometry
1990
Abstract Different systems for the introduction of alkyltin compounds in atomic absorption spectrophotometry using the vapor-phase introduction approach have been compared. Samples and standards were introduced in both quartz cell and flame atomizer using a vertical and a horizontal reactor. The better sensitivity was obtained with the quartz cell and the horizontal reactor.
Methylmercury and inorganic mercury determination in fish by cold vapour generation atomic absorption spectrometry
2000
Abstract Given that organic mercury is more dangerous than the inorganic form and that it is converted into methylmercury by biological methylation, we have studied and optimized a simple method for measuring both organic and inorganic mercury contents in fish, using a spectroscopic vapour generation technique, with a sequential reduction of the digested sample with stannous chloride and sodium tetrahydroborate. Prior to applying the method the sample was subjected to alkaline wet digestion. Due to the matrix interferences calibration curves with matrix addition were needed for mercury determinations. The analytical parameters of the method were: linearity from 10 to 200 ng of Hg in the red…