117 research outputs found

    Determination of arsenic in agricultural soil samples using High-resolution continuum source graphite furnace atomic absorption spectrometry and direct solid sample analysis

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    The authors are grateful to the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for financial support and scholarships. BW had a research scholarship from CNPq, Processo No. 303526/2016-5. The authors are also grateful to Analytik Jena for the donation of the HR-CS GF AAS Model contrAA 600 and for financial support.Peer reviewedPostprin

    Investigation of chemical modifiers for the determination of cadmium and chromium in fish oil and lipoid matrices using HR-CS GF AAS and a simple ‘dilute-and-shoot’ approach

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    The authors are grateful to the Conselho Nacional de Desenvolvimento Científico and Tecnológico (CNPq), and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for financial support and scholarships. The present research was mostly financed through Project no. CNPq 406877/2013-0. The authors are also grateful to Analytik Jena for financial support and the donation of the contrAA 600.Peer reviewedPostprin

    Development of a fast screening method for the direct determination of chlorinated persistent organic pollutants in fish oil by high-resolution continuum source graphite furnace molecular absorption spectrometry

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    The authors are grateful to the Conselho Nacional de Desenvolvimento Científico and Tecnológico (CNPq); the present research was mostly financed through Project no. CNPq 406877/2013-0. The authors are also grateful to the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for financial support and scholarships, and to Analytik Jena for financial support and donation of the contrAA 600 high-resolution continuum source atomic absorption spectrometer.Peer reviewedPostprin

    The use of high resolution graphite furnace molecular absorption spectrometry (HR -MAS) for total fluorine determination in extractable organofluorines (EOF)

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    Acknowledgment A.A. would like to thank the Ministry of Education and University of Jeddah in Saudi Arabia through the Cultural Bureau of Saudi Arabia, London for their financial support during the study period. A.O. wishes to thank the Royal Society of Chemistry Analytical Trust Fund for funding. M.S. would like to thank the Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq for the financial support. L.S., J.B. and J.F. thank Formas for financial support (Grant number 2013–00794).Peer reviewedPostprin

    Determination of sulfur in biological samples using high-resolution molecular absorption spectrometry in a graphite furnace with direct solid sampling

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    The determination of sulfur in biological materials using high-resolution continuum source molecular absorption spectrometry and electrothermal vaporization of the carbon monosulfide (CS) molecule has been investigated in detail using direct solid sampling. Best results have been obtained coating the platform with tungsten as a permanent modifier, adding 40 mg Pd in solution as a chemical modifier, and the only sulfur compound that showed sufficient sensitivity and thermal stability to be used for calibration purposes under the conditions established for biological materials was thiourea. A pyrolysis temperature of at least 900 C could be used and the optimum vaporization temperature was 2500 C. Under optimized conditions a limit of detection of 0.015 mg S absolute or 0.03 mg g À1 S in the solid sample, based on a sample mass of 0.5 mg could be obtained; the characteristic mass was m 0 ¼ 18 ng. Five certified biological reference materials have been analyzed using direct solid sampling and calibration against aqueous standards; the results were in agreement with the certified values on a 95% confidence interval

    Investigation of the feasibility to use Zeeman-effect background correction for the graphite furnace determination of phosphorus using high-resolution continuum source atomic absorption spectrometry as a diagnostic tool

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    The determination of phosphorus by graphite furnace atomic absorption spectrometry at the non-resonance line at 213.6 nm, and the capability of Zeeman-effect background correction (Z-BC) to deal with the fine-structured background absorption due to the PO molecule have been investigated in the presence of selected chemical modifiers. Two line source atomic absorption spectrometers, one with a longitudinally heated and the other with a transversely heated graphite tube atomizer have been used in this study, as well as two prototype high-resolution continuum source atomic absorption spectrometers, one of which had a longitudinally arranged magnet at the furnace. It has been found that Z-BC is capable correcting very well the background caused by the PO molecule, and also that of the NO molecule, which has been encountered when the Pd + Ca mixed modifier was used. Both spectra exhibited some Zeeman splitting, which, however, did not cause any artifacts or correction errors. The practical significance of this study is to confirm that accurate results can be obtained for the determination of phosphorus using Z-BC. The best sensitivity with a characteristic mass of m(0) = 11 ng P has been obtained with the pure Pd modifier, which also caused the lowest background level. The characteristic mass obtained with the mixed Pd + Ca modifier depended on the equipment used and was between m(0) = 9 ng P and m(0) = 15 ng P, and the background signal was higher. The major problem of Z-BC remains the relatively restricted linear working range

    Determination of mercury in airborne particulate matter collected on glass fiber filters using high-resolution continuum source graphite furnace atomic absorption spectrometry and direct solid sampling

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    A study has been undertaken to assess the capability of high-resolution continuum source graphite furnace atomic absorption spectrometry for the determination of mercury in airborne particulate matter (APM) collected on glass fiber filters using direct solid sampling. The main Hg absorption line at 253.652 nm was used for all determinations. The certified reference material NIST SRM 1648 (Urban Particulate Matter) was used to check the accuracy of the method, and good agreement was obtained between published and determined values. The characteristic mass was 22 pg Hg. The limit of detection (3σ), based on ten atomizations of an unexposed filter, was 40 ng g- 1, corresponding to 0.12 ng m- 3 in the air for a typical air volume of 1440 m3 collected within 24 h. The limit of quantification was 150 ng g-1, equivalent to 0.41 ng m-3 in the air. The repeatability of measurements was better than 17% RSD (n = 5). Mercury concentrations found in filter samples loaded with APM collected in Buenos Aires, Argentina, were between < 40 ng g-1 and 381 ± 24 ng g-1. These values correspond to a mercury concentration in the air between < 0.12 ng m-3 and 1.47 ± 0.09 ng m-3. The proposed procedure was found to be simple, fast and reliable, and suitable as a screening procedure for the determination of mercury in APM samples.Fil: Araujo, Rennan G. O.. Universidade Federal de Santa Catarina; BrasilFil: Vignola, Fabíola. Universidade Federal de Santa Catarina; BrasilFil: Castilho, Ivan N. B.. Universidade Federal de Santa Catarina; BrasilFil: Borges, Daniel L. G.. Universidade Federal de Santa Catarina; Brasil. Universidade Federal da Bahia; BrasilFil: Welz, Bernhard. Universidade Federal de Santa Catarina; Brasil. Universidade Federal da Bahia; BrasilFil: Vale, Maria Goreti R.. Universidade Federal do Rio Grande do Sul; Brasil. Universidade Federal da Bahia; BrasilFil: Smichowski, Patricia Nora. Comisión Nacional de Energía Atómica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Ferreira, Sérgio L. C.. Universidade Federal da Bahia; BrasilFil: Becker Ross, Helmut. Leibniz-Institut für Analytische Wissenschaften; Alemani

    Atomic absorption spectrometry

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    Prof. Adilson José Curtius, 21.04.1945–05.11.2012

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    Atomic Absorption Spectometry

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