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Determination of hydride forming elements (As,Sb, Se,Sn) and Hg in environmental reference materials as acid slurries by on-line hydride generation inductively coupled plasma mass spectrometry
Institution:1. Laboratório de Etnobotânica, Departamento de Botânica, Instituto de Ciências Biológicas da Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil;2. Centro de Ensino Superior de Juiz de Fora, Faculdade de Ciências Biológicas, Juiz de Fora, MG, Brazil;1. Department of Materials Science and Engineering, Tsinghua University, Beijing 100083, China;2. College of Science, Tianjin University of Science & Technology, Tianjin 300222, China;3. School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China;1. Istanbul Technical University, Faculty of Science and Letters, Department of Chemistry, Maslak, 34469 Istanbul, Turkey;2. T.C. Istanbul Aydin University, Health Services Vocational School of Higher Education, Sefakoy Kucukcekmece, 34295 Istanbul, Turkey
Abstract:A method for the determination of As, Hg, Sb, Se and Sn in environmental and in geological reference materials, as acidified slurries, by flow injection (FI) coupled to a hydride generation system (HG) and detection by inductively coupled plasma mass spectrometry (ICP-MS) is proposed. The HG unit has a gas liquid separator and a drying unit for the generated vapor. The slurries were prepared by two procedures. Approximately 50 mg of the reference material, ground to a particle size ≤50 μm, was mixed with acid solutions in an ultrasonic bath. In Procedure A, the medium was a hydrochloric acid solution while in Procedure B, the medium was aqua regia plus a hydrochloric acid solution. The conditions for the slurry formation and the instrumental parameters were optimized. Harsh conditions were used in the slurry preparation in order to reduce the hydride forming analytes to their lower oxidation states, As (III), Se(IV), Sb(III) and Sn(II), before reacting with sodium tetrahydroborate. To test the accuracy, 10 certified reference materials were analyzed (four sediments, three coals, one coal fly ash and two sewage sludges), with the analyte concentrations mostly in the μg g?1 level. Good agreements with the certified values were obtained for Hg, Sb and Sn in the sediments using Procedure A and calibration against aqueous standard solutions. Using Procedure B, good results were obtained for Hg, Se and Sn in the sediment samples, for Se in the coal and coal fly ash samples and for Hg in the sewage sludge samples, also using external calibration with aqueous standard solutions. For As in sediments, coals and coal fly ash, Procedure B and the analyte addition calibration was required, indicating matrix effects. The relative standard deviations were lower than 5%, demonstrating a good precision for slurry analysis. The limits of quantification (10 times the standard deviation; n=10), in the samples, in ng g?1, were: 20 for As, 60 for Hg, 80 for Sb, 200 for Se and 90 for Sn. The method requires small amounts of reagents and reduces contamination and losses.
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