Simultaneous determination of arsenic, cadmium, copper, chromium, nickel, lead and thallium in total digested sediment samples and available fractions by electrothermal atomization atomic absorption spectroscopy (ET AAS)

被引:48
作者
Alvarez, Maria A. [1 ]
Carrillo, Genesis [1 ]
机构
[1] Cent Univ Venezuela, Fac Ciencias, Ctr Quim Analit, Caracas 1041A, Venezuela
关键词
Modified BCR sequential extraction scheme; Sediments; Available fraction; Heavy metals; Simultaneous ET AAS; SEQUENTIAL EXTRACTION PROCEDURE; NON-SPECTRAL INTERFERENCES; TRACE-METALS; MARINE-SEDIMENTS; SLURRY SAMPLES; BCR PROTOCOL; RIVER YAMUNA; HEAVY-METALS; SPECTROMETRY; FURNACE;
D O I
10.1016/j.talanta.2012.05.006
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
This study describes the optimization and validation of a quick and simple method for the simultaneous determination of total content and available fractions of As, Cr, Cu, Ni, Pb and Tl in sediments by ET AAS, which has been proved to be useful for environmental research. The optimization was carried out using a 3(3) Box-Behnken factorial design which was applied to matrices of total digestion and to stages 1 and 2 of the modified BCR sequential extraction scheme for sediments in order to determine the appropriate atomization temperatures and masses for the chemical modifiers: Pd(NO3)(2) and Mg(NO3)(2). The simultaneous determination of the elements in all matrices considered was performed, without the use of chemical modifiers at atomization temperatures of 1700 degrees C for Cd and Tl, and 2100 degrees C for As, Cu, Cr, Ni and Pb, using a standard calibration curve for calibration purposes. The characteristic masses and limits of detection obtained were 36.5, 1.8, 6.5, 28, 34, 46.5 and 48 rho g and 0.11, 0.001, 0.022, 0.04, 0.2, 0.03 and 0.003 mu g g(-1) for As, Cd, Cr, Cu, Ni, Pb and Tl, respectively. The analytical procedure was validated by analyzing three sediment certified reference materials (CRM NCS DC 73315 and LKSD-4 for total content and BCR 701 for available fractions). Good accuracy was obtained (tested statistically, P=0.05, and shown by the high recovery for each element in each matrix), except for total As in the matrix of total digestion, where losses of the analyte could be attributed to sample treatment with HNO3. The precision of the procedure was between 0.6% and 6%. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:505 / 512
页数:8
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