Study of matrix effects and spectral interferences in the determination of lead in sediments, sludges and soils by SR-ETAAS using slurry sampling

被引:32
作者
Savio, Marianela [1 ,2 ]
Cerutti, Soledad [1 ,2 ]
Martinez, Luis D. [1 ,2 ]
Smichowski, Patricia [3 ,4 ]
Gil, Raul A. [1 ,2 ]
机构
[1] UNSL, CONICET, INQUISAL, Area Quim Analit,Inst Quim San Luis, Chacabuco, San Luis, Argentina
[2] UNSL, CONICET, INQUISAL, Area Quim Analit,Inst Quim San Luis, Pedernera, San Luis, Argentina
[3] Comis Nacl Energia Atom, San Martin Buenos Aires, DF, Argentina
[4] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
关键词
Lead; Contaminated soil analysis; Municipal sludge; Lake sediment; Slurry sampling; Self-reversal background corrector; ETAAS; ATOMIC-ABSORPTION-SPECTROMETRY; WATER SAMPLES; DIGESTION; ZN;
D O I
10.1016/j.talanta.2010.05.017
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An interference-free, fast, and simple method is proposed for Pb determination in environmental solid samples combining slurry sampling and electrothermal atomic absorption spectrometry. Samples were ground to an adequate particle size and slurries were prepared by weighing from 0.05 g to 0.20 g of dry sediment, adding nitric acid, and a solution containing 0.1% Triton X-100. Ultrasonic agitation was employed for slurries homogenization. Analytical variables including acid pre-treatment conditions, particle size, slurry stability, temperature program of the graphite furnace, and type and concentration of the chemical modifier were studied. The undesirable effects of potential non-specific and spectral interferences on Pb signal were also taken into account. Continuum source and self-reversal methods for background correction were evaluated and compared. For calibration, synthetic acid solutions of Pb were employed. Calibration was linear within the range 1-30 mu g L-1 and 5-30 mu g L-1 when the 217.0 nm and 283.3 nm analytical lines were used. Correlation coefficients of 0.9992 and 0.9997 were obtained. Using optimized conditions, limits of detection (3 sigma) of 0.025 mu g g(-1) and 0.1 mu g g(-1) were achieved for the 217.0 nm and 283.3 nm analytical lines, respectively. The method was successfully applied to the determination of lead in soil, contaminated soil, municipal sludge, and sediment samples. The accuracy was assessed by the analysis of two certified reference materials: municipal sludge (QC MUNICIPAL SLUDGE A) and lake sediment (TRAP-LRM from IJS). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:523 / 527
页数:5
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