Determination of lead in water samples by graphite furnace atomic absorption spectrometry after cloud point extraction

被引:183
|
作者
Chen, JR [1 ]
Xiao, SM
Wu, XH
Fang, KM
Liu, WH
机构
[1] Zhejiang Normal Univ, Coll Chem & Life Sci, Jinhua 321004, Zhejiang, Peoples R China
[2] Jinhua Coll Profess & Technol, Jinhua 321017, Zhejiang, Peoples R China
[3] Zhejiang Univ Technol, Coll Chem Engn & Mat Sci, Hangzhou 310032, Zhejiang, Peoples R China
关键词
cloud point extraction; GFAAS; lead;
D O I
10.1016/j.talanta.2005.04.029
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cloud point extraction (CPE) has been used for the pre-concentration of lead, after the formation of a complex with 2-(5-bromo-2-pyridylazo)-5-(diethylamino)-phenol (5-Br-PADAP), and later analysis by graphite furnace atomic absorption spectrometry (GFAAS) using octylphenoxypolyethoxyethanol (TritonX- 114) as surfactant. The chemical variables affecting the separation phase were optimized. Separation of the two phases was accomplished by centrifugation for 15 min at 4000 rpm. Under the optimum conditions i.e., pH 8.0, cloud point temperature 40 degrees C, [5-Br-PADAP] = 2.5 x 10(-5) mol l(-1), [Triton X- 114] 0.05%, added methanol volume = 0. 15 ml, pre-concentration of only 10 ml sample permitted an enhancement factor of 50-fold. The lower limit of detection (LOD) obtained under the optimal conditions was 0.08 mu g l(-1). The precision for 10 replicate determinations at 5 mu g l(-1) Pb was 2.8% relative standard deviation (R.S.D.). The calibration graph using the pre-concentration system for lead was linear with a correlation coefficient of 0.9984 at levels near the detection limits up to at least 30 mu g l(-1). The method was successfully applied to the determination of lead in water samples. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:992 / 996
页数:5
相关论文
共 50 条