On-line solid phase extraction of Ni and Pb using carbon nanotubes and modified carbon nanotubes coupled to ETAAS

被引:60
作者
Savio, Marianela [1 ]
Parodi, Belen [2 ,3 ]
Martinez, Luis D. [1 ]
Smichowski, Patricia [4 ,5 ]
Gil, Raul A. [1 ]
机构
[1] Univ Nacl San Luis, Inst Quim San Luis CCT San Luis, Area Quim Analit, Fac Quim Bioquim & Farm, San Luis, Argentina
[2] Ctr Invest & Desarrollo Mecan, INTI, Buenos Aires, DF, Argentina
[3] Univ San Martin, Inst Invest & Ingn Ambiental, San Martin, Argentina
[4] Comis Nacl Energia Atom, RA-1429 Buenos Aires, DF, Argentina
[5] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
关键词
Ni; Pb; FI-SPE-ETAAS; Carbon nanotubes; Oxidized carbon nanotubes; L-Alanine aminoacid; HEAVY-METAL IONS; ENVIRONMENTAL-SAMPLES; PRECONCENTRATION; SPECIATION; NANOSTRUCTURES; SPECTROMETRY; SEPARATION; ADSORBENT; SORBENT;
D O I
10.1016/j.talanta.2011.03.054
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A study about the capabilities of three kinds of nanomaterials namely, carbon nanotubes (CNT), oxidized carbon nanotubes (ox-CNT) and L-alanine immobilized on carbon nanotubes (ala-CNT) to serve as sorbents for preconcentrating Ni and Pb using an on-line system coupled to electrothermal atomic absorption spectroscopy (ETAAS) technique, was accomplished. The solid phase extraction was performed in a conical minicolumn used as sorbent holder. After loading a fixed volume of the analytes, they were eluted with a discrete volume (50 mu L) of nitric acid, placed directly into the platform of a L'Vov tube. After that, each analyte was determined individually. Ni and Pb retention was strongly influenced by pH but exhibiting different behaviors. The study demonstrated that the sorbent based on ox-CNTs was the one that exhibited the highest capacity and linearity for both analytes when compared with CNT or ala-CNT. The analytical performance was evaluated for the three sorbents to establish the best conditions regarding sensitivity, reproducibility and accuracy. The precision expressed as relative standard deviations (n = 6) were 3.9 and 0.5% for Ni(2+) and Pb(2+), respectively The limit of detection (LOD), calculated as the concentration required to yield a net peak equal to three times the standard deviation of the background signal (3 sigma) was 30 and 10 mu g L(-1) for Ni(2+) and Pb(2+) respectively. Alternatively, the limit of quantification (10 sigma) was calculated and resulted to be 0.79 and 0.07 mu g L(-1) for Ni(2+) and Pb(2+) respectively. After optimization, the method that involved the use of ox-CNT associated to an on-line preconcentration was tested in samples of relevant environmental importance. Accuracy was evaluated analyzing a certified reference material namely, Municipal Sludge (QC MUNICIPAL SLUDGE A) and a reference sample of Lake Sediment (TRAP-LRM from IJS). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 251
页数:7
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