Thermoresponsive polymer-mediated extraction for graphite furnace atomic absorption spectrometric determination of trace metals in high purity iron

被引:8
作者
Saitoh, Tohru [1 ]
Sakurai, Kazuki [2 ]
Hiraide, Masataka [2 ]
机构
[1] Kitami Inst Technol, Dept Biotechnol & Environm Chem, Koen Cho 165, Kitami, Hokkaido 0908507, Japan
[2] Nagoya Univ, Grad Sch Engn Mol Design & Engn, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan
关键词
Poly(N-isopropylacrylamide); High purity iron; Trace metals; Selective separation; Graphite furnace atomic absorption spectrometry; THERMALLY REVERSIBLE POLYMER; PLASMA-MASS SPECTROMETRY; ANION-EXCHANGE RESIN; EMISSION-SPECTROMETRY; TENSILE DEFORMATION; HEAVY-METALS; ELEMENTS; WATER; SEPARATION; BEHAVIOR;
D O I
10.1016/j.microc.2018.03.029
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A thermoresponsive polymer-mediated extraction was designed for the selective separation of traces metal ions from high purity iron solutions. Traces metals were extracted into the coagulum of a thermoresponsive polymer, poly(N-isopropylacrylamide) as their dibenzyldithiocarbamate chelates, while Fe(III) matrix remained in the bulk aqueous solution as its water-soluble tartrate chelate. The coagulum was readily collected from the solution and then dissolved with a small amount of N,N-dimethylformamide for the introduction to a graphite furnace of atomic absorption spectrometer. The use of 0.5 g l(-1) poly(N-isopropylacrylamide), 2.0 mM sodium dibenzyldithiocarbamate, and 0.6 M diammonium tartrate (pH 10.7) allowed nearly complete (>99.9%) collection of Co(II), Ni(II), Cu(II), Cd(II), Pb(II), and Bi(III) with reducing Fe(III) concentration from 50 mg ml(-1) to 14 +/- 1 mu g ml(-1) being lower than the tolerance limits for the determination of traces of metals. Because of effective elimination of iron matrix, six metals at fractional mu g g(-1) levels were successfully determined with high reproducibility. The accuracy and precision were evaluated by analyzing certified reference materials of high purity iron. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:410 / 415
页数:6
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