A new electrolytic dissolution of aluminum alloys and determination of some constituents by inductively coupled plasma optical emission spectrometry

被引:6
作者
Grigoletto, T
de Oliveira, E
Gutz, IGR
机构
[1] IPEN CNEN SP, BR-05422970 Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Quim, BR-05508900 Sao Paulo, Brazil
关键词
electrolytic dissolution; aluminum alloys; ICPOES; spectroscopy;
D O I
10.1016/j.talanta.2005.04.013
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The new electrolytic dissolution in batch of aluminum alloys samples as grains or turns and the determination of Fe, Cu, Mn, Mg, Cr, Ni, Zn, Pb and Ti by ICP OES was investigated. In on-line electrodissolution procedures described in the literature, samples were restricted to be in the form of solid blocks or plates with one polished flat face. Here, the sample was loaded in the barrel of a modified disposable syringe (the anodic semi-cell) and pressed with a modified plunger fitted with a platinum disk to establish electrical contact with the analyte. This arrangement was introduced in a beaker containing the electrolyte (1 mol L-1 HNO3) and a platinum wire as the cathode. The resulting solution from electrodissolution (0.6 A) was used for the ICP OES determinations. The influence of the aluminum concentration increase on the determination of the elements was evaluated. Electrodissolution of certified reference materials and commercial samples revealed relative errors lower than 10% for the elements Fe, Cu, Mg, Ni, Cr, Zn and Ti (when their content is above 0.1 %). Higher inaccuracies (> 10%) were observed for Mn and for Fe in B.C.S. 268/1 reference material certified. The proposed method presented a relative standard deviations (R.S.D.) lower or circa 10% to all of the elements (except Pb). In comparison with traditional acid dissolution, the proposed electrodissolution method is relatively fast (about 30 min), it is clean (there is no projection of solution) and simple (heating and fumes exhaust system were not necessaries). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:791 / 797
页数:7
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