VOLTAMMETRIC DETERMINATION OF TRACE AMOUNTS OF MERCURY WITH A CARBON PASTE ELECTRODE MODIFIED WITH AN ANION-EXCHANGER

被引:52
作者
CAI, X
KALCHER, K
DIEWALD, W
NEUHOLD, C
MAGEE, RJ
机构
[1] KARL FRANZENS UNIV,INST ANALYT CHEM,UNIV PL 1,A-8010 GRAZ,AUSTRIA
[2] HAINAN UNIV,COLL SCI & TECHNOL,HAIKOU 570028,PEOPLES R CHINA
[3] LA TROBE UNIV,MELBOURNE,AUSTRALIA
来源
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY | 1993年 / 345卷 / 01期
关键词
D O I
10.1007/BF00323321
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A carbon paste electrode modified with a liquid anion exchanger (Amberlite LA2) was used for the voltammetric determination of mercury(II). Mercury is pre-concentrated, as tetrachloromercurate(II), onto the surface of the modified electrode only by the ion-exchange effect of the modifier without application of potential. After exchange of the medium the accumulated amount of mercury(II) is determined by differential pulse anodic stripping voltammetry in a blank electrolyte solution. The response depends on the concentration of mercury in the bulk solution, preconcentration time, and other parameters. The detection limit was 1 mug Hg(II)/l when a suitable time for preconcentration was chosen. Preconcentration for 5 min yields a linear calibration graph for concentrations up to 1000 mug Hg(II)/l. The effect of other ions on the determination of mercury and the applicability of the method to the analysis of phenylmercury compounds in pharmaceutical preparations were investigated.
引用
收藏
页码:25 / 31
页数:7
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