Baś Bogusław
Faculty of Materials Science and Ceramics, AGH University of Science and Technology, 30-059 Kraków, al. Mickiewicza 30, Poland.
Anal Chim Acta. 2006 Jun 16;570(2):195-201. doi: 10.1016/j.aca.2006.04.013. Epub 2006 May 23.
The refreshable mercury film silver based electrode Hg(Ag)FE applied for determination of Cr(VI) traces using catalytic adsorptive striping voltammetry (CAdSV) will be presented. The film electrode is characterized by its very good surface reproducibility (not less than 2%) and long-term stability (1500-2000 measurement cycles). The mechanical refreshing of mercury film is realized in the specially constructed device, in a time shorter than 1-2s. In the paper, it will be proved that a mechanically weak hanging mercury drop electrode (HMDE) may be substituted by mercury film Hg(Ag)FE electrode with a surface area adjustable from 1.5 to 12 mm2. For the electrode surface 4 mm2 the detection limit obtained for Cr(VI) was 0.19 nM, while the linearity range measured for a 20s accumulation time was between 0.5 and 50 nM. The relative standard deviation (R.S.D.) in determination of Cr(VI) varied from 1 to 5%. The influence of the excess of Cr(III) on determination of Cr(VI) was analyzed using samples from the Dobczyce reservoir spiked with known amounts of Cr(VI) and Cr(III).
将介绍用于催化吸附溶出伏安法(CAdSV)测定痕量Cr(VI)的可更新汞膜银基电极Hg(Ag)FE。该膜电极的特点是具有非常好的表面重现性(不低于2%)和长期稳定性(1500 - 2000次测量循环)。汞膜的机械更新在专门构建的装置中实现,时间短于1 - 2秒。本文将证明,机械性能较弱的悬汞滴电极(HMDE)可以被表面积可在1.5至12平方毫米之间调节的汞膜Hg(Ag)FE电极替代。对于4平方毫米的电极表面,Cr(VI)的检测限为0.19 nM,而在20秒富集时间下测量的线性范围为0.5至50 nM。测定Cr(VI)时的相对标准偏差(R.S.D.)在1%至5%之间。使用来自多布恰尼采水库加标已知量Cr(VI)和Cr(III)的样品分析了过量Cr(III)对Cr(VI)测定的影响。