Study on the determination of trace rhenium (VII) by the adsorption differential pulse polarography
Hong‐Yuan Chen, Hui‐Qun Fang, Huangxian Ju, Huibin Li, Rolf Neeb
Abstract
Hong‐Yuan Chen, Hui‐Qun Fang, Huangxian Ju, Huibin Li, Rolf Neeb
Abstract
The determination of trace rhenium (VII) by differential pulse polarography in the system of H2SO4-(NHsOH)2 · H2SO4-TeO2−4 is markedly improved by the addition of Nitron, which is adsorbed on the surface of mercury electrode. The limit of detection is down to 2 × 1010 M. The adsorptive peak potential is −0.80 V (vs. SCE). In the ranges of 5 × 1010—10−8, 1 × 10−5—10−7 and 1 × 10−7—10−6M, there are good linear relationships between the peak current increment and the concentration, of which the relative standard deviations are 9.5, 6.6, 1.8% respectively with the correlation coefficients of linear regression of 0.995–0.999. The results relating to this polarographic wave show that it is an adsorption-catalytic wave. The mechanism of the electrode reaction is discussed.
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The determination of trace rhenium (VII) by differential pulse polarography in the system of H2SO4-(NHsOH)2 · H2SO4-TeO2−4 is markedly improved by the addition of Nitron, which is adsorbed on the surface of mercury electrode. The limit of detection is down to 2 × 1010 M. The adsorptive peak potential is −0.80 V (vs. SCE). In the ranges of 5 × 1010—10−8, 1 × 10−5—10−7 and 1 × 10−7—10−6M, there are good linear relationships between the peak current increment and the concentration, of which the relative standard deviations are 9.5, 6.6, 1.8% respectively with the correlation coefficients of linear regression of 0.995–0.999. The results relating to this polarographic wave show that it is an adsorption-catalytic wave. The mechanism of the electrode reaction is discussed.
Key concepts: Polarography, Chemistry, Dropping mercury electrode, Rhenium, Adsorption, Detection limit, Peak current, Analytical Chemistry (journal)