Catalytic polarographic determination of vanadium (V) by using double polarographic peak
Document Type
Article
Publication Date
12-1-2000
Abstract
A new catalytic polarographic method for the determination of trace amounts of vanadium(V) has been proposed. The method is based on the catalytic effect of V(V) on the oxidation reaction between ethyl orange and bromate in the medium of sulfuric acid, with tartaric acid as an activator. Ethyl orange and its oxidation product exhibits voltammetric peak at - 0.62 V and - 0.52 V (vs .SCE) in ammoniacal buffer solution respectively. Under optimal experiment condition, the reaction was monitored by measuring the peak height decrease at - 0.62V (ΔI′p1) and the peak height increase at - 0.52V (ΔI′p1). Vanadium is determined according to ΔI = (ΔI′p1 + ΔI′p2), the linear range of determination is 0.25 ∼ 3.50 μg/L for vanadium(V), the detection limit is 0.12 μg/L. The method has been used to determine trace vanadium in food samples.
Publication Source (Journal or Book title)
Fenxi Huaxue
First Page
1142
Last Page
1143
Recommended Citation
Wang, S., Du, L., Li, B., & Zhang, A. (2000). Catalytic polarographic determination of vanadium (V) by using double polarographic peak. Fenxi Huaxue, 28 (9), 1142-1143. Retrieved from https://repository.lsu.edu/ag_exst_pubs/1082