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Determination of trace heavy Metals by Sequential Injection-anodic Stripping Voltammetry using Bismuth Film Screen-printed Carbon Electrode
Author(s) -
Suchada Chuanuwatanakul,
Wijitar Dungchai,
Orawon Chailapakul,
Shoji Motomizu
Publication year - 2008
Publication title -
analytical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.392
H-Index - 73
eISSN - 1348-2246
pISSN - 0910-6340
DOI - 10.2116/analsci.24.589
Subject(s) - chemistry , anodic stripping voltammetry , bismuth , stripping (fiber) , detection limit , analytical chemistry (journal) , square wave , electrode , supporting electrolyte , hydrochloric acid , voltammetry , metal ions in aqueous solution , electrolyte , metal , working electrode , nuclear chemistry , inorganic chemistry , electrochemistry , chromatography , materials science , physics , organic chemistry , composite material , voltage , quantum mechanics
A sequential injection-square-wave anodic stripping voltammetry (SIA-SWASV) is proposed for the simultaneous determination of Pb(II), Cd(II) and Zn(II), employing an in situ plated bismuth film screen-printed carbon electrode (Bi-SPCE) as a working electrode and hydrochloric acid as a supporting electrolyte. Bi(III) and analyte metal ions were on-line deposited onto a SPCE at -1.4 V vs. Ag/AgCl for 180 s. At a stopped flow, a square-wave voltammogram was recorded from -1.3 to 0 V vs. Ag/AgCl. The experimental conditions were optimized. Under the optimum conditions, the linear ranges were 0 - 70 microg L(-1) for Pb(II) and Cd(II), and 75 - 200 microg L(-1) for Zn(II). The limits of detection (S/N = 3) were obtained at concentrations as low as 0.89 microg L(-1) for Pb(II) and 0.69 microg L(-1) for Cd(II) for a 180-s deposition time. The proposed method was applied to the determination of Pb(II), Cd(II) and Zn(II) in water samples with satisfactory results.

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