Abstract
Vanadium(IV) and vanadium(V) can be determined by using differential pulse cathodic stripping voltammetry technique (DPCSV). Cupferron (ammonium N-nitrosophenylhydroxylamine) was used as ligand to form complex compounds with vanadium ions in Britton–Robinson buffer (BRB) solution. At concentration lower than 1.0×10−6M, both V(IV) and V(V) cupferron complexes showed a single cathodic peak at −0.576V in BRB of pH 4; thus V(IV) and V(V) ions cannot be differentiated at low concentration. However, the ionic species of vanadium can be differentiated at high concentration in the presence of cupferron. Parameters including pH of BRB solution, initial potential and accumulation potential were optimized. Under the optimized parameters, the limit of detection (LOD) was 0.09nM, and the peak current was linear in the concentration range 0.01–0.9µM total vanadium ions. The determination of V(IV) and V(V) ions was carried out at higher concentration in the sample using calibration plot method. At higher concentration range of 10–60µM V(IV) and V(V) ions were determined with LOD of 1.2 and 1.1µM, respectively. The developed method was successfully applied to 10,00,000 fold diluted Benfield sample and 0.6227M total vanadium ions were determined. The determination of V(IV) and V(V) ions were also successfully carried out in artificial sample as well as Benfield sample (dilution factor, 10,000). The concentration of V(IV) and V(V) ions was 22.52µM and 38.91µM, respectively, giving total vanadium concentration of 0.6143M in Benfield sample.
[Display omitted]
•Ionic species of vanadium determined in Benfield sample.•Differential pulse cathodic stripping voltammetric techniques used.•Cupferron used as ligand and separator for V(IV) and V(V) complexes.•BR buffer with pH 4 used as supporting electrolyte.•The develop method was successfully applied to various samples.