Advanced Carbon Nanomaterials for Electrochemical Sensing in the Determination of Trace V(V) Concentrations

A new method is described for the determination of vanadium using adsorptive stripping voltammetry of V(V) complexed with cupferron at a CNTs/SGC electrode modified with a lead film. The CNTs/SGC electrode is based on carbon nanomaterials such as carbon nanotubes and spherical glassy carbon, which form the foundation of modern sensor technology. Optimal conditions of adsorptive voltammetric measurement were found to be modification/accumulation potential and time of −1.6 V and 60 s, respectively, and supporting electrolyte of 0.2 mol/L NaAc–HAc buffer (pH 5.3) containing 0.3 mmol/L cupferron and 0.15 mmol/L Pb(II). The response of the system was found to be linear in a range of V(V) concentrations from 0.25 nmol/L to 10 nmol/L. The detection limit was found to be 0.08 nmol/L. The selectivity of the procedure was determined by analysing the effect of other interfering ions on the vanadium analytical signal. The method was successfully validated by analysing natural environmental waters.

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Publication Details

Journal
Materials
Published
2026-06-30
DOI
https://doi.org/10.3390/ma19132769
Primary Topic
Electrochemical Analysis and Applications
Type
article
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Advanced Carbon Nanomaterials for Electrochemical Sensing in the Determination of Trace V(V) Concentrations

Cecylia Wardak, Małgorzata Grabarczyk
Materials
Electrochemical Analysis and Applications
article

Advanced Carbon Nanomaterials for Electrochemical Sensing in the Determination of Trace V(V) Concentrations

Cecylia Wardak, Małgorzata Grabarczyk
article en

Abstract

A new method is described for the determination of vanadium using adsorptive stripping voltammetry of V(V) complexed with cupferron at a CNTs/SGC electrode modified with a lead film. The CNTs/SGC electrode is based on carbon nanomaterials such as carbon nanotubes and spherical glassy carbon, which form the foundation of modern sensor technology. Optimal conditions of adsorptive voltammetric measurement were found to be modification/accumulation potential and time of −1.6 V and 60 s, respectively, and supporting electrolyte of 0.2 mol/L NaAc–HAc buffer (pH 5.3) containing 0.3 mmol/L cupferron and 0.15 mmol/L Pb(II). The response of the system was found to be linear in a range of V(V) concentrations from 0.25 nmol/L to 10 nmol/L. The detection limit was found to be 0.08 nmol/L. The selectivity of the procedure was determined by analysing the effect of other interfering ions on the vanadium analytical signal. The method was successfully validated by analysing natural environmental waters.

MaterialsVol. 19(13)
Maria Curie-Skłodowska University (PL)
Clean water and sanitation
Openalex Percentile: Top 17%
Electrochemical Analysis and Applications
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