4.6 Article

Voltammetric Determination of Hg2+, Zn2+, and Pb2+ Ions Using a PEDOT/NTA-Modified Electrode

Journal

ACS OMEGA
Volume 7, Issue 23, Pages 20405-20419

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.2c02682

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A novel electrochemical sensor based on a platinum electrode modified by poly(3,4-ethylenedioxythiophene) and N alpha,N alpha-bis-(carboxymethyl)-L-lysine hydrate (NTA lysine) was developed for determining trace levels of Hg2+, Pb2+, and Zn2+ ions in water using square wave voltammetry. The modified electrode was characterized and the electrochemical properties were investigated. The sensor showed linear responses and low detection limits for Hg2+, Pb2+, and Zn2+ ions.
A novel electrochemical sensor for determining trace levels of Hg2+, Pb2+, and Zn2+ ions in water using square wave voltammetry (SWV) is reported. The sensor is based on a platinum electrode (Pt) modified by poly(3,4-ethylenedioxythiophene) and N alpha,N alpha-bis-(carboxymethyl)-L-lysine hydrate (NTA lysine) PEDOT/NTA. The modified electrode surface (PEDOT/NTA) was prepared via the introduction of the lysine-NTA group to a PEDOT/N-hydroxyphthalimide NHP electrode. The (PEDOT/NTA) was characterized via cyclic voltammetry (CV), Fourier transform infrared (FTIR) spectroscopy, and scanning electron microscopy (SEM). The effects of scan rates on the electrochemical properties of the polymer electrode were also investigated. The electrochemical results were used to estimate the coverage of the electrode polymer surface and its electrostability in background electrolyte solutions. Several analytical parameters, such as polymer film thickness, metal deposition time, and pH of the electrolyte, were examined. Linear responses to Hg2+, Pb2+, and Zn2+ ions in the concentration range of 5-100 mu g L-1 were obtained. The limits of detection (LODs) for the determination of Hg2+, Pb2+, and Zn2+ ions were 1.73, 2.33, and 1.99 mu g L-1, respectively. These promising results revealed that modified PEDOT/NTA films might well represent an important addition to existing electrochemical sensor technologies.

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