Voltammetric and impedimetric determinations of selenium() by an innovative gold-free poly(1-aminoanthraquinone)/multiwall carbon nanotube-modified carbon paste electrode

• Published in: RSC advances 2022-02, Vol.12 (8), p.4988-5
• Main Authors: Ali, Asmaa Galal, Altahan, Mahmoud Fatehy, Beltagi, Amr Mohamed, Hathoot, Abla Ahmed, Abdel-Azzem, Magdi
• Format: Article
• Language: English
• Subjects: Anodic stripping; Carbon; Charge transfer; Chemical sensors; Chemistry; Electrochemical impedance spectroscopy; Electrodes; Multi wall carbon nanotubes; Polymer films; Selenium; Sensors; Spectrum analysis; Sulfuric acid; Voltammetry; Wastewater; Water pollution; Water sampling
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/d1ra07588h

Selenite (Se 4+ ), a significant source of water pollution above the permissible limits, is considered a valuable metal by environmentalists. In this study, we described a novel electrochemical sensor that utilized a carbon paste electrode (CPE) that was modified using multiwall carbon nanotubes (MWCNTs) and poly(1-aminoanthraquinone) (p-AAQ) for finding Se 4+ in water samples. Electrochemical quantification of Se 4+ depends on the formation of a selective complex (piaselenol) with p-AAQ. In this work, we prepared a CPE modified by physical embedding of MWCNTs and 1-aminoanthraquione (AAQ), while the polymer film was formed by anodic polymerization of AAQ by applying a constant potential of 0.75 V in 0.1 M HCl for 20 s followed by cyclic voltammetry (CV) from −0.2 to 1.4 V for 20 cycles. The modified CPE was used for differential pulse voltammetry (DPV) of Se 4+ in 0.1 M H 2 SO 4 from 0 to 0.4 V with a characteristic peak at 0.27 V. Further, the proposed sensor was characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, and electrochemical impedance spectroscopy (EIS). The analytical conditions regarding the electrode performance and voltammetric measurements were optimized, with the accumulation time and potential, supporting electrolyte, differential-pulse period/time, and amplitude. The EIS results indicated that the p-AAQ/MWCNTs-modified CPE sensor (p-AAQ/MWCNTs/CPE) that also exhibited low charge-transfer resistance ( R ct ) toward the anodic stripping of Se 4+ , exhibited good analytical performance toward different concentrations of Se 4+ in a linear range of 5-50 μg L −1 Se 4+ with a limit of determination (LOD) of 1.5 μg L −1 (3 σ ). Furthermore, differential-pulse voltammetry was employed to determine different concentrations of Se 4+ in a linear range of 1-50 μg L −1 Se 4+ , and an LOD value of 0.289 μg L −1 was obtained. The proposed sensor demonstrated good precision (relative standard deviation = 4.02%) at a Se 4+ concentration of 5 μg L −1 . Moreover, the proposed sensor was applied to analyze Se 4+ in wastewater samples that were spiked with Se, and it achieved good recovery values. The selenite ion is quantified electrochemically by selective complexation with poly(1-aminoanthraquione) to give a piaselenol complex on a modified p-AAQ/MWCNTs/CPE sensor.