Journal
ANALYTICA CHIMICA ACTA
Volume 1168, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.aca.2021.338595
Keywords
PCMX; Electrochemical sensing; Electropolymerization; Cyclic voltammetry; Differential pulse voltammetry; Response surface methodology
Categories
Funding
- University Grant Commission, Delhi [F1-17.1/2014-15/RGNF-2014-15-ST-ASS-80000]
- Ministry of Tribal Affairs, India [F1-17.1/2014-15/RGNF-2014-15-ST-ASS-80000]
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A rapid sensing system was developed for quantifying p-Chloro-meta-Xylenol (PCMX) in wastewater samples, utilizing a unique polymeric nanocomposite modified electrode with excellent sensitivity and stability. The optimized combination of constituents and electrochemical techniques yielded a interference-free response with good selectivity, reproducibility, and repeatability. The sensing platform demonstrated applicability for real samples and showed good correlation with standard methods.
p-Chloro-meta-Xylenol (PCMX) is an environmentally hazardous phenolic compound having biocidal and antiseptic activity. Very few research publications addressed monitoring this contaminant. This paper presents a rapid sensing system to quantify it in waste water samples. The electrochemical activity of PCMX was exploited through a unique polymeric nanocomposite modified transducer for its quantification. Poly[(3,4-Ethylenedioxythiophene)-co-(o-phenylenediamine)] [P(EDOT-co-OPD)] was deposited through one-step electropolymerization technique on the glassy carbon electrode (GCE) modified by functionalized multi-wall carbon nanotubes (fMWCNTs). An optimized combination of these constituents was evaluated using response surface methodology (RSM) based Box-Behnken experimental design. This maximized the response for PCMX using differential pulse voltammetry (DPV). The sensing matrix was characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The structural and morphological study of the modified film was conducted by Fourier transform-infrared spectroscopy (FT-IR), Raman spectroscopy, scanning electron microscopy (SEM), and field emission scanning electron microscope (FESEM). The anodic peak current could be read from a wide range of 0.5-225 mu M calibration curve with a detection limit of 0.2545 mmol L-1. Interestingly this work did not use any biomaterial in the modification but achieved interference-free response with excellent selectivity, sensitivity (0.4668 mu A mu M-1 cm(-2)), reproducibility (RSD = 2.2%), and repeatability. The sensing platform showed good stability (85.7%) of 3 months even after 150 times repetitive use. Its applicability for real samples was established by good correlation with standard methods. (C) 2021 Elsevier B.V. All rights reserved.
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