Published July 2021 | Version v1
Journal article

Interference-free electrocatalysis of p-chloro meta xylenol (PCMX) on uniquely designed optimized polymeric nanohybrid of P(EDOT-co-OPD) and fMWCNT modified glassy carbon electrode

  • 1. Pollution Control Laboratory, Department of Chemical Engineering, Jadavpur University, 188, Raja Subodh Chandra Mallick Road, Kolkata, 700032, West Bengal (India)
  • 2. Biosensor Laboratory, Department of Polymer Science and Technology, University of Calcutta, A.P.C. Road, Kolkata, 700009, West Bengal (India)
  • 3. Calcutta Institute of Technology, Uluberia, Howrah, 711316 (India)

Description

Highlights: • Novel polymeric nanohybrid of P(EDOT-co-OPD) with fMWCNT modified working electrode. • Multivariable factorial design used to optimize the sensing polymeric nanohybrid matrix. • Interference-free electrocatalysis of PCMX without using any biomaterials. • Differential pulse voltammetric analysis to quantify PCMX in environmental samples. • Excellent sensitivity, reproducibility, and stability of the sensing matrix for detection of PCMX. 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 μM calibration curve with a detection limit of 0.2545 μmol L−1. Interestingly this work did not use any biomaterial in the modification but achieved interference-free response with excellent selectivity, sensitivity (0.4668 μA μM−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.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.aca.2021.338595

Additional details

Identifiers

DOI
10.1016/j.aca.2021.338595;
PII
S0003267021004219;

Publishing Information

Journal Title
Analytica Chimica Acta
Journal Volume
1168
Journal Page Range
vp.
ISSN
0003-2670
CODEN
ACACAM

Optional Information

Copyright
Copyright (c) 2021 Elsevier B.V. All rights reserved.