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Comparative electroanalytical performance of poly o‐toulidine and polyaniline towards hydrazine oxidation supplemented by DFT.

Authors :
Liaqat, Faroha
Jamil, Madiha
Tariq, Irsa
Haider, Ali
Khan, Muhammad Abdullah
Source :
Journal of Applied Polymer Science; 8/15/2023, Vol. 140 Issue 31, p1-15, 15p
Publication Year :
2023

Abstract

This work presents a comparative experimental and theoretical study on the use of polyaniline and its derivative, poly o‐toluidine, as effective electrochemical sensor for the detection of hydrazine. Hydrazine is a toxic analytic with numerous adverse health effects on the human brain, liver and nervous system. The conducting polymers polyaniline (PANI) and poly o‐toluidine (POT) were synthesized by oxidative polymerization and characterized through x‐ray Diffraction, FT‐IR, and UV–Visible Spectroscopy. Electrochemical studies performed on the polymer modified glassy carbon electrode (GCE) using cyclic voltammetry and differential pulse voltammetry reveal strong interaction between hydrazine and the polymer through irreversible charge transfer. The oxidation current was seen to increase with increasing hydrazine concentration. The diffusion coefficients were found to be 1.89 × 10−5 cm2/s and 2.89 × 10−6 cm2/s for PANI and POT, respectively. PANI and POT based sensors show a limit of detection of 1 μM and 5.13 mM, respectively in the linear concentration range of 1–9 mM. Density functional studies on the PANI‐hydrazine and POT‐hydrazine complexes show enhanced intermolecular charge transfer from nitrogen lone pairs in hydrazine to the polymer backbone clearly identifying the donor and acceptor moieties. PANI based electrochemical sensor is shown to have a higher sensitivity for hydrazine compared to POT, where the sensing interaction is hindered by the bulky methyl group in ortho position. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00218995
Volume :
140
Issue :
31
Database :
Complementary Index
Journal :
Journal of Applied Polymer Science
Publication Type :
Academic Journal
Accession number :
164780564
Full Text :
https://doi.org/10.1002/app.54112