Conductive Carbon from Taro Stems for Simultaneous Detection of Hydroquinone and Catechol

Abstract This study shows that incorporating taro carbon (TC) into a glassy carbon electrode (GCE) significantly enhanced surface charge transfer characteristics and conductivity and successfully separated the hydroquinone (HQ) and catechol (CT). Moreover, TC on the GCE surface reduced the overpotential of HQ and CT oxidation. Using X‐ray diffraction (XRD) analysis, field‐emission scanning electron microscopy (FESEM), and energy dispersive spectroscopy (EDS), the surface morphology and elemental composition of TC was investigated. The enhanced electron transfer process at TC‐GCE was studied using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) investigation. Scan rate analysis revealed that HQ and CT exhibited a higher oxidation affinity at TC‐GCE, with diffusion‐regulated anodic processes. Quantitative analysis showed a linear detection range of 5–200 μM for both HQ and CT, with LOD values of 0.47 μM for HQ and 0.51 μM for CT respectively. The modified electrode showed excellent selectivity, stability, and high recovery rates for detecting HQ and CT in tap water.

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Publication Details

Journal
ChemistrySelect
Published
2024-08-30
DOI
https://doi.org/10.1002/slct.202402136
Citations
1
Primary Topic
Electrochemical sensors and biosensors
Type
article
Field-Weighted Citation Impact
0.21
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article

Conductive Carbon from Taro Stems for Simultaneous Detection of Hydroquinone and Catechol

Md. Aminul Haque, S. M. Abu Nayem, Nasrin Sultana, Md. Abdul Aziz et al.
1 citations
ChemistrySelect
Electrochemical sensors and biosensors
0.21
article

Conductive Carbon from Taro Stems for Simultaneous Detection of Hydroquinone and Catechol

Md. Aminul Haque, S. M. Abu Nayem, Nasrin Sultana, Md. Abdul Aziz, A. J. Saleh Ahammad, Abdul Awal, Mozammal Hoque, Nafees Ahmed
article en
1 citations

Abstract

Abstract This study shows that incorporating taro carbon (TC) into a glassy carbon electrode (GCE) significantly enhanced surface charge transfer characteristics and conductivity and successfully separated the hydroquinone (HQ) and catechol (CT). Moreover, TC on the GCE surface reduced the overpotential of HQ and CT oxidation. Using X‐ray diffraction (XRD) analysis, field‐emission scanning electron microscopy (FESEM), and energy dispersive spectroscopy (EDS), the surface morphology and elemental composition of TC was investigated. The enhanced electron transfer process at TC‐GCE was studied using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) investigation. Scan rate analysis revealed that HQ and CT exhibited a higher oxidation affinity at TC‐GCE, with diffusion‐regulated anodic processes. Quantitative analysis showed a linear detection range of 5–200 μM for both HQ and CT, with LOD values of 0.47 μM for HQ and 0.51 μM for CT respectively. The modified electrode showed excellent selectivity, stability, and high recovery rates for detecting HQ and CT in tap water.

ChemistrySelectVol. 9(33)
King Fahd University of Petroleum and Minerals (SA), Jagannath University (BD)
Clean water and sanitation
Openalex Percentile: Top 49%
Electrochemical sensors and biosensors
0.21
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