Electrochemical Determination of Chloramphenicol on Glassy Carbon Electrode Modified Activated Carbon Derived from Rice Husks

In the present article, the application of activated carbon derived from rice husks (RHAC) with high surface area as an electrode modifier for electrochemical determination of chloramphenicol (CP) is demonstrated. The RHAC was synthesized via a two-step alkaline pretreatment followed by the applicat...

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Published inECS journal of solid state science and technology Vol. 10; no. 11; pp. 117001 - 117012
Main Authors Thanh, Tran Si, Thanh Tu, Nguyen Thi, Quy, Phan Tu, Toan, Tran Thanh Tam, Thanh, Nguyen Mau, Nguyen, Vo Thang, Tuan, Nguyen Hoang, Nhiem, Dao Ngoc, Lieu, Pham Khac, Khieu, Dinh Quang
Format Journal Article
LanguageEnglish
Published IOP Publishing 01.11.2021
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Summary:In the present article, the application of activated carbon derived from rice husks (RHAC) with high surface area as an electrode modifier for electrochemical determination of chloramphenicol (CP) is demonstrated. The RHAC was synthesized via a two-step alkaline pretreatment followed by the application of ultrasound radiation. The obtained carbon materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen adsorption/desorption isotherms, Fourier transformation Infrared (FT-IR) spectroscopy and Raman spectroscopy. It was found that the ultrasonic activation process plays a critical role in improving the textural properties of AC by removing fine particles to clean capillaries and transforming a graphitic structure to a turbostratic one. The RHAC synthesized in suitable conditions displayed a specific surface area up to 1710 m 2 g −1 . The glassy carbon electrode modified with RHAC exhibited an excellent electroactivity towards CP as compared to bare GCE. The voltammetry characteristics of the electrochemical sensor were studied by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). This electrode had a good performance with a linear response range of 0.95–5.76 μ M and a low detection limit of 0.66 μ M (S/N = 3). The present promising sensor displayed high selectivity, great stability and expectable recovery for CP detection in real samples.
Bibliography:JSS-101679.R1
ISSN:2162-8769
2162-8777
DOI:10.1149/2162-8777/ac372c