A novel voltammetric platform based on dysprosium oxide for the sensitive determination of sunset yellow in the presence of tartrazine.

检出限 分析化学(期刊) 色谱法 微分脉冲伏安法 伏安法 循环伏安法
作者
Aysegul Kutluay Baytak,Emine Akbaş,Mehmet Aslanoglu
出处
期刊:Analytica Chimica Acta [Elsevier BV]
卷期号:1087: 93-103 被引量:7
标识
DOI:10.1016/j.aca.2019.08.055
摘要

Abstract This study reports the preparation of a novel voltammetric platform based on the modification of a glassy carbon electrode (GCE) with carbon nanotubes (MWCNTs) and dysprosium oxide (Dy2O3) nanoparticles. The electrode material was characterized by means of scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction method (XRD). The novel platform (Dy2O3NPs/MWCNTs/GCE) was applied for the voltammetric determination of sunset yellow (SY) in the presence of tartrazine (TAR). SY was first adsorbed at the surface of Dy2O3NPs/MWCNTs/GCE by keeping it into a solution of SY for 200 s. Afterwards, the proposed platform was washed with ultrapure water and transferred with the adsorbed species in a voltammetric cell containing only 0.1 M phosphate buffer solution (PBS). Then, the novel platform (Dy2O3NPs/MWCNTs/GCE) exhibited excellent electrocatalytic activity and presented improved voltammetric responses when compared to other electrodes. The novel platform produced an improved anodic peak at 0.705 V and a corresponding cathodic peak at 0.690 V for SY and an irreversible anodic peak at 0.957 V for TAR. When compared to the electrode modified with only MWCNTs, a remarkable increase in current response and a electrocatalytic activity of the proposed platform were observed for SY and TAR at a GCE modified with both MWCNTs and Dy2O3NPs. A linear relationship was obtained between the current response and the concentration of SY over range of 1.0 × 10−9 M −  1.4 × 10−7 M with an LOD of 3.5 × 10−10 M using square wave voltammetry (SWV). The proposed procedure provided an accurate and a precise quantification to the analysis of food and pharmaceutical samples.
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