Differential Pulse Voltammetric Determination of Quercetin with Ferrocene Modified Carbon Paste Electrode
摘 要
制备了二茂铁修饰碳糊电极,并采用循环伏安法研究了槲皮素在该修饰电极上的电化学行为。研究发现:在pH 6.2磷酸盐缓冲溶液中,修饰电极对槲皮素有良好的电催化作用,得到了一对氧化还原峰,其氧化反应是受吸附控制的两电子、两质子电极过程。并在此基础上提出了一种测定槲皮素的示差脉冲伏安法。试验结果表明:槲皮素的氧化峰电流与其浓度在8×10-4~2×10-6mol·L-1范围内呈线性关系,检出限(3S/N)为7×10-6mol·L-1。
Abstract
Ferrocene modified carbon paste electrode was prepared, and the electrochemical behavior of quercetin of this modified electrode was studied by cyclic voltammetry. It was found that significant electro-catalytic action of the modified electrode was observed on the reaction of quercetin at the electrode, giving a pair of oxidation and reduction peak in PBS of pH 6.2. The oxidation of quercetin at the modified electrode is controlled mainly by adsorption in an electrode process involved with 2 electrons and 2 protons. Based on this fact, a method of differential pulse voltammetry was proposed for the determination of quercetin. Linear relationship between values of oxidation peak current and concentration of quercetin was obtained in the range from 8×10-4 to 2×10-6mol·L-1, with detection limit (3S/N) of 7×10-6mol·L-1.
中图分类号 O657.1
所属栏目 试验与研究
基金项目
收稿日期 2012/5/26
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联系人作者顾玲(anmslqwt@163.com)
备注顾玲(1962-),女,上海人,副教授,硕士,研究方向为电分析化学。
引用该论文: GU Ling,HE Ya-mei,ZHANG Miao,YUAN Miao-miao. Differential Pulse Voltammetric Determination of Quercetin with Ferrocene Modified Carbon Paste Electrode[J]. Physical Testing and Chemical Analysis part B:Chemical Analysis, 2013, 49(3): 266~269
顾玲,贺亚梅,张苗,袁苗苗. 二茂铁修饰碳糊电极示差脉冲伏安法测定槲皮素[J]. 理化检验-化学分册, 2013, 49(3): 266~269
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【9】邓湘辉,阚显文,尉艳,等.二茂铁/L-半胱氨酸修饰电极的电化学行为及电催化性能[J].物理化学学报, 2005,21(12):1399-1402.
【10】白莉,郑志祥,高作宁.二茂铁修饰碳糊电极对抗坏血酸的电催化氧化及电分析方法研究[J].化学传感器, 2007,27(3):53-57.
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【13】曾恚恚,林辉概,俞汝勤.槲皮素荧光光度测定法的研究[J].分析试验室, 1993,12(6): 1-3.
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【15】XIAO Ping, ZHAO Fa-qiong, ZENG Bai-zhao. Voltammetric determination of quercetin at a multi-walled carbon nanotubes paste electrode[J]. Microchemical Journal, 2007,85(2):244-249.
【16】BRETT A M O, GHICA M E. Electrochemical oxidation of quercetin[J]. Electroanalysis, 2003,15(22):1745-1750.
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