Wang Liang, Huang Peng-Fei, Wang Hong-Jing, Bai Jun-Yue, Zhang Li-Ying, Zhao Yu-Qing
College of Life Science, Dalian Nationalities University, Dalian 116600, China.
Ann Chim. 2007 May-Jun;97(5-6):395-404. doi: 10.1002/adic.200790024.
Glassy carbon electrode (GCE) is covalently modified with aspartic acid (Asp). The modified electrode is used for the simultaneous electrochemical determination of hydroquinone (HQ) and catechol (CC) and shows an excellent electrocatalytical effect on the oxidation of HQ and CC by cyclic voltammetry (CV) in 0.1 mol/L acetate buffer solution (pH 4.5). In differential pulse voltammetric (DPV) measurements, the modified electrode could separate the oxidation peak potentials of HQ and CC present in binary mixtures by about 101 mV though the bare electrode gave a single broad response. A successful elimination of the fouling effect by the oxidized product of HQ on the response of CC has been achieved at the modified electrode. The determination limit of HQ in the presence of 0.1 mmol/L CC was 9.0 x 10(-7) mol/L and the determination limit of CC in the presence of 0.1 mmol/L HQ was 5.0 x 10(-7) mol/L. The proposed method has been applied to the simultaneous determination of HQ and CC in a water sample with simplicity and high selectivity.
玻碳电极(GCE)用天冬氨酸(Asp)进行共价修饰。修饰后的电极用于同时电化学测定对苯二酚(HQ)和邻苯二酚(CC),在0.1 mol/L醋酸盐缓冲溶液(pH 4.5)中通过循环伏安法(CV)对HQ和CC的氧化显示出优异的电催化效果。在差分脉冲伏安法(DPV)测量中,尽管裸电极给出单一的宽响应,但修饰后的电极可将二元混合物中HQ和CC的氧化峰电位分开约101 mV。在修饰电极上已成功消除了HQ氧化产物对CC响应的污垢效应。在存在0.1 mmol/L CC的情况下,HQ的测定限为9.0×10⁻⁷ mol/L,在存在0.1 mmol/L HQ的情况下,CC的测定限为5.0×10⁻⁷ mol/L。所提出的方法已被应用于简单且高选择性地同时测定水样中的HQ和CC。