Simultaneous electrochemical determination of hydroquinone, catechol and resorcinol at Nafion/multi-walled carbon nanotubes/carbon dots/multi-walled carbon nanotubes modified glassy carbon electrode

被引:112
|
作者
Wei, Chan [1 ]
Huang, Qitong [2 ]
Hu, Shirong [1 ]
Zhang, Hanqiang [1 ]
Zhang, Wuxiang [1 ]
Wang, Zhaoming [1 ]
Zhu, Menglin [1 ]
Dai, Pingwang [3 ]
Huang, Lizhang [3 ]
机构
[1] Minnan Normal Univ, Coll Chem & Environm, Zhangzhou 363000, Peoples R China
[2] Zhangzhou Inst Technol, Dept Food & Biol Engn, Zhangzhou 363000, Peoples R China
[3] Zhangzhou Prod Qual Supervis Inst, Zhangzhou 363000, Peoples R China
关键词
simultaneous determination; dihydroxybenzene isomers; electrochemical sensor; carbon dots; multi-walled carbon nanotubes; DIHYDROXYBENZENE ISOMERS; HYBRID MATERIALS; IONIC LIQUID; DOTS; PHENOL; SENSOR; FILMS;
D O I
10.1016/j.electacta.2014.10.051
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this work, an excellent electrochemical sensor based on Nafion/multi-walled carbon nanotubes/carbon dots/multi-walled carbon nanotubes (Nafion/MWCNTs/CDs/MWCNTs) for simultaneous determination of hydroquinone (HQ), catechol (CC) and resorcinol (RS) in 0.1 M phosphate buffer solutions (PBS, pH = 7.0) was found. The functioned MWCNTs, which contained amido bond, were combined to CDs via the electrostatic interaction to build the Nafion/MWCNTs/CDs/MWCNTs modified electrode. As we know, MWCNTs have large specific surface area and CDs have electrical conductivity, which were benefited to build the composite modified electrode. The three dihydroxybenzene isomers could well separate from each other at the scan rate of 100 mV s (1) with a potential difference of 119 mV and 419 mV for the oxidation peak potentials of HQ-CC and CC-RS, respectively. Differential pulse voltammetry (DPV) was used for the simultaneous determination of HQ, CC and RS in their ternary mixture. The peak current obtained was linearly dependent on the HQ, CC and RS concentrations in the range of 1.0 to 200.0 mu M, 4.0 to 200.0 mu M and 3.0 to 400.0 mu M and the detection limits for HQ, CC and RS were 0.07 mu M, 0.06 mu M and 0.15 mu M (S/N = 3), respectively. The modified electrode was applied to detect the tap water, well water and river water and the recoveries of tap water, well water and river water samples were 100.3-109.8% for HQ, 96.0-105.8% for CC and 83.4-101.6% for RS, respectively. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:237 / 244
页数:8
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