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基于电聚合微孔聚(2-巯基苯并噻唑)修饰玻碳电极表面离子印迹策略的示差脉冲溶出伏安法检测汞(II)。

Stripping voltammetric detection of mercury(II) based on a surface ion imprinting strategy in electropolymerized microporous poly(2-mercaptobenzothiazole) films modified glassy carbon electrode.

机构信息

Research Center for Biomimetic Functional Materials and Sensing Devices, Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei, Anhui, 230031, PR China.

出版信息

Anal Chim Acta. 2011 Jan 24;685(1):21-8. doi: 10.1016/j.aca.2010.11.020. Epub 2010 Nov 21.

DOI:10.1016/j.aca.2010.11.020
PMID:21168547
Abstract

This work reports a surface ion imprinting strategy in electropolymerized microporous poly(2-mercaptobenzothiazole) (MPMBT) films at the surface of glassy carbon electrode (GCE) for the electrochemical detection of Hg(II). The Hg(II)-imprinted MPMBT/GCE exhibits larger binding to functionalized capacity, faster binding kinetics and higher selectivity to template Hg(II) due to their high ratio of surface-imprinted sites, larger surface-to-volume ratios, the complete removal of Hg(II) templates and larger affinity to Hg(II). The square wave anodic stripping voltammetry (SW ASV) response of the Hg(II)-imprinted MPMBT/GCE to Hg(II) is ca. 3.0 and 5.9 times larger than that at the direct imprinted poly(2-mercaptobenzothiazole) modified GCE and non-imprinted MPMBT/GCE sensor, respectively; and the detection limit for Hg(II) is 0.1nM (which is well below the guideline value given by the World Health Organization). Excellent wide linear range (1.0-160.0nM) and good repeatability (relative standard deviation of 2.5%) were obtained for Hg(II). The interference experiments showed that mercury signal was not interfered in the presence of Pb(II), Cd(II), Zn(II), Cu(II) and Ag(I), respectively. These values, particularly the high sensitivity and excellent selectivity compared favorably with previously reported methods in the area of electrochemical Hg(II) detection, demonstrate the feasibility of using the prepared Hg(II)-imprinted MPMBT/GCE for efficient determination of Hg(II) in aqueous environmental samples.

摘要

本工作报道了一种在玻碳电极表面电聚合微孔聚(2-巯基苯并噻唑)(MPMBT)薄膜中的表面离子印迹策略,用于电化学检测 Hg(II)。由于其高比例的表面印迹位点、更大的比表面积、完全去除 Hg(II)模板和对 Hg(II)更大的亲和力,Hg(II)印迹的 MPMBT/GCE 对功能化容量表现出更大的结合能力、更快的结合动力学和更高的模板 Hg(II)选择性。Hg(II)印迹的 MPMBT/GCE 对 Hg(II)的方波阳极溶出伏安法(SW ASV)响应分别比直接印迹的聚(2-巯基苯并噻唑)修饰的 GCE 和非印迹的 MPMBT/GCE 传感器大约 3.0 和 5.9 倍;Hg(II)的检测限为 0.1nM(远低于世界卫生组织给出的指导值)。Hg(II)的线性范围很宽(1.0-160.0nM),重现性良好(相对标准偏差为 2.5%)。干扰实验表明,在存在 Pb(II)、Cd(II)、Zn(II)、Cu(II)和 Ag(I)时,汞信号没有受到干扰。与电化学 Hg(II)检测领域的先前报道方法相比,这些值,特别是高灵敏度和出色的选择性,证明了制备的 Hg(II)印迹的 MPMBT/GCE 用于高效测定水相环境样品中 Hg(II)的可行性。

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