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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Electrochemically induced regioregularity of the binding sites of a polyaniline membrane as a powerful approach to produce selective recognition sites for silver ion
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Electrochemically induced regioregularity of the binding sites of a polyaniline membrane as a powerful approach to produce selective recognition sites for silver ion

机译:电化学诱导的聚苯胺膜结合位点的区域规则性是产生银离子选择性识别位点的有力方法

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Polyaniline (PANI) modified electrodes based on the electrochemical polymerization of aniline in the presence of a chelating agent, 5-sulfosalicylic acid (SSA), were prepared. The resulting PANI/SSA membrane was templated with respect to silver ion by applying consecutive reduction/oxidation steps. The electrochemically mediated templating causes doping/undoping of silver ions into the polymeric membrane. It seems that repeated addition/removal of silver ions into/from the membrane, induces conformational changes in the binding sites of the PANI and SSA, and increases the number of proper binding sites. This electrochemically induced regioregularity of the binding sites of the membrane components was found to be a powerful approach to produce selective recognition sites for silver ions in the PANI/SSA membrane. The system was able to fulfill four main criteria of the recognition process, including selectivity, sensitivity, rapidity and chemical reversibility in the voltammetric and potentiometric detection of silver ion. The prepared sensor was employed for preconcentration and differential pulse anodic stripping voltammetric (DPASV) measurement of silver ion. The stripping peak current was found to be dependent on the silver ion concentration over the range 1.0 x 10(-10) to 1.0 x 10(-4) M. Several metal ions did not show appreciable interference in the voltammetric determination of Ag+, however, mercury ion led to a significant interference. During potentiometric measurements, the sensor demonstrated reproducible response with a near-Nernstian slope of 57.1 +/- 0.4 mV per decade of silver ion activity over a linear range extending five orders of magnitude (1.0 x 10(-8) to 1.0 x 10(-3) M Ag+), with a detection limit of 1.0 x 10(-9) M Ag+. The templated electrode provided improved potentiometric selectivity for silver ion with respect to various metal ions and could be used over a pH range of 3.0-5.5. (C) 2016 Elsevier B.V. All rights reserved.
机译:在螯合剂5-磺基水杨酸(SSA)存在下,基于苯胺的电化学聚合反应制备了聚苯胺(PANI)修饰电极。通过施加连续的还原/氧化步骤,相对于银离子对所得的PANI / SSA膜进行模板化。电化学介导的模板导致银离子掺杂/去掺杂到聚合物膜中。似乎反复向膜中添加银离子/从膜中去除银离子会引起PANI和SSA结合位点的构象变化,并增加适当结合位点的数量。发现膜成分结合位点的这种电化学诱导的区域规则性是在PANI / SSA膜中产生银离子的选择性识别位点的有效方法。该系统能够满足识别过程的四个主要标准,包括银离子伏安法和电位法检测中的选择性,灵敏度,快速性和化学可逆性。所制备的传感器用于银离子的预浓缩和差分脉冲阳极溶出伏安法(DPASV)测量。发现在1.0 x 10(-10)到1.0 x 10(-4)M范围内,溶出峰电流取决于银离子浓度。几种金属离子在伏安法测定Ag +中没有明显的干扰,但是,汞离子导致严重干扰。在电位测量过程中,该传感器表现出可重现的响应,在十个线性范围(1.0 x 10(-8)至1.0 x 10(10) -3)M Ag +),检出限为1.0 x 10(-9)M Ag +。模板化电极相对于各种金属离子提供了改进的银离子电位选择性,可以在3.0-5.5的pH范围内使用。 (C)2016 Elsevier B.V.保留所有权利。

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