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首页> 外文期刊>Electrochimica Acta >Sensitive simultaneous determination of nitrophenol isomers at poly (p-aminobenzene sulfonic acid) film modified graphite electrode
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Sensitive simultaneous determination of nitrophenol isomers at poly (p-aminobenzene sulfonic acid) film modified graphite electrode

机译:聚对氨基苯磺酸膜修饰石墨电极同时灵敏测定硝基苯酚异构体

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Poly(p-aminobenzene sulfonic acid)-modified graphite electrode [poly(p-ABSA)/GE] was prepared via a straightforward one-step electropolymerization and was employed to investigate the electrochemical behavior of o-nitrophenol (o-NP), m-nitrophenol (m-NP) and p-nitrophenol (p-NP), for the purpose of realizing the simultaneous determination of nitrophenol isomers. Semi-derivative voltammetry (SDV) was adopted to enhance the resolution and sensitivity. Compared with the bare GE, poly(p-ABSA)/GE exhibited excellent electrocatalytic activity towards the oxidation process of the intermediate products of nitrophenol isomers. Thus, o-, m- and p-NP can be clearly identified and successfully separated at 0.119V, -0.125V and 0.027V (vs. saturated calomel electrode). Under the optimized experimental conditions, the linear ranges of the calibration curves were 3 similar to 800 mu mol L-1 for o-NP, and 3 similar to 700 mu mol L-1 for both m-NP and p-NP. In addition, the low detection limits for o-, m- and p-NP were 0.28, 0.5 and 0.3 mu mol L-1, respectively (S/N = 3). The proposed method is novel and has many advantages such as simple, sensitive, selective, reproducible and cost-effective. Therefore, it can be considered a promising sensing platform for direct simultaneous determination of nitrophenol isomers in water samples. (C) 2015 Published by Elsevier Ltd.
机译:聚(对氨基苯磺酸)修饰的石墨电极[poly(p-ABSA)/ GE]是通过简单的一步电聚合制备的,并用于研究邻硝基苯酚(o-NP)的电化学行为-硝基苯酚(m-NP)和对硝基苯酚(p-NP),以实现同时测定硝基苯酚异构体的目的。采用半导数伏安法(SDV)来提高分辨率和灵敏度。与裸GE相比,聚(p-ABSA)/ GE对硝基酚异构体中间产物的氧化过程表现出优异的电催化活性。因此,o-,m-和p-NP可以清晰识别,并可以在0.119V,-0.125V和0.027V的条件下成功分离(相对于饱和甘汞电极)。在优化的实验条件下,对于o-NP,校准曲线的线性范围分别为3和800μmol L-1,对于m-NP和p-NP而言,其线性范围为3类似于700μmol L-1。另外,o-,m-和p-NP的低检测限分别为0.28、0.5和0.3μmolL-1(S / N = 3)。所提出的方法是新颖的并且具有许多优点,例如简单,灵敏,选择性,可重现和成本有效。因此,它可以被认为是直接同时测定水样品中硝基苯酚异构体的有前途的传感平台。 (C)2015由Elsevier Ltd.出版

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