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首页> 外文期刊>Bulletin of the Korean Chemical Society >Trace Mercury Determination by Differential Pulse Anodic Stripping Voltammetry Using Polythiophene-Quinoline/Glassy Carbon Modified Electrode
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Trace Mercury Determination by Differential Pulse Anodic Stripping Voltammetry Using Polythiophene-Quinoline/Glassy Carbon Modified Electrode

机译:聚噻吩-喹啉/玻璃状碳修饰电极的差分脉冲阳极溶出伏安法测定痕量汞

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A Polythiophene-quinoline/glassy carbon (PTQ/GC) modified electrode was developed for the determination of trace mercury in industrial waste water, natural water, soil, and other media. The electrode was prepared by the cyclic voltammetric polymerization of thiophene and quinoline on glassy carbon (GC) electrode by the potential application from -0.6 V to +2.0 V (50 mV/sec) in a solution of 0.1 M thiophene, quinoline and tetrabutyl ammonium perchlorate (TBAP) in acetonitrile. Optimum thickness of the polymer membrane on the GC electrode was obtained with 20 repeated potential cyclings. The redox behavior of Cu(II) and Hg(II) were almost identical on this electrode. The addition of 4-(2-pyridylazo)resorcinol (PAR) to the solution containing Cu(II) and Hg(II) allowed the separation of the components due to the formation of the Cu(II)-PAR complex reduced at -0.8V, which was different from the Hg(II) reduced at -0.5 V on a saturated calomel electrode (SCE). The calibration graph of Hg(II) shows good linear relationship with the correlation factor of 0.9995 and the concentration gradient of 0.33 mA/cm2/ppb down to 0.4 ppb Hg. The method developed was successfully applied to the determination of mercury in samples such as river, waste water, and sea water.
机译:开发了一种聚噻吩喹啉/玻碳(PTQ / GC)修饰电极,用于测定工业废水,天然水,土壤和其他介质中的痕量汞。通过在0.1 M噻吩,喹啉和四丁基铵的溶液中从-0.6 V到+2.0 V(50 mV / sec)施加电压,通过噻吩和喹啉在玻璃碳(GC)电极上的循环伏安聚合制备电极乙腈中的高氯酸盐(TBAP)。通过20次重复的电势循环,可以获得GC电极上聚合物膜的最佳厚度。 Cu(II)和Hg(II)在该电极上的氧化还原行为几乎相同。在含Cu(II)和Hg(II)的溶液中添加4-(2-吡啶基偶氮)间苯二酚(PAR)可以分离组分,因为形成的Cu(II)-PAR配合物在-0.8时减少V与在饱和甘汞电极(SCE)上在-0.5 V下还原的Hg(II)不同。 Hg(II)的校正曲线与相关因子为0.9995,浓度梯度为0.33 mA / cm2 / ppb,降至0.4 ppb Hg时,显示出良好的线性关系。所开发的方法已成功应用于河流,废水和海水等样品中汞的测定。

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