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Anodic Stripping Voltammetric Determination of Lead(II) Using Glassy Carbon Electrode Modified with Novel Calix[4]arene

机译:新型杯[4]芳烃修饰的玻碳电极阳极溶出伏安法测定铅(II)

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摘要

A new glassy carbon electrode modified with novel calix[4]arene derivative was prepared and then applied to the selective recognition of lead ion in aqueous media by cyclic and square wave voltammtry. A new anodic stripping peak at - 0.92 V (vs. Ag/Ag~+) in square wave voltammogram can be obtained by scanning the potential from -1.5 to -1.6 V, of which the peak current is proportional to the concentration of Pb~(2+). The modified electrode in 0.1 mol/L HNO_3 solution showed a linear voltammetric response in the range of 2.0 * 10~(-8)-1.0 * 10~(-6) mol/L and a detection limit of 6.1 * 10~(-9) mol/L. In the modified glassy carbon electrode no significant interference occurred from alkali, alkaline and transition metal ions except Hg~(2+), Ag~(2+) and Cu~(2+) ions, which can be eliminated by the addition of KSCN. The proposed method was successfully applied to determine lead in aqueous samples.
机译:制备了一种用新型杯[4]亚芳基衍生物修饰的玻璃碳电极,然后通过循环和方波伏安法将其用于水介质中铅离子的选择性识别。通过在-1.5至-1.6 V范围内扫描电势,可以获得方波伏安图中-0.92 V(vs. Ag / Ag〜+)的新阳极剥离峰,其中峰值电流与Pb〜的浓度成正比。 (2+)。修饰电极在0.1 mol / L HNO_3溶液中的线性伏安响应范围为2.0 * 10〜(-8)-1.0 * 10〜(-6)mol / L,检出限为6.1 * 10〜(- 9)摩尔/升在改性玻璃碳电极中,除Hg〜(2 +),Ag〜(2+)和Cu〜(2+)离子外,碱金属,碱金属和过渡金属离子均无明显干扰,可通过添加KSCN消除。 。所提出的方法已成功地用于测定水性样品中的铅。

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