Volume 21, Issue 6 pp. 687-692
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Anodic Stripping Voltammetric Determination of Lead (II) Using Glassy Carbon Electrode Modified with Novel Calix[4]arene

Lüu Jian-Quan

Lüu Jian-Quan

State Key Laboratory of Elemento-Organic Chemistry, Department of Chemistry, Nankai University, Tianjin 300071, China

Department of Chemistry, Hubei Normal University, Huangshi, Hubei 435002, China

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He Xi-Wen

He Xi-Wen

State Key Laboratory of Elemento-Organic Chemistry, Department of Chemistry, Nankai University, Tianjin 300071, China

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Zeng Xian-Shun

Zeng Xian-Shun

State Key Laboratory of Elemento-Organic Chemistry, Department of Chemistry, Nankai University, Tianjin 300071, China

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Zhang Hai-Li

Zhang Hai-Li

State Key Laboratory of Elemento-Organic Chemistry, Department of Chemistry, Nankai University, Tianjin 300071, China

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Zhang Zheng-Zhi

Zhang Zheng-Zhi

State Key Laboratory of Elemento-Organic Chemistry, Department of Chemistry, Nankai University, Tianjin 300071, China

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First published: 26 August 2010
Citations: 6

Abstract

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 voltammetry. 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 − 0.6 V, of which the peak current is proportional to the concentration of Pb2+. The modified electrode in 0.1 mol/L HNO3 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 Hg2+, Ag+ and Cu2+ ions, which can be eliminated by the addition of KSCN. The proposed method was successfully applied to determine lead in aqueous samples.

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