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Differential Pulse Anodic Stripping Voltammetric Determination of Lead with Heparin Modified Electrode
作者姓名:李念兵  段建平  陈国南
作者单位:Department of Chemistry,Fuzhou University,Fuzhou,Fujian 350002,China,College of Chemistry and Chemical Engineering,Southwest China Normal University,Chongqing 400715,China,Analytical and Testing Center,Fuzhou University,Fuzhou,Fujian 350002,China,Department of Chemistry,Fuzhou University,Fuzhou,Fujian 350002,China
基金项目:Project supported by the National Natural Science Foundation of China (No. 20377007).
摘    要:Introduction Overall exposure to lead is of public health concern because of several hazardous effects that may occur to human beings. Lead poisoning may provoke irritability, anorexia, malaise and headache. Intoxication progress may lead to attacks of abdominal pain until coma and death.1 The determination of trace lead in variety of en-vironmental samples is of great importance since lead is recognized as a cumulative poison to animals and hu-mans. There is a constant demand for improved an…

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Differential Pulse Anodic Stripping Voltammetric Determination of Lead with Heparin Modified Electrode
LI,Nian-Binga,b DUAN,Jian-Pingc.Differential Pulse Anodic Stripping Voltammetric Determination of Lead with Heparin Modified Electrode[J].Chinese Journal of Chemistry,2004,22(6):553-557.
Authors:LI  Nian-Binga  b DUAN  Jian-Pingc
Abstract:A novel differential pulse anodic stripping voltammetry for the determination of trace amounts of lead, using a biomacromolecule heparin drop‐coated modified glassy carbon electrode, has been described. Pb2‐ was deposited on the surface of a heparin‐modified electrode at ‐1.0 V (vs. SCE) via forming Pb2‐heparin and subsequent reduction at the electrode. In the following step, Pb‐heparin was oxidized, and voltammograms were recorded by scanning the potential in a positive direction. Conditions were optimized with respect to the pH of the medium, the mass of drop‐coated heparin, accumulation potential and accumulation time. The peak current was proportional to the Pb2‐ concentration in the range of 2.0X 10?9 to 7.0X 10?7 mol/L. The detection limit was 3.0X 10?10 mol/L. The relative standard deviation was 4.83% for 1.0X 10?8 mol/L Pb2‐ (n = 10). The developed method has been applied to the determination of Pb2‐ in water samples with satisfactory results.
Keywords:heparin  chemically modified electrode  lead  differential pulse anodic stripping
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