Voltammetric Behavior of Lead(lI) at N-p-Chlorophenylcinhamohydroxamic Acid Modified Carbon Paste Electrode

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Date

1999-06

Authors

Hailu Tesfaye

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Publisher

Addis Ababa Universty

Abstract

A sensitive and selective method for the determination of lead(ll) with N-pchlorophenylcinnamohydroxamic acid modified carbon paste electrode has been developed. The iead(ll) is accumulated on the electrode surface by the formation of the complex in an open-circuit/ and the resulting surface is characterized by medium exchange, potential reduction, and differential pulse anodic stripping voltammetry. The electrochemical response was evaluated with respect to carbon paste composition,pH and concentration of accumulating and stripping solutions, preconcentration time, lead(ll) concentration, and other variables. Two linear ranges were obtained in the concentration ranges 1.00 x 10-6 - 2.40 x 10'5MPb(ll) with 2 min preconcentration time and 2.00 x 10-8 - 1.00 x 10’6MPb(ll) with 6 min preconcentration time. The detection limit was found to be 1.00 x 10 s M with 6 min preconcentration time. For six preconcentration/medium exchange/voltammetric determination/renewal cycles, the differential pulse voltammetric response was reproduced with 5.3% and 4.9% relative standard deviations at 4.00 x 10*6Mand 8.00 x 104MPb(ll), respectively. Rapid and convenient renewal allows the use of a single modified electrode surface in multiple analytical determinations over several weeks. Many coexisting metal ions had little or no effect on the determination of lead(ll). The developed method was applied to lead determination in potable water

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N-p-Chlorophenylcinhamohydroxamic Acid

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