Polarographic behavior and analysis of Flumetralin in formulations and environmental samples


ABSTRACT:

A differential pulse polarographic (DPP) method for the determination of Flumetralin is described based on the reduction of a nitro group at a dropping mercury electrode (DME) in Briton-Robinson buffers of pH 2.0 to 12.0 using 25% acetone-water mixture as a solvent. Also a cyclic voltammetric (CV) technique has been used to study the behaviour of Flumetralin at a hanging mercury drop electrode (HMDE). The DPP method described here has been applied to the analysis of Flumetralin in formulations, grains, soils and spiked water samples. Both standard addtion and calibration methods were used for the analytical measurements. The lower detection limit was found to be 1.87x10-8 M.

Introduction:

Pesticides containing nitro substituents are extensively used in agriculture throughout the world. Flumetralin is one of the dinitroaniline pesticide families and is an economically important class of agricultural compound used to prevent the growth of grasses and weeds in cultivated crops. The volatility persistence of Flumetralin, together with the variability under environmental conditions among different areas, results in a residual amount of herbicide in soil that can be phytotoxic to sensitive corps, in soil plants  and in air. There are several methods available for the determination of Flumetralin; mostly chromatographic methods are reported to be used for the determination of the dinitroaniline herbicide in various matrices. This includes HPLC, GC with mass selective detection and with electron capture detection and LC with fluorescence detection.

Further details @ http://www.jocpr.com/


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