A. Guiberteau et al., Study and determination of the pesticide Imidacloprid by square wave adsorptive stripping voltammetry, TALANTA, 53(5), 2001, pp. 943-949
An electroanalytical method has been developed for the detection and determ
ination of the pesticide 1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2
ylidineamine (Imidacloprid) by square wave adsorptive stripping voltammetry
on a hanging mercury drop electrode (HMDE) in aqueous solution with Britto
n Robinson buffer as supporting electrolyte. The best adsorption conditions
were found to be pH 7.2, an accumulation potential of - 1050 mV (HMDE vs.
Ag/AgCl-KCl 3M) and an accumulation time of 50 s. Effects of square wave fr
equency, step potential and pulse amplitude were examined for the optimizat
ion of instrumental conditions. Calibration curve is linear in the range 2
x 10(-8)-5 x 10(-7) M with a detection limit of 1.6 x 10(-8) M (Clayton et
al. method). The method is applied to the direct determination of the pesti
cide in river water samples. For a concentration of 4.1 x 10(-8) M a recove
ry value of 104 +/- 3% is obtained. In order to determine lon er concentrat
ions, previous preconcentration and cleaning steps (liquid-liquid extractio
n into CH2Cl2 and solid-phase extraction with Sep-Pak C-18 cartridges) are
carried out. The recovery values obtained in spiked river water are 89 +/-
4%, for 2 x 10(-8) M and 90 +/- 6% for 8 x 10(-9) M. (C) 2001 Elsevier Scie
nce B.V. All rights reserved.