Electrocatalytic behaviour of carbon paste electrode modified with iron(II) phthalocyanine (FePc) nanoparticles towards the detection of amitrole

Talanta. 2006 Jul 15;69(5):1136-42. doi: 10.1016/j.talanta.2005.12.014. Epub 2006 Jan 10.

Abstract

This paper describes the construction of a carbon paste electrode (CPE) impregnated with nanoparticles of iron(II) phthalocyanine (nanoFePc). The new electrode (nanoFePc-CPE) revealed interesting electrocatalytic behaviour towards amitrole; pure catalytic diffusion-controlled process, with high Tafel slope (235 mV/decade) suggesting strong binding of amitrole with nanoFePc catalyst. The effects of catalyst loading, varying pH and electrolytes were studied. The mechanism for the interaction of amitrole with the nanoFePc is proposed to involve the Fe((III))Pc/Fe((II))Pc redox process. Using chronoamperometry (E=+0.42V versus Ag/AgCl) technique, the sensor was reliably employed for amitrole assay at pH 12.0 phosphate buffer (with sodium sulphate as the supporting electrolyte) for up to 12 nM amitrole with excellent sensitivity (ca. 3.44 microA/nM) and low detection limit (3.62+/-0.11 nM, i.e. 0.305 microgL(-1) using the Y(B)+3(sigmaB) criterion and 0.85+/-0.03 nM, i.e. 70 ng/L with the Y(B)+2(sigmaB) criterion) as well as satisfactory amperometric selectivity coefficient (K(amp) approximately equal to 7.4 x 10(-4) for ammonium thiocyanate, a component of many amitrole herbicides, and 3.2 x 10(-3) for asulam pesticide). The surface of the electrode can easily be regenerated by simple polishing on an alumina paper, obtaining a fresh surface ready for use in a new assay. The proposed electrode was successfully applied in the quantification of amitrole in its commercial formulation as well as in tap water samples.