Electrochemical detection of nitrate and nitrite at a copper modified electrode

The development of a reagentless electrode system for the determination of nitrate is presented. The approach is based upon the deposition of a macrop orous copper deposit which shows marked selectivity for nitrate ion under m ildly acidic conditions (pH 3) with a linear range extending from 10 to 200 mu M nitrate. Fabrication of the layer is both inexpensive and simple and is relatively substrate independent (Cu, Au, glassy carbon) as the response is attributed to the electrodeposited support. The influence of potential interferents such as chloride, nitrite and complexing agents such as citric acid were examined. In particular, the reduction of nitrite was found to o ccur at potentials significantly less negative than those required for nitr ate reduction and as a result clear resolution of both voltammetric peaks i s obtainable. The lack of direct interference between the two ions combined with wide peak separation (200 mV) provides a system that may offer some p otential in speciation studies. The analytical applicability of the propose d system was demonstrated through the standard addition determination of ni trate in a number of authentic samples with the nitrate concentrations inde pendently corroborated using established Griess assay spectroscopic protoco ls.