A method for the voltammetric determination of nitrate in drinking wat
er is presented. Nitrate exerts a catalytic effect on the reduction an
d reoxidation of thallium (1 <-- --> 0) in cyclic and differential pul
se voltammetry leading to a peak enhancement. Nitrate can be preconcen
trated together with tetrachlorothallate(III) from hydrochloric acid s
olutions onto a carbon paste electrode modified with a liquid anion ex
changer (Amberlite LA2) under open circuit conditions. After reduction
of the TI(III) to Tl(0) at the electrode surface at a potential of -1
.2 V (vs. SCE), the increase of the reoxidation current of Tl(0) to Tl
(I) by nitrate is exploited for analytical purposes. Linearity between
current and concentration exists for 0.5 to 60 mug . mL-1 nitrate whe
n applying anodic differential pulse voltammetry. Mechanical regenerat
ion of the electrode surface is necessary after each measurement. The
interference of other anions and the influence of methodical parameter
s are investigated. The applicability of this method for the determina
tion of nitrate in drinking water is demonstrated. A concise overview
on the electroanalytical techniques for the quantitative determination
of nitrate is also presented.