Utilization of activating and masking effects by ligands for highly selective catalytic spectrophotometric determination of copper and iron in natural waters.

A kinetic-catalytic spectrophotometric method is proposed for the successive determination of nanogram levels of copper and iron, which is based on their catalytic effects on the oxidative coupling of p-anisidine with N,N-dimethylaniline (DMA) to form a colored compound (lambda(max)=740 nm) in the presence of hydrogen peroxide at pH 3.2. 2,9-Dimethyl-1,10-phenanthroline (neocuproine) acted as an activator for the copper catalysis, and 1,10-phenanthroline (phen) acted as an activator for the iron catalysis. The selectivity was improved in the presence of diphosphate as a masking agent. The determinable ranges were 0.16-10 ppb for copper and 1-100 ppb for iron, respectively. The relative standard deviations of copper and iron were 1.1 and 0.97% for five determinations of 10 ppb copper and 40 ppb iron. The method was successfully applied to the analyses of copper and iron in tap, well, river and pond waters.