Particle discrimination effects in the determination of trace metals in natural fresh waters

Instrumental neutron activation analysis (i.n.a.), atomic absorption spectrometry (a.a.s.), and inductively-coupled plasma atomic emission spectrometry (i.c.p.a.e.s.) have been applied to the determination of Na, K, Mg, Ca, Al, Mn, Fe and Zn in fresh waters containing naturally occurring particles. Scattered results were obtained for the total concentrations of trace metals which were associated to some extent with particles retainable by 0.45-μm filter membranes. Particle discrimination effects are indicated and the fraction of elements included in the final result depends on the method used. For the simultaneous determination of the total concentrations of Al, Mn, Fe and Zn, i.n.a.a. is preferred, as all element fractions present are included in the result. When a.a.s. or i.c.p.a.e.s. is applied, lower results are obtained when particulate matter is present, the results referring only to the acid-soluble low-molecular-weight fraction (< 0.45 μm diameter). When particles are removed prior to the quantifying step, the results obtained on the filtrates by all methods are in good agreement. However, considering the low concentrations of several elements in the separated fractions, i.n.a.a. is most favourable for the determination of aluminium while graphite-furnace a.a.s. is most suitable for zinc. Both methods are applicable for manganese. For Ca, Fe, K, Mg and Na, i.c.p.a.e.s. is recommended.