Abstract
Size fractionation techniques used in speciation studies of trace metals in natural waters have been reviewed. Centrifugation, filtration, ultrafiltration (UF), dialysis and gel filtration chromatography (GFC) have been considered with respect to trace metal contamination, adsorption effects and size selectivity. Size differentiation during centrifugation is impeded due to density effects on particle settling rates. Filtration is the most commonly used method to fractionate trace metal species, but often only “issolved” and “particulate” fractions are identified. Filters may be decontaminated with dilute nitric acid and adsorption effects may be minimised by preconditioning with a dilute calcium nitrate solution. Several studies concerning the size selectivity of filters indicate that at present only Nuclepore polycarbonate filters are suitable for size spectrum investigations. Those difficulties outlined above are also experienced with UF methods but generally have not been so well resolved. particularly with respect to adsorption. Adsorption during UF causes an overestimation of the molecular size of metal complexes. Dialysis techniques have been utilized with some success in order to isolate trace metal species in true solution but have seen only limited applications in comprehensive speciation schemes. GFC offers considerable potential in physicochemical speciation studies. The major advantage lies with the ability to determine metal concentrations over a continuous size spectrum rather than at discrete size ranges. In contrast to other methods, adsorption during GFC will cause the molecular weight of organometallic complexes to be underestimated. Several examples of the environmental application of each technique have been considered, thereby illustrating the value of examining the size distribution of metal species in natural waters.