Membrane filtration studies of aquatic humic substances and their metal species: a concise overview Part 1. Analytical fractionation by means of sequential-stage ultrafiltration.

A concise overview (75 references) of the analytical fractionation of aquatic humic substances using sequential-stage ultrafiltration is presented. First, humic substances in aquatic environments and actual problems connected with their fractionation and analysis are briefly considered. The molecular size classification of dissolved humic substances by means of multistage ultrafiltration, with special emphasis on on-line techniques, is the focal point of the discussion.

Bioaccumulation of platinum group elements and characterization of their species in Lolium multiflorum by size-exclusion chromatography coupled with ICP-MS.

The bioaccumulation of Pt, Pd and Rh by grass grown hydroponically with nutrient solutions containing these ions at elevated (38.7 mg l(-1) Pt, 21.7 mg l(-1) Pd and 7.

Determination of Cr(VI) in ambient airborne particulate matter by a species-preserving scrubber-sampling technique.

Airborne particulate matter has been sampled at a location close to a metallurgical plant in North-Rhine-Westphalia, Germany, and first results on the chromium(VI) content in the collected dust are presented. A special procedure using a scrubber as sampling device was used to preserve Cr(VI) during the sampling procedure. The scrubber solution which consisted of 0.

Application of femtosecond laser ablation time-of-flight mass spectrometry to in-depth multilayer analysis.

A femtosecond laser system was used in combination with a time-of-flight mass spectrometer (TOF-MS) for in-depth profiling of semiconductor and metal samples. The semiconductor sample was a Co-implanted (10(17) ions/cm3) silicon wafer that had been carefully characterized by other established techniques. The total depth of the shallow implanted layer was 150 nm.

Analytical fractionation of aquatic humic substances and their metal species by means of multistage ultrafiltration.

The molecular-size fractionation of aquatic humic substances (HS) and their metal species by means of a novel sequential-stage ultrafiltration (UF) device equipped with five appropriate ultramembranes (1, 5, 10, 50 and 100 kD) is described. First of all, the concentration dynamics of macromolecules, particulary HS, during five-stage UF and its subsequent washing step has been modelled. Based on these results, the fractionation of aquatic HS (from ground and bog water) by means of multistage UF has been optimized for an analytical scale (10 ml sample, 1 mg/ml HS, 10 ml washing solution, pH 6.