Survey of the occurrence of residues of methyl tertiary butyl ether (MTBE) in Dutch drinking water sources and drinking water

An indicative survey has been carried out in The Netherlands investigating the presence of methyl tertiary butyl ether (MTBE) in drinking water and the corresponding sources. In total, 71 different sites used for the preparation of drinking water in The Netherlands were sampled in two successive seasons in 2001 involving the analysis of 156 samples. (ground water (n = 88), surface water (n = 17), bank filtrate water (n = 6) and drinking water (n = 45)). To combine high sample throughput with high selectivity and sensitivity, off-line purge and trap for sampling and gas chromatography mass spectrometry equipped with an automated thermal desorption sampler (TDS-GC-MS) was selected as the preferred analytical methodology. The developed procedure enabled the analysis of at least 40 samples per day and provided a limit of quantification of 2 ng l(-1). In the first period 63 samples of raw water were analyzed. Concentrations ranged between < 10 ng l(-1) and 420 ng l(-1) with a median concentration below 10 ng l(-1). The second period was focused at the re-sampling of positive locations (MTBE > 10 ng l(-1)) and a few additional drinking water utilities of which both the raw and drinking water of the utilities were analyzed. The median concentration of MTBE in the selected set of drinking water samples was 20 ng l(-1) (n = 45). At one location MTBE was found at a level of 2900 ng l(-1) caused by point source contamination of the ground water (11 900 ng l(-1)). Special attention has been paid to the quality of the results by analyzing all samples in duplicate and the analysis of control samples during each series of analyses.     

A Strategy for Reduction of Particulate Emissions in the Boston Area

Initial implementation plans provided for particulate reduction largely through the imposition of emission limitations on industrial processes, large steam generators, and solid waste disposal, requiring, in turn, application of control equipment for compliance. In many urban areas, this approach is not adequate to achieve the secondary air quality standards so that a more general strategy must be employed. Such strategy may include restrictions on fuel burning, combustion equipment, maintenance programs, utility steam distribution, etc. The potential abatement achievable through such strategies is described using Boston as a case study. Cost and technical factors associated with each strategy are discussed.     

Complexation-flocculation of organic contaminants by the application of oxyhumolite-based humic organic matter

Control of hazardous organic micropollutants is a challenging water quality issue. Dissolved humic organic matter (DOM) isolated from oxyhumolite coal mined in Bohemia was investigated as a complexation agent to remove polycyclic aromatic hydrocarbons (PAHs) and functionalized phenols from water by a two-stage process involving complexation and flocculation. After the formation of humic-contaminant complexes, ferric salts were added resulting in the precipitation and flocculation of the DOM and the associated pollutants. Flocculation experiments with ferric ion coagulants indicated that precipitation of oxyhumolite DOM together with the complexed contaminants occurred at lower ferric ion concentrations than with the reference DOM in acidic environments (pH approximately 3.5). The complexation-flocculation removal rates for non-reactive PAHs characterized by small localization energies of pi-electrons correlated well with the complexation constants. On the other hand, the combined complexation-flocculation removal rates for activated PAHs including trans-stilbene, anthracene and 9-methyl anthracene, as well as functionalized polar phenols, were higher than predicted from the complexation coefficients. Methodological studies revealed for the first time that the ferric ion coagulant contributed to enhanced removal rates, most probably due to ferric ion-catalyzed pollutant degradation resulting in oxidized products.     

Modeling Analysis of Power Plants for Compliance Extensions in 51 Air Quality Control Regions

Past studies indicate a nationwide potential low-sulfur coal supply deficit in 1975 arising from extremely low-sulfur State Implementation Plan requirements which cannot ail be met in time by available coal and gas cleaning technology. One means to alleviate this net deficit would be to grant variances where at least primary air quality standards would be maintained.

An extensive modeling analysis was conducted by EPA and Walden Research on a large number of power plants in 51 AQCRs located in 20 states to determine if compliance extensions at these plants could significantly reduce the projected deficit of lowsulfur coal. Using simulation modeling, air quality impact at each plant for projected 1975 operations was determined with application of SIP regulatory requirements and with a full variance from SIP requirements for coal-fired boilers. The results from this investigation indicate that the attainment of primary SO2 air quality standards for the coal-fired plants would probably not be jeopardized by the application of full variance status to 34% of the plants and limited variance status to an additional 22% of the plants. No variance is appropriate for the remaining plants. The projected annual reduction In low-sulfur coal demand (less than 1.0% sulfur) is approximately 137 million tons. The projected shift in the average coal sulfur distribution is from 1.2% under SIP status to 2.1% under the applicable variance status. The power plant variance strategy appears, then, to offer a potentially feasible approach toward alleviating the low-sulfur coal deficit problem without jeopardizing attainment of primary air quality standards. It should be emphasized that compliance extensions are not the only way, or the most desirable way, of dealing with this problem. The final selection of a strategy for a given state or AQCR and the implementation of that strategy involve many questions and policy matters beyond the scope of this study.     

Hochwasser 2002

In August 2002, highly contaminated areas in the region of Bitterfeld, e.g. the floodplain of the creek Spittelwasser, as well as the adjacent regions of Jeßnitz and Raguhn, were submerged by the river Mulde. An input of mobilized contaminated sediments in residential areas was the matter of concern. The objective of the present study was to estimate the pollutants load on the basis of chemical and biological data and identify the sources of pollutants. Deposited sludge and flood water samples were assessed on the basis of biological and chemical analyses and in comparison with administrative reference values. The pollution of the investigated sites was rather heterogeneous. At several sites, tolerance limits of the German Klärschlammverordnung or the Bundesbodenschutzverordnung were clearly exceeded, e.g. for Pb, As and HCH. Organic extracts exhibited significant effects in several biotests. This may be relevant with respect to direct particle uptake via ingestion or respiration. Pollution patterns for heavy metals as well as for organic pollutants differed significantly from the pattern found in the Spittelwasser flood plain before the inundation, which is in contrast to the initial hypothesis of a possible transport of contaminated Spittelwasser sediments into residential areas. Interestingly, a correlation of chemical load and the overall biological effect could be shown. From the viewpoint of the precautionary principle, the identification of the compounds exerting toxic effects and of the respective pollutant sources would be desirable.     

Anwendung des Röntgenbildverstärkers für Feinstrukturuntersuchungen

The Science of Nature -     

Spatial and temporal variability of sediment deposition on artificial-lawn traps in a floodplain of the River Elbe

Artificial-lawn mats were used as sediment traps in floodplains to measure sediment input and composition during flood events. To estimate the natural variability, 10 traps were installed during two flood waves at three different morphological units in a meander loop of the River Elbe. The geochemical composition of deposited and suspended matter was compared. The sediment input showed weak correlations with concentration and composition of river water. It also correlated poorly with flood duration and level as well as distance of trap position from the main river. This is due to the high variability of the inundation, different morphological conditions and the variability of sources. The composition of the deposits and the suspended matter in the river water was comparable. Hence, for the investigated river reach, the expected pollution of the floodplain sediments can be derived from the pollution of the suspended matter in the river during the flood wave.     

Toxic oxide deposits from the combustion of landfill gas and biogas

Oxide deposits found in combustion systems of landfill gas fired power stations contain relatively high concentrations of elements which form volatile species such as P, As, Sb and Sn. These deposits should be handled with care because of their potential toxicity. By contrast, deposits in biogas system engines were found to contain much lower levels of such elements. The enrichment of these elements can be attributed to a hypothetical multistage process. The elements form volatile species in the landfill body. They are selectively transported as part of the landfill gas into the gas-burning devices. Inside the burners, they are immobilized as nonvolatile oxides.