Influence of platinum, palladium and rhodium as compared with cadmium, nickel and chromium on cell viability and oxidative stress in human bronchial epithelial cells

The platinum group elements (PGE) Pt, Pd and Rh are increasingly emitted into the environment by automobile catalytic converters. Whereas the biological availability of PGE to plants and animals has been demonstrated, only few studies concentrate on the influence of PGE on a cellular level. The effects of Pt, Pd and Rh compared with Cd, Ni and Cr on cell viability and oxidative stress response using soluble metal salts were studied in the human bronchial epithelial cell line BEAS-2B. Whilst Rh(III) showed little influence, both Pt(II) and Pt(IV) as well as Pd(II) had significant effects on cell viability at levels comparable to Cd(II) and Cr(VI). Arranging metal species in order of increasing toxicity as determined by LC50 yields: Rh(III)=1.2 mmol/L相似文献   

Hydraulic characterisation of the Stuttgart formation at the pilot test site for CO2 storage, Ketzin, Germany

The paper presents an approach for the interpretation of hydraulic tests of a CO₂ storage reservoir. The sandstone reservoir is characterised by a fluviatile channel structure embedded in a low-permeability matrix. Pumping tests were carried out in three wells, with simultaneous pressure monitoring in each well.The hydraulic parameters (permeability and storativity) and the boundary configurations were calibrated using three different approaches: (i) parameter calibration and type curve interpretation for single-hole tests, (ii) calibration of the entire build-up phase for cross-hole tests, and (iii) calibration of the initial pressure response for cross-hole pumping tests. In addition, the arrival time of the pressure response was determined and provides additional information about the pathways of hydraulic connection.The measured pumping test permeabilities of the formation were much lower than those measured on the cores, which is very unusual. The pumping test permeabilities are mainly between 50 mD and 100 mD (millidarcy), while core samples show a mean aquifer permeability of 500–1100 mD. Based on this it was concluded that some kind of continuous low-permeability structure exists, which was supported by core material. Three possible aquifer configurations were considered. The first and second were derived from traditional pumping test analysis and were conceptualised using flow boundaries. Each of the analyses provides a different result. A method was developed in which these differences were resolved by interpreting the pressure response with respect to its spatial and temporal sensitivity. This solution lead to a third configuration which was mainly based on spatially-variable permeabilities. Taking into account the pumping test results, the geological background and the behaviour of injected CO₂, we consider only the third configuration to be realistic. The results are in good agreement with modelled CO₂ arrival times and pressure history.     

Impact of humic substances on the aqueous solubility, uptake and bioaccumulation of platinum, palladium and rhodium in exposure studies with Dreissena polymorpha

Zebra mussels (Dreissena polymorpha) were exposed to different types of water containing PGE salts (PtCl4, PdSO4, RhCl3) to investigate the influence of humic substances on the aqueous solubility, uptake and bioaccumulation of noble metals. The results showed a time dependent decrease of the aqueous PGE concentrations in tank water for all groups. This could mainly be related to non-biological processes. The aqueous solubility of Pd and Rh was higher in humic water compared with non-chlorinated tap water, whereas Pt showed opposing results. Highest metal uptake rates and highest bioaccumulation plateaus were found for Pd, followed by Pt and Rh. Pd uptake and bioaccumulation was significantly hampered by humic substances, whose presence appear to increase Pt uptake and bioaccumulation. No clear trend emerged for Rh. Differences in effects of humic matter among the PGE may be explained by formation of metal complexes with different fractions of humic substances.     

Experimental and statistical determination of indicator parameters for the evaluation of fly ash and boiler ash PCDD/PCDF concentration from municipal solid waste incinerators

On-line detectable indicator parameters in the flue gas of municipal solid waste incinerators (MSWI) such as chlorinated benzenes (PCBz) are well known surrogate compounds for gas-phase PCDD/PCDF concentration. In the here presented work derivation of indicators is broadened to the detection of fly and boiler ash fractions with increased PCDD/PCDF content. Subsequently these fractions could be subject to further treatment such as recirculation in the combustion chamber to destroy their PCDD/PCDF and other organic pollutants' content. Aim of this work was to detect suitable on-line detectable indicator parameters in the gas phase, which are well correlated to PCDD/PCDF concentration in the solid residues. For this, solid residues and gas-phase samples were taken at three MSWI plants in Bavaria. Analysis of the ash content from different plants yielded a broad variation range of PCDD/PCDF concentrations especially after disturbed combustion conditions. Even during normal operation conditions significantly increased PCDD/PCDF concentrations may occur after unanticipated disturbances. Statistical evaluation of gas phase and ash measurements was carried out by means of principal component analysis, uni- and multivariate correlation analysis. Surprisingly, well known indicators for gas-phase PCDD/PCDF concentration such as polychlorinated benzenes and phenols proved to be insufficiently correlated to PCDD/PCDF content of the solid residues. Moreover, no single parameter alone was found appropriate to describe the PCDD/PCDF content of fly and boiler ashes. On the other hand, multivariate fitting of three or four parameters yielded convenient correlation coefficients of at least r=0.8 for every investigated case. Thereby, comprehension of plant operation parameters such as temperatures and air flow alongside concentrations of inorganic compounds in the gas phase (HCl, CO, SO2, NOx) gave the best results. However, the suitable set of parameters suited best for estimation of PCDD/PCDF concentration in solid residues has to be derived anew for each individual plant and type of ash.