Targeting arsenic-safe aquifers for drinking water supplies

At present, 70 countries worldwide are affected by groundwater contamination by arsenic (As) released from predominantly geogenic sources. Consequently, the As problem is becoming a global issue. The option to target As-safe aquifers, which uses geological, geochemical, hydrogeological, morphological and climatic similarities to delimit As-safe aquifers, appears as a sustainable mitigation option. Two pilot areas, Meghna Flood Plain in Matlab Upazila, representative of Bengal Delta in Bangladesh, and Río Dulce Alluvial Cone, representing a typical aquifer setting in the Chaco-Pampean Plain in Argentina groundwater As occurrence, were compared. In rural Bangladesh, As removal techniques have been provided to the population, but with low social acceptance. In contrast, “targeting As-safe aquifers” was socially accepted in Bangladesh, where sediment color could be used to identify As-safe aquifer zones and to install safe wells. The investigation in Argentina is more complex because of very different conditions and sources of As. Targeting As-safe aquifers could be a sustainable option for many rural areas and isolated peri-urban areas.     

Comprehensive study of endocrine disrupting compounds using grab and passive sampling at selected wastewater treatment plants in South East Queensland, Australia

Chemical (gas chromatography-mass spectrometry, GC-MS) and biological (E-Screen assay) analyses were used to determine the concentrations of 15 endocrine disrupting compounds (EDCs) and estrogen equivalent (EEq) in grab and passive samples from five municipal wastewater treatment plants (WWTPs) in South East Queensland, Australia. EEq concentrations derived by E-Screen assays for the grab samples were between 108-356 ng/L for the influents and < 1-14.8 ng/L for the effluents with the exception of one effluent sample which was at 67.8 ng/L EEq. The EDC concentrations and EEq values for the passive samples were several times lower than those of the grab samples: a decrease probably caused by, but not limited to biofouling, low flow rate, biodegradation and temperature which can progressively reduce the uptake of compounds into the sampler. At this stage, grab sampling is the most reliable method for field monitoring; nevertheless, passive sampler is a useful sampling tool but the method requires more research to ensure that the information obtained can be interpreted appropriately. Although alkylphenols and phthalates were detected at higher concentrations in the wastewater samples as compared to natural hormones, the environmental risk may be negligible as their estrogenic potencies are several orders of magnitude lower than that of the natural estrogens. In most wastewater samples, the natural estrogens contributed to 60% or more of the EEq value. Removal efficacy of most estrogenic and xenoestrogenic compounds from the conventional activated sludge or biological nutrient removal (BNR) WWTPs monitored in this study was in the range of 80-> 99%. The efficiency of the WWTPs in removing estrogenic activity was > 95%. The EEqs of the E-Screen and those calculated from the results of extensive chemical analyses using the estradiol equivalency factors were comparable for most of the WWTPs samples.     

Mercury removal from incineration flue gas by organic and inorganic adsorbents

Experiments were performed to investigate various adsorbents for their mercury removal capabilities from incineration flue gases. Four different materials were tested; Zeolite, Bentonite, activated carbon (AC), and wood char. Real incineration off-gas and in-lab simulated combustion flue gases (N2 + Hg) were used. Three cylindrical-shaped sorbent columns with 5 cm in diameter and 20 cm in length were used. The gas flow rate was fixed at 660 l/h at all times. Concentrations of NO, CO, O2, CO2, SO2, H2O, HCl, and mercury were continuously monitored. Mercury removal efficiencies of natural Zeolite and Bentonite were found to be much lower than those of the referenced AC. Amount of Hg removed were 9.2 and 7.4 microg/g of Zeolite and Bentonite, respectively. Removal efficiencies of each layer consisted of inorganic adsorbents were no higher than 7%. No significant improvement was observed with sulfur impregnation onto the inorganic adsorbents. Organic adsorbents (wood char and AC) showed much higher mercury removal efficiencies than those of inorganic ones (Zeolite and Bentonite). Mercury removal efficiency of wood char reached over 95% in the first layer, showing almost same effectiveness as AC which currently may be the most effective adsorbents for mercury. Amount of mercury captured by wood char was approximately 0.6 mg/g of wood char, close to the amount captured by AC tested in this study. Hence, wood char, made from the waste woods through a gasification process, should be considered as a possible alternative to relatively expensive AC.     

Mobilität von Nitroaromaten im Sandstein infolge Schwefelsäureeintrag zur Uranlaugung

As a result of former in situ leaching activities with sulfphuric acid, nitroaromatic compounds have invaded into cenomanian and turonian sandstone aquifers and mining waters in parts of the uranium mining of Königstein, Germany (Saxony). In the mining area contamination levels of nitrobenzene, mononitrotoluene and dinitrotoluene lead to a partial excess in the drining water guide values. For environmental protection, control and remediation efforts by flooding, more knowledge about contaminant mobility in sandstone, and in intercalated clays and silts, is demanded. A selected experimental area has been flooded to realize and study transport processes under real mining conditions. In this work, we have examined the mobilization of nitroaromatic compounds by flooding waters. The interactions between the nitroaromatic compounds, which are dissolved in the mining water, and the host rocks are discussed. The existing data for strata of varying lithologic conditions suggest that the sorption processes of the compounds investigated are negligible in pure sandstone aquifer layers and significant in the lithologic conditions with a complex mixture of mudstone, siltstone and clay. Several lithologic conditions are demonstrated in contaminant sinks and sources caused by adsorption processes and mobilization of newly connected stagnant pore waters.     

The Kyoto Protocol and non-CO2 Greenhouse Gases and Carbon Sinks

Many trace constituents other than carbon dioxide affect the radiative budget of the atmosphere. The existing international agreement to limit greenhouse gases, the Kyoto Protocol, includes carbon dioxide (CO₂), methane (CH₄), nitrous oxide (N₂O), hydrofluorocarbons (HFCs), perfluorocarbons (PFCs), sulfur hexafluoride (SF₆) and credit for some carbon sinks. We investigate technological options for reducing emissions of these gases and the economic implications of including other greenhouse gases and sinks in the climate change control policy. We conduct an integreated assessment of costs using the MIT Emissions Prediction and Policy Analysis (EPPA) model combined with estimates of abatement costs for non-CO₂ greenhouse gases and sinks. We find that failure to take advantage of the other gas and sink flexibility would nearly double aggregate Annex B costs. Including all the GHGs and sinks is actually cheaper than if only CO₂ had been included in the Protocol and their inclusion achieves greater overall abatement. There remains considerable uncertainty in these estimates, the magnitude of the savings depends heavily on reference projections of emissions, for example, but these uncertainties do not change the overall conclusion that non-CO₂ GHGs are an important part of a climate control policy.