25 research outputs found

    Developments since 2005 in understanding potential environmental impacts of CO2 leakage from geological storage

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    This paper reviews research into the potential environmental impacts of leakage from geological storage of CO2 since the publication of the IPCC Special Report on Carbon Dioxide Capture and Storage in 2005. Possible impacts are considered on onshore (including drinking water aquifers) and offshore ecosystems. The review does not consider direct impacts on man or other land animals from elevated atmospheric CO2 levels. Improvements in our understanding of the potential impacts have come directly from CO2 storage research but have also benefitted from studies of ocean acidification and other impacts on aquifers and onshore near surface ecosystems. Research has included observations at natural CO2 sites, laboratory and field experiments and modelling. Studies to date suggest that the impacts from many lower level fault- or well-related leakage scenarios are likely to be limited spatially and temporarily and recovery may be rapid. The effects are often ameliorated by mixing and dispersion of the leakage and by buffering and other reactions; potentially harmful elements have rarely breached drinking water guidelines. Larger releases, with potentially higher impact, would be possible from open wells or major pipeline leaks but these are of lower probability and should be easier and quicker to detect and remediate

    Geochemical detection of carbon dioxide in dilute aquifers

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    <p>Abstract</p> <p>Background</p> <p>Carbon storage in deep saline reservoirs has the potential to lower the amount of CO<sub>2 </sub>emitted to the atmosphere and to mitigate global warming. Leakage back to the atmosphere through abandoned wells and along faults would reduce the efficiency of carbon storage, possibly leading to health and ecological hazards at the ground surface, and possibly impacting water quality of near-surface dilute aquifers. We use static equilibrium and reactive transport simulations to test the hypothesis that perturbations in water chemistry associated with a CO<sub>2 </sub>gas leak into dilute groundwater are important measures for the potential release of CO<sub>2 </sub>to the atmosphere. Simulation parameters are constrained by groundwater chemistry, flow, and lithology from the High Plains aquifer. The High Plains aquifer is used to represent a typical sedimentary aquifer overlying a deep CO<sub>2 </sub>storage reservoir. Specifically, we address the relationships between CO<sub>2 </sub>flux, groundwater flow, detection time and distance. The CO<sub>2 </sub>flux ranges from 10<sup>3 </sup>to 2 × 10<sup>6 </sup>t/yr (0.63 to 1250 t/m<sup>2</sup>/yr) to assess chemical perturbations resulting from relatively small leaks that may compromise long-term storage, water quality, and surface ecology, and larger leaks characteristic of short-term well failure.</p> <p>Results</p> <p>For the scenarios we studied, our simulations show pH and carbonate chemistry are good indicators for leakage of stored CO<sub>2 </sub>into an overlying aquifer because elevated CO<sub>2 </sub>yields a more acid pH than the ambient groundwater. CO<sub>2 </sub>leakage into a dilute groundwater creates a slightly acid plume that can be detected at some distance from the leak source due to groundwater flow and CO<sub>2 </sub>buoyancy. pH breakthrough curves demonstrate that CO<sub>2 </sub>leaks can be easily detected for CO<sub>2 </sub>flux ≥ 10<sup>4 </sup>t/yr within a 15-month time period at a monitoring well screened within a permeable layer 500 m downstream from the vertical gas trace. At lower flux rates, the CO<sub>2 </sub>dissolves in the aqueous phase in the lower most permeable unit and does not reach the monitoring well. Sustained pumping in a developed aquifer mixes the CO<sub>2</sub>-affected water with the ambient water and enhances pH signal for small leaks (10<sup>3 </sup>t/yr) and reduces pH signal for larger leaks (≥ 10<sup>4</sup>t/yr).</p> <p>Conclusion</p> <p>The ability to detect CO<sub>2 </sub>leakage from a storage reservoir to overlying dilute groundwater is dependent on CO<sub>2 </sub>solubility, leak flux, CO<sub>2 </sub>buoyancy, and groundwater flow. Our simulations show that the most likely places to detect CO<sub>2 </sub>are at the base of the confining layer near the water table where CO<sub>2 </sub>gas accumulates and is transported laterally in all directions, and downstream of the vertical gas trace where groundwater flow is great enough to transport dissolved CO<sub>2 </sub>laterally. Our simulations show that CO<sub>2 </sub>may not rise high enough in the aquifer to be detected because aqueous solubility and lateral groundwater transport within the lower aquifer unit exceeds gas pressure build-up and buoyancy needed to drive the CO<sub>2 </sub>gas upwards.</p

    Soil gas radon assessment and development of a radon risk map in Bolsena, Central Italy

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    Vulsini Volcanic district in Northern Latium (Central Italy) is characterized by high natural radiation background resulting from the high concentrations of uranium, thorium and potassium in the volcanic products. In order to estimate the radon radiation risk, a series of soil gas radon measurements were carried out in Bolsena, the principal urban settlement in this area NE of Rome. Soil gas radon concentration ranges between 7 and 176 kBq/m(3) indicating a large degree of variability in the NORM content and behavior of the parent soil material related in particular to the occurrence of two different lithologies. Soil gas radon mapping confirmed the existence of two different areas: one along the shoreline of the Bolsena lake, characterized by low soil radon level, due to a prevailing alluvial lithology; another close to the Bolsena village with high soil radon level due to the presence of the high radioactive volcanic rocks of the Vulsini volcanic district. Radon risk assessment, based on soil gas radon and permeability data, results in a map where the alluvial area is characterized by a probability to be an area with high Radon Index lower than 20 %, while probabilities higher than 30 % and also above 50 % are found close to the Bolsena village

    Metal release from contaminated estuarine sediment under pH changes in the marine environment

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    The contaminant release from estuarine sediment due to pH changes was investigated using a modified CEN/TS 14429 pH-dependence leaching test. The test is performed in the range of pH values of 0-14 using deionised water and seawater as leaching solutions. The experimental conditions mimic different circumstances of the marine environment due to the global acidification, carbon dioxide (CO2) leakages from carbon capture and sequestration technologies, and accidental chemical spills in seawater. Leaching test results using seawater as leaching solution show a better neutralisation capacity giving slightly lower metal leaching concentrations than when using deionised water. The contaminated sediment shows a low base-neutralisation capacity (BNCpH 12 = -0.44 eq/kg for deionised water and BNCpH 12 = -1.38 eq/kg for seawater) but a high acid-neutralisation capacity when using deionised water (ANCpH 4 = 3.58 eq/ kg) and seawater (ANCpH 4 = 3.97 eq/kg). Experimental results are modelled with the Visual MINTEQ geochemical software to predict metal release from sediment using both leaching liquids. Surface adsorption to iron- and aluminium- (hydr)oxides was applied for all studied elements. The consideration of the metal-organic matter binding through the NICA-Donnan model and Stockholm Humic Model for lead and copper, respectively, improves the former metal release prediction. Modelled curves can be useful for the environmental impact assessment of seawater acidification due to its match with the experimental values.This work was supported by the Spanish Ministry of Economy and Competitiveness, Project No. CTM 2011-28437-C02-01, ERDF included. M. C. Martı´n-Torre was funded by the Spanish Ministry of Economy and Competitiveness by means of FPI. Fellowship No. BES-2012-053816

    Controlling in der Echtzeit-Economy: Auswirkungen der digitalen Transformation auf die Unternehmenssteuerung

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    Allein für Deutschland weist die amtliche Statistik rund 2,5 Mio. Unternehmen aus, die eine Bruttowertschöpfung von knapp 1,6 Bio. € erbringen. Dazu gehören große multinationale Konzerne mit mehreren Hunderttausend Mitarbeitern genauso wie Kleinstunternehmen, Traditionsunternehmen mit einer über 100-jährigen Firmengeschichte genauso wie Start-ups, die am Anfang der Umsetzung ihrer Geschäftsideen stehen
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