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Andrea D'Aniello Sigrún Tómasdóttir Bergur Sigfússon Massimiliano Fabbricino 《Ground water》2021,59(5):677-693
Particular attention is paid to the risk of carbon dioxide (CO2) leakage in geologic carbon sequestration (GCS) operations, as it might lead to the failure of sequestration efforts and to the contamination of underground sources of drinking water. As carbon dioxide would eventually reach shallower formations under its gaseous state, understanding its multiphase flow behavior is essential. To this aim, a hypothetical gaseous leak of carbon dioxide resulting from a well integrity failure of the GCS system in operation at Hellisheiði (CarbFix2) is here modeled. Simulations show that migration of gaseous carbon dioxide is largely affected by formation stratigraphy, intrinsic permeability, and retention properties, whereas the initial groundwater hydraulic gradient (0.0284) has practically no effect. In two different scenarios, about 18.3 and 30.6% of the CO2 that would have been injected by the GCS system for 3 days could be potentially released again into the atmosphere due to a sustained leakage of the same duration. As the gaseous leak occurs, the aquifer experiences high pressure buildups, and the presence of a less conductive layer further magnifies these. Strikingly, the dimensional analysis showed that buoyant and viscous forces can be comparable over time within the predicted gaseous plumes, even far from the leakage source. Local pressure gradients, buoyant, viscous, and capillary forces all play an important role during leakage. Therefore, neglecting one or more of these contributions might lead to a partial prediction of gaseous CO2 flow behavior in the subsurface, giving space to incorrect interpretations and wrong operational choices. 相似文献
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Bergur Sigfusson Sigurdur R. Gislason Graeme I. Paton 《Journal of Geochemical Exploration》2006,88(1-3):321
Histic Andosol in Western Iceland was studied using laboratory based repacked microcosms conjointly with sampling of field soil solution. The main primary phase of the 205 cm thick soil profile was basaltic glass, allophane content ranged from 2 to 22 wt.% and the soil carbon content ranged from 11 to 42 wt.%. At constant temperature, the dissolution rate of the basaltic glass, and probably allophane and imogolite, was dictated by the aH+3 / aAl3+ activity ratio only, which in turn is governed by the pH, total dissolved Al and the anions capable of complexing Al3+; SO42−, F− and organic anions (DOC). Dissolution rate was slowed down by up to 20% by decreasing undersaturation in the field. Dissolution rate of basaltic glass was stable after an initial flushing event at the beginning of microcosm experiments. Predicted dissolution rates increased up to a factor of 7 and 30 by speciating Al3+ with oxalate in field and microcosms respectively. Speciation with oxalate generally had more effect in shallow horizons than deep horizons. 相似文献
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Direct evidence of the feedback between climate and weathering 总被引：1，自引：0，他引：1
Sigurdur R. Gislason Eric H. Oelkers Eydis S. Eiriksdottir Marin I. Kardjilov Gudrun Gisladottir Bergur Sigfusson Arni Snorrason Sverrir Elefsen Jorunn Hardardottir Peter Torssander Niels Oskarsson 《Earth and Planetary Science Letters》2009,277(1-2):213-222
Long-term climate moderation is commonly attributed to chemical weathering; the higher the temperature and precipitation the faster the weathering rate. Weathering releases divalent cations to the ocean via riverine transport where they promote the drawdown of CO2 from the atmosphere by the precipitation and subsequent burial of carbonate minerals. To test this widely-held hypothesis, we performed a field study determining the weathering rates of 8 nearly pristine north-eastern Iceland river catchments with varying glacial cover over 44 years. The mean annual temperature and annual precipitation of these catchments varied by 3.2 to 4.5 °C and 80 to 530%, respectively during the study period. Statistically significant linear positive correlations were found between mean annual temperature and chemical weathering in all 8 catchments and between mean annual temperature and both mechanical weathering and runoff in 7 of the 8 catchments. For each degree of temperature increase, the runoff, mechanical weathering flux, and chemical weathering fluxes in these catchments are found to increase from 6 to 16%, 8 to 30%, and 4 to 14% respectively, depending on the catchment. In contrast, annual precipitation is less related to the measured fluxes; statistically significant correlations between annual precipitation and runoff, mechanical weathering, and chemical weathering were found for 3 of the least glaciated catchments. Mechanical and chemical weathering increased with time in all catchments over the 44 year period. These correlations were statistically significant for only 2 of the 8 catchments due to scatter in corresponding annual runoff and average annual temperature versus time plots. Taken together, these results 1) demonstrate a significant feedback between climate and Earth surface weathering, and 2) suggest that weathering rates are currently increasing with time due to global warming. 相似文献
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