A geological database for parameterization in numerical modeling of subsurface storage in northern Germany

Underground land use can play a significant role in future concepts of energy and gas storage and requires an improved understanding of the parameters of potential storage formations (saline aquifers), for instance of porosity and permeability, and also of mineralogical and gas compositions. This study aims at providing data examples and calculating vertical spatial variations through variogram analyses of important North German geological reservoirs from Dogger, Rhaetian, Middle Buntsandstein, and Rotliegend (Sub)Groups and Formations, focusing on the western part of the North German Basin. Vertical correlation lengths of porosity and permeability data range between 0 and 30 m, while most results are calculated at approximately 2–4 m and do not show relevant differences among the evaluated formations. In the majority of the regarded formations, the Kozeny–Carman relationship between porosity and permeability is supported as long as low porosity and permeability values are excluded from the evaluation. Mineral percentages varied significantly among the evaluated sediments. Besides quartz, ankerite is the main compound in the Dogger Group, while feldspars and clay minerals were more frequent in the Rhaetian, Middle Buntsandstein, and Rotliegend sediments. Methane was the main gas compound in the reservoirs, followed by nitrogen, ethane, and carbon dioxide. This study serves as preparatory work to allow for the parameterization of geological models and a subsequent simulation of fluid transport to evaluate (long-term) safety and impacts of geothermal and gas storage projects.     

Determination of bioavailable Fe(III) content in column experiments with the reactive tracer phosphate

Different methods were compared to evaluate the oxidation capacity of ferric iron in column studies. The specific adsorption of the reactive tracer phosphate on the Fe(III) oxide surface was used as an alternative approach to determine the oxidation capacity utilizing the linear correlation between the long-term extent of Fe(III) reduction and the specific surface area of the oxide. Although a low crystalline form of ferric iron (two-line ferrihydrite) was used as electron acceptor and toluene as a carbon source, only 31 and 24% respectively of the total iron was reduced by Geobacter metallireducens in parallel experiments. The results of the phosphate tracer tests were in good agreement with the Fe(III) that was actually reduced and the microbially oxidized toluene. The oxidation capacity of ferric iron is therefore overestimated by the chemical extraction methods, which completely dissolve the ferrihydrite and neglect surface-dependent limitations.