Abstract

The Upper Rhine Graben (URG) is a Tertiary rift structure in central Europe offering favorable conditions for geothermal energy utilization. Relatively high heat flow combines with sufficiently high permeability of the hydrothermal reservoirs. One of the target stratigraphic levels is the lower Triassic sandstone formation (Buntsandstein), where hot water resources at temperatures up to 250 °C can be utilized. Extensional neotectonics and hydraulic stimulation form new fracture surfaces in the reservoir rocks (enhanced geothermal system, EGS). The exposed fresh rock fracture surface reacts with the highly saline reservoir brines (Na-Cl up to 200 g l−1) with consequences for the permeability of the reservoir.In order to better understand the dynamic evolution of fault systems caused by fluid-rock interaction, we conducted batch-type experiments in a stirred autoclave system and reacted arkosic sandstone with synthetic 2 molal Na-Cl solution at temperatures of 200 °C and 260 °C. After 45–55 days reaction time altered rock samples were compared with the starting material and the geochemical-mineralogical processes were deduced with the help of XRD, SEM methods and EMP measurements. Fluid compositions were examined by ICP-MS, ICP-OES and IC.The arkosic sandstones show a surprisingly high reactivity during the experiments. Quartz grain surfaces show deep dissolution features and all reaction fluids were saturated with respects to quartz. Illite and kaolinite from the primary sandstone cementation completely dissolved from the sample surface. Perfectly euhedral crystals of metastable analcime formed during the experiment as separate crystals on quartz, as groups or clusters and as surface covering mats. The overall net transfer process dissolves quartz + illite + kaolinite ± K-feldspar and precipitates analcime + chlorite ± albite. The process is accompanied by a total volume increase of the solids of 20–30 vol%. K-feldspar dissolution is hampered by albitization rims shielding K-feldspar and efficiently preventing an equilibration of the Na–K exchange with the fluid. The experiments show changes on the rock surface, leading to an increase of the aperture of a single fracture during the early phases of reaction and later to a decrease as the fluid-rock reaction progresses. Alteration of the fracture surface also generates loose fragments and altered minerals. This fine material may efficiently reduce the fracture aperture at narrow points along the fracture.

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