Micromechanics of High-Pressure Compaction in Granular Quartz Aggregates

The mechanical behavior of porous sandstones is generally modeled using concepts from granular mechanics, often overlooking the effect of cementation. To probe the key differences between sand and sandstone mechanics, we performed triaxial deformation experiments on Ottawa quartz sand at 5- to 40 MPa effective confining pressure. At 5 MPa, the samples are able to dilate. At higher confinement, the aggregates show continuous compaction, displaying strain hardening. The stress-strain behavior is nonlinear, and the exact onset of inelastic compaction could not be determined accurately. Measured P-wave velocities show the development of anisotropy. With increasing axial strain, the along-axis velocities tend to increase, while velocities perpendicular to the compression axis tend to decrease (at low pressure) or remain constant (at high pressure). In samples deformed under elevated pressure conditions, acoustic emission event locations are diffuse. Microstructural investigations show an increase in grain chipping and crushing with increasing confining pressure, but no evidence of localized compaction could be observed. The nature of the pore fluid, either decane or water, does not significantly influence the mechanical behavior at strain rates of 10−6 to 10−4 s−1. Grain angularity and grain-size distribution also did not significantly change the mechanical behavior. We infer that our observations indicate that the lack of cementation introduces additional degrees of freedom for grains to slide, rotate, and reorganize at the sample scale, precluding the existence and sustainability of stress concentrations beyond the grain scale. This results in progressive compaction and hardening, and lack of compaction localization

The Geomechanics of CO2 Storage in Deep Sedimentary Formations

This paper provides a review of the geomechanics and modeling of geomechanics associated with geologic carbon storage (GCS), focusing on storage in deep sedimentary formations, in particular saline aquifers. The paper first introduces the concept of storage in deep sedimentary formations, the geomechanical processes and issues related with such an operation, and the relevant geomechanical modeling tools. This is followed by a more detailed review of geomechanical aspects, including reservoir stress-strain and microseismicity, well integrity, caprock sealing performance, and the potential for fault reactivation and notable (felt) seismic events. Geomechanical observations at current GCS field deployments, mainly at the In Salah CO2 storage project in Algeria, are also integrated into the review. The In Salah project, with its injection into a relatively thin, low-permeability sandstone is an excellent analogue to the saline aquifers that might be used for large scale GCS in parts of Northwest Europe, the U.S. Midwest, and China. Some of the lessons learned at In Salah related to geomechanics are discussed, including how monitoring of geomechanical responses is used for detecting subsurface geomechanical changes and tracking fluid movements, and how such monitoring and geomechanical analyses have led to preventative changes in the injection parameters. Recently, the importance of geomechanics has become more widely recognized among GCS stakeholders, especially with respect to the potential for triggering notable (felt) seismic events and how such events could impact the long-term integrity of a CO{sub 2} repository (as well as how it could impact the public perception of GCS). As described in the paper, to date, no notable seismic event has been reported from any of the current CO{sub 2} storage projects, although some unfelt microseismic activities have been detected by geophones. However, potential future commercial GCS operations from large power plants will require injection at a much larger scale. For such largescale injections, a staged, learn-as-you-go approach is recommended, involving a gradual increase of injection rates combined with continuous monitoring of geomechanical changes, as well as siting beneath a multiple layered overburden for multiple flow barrier protection, should an unexpected deep fault reactivation occur

Effect of injected CO2 on geochemical alteration of the Altmark gas reservoir in Germany

Capturing CO2 from point sources and storing it into geologic formations is a potential option to allaying the CO2 level in the atmosphere. In order to evaluate the effect of geological storage of CO2 on rock-water interaction, batch experiments were performed on sandstone samples taken from the Altmark reservoir, Germany, under insitu conditions of 125°C and 50 bar CO2 partial pressure. Two sets of experiments were performed on pulverized sample material placed inside a closed batch reactor in a) CO2 saturated and b) CO2 free environment for 5, 9 and 14 days. A 3M NaCl brine was used in both cases to mimic the reservoir formation water. For the "CO2 free" environment, Ar was used as a pressure medium. The sandstone was mainly composed of quartz, feldspars, anhydrite, calcite, illite and chlorite minerals. Chemical analyses of the liquid phase suggested dissolution of both calcite and anhydrite in both cases. However, dissolution of calcite was more pronounced in the presence of CO2. In addition, the presence of CO2 enhanced dissolution of feldspar minerals. Solid phase analysis by X-ray diffraction and Mössbauer spectroscopy did not show any secondary mineral precipitation. Moreover, Mössbauer analysis did not show any evidence of significant changes in redox conditions. Calculations of total dissolved solids concentrations indicated that the extent of mineral dissolution was enhanced by a factor of approximately 1.5 during the injection of CO2, which might improve the injectivity and storage capacity of the targeted reservoir. The experimental data provide a basis for numerical simulations to evaluate the effect of injected CO2 on long term geochemical alteration at reservoir scale

Enhanced weathering strategies for stabilizing climate and averting ocean acidification

Chemical breakdown of rocks, weathering, is an important but very slow part of the carbon cycle that ultimately leads to CO2 being locked up in carbonates on the ocean floor. Artificial acceleration of this carbon sink via distribution of pulverized silicate rocks across terrestrial landscapes may help offset anthropogenic CO2 emissions. We show that idealized enhanced weathering scenarios over less than a third of tropical land could cause significant drawdown of atmospheric CO2 and ameliorate ocean acidification by 2100. Global carbon cycle modelling driven by ensemble Representative Concentration Pathway (RCP) projections of twenty-first-century climate change (RCP8.5, business-as-usual; RCP4.5, medium-level mitigation) indicates that enhanced weathering could lower atmospheric CO2 by 30–300 ppm by 2100, depending mainly on silicate rock application rate (1 kg or 5 kg m−2 yr−1 ) and composition. At the higher application rate, end-of-century ocean acidification is reversed under RCP4.5 and reduced by about two-thirds under RCP8.5. Additionally, surface ocean aragonite saturation state, a key control on coral calcification rates, is maintained above 3.5 throughout the low latitudes, thereby helping maintain the viability of tropical coral reef ecosystems. However, we highlight major issues of cost, social acceptability, and potential unanticipated consequences that will limit utilization and emphasize the need for urgent efforts to phase down fossil fuel emissions

Cordierite formation during the experimental reaction of plagioclase with Mg-rich aqueous solutions

The reaction between plagioclase (labradorite and oligoclase) and Mg-rich aqueous solutions was studied experimentally at hydrothermal conditions (600–700 °C, 2 kbar). During the experiments, plagioclase grains were readily converted to cordierite and quartz within 4 days. The cordierite crystals had well-developed polyhedral shapes, but showed skeletal internal morphologies suggestingthat the initial growth occurred fast under high-driving-force conditions. In pure MgCl2 solutions (0.5–5 M), plagioclase dissolution and cordierite precipitation were spatially uncoupled indicating that Al was to some extent mobile in the fluid. Cordierite crystals formed at 700 °C showed orthorhombic symmetry, whereas those formed at 600 °C dominantly persisted in the metastable hexagonal form suggesting a strong increase in Al, Si ordering speed between 600 and 700 °C. The thermodynamic evolution of the fluid–solid system ultimately resulted in stabilization of Ca-rich plagioclase as demonstrated by partial anorthitization of unreacted plagioclase grains. Cordierite was also observed to form when Mg was added to a potentially albitizing Na-silicate-bearing solution. In that case, cordieriteprecipitation appeared to be more closely coupled to plagioclase dissolution, and secondary alteration of remnant plagioclase grains did not occur most likely due to armouring of the plagioclase by the cordierite overgrowth. The fast reaction rates observed in our experimental study have potential implications for Mg-metasomatism as a rockforming process