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Drilling and sampling a natural CO2 reservoir: Implications for fluid flow and CO2-fluid–rock reactions during CO2 migration through the overburden
Chemical Geology (2014)
  • Nico Kampman, University of Cambridge
  • Andrea Maskell, University o Lancaster
  • H J Chapman, University of Cambridge
  • Michael J Bickle, University of Cambridge
  • James P. Evans
  • Gemma Purser, British Geological Survey
  • J Zhou, University of Lancaster
  • Jerome Gattacceca
  • Morgan Schaller, Rutgers University - New Brunswick/Piscataway
  • P Bertier, RWTH Aachen University
  • F. Chen, University of Cambridge
  • A S Turchyn, University of Cambridge
  • N. Assayag, University of Cambridge
  • Andreas Busch
Abstract
This paper presents the initial results of a scientific drilling project to recover core and pressurized fluid samples from a natural CO2 reservoir, near the town of Green River, Utah. The drilling targeted a stacked sequence of CO2-charged Jurassic sandstone reservoirs  and caprocks, situated adjacent to a CO2-degassing normal fault. This site has actively  leaked CO2 from deep supercritical CO2 reservoirs at depth >2km within the basin for over  400,000 years. The project objectives were to gather samples to examine reactive fluid flow  in the reservoirs, caprocks and faults, during migration of CO2 through the geological overburden from the deep supercritical CO2 reservoirs. Downhole fluid sampling and fluid  element and isotope geochemistry show that the shallow reservoirs are being actively fed  by inflow of CO2-saturated brines through the faults. Comparisons of shallow and deep fluid  geochemistry suggests that: (i) CO2 and CO2-charged brines co-migrated from the deep reservoirs, (ii) the CO2-saturated brines migrating from depth interact with significant volumes of meteoric groundwater in aquifers in the shallower Permian and Jurassic sandstones, diluting the brine composition, and (iii) that a significant fraction of the CO2 migrating from depth is dissolved in these brine-meteoric water mixtures, with >99% of the CO2 in fluids sampled from the shallow reservoirs being derived during fluid migration, after the fluids left their source reservoir. The 87Sr/86 40 Sr ratio of the brine flowing through the faults is significantly elevated due to the addition of Sr from silicate mineral dissolution during fluid migration. The association of bleached sandstones in the core with CO2-rich fluids supports interpretations from elsewhere that CO2-charged brines with CH4 or H2S reductants can dissolve hematite present within the sediment. Analysis of fluid geochemistry and sandstone petrology suggest that the CO2-rich fluids dissolve carbonate, hematite and  gypsum in the reservoirs, as they flow away from the faults. Element and isotope geochemistry of fluid samples from the drillhole and Crystal Geyser constrain mixing models which show that, within the Navajo Sandstone, the reservoir fluids are undergoing complex mixing of: (i) CO2-saturated brine inflowing from the fault, (ii) CO2-undersaturated meteoric groundwater flowing through the reservoir and (iii) reacted CO2-charged brines flow through fracture zones in the overlying Carmel Formation caprock, into the formations above. Such multi-scale mixing processes may  significantly improve the efficiency with which groundwaters dissolve the migrating CO2.
Publication Date
2014
DOI
10.1016/j.chemgeo.2013.11.015
Citation Information
Nico Kampman, Andrea Maskell, H J Chapman, Michael J Bickle, et al.. "Drilling and sampling a natural CO2 reservoir: Implications for fluid flow and CO2-fluid–rock reactions during CO2 migration through the overburden" Chemical Geology Vol. 369 (2014) p. 51 - 82 ISSN: 0009-2541
Available at: http://works.bepress.com/james_evans/134/
Creative Commons license
Creative Commons License
This work is licensed under a Creative Commons CC_BY International License.