SUITABILITY OF THE NAVAJO SANDSTONE FOR CO2 SEQUESTRATION IN CENTRAL UTAH
Based on the geochemical results, no mixing appears to be taking place between the deep, salt-water disposal formations and the overlying, fresh-water aquifers. A graph of delta-D/H versus delta-18O/16O values shows that the salt- and fresh-water samples plot in separate portions of the graph. The salt water has high delta-13C/12C values (isotopically heavy), indicating that the carbon source likely is calcite. Water from the shallow aquifers is isotopically light, thus the source most likely is atmospheric and/or soil CO2 gas. The major ion and trace metal geochemistry of the injected salt water and the shallow groundwater are drastically different. The chemistry of the shallow groundwater samples is nearly uniform, and the injected salt water samples have much higher concentrations for nearly every constituent analyzed, indicating that mixing does not appear to be occurring on either a local or a regional scale.
A geologic analysis of the area will be done using geologic and topographic maps and aerial photos. These will be examined with an eye toward locating faults that may exist in the subsurface but do not displace rocks at the surface, as is common in areas where sandstones, which are brittle and fracture, are overlain by shales, which are ductile and fold rather than fracture, as is the case in the study area.