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W.D. Gunter

Publications and source records attributed to W.D. Gunter.

3 recordsLinked to original sources

Gas-water-rock interactions in Frio Formation following CO 2 injection: Implications for the storage of greenhouse gases in sedimentary basins

To investigate the potential for the geologic storage of CO 2 in saline sedimentary aquifers, 1600 t of CO 2 were injected at 1500 m depth into a 24-m-thick sandstone section of the Frio Formation, a regional brine and oil reservoir in the U.S. Gulf Coast. Fluid samples obtained from the injection and observation wells before CO 2 injection showed a Na-Ca-Cl–type brine with 93,000 mg/L total dissolved solids (TDS) at near saturation with CH 4 at reservoir conditions. Following CO 2 breakthrough, samples showed sharp drops in pH (6.5–5.7), pronounced increases in alkalinity (100–3000 mg/L as HCO 3 ) and Fe (30–1100 mg/L), and significant shifts in the isotopic compositions of H 2 O, dissolved inorganic carbon (DIC), and CH 4 . Geochemical modeling indicates that brine pH would have dropped lower but for the buffering by dissolution of carbonate and iron oxyhydroxides. This rapid dissolution of carbonate and other minerals could ultimately create pathways in the rock seals or well cements for CO 2 and brine leakage. Dissolution of minerals, especially iron oxyhydroxides, could mobilize toxic trace metals and, where residual oil or suitable organics are present, the injected CO 2 could also mobilize toxic organic compounds. Environmental impacts could be major if large brine volumes with mobilized toxic metals and organics migrated into potable groundwater. The δ 18 O values for brine and CO 2 samples indicate that supercritical CO 2 comprises ∼50% of pore-fluid volume ∼6 mo after the end of injection. Postinjection sampling, coupled with geochemical modeling, indicates that the brine gradually will return to its preinjection composition.

Geology↗

Phase relations in the system NaCl-KCl-H 2 O II: Differential thermal analysis of the halite liquidus in the NaCl-H 2 O binary above 450°c

Thermal analysis of the halite liquidus in the system NaCl-H 2 O has been conducted for NaCl mole fractions ( X NaCl ) greater than 0.25 ( i.e. , > 50 wt. % NaCl) at pressures between 0.3 and 4.1 kb and temperatures greater than 450&deg;C. The position of the liquidus was located by differential thermal analysis (DTA) of cooling scans only, as heating scans did not produce definitive DTA peaks. The dP/dT slope of the liquidus is positive and steep at high pressures, but at high X NaCl , and pressures below 0.5 kb it appears to reverse slope and intersects the three-phase curve (liquid-halite-vapour) at a shallow angle. However, due to the complex nature of the DTA signal when P <- 0.5 kb, there is considerable doubt about exactly what event has been recorded in the experiments conducted at these low pressures. The solubility of halite can be expressed as a function of the mole-fractional-based activity of NaCl in the liquid phase ( L ) in temperature (T, &deg;K) and pressure (P, bars) In Our liquidus data (based on 10 compositions) above 500 bars for these brines were combined with this equation to generate activity coefficients of NaCl which were fit within their experimental uncertainties to the following one parameter Margules equation In . Concentrated solutions of NaCl show negative deviations from ideality which rapidly increase in magnitude with decreasing X NaCl .

Geochimica et Cosmochimica Acta↗