2004 Denver Annual Meeting (November 7–10, 2004)

Paper No. 14
Presentation Time: 11:40 AM

QUANTIFYING THE IMPACT OF ION EXCHANGE ON LONG-TERM SOLUTE TRANSPORT IN CLAY AQUITARDS USING CENTRIFUGATION AND GEOCHEMICAL MODELING


TIMMS, W.A., Geological Sciences, Univ of Saskatchewan, 114 Science Pl, Saskatoon, SK S7N 5E2 and HENDRY, M. Jim, Geological Sciences, Univ Saskatchewan, 114 Science Pl, Saskatoon, SK S7N 5E2, Canada, w.timms@wrl.unsw.edu.au

Characterizing and predicting reactive solute transport in low hydraulic conductivity (K) clay-rich aquitards is challenging because the very long transport time for solutes (about 0.5 to 0.8 m per 10,000 years) renders conventional column tests impractical. Furthermore, standard cation exchange batch techniques may not provide realistic data due to higher liquid:solid ratio (200:1) than in situ conditions (1:5) and the impact of carbonate mineral dissolution (~8 wt. % calcite). In this study, a centrifugation technique was developed to accelerate solute flux through low K (1.1x10-11 m/s) clay-rich core samples to quantify ion exchange processes in a scale model for comparison with observations at the field scale. Duplicate cores (52 mm length x 33 mm dia.) were centrifuged at 330 x g for 3 months to simulate the migration of saline pore water (0.5 M NaCl) through ~17 m thick clay aquitard over ~27,000 years under in situ conditions. Importantly, a liquid:solid ratio of 1:5 was maintained by centrifugation at stresses equivalent to pre-consolidation stress in the aquitard. Effluent breakthrough over the experimental period was simulated with a PHREEQC 1D reactive solute transport model using measured cation exchange capacity (CEC) of ~20 meq/100g. Best fit simulations for breakthrough and exchangeable cations indicated that exchange coefficients KNa/Ca and KNa/Mg were lower than determined by static cation exchange batch tests. PHREEQC simulations of the field solute profile obtained from 13 piezometers installed between 3 and 20 m below ground, indicated that despite high CEC, chromatographic separation of Na+ and Mg2+ was limited to ~1 m by diffusive dominated solute transport. Migration of K+ and Sr2+ was also delayed. High apparent Ca2+ exchange affinity was attributed in part to high Na/Ca molar ratios in porewater. Similar KNa/Mg and KNa/Ca for centrifugation and field results indicated that centrifugation may be used to determine long-term reactive solute transport controlled by ion exchange in clay-rich aquitards.