2005 Salt Lake City Annual Meeting (October 16–19, 2005)

Paper No. 8
Presentation Time: 3:35 PM

USING REACTIVE TRANSPORT MODELING TO QUANTIFY LONG-TERM REACTION RATES IN PERMEABLE REACTIVE BARRIERS FOR THE TREATMENT OF MINE DRAINAGE


MAYER, K. Ulrich1, BENNER, Shawn G.2, BLOWES, David W.3, WILLIAMS, Randi L.1, BAIN, Jeff G.3 and DAIGNAULT, Eugenie3, (1)Earth and Ocean Sciences, Univ of British Columbia, 6339 Stores Rd, Vancouver, BC V6T 1Z4, Canada, (2)Department of Geology, Boise State University, Boise, ID 83705, (3)Earth Sciences, Univ of Waterloo, 200 University Avenue W, Waterloo, ON N2L 3G1, umayer@eos.ubc.ca

Organic-carbon based permeable reactive barriers are useful for the treatment of mine drainage impacted waters, which are rich in SO4 and Fe(II). In order to quantitatively assess the long-term the performance of these systems, it is of importance to understand the processes controlling rates of SO4-reduction and organic matter consumption. Reactive transport modeling of a permeable reactive barrier for the treatment of mine drainage was used to integrate a comprehensive field data set including pore water chemistry, solid phase and dissolved gas data from several sampling events over a >7-year time period. The simulations consider the reduction of sulfate by the organic carbon-based treatment material and the removal of sulfate and iron by precipitation of reduced mineral phases including iron monosulfides and siderite. Additional parameters constraining the model include dissolved gases (H2S, CO2, CH4, N2, Ar), alkalinity and pH, as well as a suite of solid phase S-fractions identified by extractions. Influences of spatial heterogeneity necessitated the use of a 2-D modeling approach. Simulating observed seasonal fluctuations and long-term changes in barrier reactivity, required the use of temperature-dependent rate coefficients and a multimodal Monod-type rate expression accounting for the variable reactivity of different organic carbon fractions. Simulated concentrations of SO4, Fe, alkalinity, pH, dissolved gases, and solid phase accumulations of reduced sulfur phases generally compare well to observed trends. Spatial variations, seasonal fluctuations and the time-dependent decline in reactivity were also captured. The modeling results indicate that only a relatively small fraction of the treatment material is consumed by methanogenesis. Overall sulfate reduction and S-accumulation rates are constrained with confidence within a factor of 1.5.