2009 Portland GSA Annual Meeting (18-21 October 2009)

Paper No. 21
Presentation Time: 9:00 AM-6:00 PM

SULFUR ISOTOPIC EVALUATION OF A SULFATE-REDUCING BIOREACTOR TREATING ACID MINE DRAINAGE


REEDER, Matthew, Department of Geological Sciences, Indiana University, Bloomington, IN 47405 and OLYPHANT, Greg A., Geological Sciences, Indiana University, Center for Geospatial Data Analysis, 1001 East Tenth Street, Bloomington, IN 47405, mdreeder@indiana.edu

Sulfate-reducing bioreactor cells (SRBCs) hold promise as a cost-effective option in the treatment of acid mine drainage (AMD). They are designed to promote bacterial sulfate reduction by providing the needed conditions for the bacteria to thrive. Laboratory and small-scale field studies have shown that these systems are capable of simultaneously removing sulfate and sequestering metal sulfides while generating excess alkalinity. However, there have been few studies of these systems in large-scale field settings that go beyond monitoring the inflow and outflow chemistry. Here we provide preliminary data on the internal workings of a large (2,100 m3) SRBC built to treat a low-flow AMD seep in Indiana.

Beginning in January, 2009 samples were collected from the inflow and outflow of the system as well as from an array of monitoring ports located at varying depths inside the cell. The internal sampling ports were placed in such a way as to observe 3D trends in activity occurring within the system. The AMD flowing into the SRBC has [SO4] = 2840 mg/L with a δ34SVCDT of -6.55‰. By the time the water leaves the system, [SO4] = 940 mg/L with a δ34SVCDT of -4.48‰, indicating that the dominate sulfate removal mechanism is unlikely to be bacterial sulfate reduction. At the same time, samples collected from the deepest portion of cell have δ34SVCDT of up to +35.71‰ for the residual sulfate ([SO4] = 350 mg/L), signifying that bacterial sulfate reduction is occurring. Other sections, particularly near where the AMD enters the SRBC ([SO4] = 1390 mg/L; δ34SVCDT -5.21‰), near the surface ([SO4] = 1350 mg/L; δ34SVCDT -6.34‰), and along the perimeter ([SO4] = 1600 mg/L; δ34SVCDT -2.87‰) have significantly lighter δ34SVCDT values. These findings suggest that while bacterial sulfate reduction is taking place (as evidenced by a fractionation of up to +42‰), it’s not occurring in a uniform manner throughout the system. The observed range in fractionation values may reflect an influence by gypsum precipitation or the development of preferential flow within the system. The information presented in this study highlights observations not typically attainable in smaller laboratory scale studies that need to be accounted for in future installations of this technology.