You are here:
MTBE BIOREMEDIATION WITH BIONETS(TM) CONTAINING ISOLITE, PM1, SOLD OXYGEN SOURCE (SOS) OR AIR
Citation:
Stavnes, S. A., J. J. Fleischman, S. C. Hunt, J Goetz*, W J. DavisHoover*, AND et al. MTBE BIOREMEDIATION WITH BIONETS(TM) CONTAINING ISOLITE, PM1, SOLD OXYGEN SOURCE (SOS) OR AIR. Presented at Third International Conference on Remediation of Chlorinated and Recalcitrant Compounds, Monterey, CA, 5/20-23/02.
Description:
MTBE, a gasoline additive, is a persistent and foul tasting contaminant that is more mobile in groundwater than BTEX (benzene, toluene, ethylbenzene, xylenes). It is turning up at many American crossroads. The objective of this well controlled study was to determine if biologically active in situ BioNets could bioremediate MTBE contaminated groundwater. Seven BioNets, most containing 3 fractures each, were placed in a site on the Flathead Indian Reservation in Montana. The MTBE and BTEX plume from a retail gasoline station was contaminating
farmland and threatening Native American owned surface waters. The BioNets contained:
1)sand or Isolite as a fracture material, which created bioremediation zones by facilitating inoculation, allowing attachment of the bacteria, presenting a zone for addition of oxygen by way of aeration or addition of Solid Oxygen Source (SOS) and enhancing the porosity/permeability ofthe subsurface; 2) PMl, an aerobic bacteria known to degrade MTBE, which can be monitored with a genetic probe; 3) nutrients; and 4) oxygen as air or SOS.
Results indicate that 12 months after inoculation the reductions ofMTBE in the groundwater samples were as high as 85 percent where optimum conditions existed for biodegradation, which included PM1 inoculated Isolite with SOS or air. The use of SOS stimulates more or as much reduction as the use of oxygen as supplied air at various flow rates. After 12 months, DNA of PM 1 was isolated from soils from the inoculated BioNets, but not' the un inoculated BioNet. PM 1 and naturally occurring MTBE degraders were consistently identified on subsurface soil samples using Taqman geneprobe and standard microbial techniques.