Anaerobic MTBE and TBA
Biodegradation under Different Terminal Electron Accepting
Processes
Student Presenter
Na Wei, University of Illinois - Urbana Champaign, Dept of Civil and
Environmental Engineering, NCEL 205 N. Mathews, Urbana,
IL, 61801, Tel: 217-333-8121, Email: nawei2@uiuc.edu
Kevin T. Finneran, Assistant Professor,
University of Illinois - Urbana Champaign, Dept of Civil
and Environmental Engineering, NCEL 205 N. Mathews,
Urbana, IL, 61801, Tel: 217-333-1514, Fax: 217-333-6967,
Email: finneran@uiuc.edu
The fuel oxygenate methyl tert-butyl ether (MTBE) is a
prevalent groundwater contaminant, and its key degradation
intermediate tert-butyl alcohol (TBA) often accumulates in
subsurface environments. Although studies have reported
potential for aerobic microbial degradation of MTBE and
TBA, in situ conditions within proximity of source areas
are typically anaerobic, and moreover, oxygen introduced
artificially can be consumed quickly by chemical oxidation
of Fe (II) and sulfides. Source area bioremediation
strategies must encompass anaerobic conditions from
nitrate reduction, Fe (III) reduction, sulfate reduction
to methanogenesis, as these processes shift from higher to
lower redox processes. This research has investigated the
mechanisms and kinetics of MTBE and TBA biodegradation
under shifting anaerobic conditions.
Microcosm experiments were initiated using petroleum
contaminated sediment, river sediment, and anaerobic
digester sludge. Radiolabeled (14C) and non-radiolabeled
MTBE and TBA were amended to different incubations to
quantify MTBE/TBA biodegradation. Different electron
acceptor amendments and electron shuttling amendments were
added to identify the MTBE degradation (and potential TBA
accumulation) dynamics as conditions shift from one
dominant process to another. To date the microcosms are in
acclimation stage with up to 5% recovery of [U
-14C
]-MTBE or [U
-14C
]-TBA as 14CO2. Data
suggest that fumarate and electron shuttles increase the
extent of MTBE biodegradation; however, TBA degradation is
slower than corresponding MTBE incubations.
Sulfate increases the rate of MTBE and TBA
biodegradation, but is very dependent on the starting
material. Liquid enrichments with petroleum contaminated
sediment degraded MTBE and TBA in less than one month
under nitrate reducing, Fe (III) reducing, sulfate
reducing and fumerate reducing conditions. These liquid
enrichments may provide a model, anaerobic microbial
culture for investigating basic cellular processes related
to anaerobic MTBE and TBA biodegradation – currently, no
such anaerobic culture has been reported.
These data suggest that anaerobic MTBE/TBA
biodegradation is influenced by shifting electron
accepting processes, and the effects of these geochemical
factors on MTBE/TBA degradation continue to be
investigated.
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