Abstract
This study investigated the use of hollow-fiber membranes for hydrogen (H 2) delivery to support the biological reductive dechlorination of tetrachloroethene (PCE). Two experiments were performed in which H 2 was supplied through membranes placed in stirred batch reactors containing a mixed methanogenic/dechlorinating culture and PCE (≤10 μM). Reductive dechlorination of PCE to cis-dichloroethene was sustained in the reactors receiving H 2 (1% H 2 and 50% H 2), while negligible dechlorination was observed in control reactors (100% N 2). The 1%-H 2-fed reactor outperformed the 50%-H 2-fed reactor in the first experiment. However, the dechlorinating performance in the two reactors was similar in the second experiment. Despite relatively high H 2 concentrations (4.6 to 178 μM) that led to H 2 consumption (and CH 4 production) by methanogens, dechlorination was effectively maintained for the duration of the experiments (35 to 62 days). The results of this study are significant in that dechlorination was sustained in a minimal medium by membrane-delivered H 2. Dechlorination was also maintained at aqueous H 2 concentrations that exceeded the thermodynamic thresholds for not only dechlorination (<0.1 to 2 nM), but also methanogenesis (∼10 nM) and homoacetogenesis (94 to 400 nM). The results of these experiments suggest that membranes are a promising H 2 delivery technology for stimulating the bioremediation of chlorinated ethene-contaminated aquifers.
Original language | English (US) |
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Pages (from-to) | 337-350 |
Number of pages | 14 |
Journal | Bioremediation Journal |
Volume | 6 |
Issue number | 4 |
DOIs | |
State | Published - 2002 |
Bibliographical note
Funding Information:This work was principally funded by the United States Department of Defense’s Strategic Environmental Research and Development Program, with additional support provided by the University of Minnesota.
Keywords
- Electron donor
- Groundwater
- Hydrogen
- In situ
- Membranes
- PCE
- Reductive dechlorination
- Tetrachloroethene