Comparative kinetics of hydrogen utilization for reductive dechlorination of tetrachloroethene and methanogenesis in an anaerobic enrichment culture

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School of Civil Engineering, Hollister Hall, Cornell University, Ithaca, NY 14853, United States [1 ]
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ENVIRON. SCI. TECHNOL. | / 9卷 / 2850-2858期
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Biological water treatment - Hydrogen - Mass transfer - Methanogens - Organic compounds - Reaction kinetics;
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Anaerobic microorganisms that reductively dechlorinate tetrachloroethene (PCE) must often compete with methanogens for H2. This study compared the kinetics of H2 utilization between the two types of organisms at 35 °C under conditions of continuous agitation. Limiting levels of H2 were administered to 160-mL serum bottles seeded with a PCE/butyric acid enrichment culture; H2, methane, and vinyl chloride were tracked over time using headspace samples. Measured half-velocity constants with respect to H2 - Ks(H2) values ±95% Cl - for methanogenesis and dechlorination were 960±180 and 100±50 nM, respectively. Mass-transfer equations were used to calculate aqueous H2 concentrations at the half-velocity point from headspace measurements. The possible effect on Ks(H2) values arising from interconversion between H2 and formate through an active formate/H2 lyase system was examined by comparing results from formate-fed and H2-fed bottles. Only methanogens in the culture were apparently capable of using formate; hence, the measured methanogenic Ks(H2) was dependent on which electron donor was administered. The nearly 10-fold difference in Ks(H2) between methanogens and dechlorinators suggests that the deliberate choice of an electron donor whose fermentation results in a slow, steady, and low-level release of H2 over time could maximize dechlorination potential while minimizing methanogenic competition for H2.
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