Electrolytic methanogenic - Methanotrophic coupling for tetrachloroethylene bioremediation: Proof of concept

Guiot, SR; Cimpoia, R; Kuhn, R; Alaplantive, A

HERO ID

1960312

Reference Type

Journal Article

Year

2008

Language

English

PMID

18497159

HERO ID 1960312
In Press No
Year 2008
Title Electrolytic methanogenic - Methanotrophic coupling for tetrachloroethylene bioremediation: Proof of concept
Authors Guiot, SR; Cimpoia, R; Kuhn, R; Alaplantive, A
Journal Environmental Science & Technology
Volume 42
Issue 8
Page Numbers 3011-3017
Abstract Coupling of methanogenic and methanotrophic catabolisms was performed in a single-stage technology equipped with a water electrolysis cell placed in the effluent recirculation loop. The electrolysis-generated hydrogen served as an electron donor for both bicarbonate reduction into CH4 and reductive dechlorination, while the O2 and CH4, supported the cometabolic oxidation of chlorinated intermediates left over by the tetrachloroethylene (PCE) transformation. The electrolytical methanogenic/methanotrophic coupled (eMaMoC) process was tested in a laboratory-scale setup at PCE loads ranging from 5 to 50 micromol/L(rx) x d (inlet concentrations from 4 to 11 mg/L), and at various hydraulic residence times (HRT). Degradation followed essentially a reductive dechlorination pathway from PCE to cis-1,2-dichloroethene (DCE), and an oxidative pathway from DCE to CO2. PCE reductive dechlorination to DCE was consistently over 98% while a maximum oxidative DCE mineralization of 89% was obtained at a load of 4.3 micromol PCE/ L(rx) x d and an HRT of 6 days. Controlling dissolved oxygen concentrations within a relatively low range (2-3 mg/L) seemed instrumental to sustain the overall degradation capacity. Degradation kinetics were further evaluated: the apparent half-saturation constant (K(s)) had to be set relatively high (29 microM) for the simulated data to best fit the experimental ones. In spite of such kinetic limitations, the eMaMoC system, while fueled by water electrolysis, was effective in building and sustaining a functional methanogenic/methanotrophic consortium capable of significant PCE mineralization in a single-stage process. Hence, degradation standards are within reach so long as the methanotrophic DCE-oxidizing potential, including substrate affinity, are optimized and HRT accordingly adjusted.
Doi 10.1021/es702121u
Pmid 18497159
Wosid WOS:000254890400055
Url https://search.proquest.com/docview/70736014?accountid=171501
Is Certified Translation No
Dupe Override No
Comments Journal: ISSN:
Is Public Yes
Language Text English
Keyword Methane; OP0UW79H66; S88TT14065; Tetrachloroethylene; TJ904HH8SN; Index Medicus; Anaerobiosis; Biodegradation, Environmental; Electrolysis; Oxygen -- metabolism; Methane -- metabolism; Bioreactors; Tetrachloroethylene -- metabolism
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