Study of an aquifer contaminated by ethyl tert-butyl ether (ETBE): Site characterization and on-site bioremediation
► Ethyl tert-butyl ether (ETBE) (>300 mg L −1) found in a groundwater (gas-station). ► No significant carbon or hydrogen isotopic fractionation of ETBE along the plume. ► MC-IFP culture degraded ETBE (0.91 mg L −1 h −1) and BTEX (0.64 mg L −1 h −1). ► A pilot plant (2 m 3) inoculated with MC-IFP...
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Published in | Journal of hazardous materials Vol. 201; no. 30; pp. 236 - 243 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
30.01.2012
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | ► Ethyl
tert-butyl ether (ETBE) (>300
mg
L
−1) found in a groundwater (gas-station). ► No significant carbon or hydrogen isotopic fractionation of ETBE along the plume. ► MC-IFP culture degraded ETBE (0.91
mg
L
−1
h
−1) and BTEX (0.64
mg
L
−1
h
−1). ► A pilot plant (2
m
3) inoculated with MC-IFP degraded ETBE in groundwater (15
°C). ►
ethB gene (ETBE biodegradation) amplified during bioaugmentation (5
×
10
6
ethB gene copies
L
−1).
Ethyl
tert-butyl ether (ETBE) was detected at high concentration (300
mg
L
−1) in the groundwater below a gas-station. No significant carbon neither hydrogen isotopic fractionation of ETBE was detected along the plume. ETBE and BTEX biodegradation capacities of the indigenous microflora Pz1-ETBE and of a culture (MC-IFP) composed of
Rhodococcus wratislaviensis IFP 2016,
Rhodococcus aetherivorans IFP 2017 and
Aquincola tertiaricarbonis IFP 2003 showed that ETBE and BTEX degradation rates were in the same range (ETBE: 0.91 and 0.83
mg
L
−1
h
−1 and BTEX: 0.64 and 0.82
mg
L
−1
h
−1, respectively) but
tert-butanol (TBA) accumulated transiently at a high level using Pz1-ETBE (74
mg
L
−1). An on-site pilot plant (2
m
3) filled with polluted groundwater and inoculated by MC-IFP, successfully degraded four successive additions of ETBE and gasoline. However, an insignificant ETBE isotopic fractionation was also accompanying this decrease which suggested the involvement of low fractionating-strains using EthB enzymes, but required of additional proofs. The
ethB gene encoding a cytochrome P450 involved in ETBE biodegradation (present in
R. aetherivorans IFP 2017) was monitored by quantitative real-time polymerase chain reaction (q-PCR) on DNA extracted from water sampled in the pilot plant which yield up to 5
×
10
6 copies of
ethB gene per L
−1. |
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Bibliography: | http://dx.doi.org/10.1016/j.jhazmat.2011.11.074 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0304-3894 1873-3336 |
DOI: | 10.1016/j.jhazmat.2011.11.074 |