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Enhanced reductive dechlorination of PCE DNAPL with TBOS as a slow-release electron donor

Tetrabutoxysilane (TBOS), which yields 1-butanol upon abiotic hydrolysis, was evaluated as a slow-release substrate for the reductive dechlorination of tetrachloroethylene (PCE) as a dense non-aqueous-phase liquid (DNAPL). Dechlorination was achieved using an anaerobic binary mixed (BM) culture, whi...

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Published in:Journal of hazardous materials 2009-08, Vol.167 (1), p.97-104
Main Authors: Yu, Seungho, Semprini, Lewis
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description Tetrabutoxysilane (TBOS), which yields 1-butanol upon abiotic hydrolysis, was evaluated as a slow-release substrate for the reductive dechlorination of tetrachloroethylene (PCE) as a dense non-aqueous-phase liquid (DNAPL). Dechlorination was achieved using an anaerobic binary mixed (BM) culture, which consisted of the Pt. Mugu (PM) and the Evanite (EV) mixed cultures. In batch reactor experiments, TBOS was mixed with PCE DNAPL to achieve different PCE mol fractions (PCE mol/(PCE mol + TBOS mol)), and different PCE aqueous concentrations based on Raoult's Law. The reductive dechlorination activity was determined based on the amount of chloride ions released and the mass balances of the transformation products formed. The mass balances of the total chlorinated aliphatic hydrocarbons (CAHs) between water, NAPL and gas phases were performed using independently measured NAPL/water partition coefficients. The amounts of chloride released (directly measured in aqueous samples) agreed with the total chloride produced based on the mass balances. The abiotic rates of TBOS hydrolysis were first-order with respect to TBOS NAPL concentration. A higher electron transfer efficiency to dechlorination was correlated with lower rates of TBOS hydrolysis. The total amounts of PCE DNAPL and TBOS were important factors for the reductive dechlorination of PCE. The dechlorination activity was suppressed at high NAPL concentrations. Direct contact of the PCE/TBOS NAPL mixture may have caused toxicity to the dechlorinating bacteria. Decreases in pH likely lowered the microbial activity for reductive dechlorination due to the accumulation of acetate and/or butyrate. These studies showed the potential of TBOS as a slow-release substrate for enhancing bioremediation of DNAPL contaminated sites.
doi_str_mv 10.1016/j.jhazmat.2008.12.087
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Dechlorination was achieved using an anaerobic binary mixed (BM) culture, which consisted of the Pt. Mugu (PM) and the Evanite (EV) mixed cultures. In batch reactor experiments, TBOS was mixed with PCE DNAPL to achieve different PCE mol fractions (PCE mol/(PCE mol + TBOS mol)), and different PCE aqueous concentrations based on Raoult's Law. The reductive dechlorination activity was determined based on the amount of chloride ions released and the mass balances of the transformation products formed. The mass balances of the total chlorinated aliphatic hydrocarbons (CAHs) between water, NAPL and gas phases were performed using independently measured NAPL/water partition coefficients. The amounts of chloride released (directly measured in aqueous samples) agreed with the total chloride produced based on the mass balances. The abiotic rates of TBOS hydrolysis were first-order with respect to TBOS NAPL concentration. A higher electron transfer efficiency to dechlorination was correlated with lower rates of TBOS hydrolysis. The total amounts of PCE DNAPL and TBOS were important factors for the reductive dechlorination of PCE. The dechlorination activity was suppressed at high NAPL concentrations. Direct contact of the PCE/TBOS NAPL mixture may have caused toxicity to the dechlorinating bacteria. Decreases in pH likely lowered the microbial activity for reductive dechlorination due to the accumulation of acetate and/or butyrate. 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Dechlorination was achieved using an anaerobic binary mixed (BM) culture, which consisted of the Pt. Mugu (PM) and the Evanite (EV) mixed cultures. In batch reactor experiments, TBOS was mixed with PCE DNAPL to achieve different PCE mol fractions (PCE mol/(PCE mol + TBOS mol)), and different PCE aqueous concentrations based on Raoult's Law. The reductive dechlorination activity was determined based on the amount of chloride ions released and the mass balances of the transformation products formed. The mass balances of the total chlorinated aliphatic hydrocarbons (CAHs) between water, NAPL and gas phases were performed using independently measured NAPL/water partition coefficients. The amounts of chloride released (directly measured in aqueous samples) agreed with the total chloride produced based on the mass balances. The abiotic rates of TBOS hydrolysis were first-order with respect to TBOS NAPL concentration. 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subjects Acetates
Anaerobiosis
Applied sciences
Atmospheric pollution
Bacteria
Biodegradation, Environmental
Bioremediation
CAH
Chemical engineering
Chlorides
Culture
Dechlorination
DNAPL
Electrons
Exact sciences and technology
Halogenation
Hydrolysis
Microorganisms
Pollution
Reactors
Silanes - chemistry
Tetrabutoxysilane
Tetrachloroethylene - chemistry
Tetrachloroethylene - metabolism
Toxicity
Transformations
title Enhanced reductive dechlorination of PCE DNAPL with TBOS as a slow-release electron donor
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