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Anaerobic microbial transformation of aromatic hydrocarbons and mixtures of aromatic hydrocarbons and halogenated solvents. Final report, 30 September 1988-31 March 1992

Technical Report ·
OSTI ID:6599419
Anaerobic microbial transformation of monoaromatic hydrocarbons (NM), chlorinated benzenes (CB), and mixtures of MAH and CB, as well as MAH and chlorinated aliphatic solvents (tetrachloroethylene -- PCE, and carbon tetrachloride -CT) was studied in laboratory microcosms derived from hydrocarbon-contaminated groundwater aquifers. Some MAH , such as toluene and o-xylene, were completely degraded to CO 2 and CH by mixed methanogenic cultures from a creosote-contaminated aquifer. This degradation was inhibited by the addition of accessory electron acceptors (oxygen, nitrate, sulfate), indicating acclimation of the microbial community to methanogenic conditions. The addition of preferred substrates, such as acetate, propionate, methanol, fatty acids, glucose, casamino acids, pepton, yeast extract, or acetone also inhibited MAH degradation, indicating that the presence of natural organic substrates may preclude anaerobic biodegradation of in situ. Cyclohexane, CT, and high concentrations of toluene and o-xylene had a toxic effect. Under sulfate-reducing conditions, several MAH -- toluene, all three xylene isomers, and benzene were mineralized to CO by microorganisms from a petroleum-contaminated, sulfidogenic aquifer. Whereas 2 toluene and xylenes were sequentially degraded in a mixture, benzene was degraded only if alone, or slowly transformed in a mixture with toluene. This explains previously reported recalcitrance of benzene under anaerobic conditions. The addition of preferred substrates (lactate, glucose, or yeast extract) to the cultures temporarily inhibited the degradation of MAH. Methanogenic microcosms from the creosote-contaminated aquifer reductively dechlorinated hexa-, penta-, tetra-, tri-, and di-chlorobenzene.
Research Organization:
Stanford Univ., CA (United States). Dept. of Civil Engineering
OSTI ID:
6599419
Report Number(s):
AD-A-260498/1/XAB; CE--319; CNN: AFOSR-88-0351
Country of Publication:
United States
Language:
English

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