RESUMEN
The biodegradation of polycyclic aromatic hydrocarbons (PAHs) has been reported to occur under aerobic, sulfate reducing, and denitrifying conditions. PAHs present in contaminated sites, however, are known for their persistence. Most published studies were conducted in systems where PAHs were freshly spiked, and biodegradation was often tested using pure cultures or enrichments. This paper investigated the degradation potentials of PAHs that were present in aged contaminated sediment by indigenous bacteria, where the limited bioavailability of PAHs due to aging played an important role. The sediment and the overlaying water were collected from a contaminated site to prepare sediment-water slurries, and the sediment served as both the media containing PAH substrates and the habitat for the indigenous microorganisms. Reduced sulfur compounds present in the sediment caused rapid oxygen depletion due to extensive activities of sulfur-oxidizing bacteria and could result in a dramatic pH drop. Once oxygen depletion and acidification problems were avoided, substantial removals of two-, three-, four-, and five-ring PAHs were achieved aerobically, though the extent of degradations was smaller than what was reported for freshly spiked PAHs. The amendment of inorganic N and P, co-substrates, or surfactant Triton X-100 did not enhance the level of degradations appreciably. Under denitrifying conditions, no distinct PAH degradation was observed, while the complete denitrification of nitrate to nitrogen occurred stoichiometrically with a concomitant increase in sulfate concentration, indicating the dominance of autotrophic denitrifiers. The addition of ethanol or acetic acid did not stimulate PAH degradation. Substantial PAH degradation attributed to sulfate reduction was only observed for phenanthrene, the low-ring PAH existing in a highest initial concentration. Addition of ethanol or acetic acid did not change this finding. This is the first study to our knowledge that revealed the importance of indigenous bacteria involved in natural sulfur cycling in determining degradation behavior of PAHs.
Asunto(s)
Biodegradación Ambiental , Sedimentos Geológicos/química , Sedimentos Geológicos/microbiología , Hidrocarburos Policíclicos Aromáticos/metabolismo , Aerobiosis , Electrones , Concentración de Iones de Hidrógeno , Nitritos/química , Nitritos/metabolismo , Nitrógeno/química , Oxígeno/química , Sulfatos/química , Azufre/química , Factores de TiempoRESUMEN
An integrated system has been developed to remediate soils contaminated with pentachlorophenol (PCP) and polycyclic aromatic hydrocarbons (PAHs). This system involves the coupling of two treatment technologies, soil-solvent washing and anaerobic biotreatment of the extract. Specifically, this study evaluated the effectiveness of a granular activated carbon (GAC) fluidized-bed reactor to treat a synthetic-waste stream of PCP and four PAHs (naphthalene, acenaphthene, pyrene, and benzo(b)fluoranthene) under anaerobic conditions. This waste stream was intended to simulate the wash fluids from a soil washing process treating soils from a wood-preserving site. The reactor achieved a removal efficiency of greater than 99.8% for PCP with conversion to its dechlorination intermediates averaging 46.5%. Effluent, carbon extraction, and isotherm data also indicate that naphthalene and acenaphthene were removed from the liquid phase with efficiencies of 86 and 93%, respectively. Effluent levels of pyrene and benzo(b)fluoranthene were extremely low due to the high-adsorptive capacity of GAC for these compounds. Experimental evidence does not suggest that the latter two compounds were biochemically transformed within the reactor.
Asunto(s)
Reactores Biológicos , Pentaclorofenol/análisis , Hidrocarburos Policíclicos Aromáticos/aislamiento & purificación , Contaminantes del Suelo/análisis , Contaminantes Químicos del Agua/análisis , Acenaftenos/análisis , Anaerobiosis , Carbón Orgánico/química , Cinética , Modelos Estadísticos , Naftalenos/análisis , Pentaclorofenol/química , Pirenos/análisisRESUMEN
Removal of PAHs from highly contaminated soil found at a manufactured gas site was evaluated using solvent washing with mixed solvents. The following solvents were considered as water miscible co-solvents in mixed solvents: ethanol, 2-propanol, acetone, and 1-pentanol. In batch solvent extraction of soil, ethanol and 2-propanol were selected as primary components of mixed solvents in addition to 1-pentanol. Using ternary solutions containing either ethanol or 2-propanol with a volume fraction of 1-pentanol ranging from 5 to 25% and a water volume fraction ranging from 5 to 30%, ethanol was more effective than 2-propanol in extracting PAHs from soil. A solvent mixture of 5% 1-pentanol, 10% water and 85% ethanol was selected as the extraction solvent. Using a 1g:4ml soil:solvent extraction ratio, extraction kinetics showed that from 65 to 90% of the extractable PAHs were removed within an hour of contact between soil and solvent. Using this 1g:4ml extraction ratio, PAHs were removed in a three-stage cross-current solvent washing process where the same batch of soil was extracted with clean solvent for 1h in each stage. PAH removals in three-stage cross-current solvent washing were comparable to PAH removals obtained with Soxhlet extraction.