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2,4,6‐Trichlorophenol and phenol removal in methanogenic and partially‐aerated methanogenic conditions in a fluidized bed bioreactor
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Citations
26
References
2005
Year
EngineeringPhenol RemovalBiological Waste TreatmentAnaerobic DigestionSimilar TcpWastewater TreatmentPartially‐aerated Methanogenic ConditionsChemical EngineeringBioremediationBiochemical EngineeringWater TreatmentEnvironmental MicrobiologyPam Conditions 4CpSeparation TechnologyWastewater ManagementIndustrial WastewaterWaste ManagementWater TechnologyEnvironmental EngineeringPretreatmentEnvironmental RemediationWater PurificationFluidized Bed Bioreactor
Abstract A fluidized bed bioreactor (FBBR) was operated for more than 575 days to remove 2,4,6‐trichlorophenol (TCP) and phenol (Phe) from a synthetic toxic wastewater containing 80 mg L −1 of TCP and 20 mg L −1 of Phe under two regimes: Methanogenic (M) and Partially‐Aerated Methanogenic (PAM). The mesophilic, laboratory‐scale FBBR consisted of a glass column (3 L capacity) loaded with 1 L of 1 mm diameter granular activated carbon colonized by an anaerobic consortium. Sucrose (1 g COD L −1 ) was used as co‐substrate in the two conditions. The hydraulic residence time was kept constant at 1 day. Both conditions showed similar TCP and Phe removal (99.9 + %); nevertheless, in the Methanogenic regime, the accumulation of 4‐chlorophenol (4CP) up to 16 mg L −1 and phenol up to 4 mg L −1 was observed, whereas in PAM conditions 4CP and other intermediates were not detected. The specific methanogenic activity of biomass decreased from 1.01 ± 0.14 in M conditions to 0.19 ± 0.06 mmolCH 4 h −1 gTKN −1 in PAM conditions whereas the specific oxygen uptake rate increased from 0.039 ± 0.008 in M conditions to 0.054 ± 0.012 mmolO 2 h −1 gTKN −1 , which suggested the co‐existence of both methanogenic archaea and aerobic bacteria in the undefined consortium. The advantage of the PAM condition over the M regime is that it provides for the thorough removal of less‐substituted chlorophenols produced by the reductive dehalogenation of TCP rather than the removal of the parent compound itself. Copyright © 2005 Society of Chemical Industry
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