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Received July 20, 2007
Accepted September 20, 2007
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Removal of volatile fatty acids (VFA) by microbial fuel cell with aluminum electrode and microbial community identification with 16S rRNA sequence
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology, 335 Gwahang-no, Yuseong-gu, Daejeon 305-701, Korea 1Department of Environmental Engineering, Dong-A University, 840 Hadan2-dong, Saha-gu, Busan 614-753, Korea
hnchang@kaist.ac.kr
Korean Journal of Chemical Engineering, May 2008, 25(3), 535-541(7), 10.1007/s11814-008-0090-6
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Abstract
Removal of volatile fatty acids in anaerobic digestion of organic wastes can accelerate eventual decomposition of organic wastes to CO2 and H2O using a recovery of electric energy by a microbial fuel cell. The fuel cell anode chamber was a 10 cm (I.D.)×20 cm long cylindrical Plexiglass having an ion ceramic cylinder separator (I.D.10 mm, O.D.12 mm, 0.3 μm average pore size). The aluminum foil cathode (12 cm2 surface area) was located inside the ceramic cylinder. Between the two cylinders, 1 liter of activated carbon particles was packed as anode electrode having a void fraction of 0.4. This fuel cell was connected to a 5 liter bioreactor (working volume 1.5 liter), and the bioreactor was run in batch mode by re-circulating a synthetic wastewater of 5 g/L glucose. Maximum TVFA (total volatile fatty acids) and SCOD (soluble chemical oxygen demand) removal rate were 3.79 g/L·day, 5.88 g/L·day, respectively. TVFA removal efficiency (92.7%) and SCOD removal efficiency (94.7%) under maximum current density operation were higher than the operation with maximum power density. In acid fermentation, butyric acid concentration was highest because Clostridium butyricum was a dominant microbial communitiy in the inoculum. The microbial cells collected from the anode bio-film samples were affiliated with Bacillus cereus based on the nucleotide sequences of dominant DGGE (denaturing gradient gel electrophoresis) bands.
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Daniel RB, Lovley DR, Appl. Environ. Microbiol., 71, 4 (2005)
Korneel R, Geert L, Steven DS, Willy V, Biotechnol. Lett., 25 (2003)
Park DH, Zeikus JG, Appl. Environ. Microbiol., 66, 4 (2000)
Kim HJ, Park HS, Hyun MS, Chang IS, Kim M, Kim BH, Enzyme Microb. Technol., 30 (2002)
Swades KC, Lovley DR, Nat. Biotechnol., 21, 10 (2003)
Lloyd JR, Sole VA, Lovley DR, Appl. Environ. Microbiol., 66, 9 (2000)
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DuVall SH, McCreery RL, Anal. Chem., 71 (1999)
Hernandez ME, Newman DK, Cell. Mol. Life Sci., 58 (2001)
Jaffari SA, Turner APF, Biosens. Bioelectron., 12 (1997)
Madigan MT, Brock biology of microorganisms, Prentice Hall (2000)
Larminie J, Dicks A, Fuel cell systems explained, John Wiley & Sons (2000)
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Gillan DC, Speksnijder AG, Zwart G, Ridder C, Appl. Environ. Microbiol., 64 (1998)
Shiru J, Haifeng Y, Yongxian L, Yujie D, Biotechnol. Bioprocess Eng., 12, 3 (2007)
Jung YJ, Yoo JS, Lee YS, Park IH, Kim SH, Lee SC, Masaaki Y, Chung SY, Choi YL, Biotechnol. Bioprocess Eng., 12, 3 (2007)
Ahn YH, Park EJ, Oh YK, Park SH, Webster G, Weightman AJ, FEMS Microbiol. Lett., 249, 1 (2005)
Anderson KL, Tayne TA, Ward DM, Appl. Environ. Microbiol., 53 (1987)
Choi YJ, Jung EK, Park HJ, Paik SR, Jung SH, Kim SH, Bull. Korean Chem. Soc., 25, 6 (2004)
Hur W, Chung YK, Biotechnol. Bioprocess Eng., 11, 6 (2006)
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