Production of hydrogen from domestic wastewater using a bioelectrochemically assisted microbial reactor (BEAMR)

被引:261
作者
Ditzig, Jenna [1 ]
Liu, Hong [1 ]
Logan, Bruce E. [1 ]
机构
[1] Penn State Univ, Penn State Hydrogen Energy H2E Ctr, University Pk, PA 16802 USA
基金
美国国家科学基金会;
关键词
hydrogen; wastewater; treatment; electrochemical; electrolysis; bacteria;
D O I
10.1016/j.ijhydene.2007.02.035
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrogen production from domestic wastewater was examined using a plain carbon electrode or graphite-granule packed-bed bioelectrochemically assisted microbial reactors (BEAMRs) capable of continuous or intermittent hydrogen release. When graphite granules were added to the anode chamber (packed-bed mode) current density was increased when the domestic wastewater had a high initial chemical oxygen demand (COD > 360 mg/L), and produced a maximum Coulombic efficiency of 26% (applied voltage of 0.41 V) and a maximum hydrogen recovery of 42% (applied voltage of 0.5 V). The packed-bed system successfully treated the wastewater, with removal efficiencies of biochemical oxygen demand (BOD), chemical oxygen demand (COD), and dissolved organic carbon (DOC) in the range of 87-100%. The final BOD of the treated wastewater was always reduced to less than 7.0 +/- 0.2 mg/L. Overall hydrogen production based on COD removal was a maximum of 0.0125 mg-H-2/mg-COD (154 mL-H-2/g-COD versus a maximum possible conversion of 0.126 mg-H-2/mg-COD), with an energy requirement equivalent to 0.0116 mg-H-2/mg-COD, producing an 8% net yield of H-2. These results demonstrate that a wastewater treatment based on a BEAMR reactor is feasible, but improvements are needed in hydrogen recoveries and Coulombic efficiencies to increase the overall hydrogen yield. (C) 2007 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2296 / 2304
页数:9
相关论文
共 20 条
[1]  
*AM PUBL HLTH ASS, 1995, WAT POLL CONTR FED
[2]  
*EPA, EPA ONS WAST TREATM
[3]   Electricity generation from artificial wastewater using an upflow microbial fuel cell [J].
He, Z ;
Minteer, SD ;
Angenent, LT .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (14) :5262-5267
[4]  
HEILMANN J, 2005, MICROBIAL FUEL CELLS
[5]   Production of electricity from proteins using a microbial fuel cell [J].
Heilmann, Jenna ;
Logan, Bruce E. .
WATER ENVIRONMENT RESEARCH, 2006, 78 (05) :531-537
[6]   HALIDE AND SULFATE ION DIFFUSION IN NAFION MEMBRANES [J].
HERRERA, A ;
YEAGER, HL .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1987, 134 (10) :2446-2451
[7]   A mediator-less microbial fuel cell using a metal reducing bacterium, Shewanella putrefaciense [J].
Kim, HJ ;
Park, HS ;
Hyun, MS ;
Chang, IS ;
Kim, M ;
Kim, BH .
ENZYME AND MICROBIAL TECHNOLOGY, 2002, 30 (02) :145-152
[8]   Electrochemically assisted microbial production of hydrogen from acetate [J].
Liu, H ;
Grot, S ;
Logan, BE .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (11) :4317-4320
[9]   Production of electricity from acetate or butyrate using a single-chamber microbial fuel cell [J].
Liu, H ;
Cheng, SA ;
Logan, BE .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (02) :658-662
[10]   Electricity generation using an air-cathode single chamber microbial fuel cell in the presence and absence of a proton exchange membrane [J].
Liu, H ;
Logan, BE .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (14) :4040-4046