Liu Hong, Cheng Shaoan, Logan Bruce E
Department of Civil and Environmental Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Environ Sci Technol. 2005 Jan 15;39(2):658-62. doi: 10.1021/es048927c.
Hydrogen can be recovered by fermentation of organic material rich in carbohydrates, but much of the organic matter remains in the form of acetate and butyrate. An alternative to methane production from this organic matter is the direct generation of electricity in a microbial fuel cell (MFC). Electricity generation using a single-chambered MFC was examined using acetate or butyrate. Power generated with acetate (800 mg/L) (506 mW/m2 or 12.7 mW/ L) was up to 66% higher than that fed with butyrate (1000 mg/L) (305 mW/m2 or 7.6 mW/L), demonstrating that acetate is a preferred aqueous substrate for electricity generation in MFCs. Power output as a function of substrate concentration was well described by saturation kinetics, although maximum power densities varied with the circuit load. Maximum power densities and half-saturation constants were Pmax = 661 mW/m2 and Ks = 141 mg/L for acetate (218 ohms) and Pmax = 349 mW/m2 and Ks = 93 mg/L for butyrate (1000 ohms). Similar open circuit potentials were obtained in using acetate (798 mV) or butyrate (795 mV). Current densities measured for stable power outputwere higher for acetate (2.2 A/m2) than those measured in MFCs using butyrate (0.77 A/m2). Cyclic voltammograms suggested that the main mechanism of power production in these batch tests was by direct transfer of electrons to the electrode by bacteria growing on the electrode and not by bacteria-produced mediators. Coulombic efficiencies and overall energy recovery were 10-31 and 3-7% for acetate and 8-15 and 2-5% for butyrate, indicating substantial electron and energy losses to processes other than electricity generation. These results demonstrate that electricity generation is possible from soluble fermentation end products such as acetate and butyrate, but energy recoveries should be increased to improve the overall process performance.
富含碳水化合物的有机物质通过发酵可回收氢气,但大部分有机物质仍以乙酸盐和丁酸盐的形式存在。利用这种有机物质生产甲烷的替代方法是在微生物燃料电池(MFC)中直接发电。使用单室MFC,以乙酸盐或丁酸盐为原料进行发电实验。以乙酸盐(800毫克/升)发电时的功率(506毫瓦/平方米或12.7毫瓦/升)比以丁酸盐(1000毫克/升)发电时的功率(305毫瓦/平方米或7.6毫瓦/升)高出66%,这表明乙酸盐是MFC中发电的首选水性底物。尽管最大功率密度随电路负载而变化,但功率输出与底物浓度的函数关系可用饱和动力学很好地描述。乙酸盐(218欧姆)的最大功率密度和半饱和常数分别为Pmax = 661毫瓦/平方米和Ks = 141毫克/升,丁酸盐(1000欧姆)的最大功率密度和半饱和常数分别为Pmax = 349毫瓦/平方米和Ks = 93毫克/升。使用乙酸盐(798毫伏)或丁酸盐(795毫伏)时获得了相似的开路电位。对于稳定功率输出,乙酸盐的电流密度(2.2安/平方米)高于使用丁酸盐的MFC中的电流密度(0.77安/平方米)。循环伏安图表明,这些分批试验中发电的主要机制是在电极上生长的细菌将电子直接转移到电极上,而不是通过细菌产生的介质。乙酸盐的库仑效率和总能量回收率分别为10 - 31%和3 - 7%,丁酸盐的库仑效率和总能量回收率分别为8 - 15%和2 - 5%,这表明除发电外,电子和能量在其他过程中大量损失。这些结果表明,利用乙酸盐和丁酸盐等可溶性发酵终产物发电是可行的,但应提高能量回收率以改善整体工艺性能。