期刊文献+

铝阳极海底沉积物电池的产电性能与应用 被引量:1

Power production of performance and application research of aluminum anode in submarine sediments
下载PDF
导出
摘要 普通海水电池,由于阳极金属的腐蚀速率过快,限制了该类电池的使用寿命。采用铝合金作阳极材料,分别置于海底沉积物与海水中,使用同种阴极来构建电池,测试了电池的相关性能并观察铝阳极沉积物电池驱动仪器运行的情况。对比结果表明沉积物中铝阳极腐蚀速率V-为0.966 g/(m2h),海水中为1.207 g/(m2h);沉积物中库仑效率CE为0.710,海水中为0.531。说明沉积物中电极的腐蚀速率减慢,使用寿命可被延长,产能效率提高。铝阳极沉积物电池开路电压1.35 V,比实验中的海水电池高约0.10 V,最大功率密度Pmax为20 W/m2,内阻28 W;外接升压器件后,输出电压至6 V以上,且升压器件最高功率转化率达0.608,表明升压效果良好且具有较高的功率转化效率。同时验证了铝阳极沉积物电池可有效驱动海洋仪器的运行,为以后的海洋实际应用提供了理论依据。 In consideration of the high corrosion rate, the calendar lifetime was limited for the seawater battery with sacrificial anode. Two type of battery using the same cathode were designed in the premise of aluminum anode, including the anode embedded in marine sediment and in seawater. The date of power performance was obtained by multimeter and the operation of instrument driven by the former was observed. The results demonstrate that the corrosion rates of aluminum anode is 0.966 g/(m^2h) in sediment, 1.207 g/(m^2h) in seawater, and the former is about 4/5 of it in seawater; the coulomb efficiency (CE) in sediment is 0.710, in seawater 0.531, respectively. The working time was increased and the replacement frequency of the anode was reduced. For sediment battery with aluminum anode, open circuit potential (OCP) was 1.35 V, 0.10 V higher than the seawater battery; the maximum power density (Pm) was 20 W/m^2, and the internal resistance was 28 Ω. The output voltage could reach up to 6 V by connecting the DC-DC converter, power conversion efficiency reached up to 0.608. By the experiment, the operation of the instrument can be driven by the aluminum anode in sediment. It was a basic a theory for the field application.
出处 《电源技术》 CAS CSCD 北大核心 2014年第11期2016-2018,2046,共4页 Chinese Journal of Power Sources
基金 国家海洋局可再生能源专项资金(GHME2011GD04)
关键词 铝阳极 沉积物电池 产电性能 仪器 aluminum anode sediment battery electrical performance instrument
  • 相关文献

参考文献17

  • 1AVINASH S, HALUK B, ZBIGNIEW L. Wireless sensors powered by microbial fuel cells [J]. Environmental Science & Technology, 2005,39 : 5037-5042.
  • 2TENDER L M, RIMERS C E, STECHER H A, et al. Harnessing mi- crobially generated power on the seafloor[J]. Nature Biotechnology, 2002,20(8): 821-825.
  • 3MATTHEW P, SEIDEL M D, DEGRANDPRE A G. A sensor for in situ indicator-based measurements of seawater pH[J]. Marine Che- mistry, 2008,109 : 18-28.
  • 4DELONG E F, CHANDLER P. Power from the deep [J]. Nature Biotechnology, 2002,20(8) : 788-789.
  • 5REIMERS C E, TENDER L M, FERTIG S, et al. Harvesting energy from the marine sediment-water interface[J].Environmental Science & Technology,2001,35(1) : 192-195.
  • 6DUMASA C, MOLLICA A, FERON D, et al.Marine microbial fuel cell:use of stainless steel electrodes as anode and cathode materials [J]. Electrochimica Acta, 2007,53 : 468-473.
  • 7LOGAN B E. Scaling up microbial fuel cells and other bio electro- chemical systems [J]. Applied Microbiology and Biotechnology, 2010, 85 : 1665-1671.
  • 8ZHISHENG L, DAOHAI X, XIANJUN Y, et al. Ruthenium oxide- coated carbon felt electrode: a highly active anode for microbial fuel cell applications[J]. Journal of Power Sources, 2012,210 : 26-31.
  • 9JESSICA K, SOUREN S, SKY M, et al. Microbial fuel cell biofilm characterization with thermogravimetrie analysis on bare and polye- thyleneimine surface modified carbon foam anodes [J]. Journal of Power Sources,2010,210: 122-128.
  • 10BESTAMIN O, BUSRA A, DOGAN K, et al.Bioelectricity produc- tion using a new electrode in a microbial fuel cell [J]. Bioprocess and Biosystems Engineering, 2012,35 : 1219-1227.

同被引文献17

  • 1Holmes D E, Bond D R, Oniel R A, et al. Microbial communities associated with electrodes harvesting e- lectricity from a variety of aquatic sediments [ J ]. Microbial Ecology,2004,48 : 178-190.
  • 2Yong J Z, Cui L X,Li N Y, et al. A mediatorless mi- crobial fuel cell using polypyrrole coated carbon nano- tubes composite as anode material [ J ]. International Journal of Hydrogen Energy,2008,33:4856-4862.
  • 3Dan Z, Qi Qi D, Xiang W, et al. Preparation of a three-dimensional ordered macroporous carbon nano- tube/polypyrrole composite for supercapacitors and diffusion modeling [J]. J. Phys. Chem. C. ,2013,9 (9) :1021-1031.
  • 4Xin Y Z, Sanjeev K M. Narrow Pore-Diameter Poly- pyrrole Nanotubes [ J ]. J. Am. Chem. Soc. , 2005, 127 : 14156-14157.
  • 5Kirk J Z, Zhen N G, Hai Q P, et al. Controlled oxida- tive cutting of single-walled carbon nanotubes [ J ]. J. Am. Chem. Soc. ,2005,127:1541 J1547.
  • 6Min L, Shailesh K, How Y N, et al. Carbon nanotube supported MnO2 catalysts for oxygen reduction reac-tion and their applications in microbial fuel cells [ J ]. Biosensors and Bioelectronics ,2011,26:4728-4732.
  • 7Pejman H T, George P S. Electropolymerization of polypyrrole/carbon nanotube nanocomposite films o- ver an electrically nonconductive membrane [ J ]. Phys. Chem. C. ,2010,114:13962-13966.
  • 8Mark H, George Z C, Milo S P S, et al. Electrochem- ical capacitance of a nanoporous composite of carbon nanotubes and polypyrrole [ J ] . Chem. Mater. , 2002,14 : 1610-1613.
  • 9Junyeong A, Bongkyu K, Jonghyeon N, et al. Com- parison in performance of sediment microbial fuel cells according to depth of embedded anode [ J ]. Bioresource Technology,2013,127 : 138-142.
  • 10傅清宾,高博,苏凌浩,原长洲,卢向军,张校刚.氢键诱导的聚吡咯/苯磺酸功能化多壁碳纳米管的制备及其电化学行为[J].物理化学学报,2009,25(11):2199-2204. 被引量:4

引证文献1

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部