4.6 Article

Enhanced bioelectrochemical reduction of p-nitrophenols in the cathode of self-driven microbial fuel cells

期刊

RSC ADVANCES
卷 6, 期 35, 页码 29072-29079

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra04293g

关键词

-

资金

  1. National Science Foundation of China [51348007, 51508275, 51378261]
  2. Specialized Research Fund for the Doctoral Program of Higher Education [2013321912001]
  3. China Postdoctoral Science Foundation [2014M560426]
  4. Jiangsu Postdoctoral Science Foundation [1302100C]

向作者/读者索取更多资源

Reduction from p-nitrophenol (PNP) to p-aminophenol (PAP) was studied in the cathodes of self-driven microbial fuel cells (MFCs), and the influence of electron donor (CH3COONa) & acceptor concentration, external resistance and electrolyte conductivity were investigated. The results showed that PNP reduction efficiencies reached 100% when initial concentrations were lower than 50 mg L-1. PAP formation efficiencies were promoted from 31.7 + 2.1% to 76.4 + 4.1%, by increasing CH3COONa concentration from 2000 mg L-1 to 4000 mg L-1. Decreasing the external resistance from 1000 Omega to 240 Omega improved the PAP formation by 4-5 times for higher currents. Increasing the electrolyte conductivity (controlled by total dissolved solids, TDS) could accelerate the PNP degradation process within 24 h. Illumina high-throughput sequencing showed the dominating bacteria on the biocathodes were: Ignavibacterium 14.37%, Ottowia 4.04%, Pseudomonas 3.66%, Proteiniphilum 2.50%, Chlorobaculum 1.67%, Nitrospira 1.62% (at the genera level). The bacteria might play vital roles in more efficient nitrophenol degradation in biocathode MFCs. Compared to the abiotic control, the main advantages of PNP degradation in biocathodes are higher PNP reduction & PAP formation efficiencies, less electron donor consumption and higher system efficiency. The self-driven MFC system could be a promising way to deal with nitroaromatic pollutants.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据