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表面活性剂改性沉积物基生物电化学系统中阴极生物膜的电化学特性及随时间变化的细菌群落特征对增强 2,3,4,5-四氯联苯脱氯的影响。

Time-dependent bacterial community and electrochemical characterizations of cathodic biofilms in the surfactant-amended sediment-based bioelectrochemical reactor with enhanced 2,3,4,5-tetrachlorobiphenyl dechlorination.

机构信息

The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, School of Environment and Energy, South China University of Technology, Guangzhou 510006, PR China.

The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, School of Environment and Energy, South China University of Technology, Guangzhou 510006, PR China; Guangdong Provincial Engineering and Technology Research Center for Environmental Risk Prevention and Emergency Disposal, South China University of Technology, Guangzhou 510006, PR China.

出版信息

Environ Pollut. 2018 May;236:343-354. doi: 10.1016/j.envpol.2018.01.048.

DOI:10.1016/j.envpol.2018.01.048
PMID:29414357
Abstract

Applying an electric field to stimulate the microbial reductive dechlorination of polychlorinated biphenyls (PCBs) represents a promising approach for bioremediation of PCB-contaminated sites. This study aimed to demonstrate the biocathodic film-facilitated reduction of PCB 61 in a sediment-based bioelectrochemical reactor (BER) and, more importantly, the characterizations of electrode-microbe interaction from microbial and electrochemical perspectives particularly in a time-dependent manner. The application of a cathodic potential (-0.45 V vs. SHE) significantly improved the rate and extent of PCB 61 dechlorination compared to the open-circuit scenario (without electrical stimulation), and the addition of an external surfactant further increased the dechlorination, with Tween 80 exerting more pronounced effects than rhamnolipid. The bacterial composition of the biofilms and the bioelectrochemical kinetics of the BERs were found to be time-dependent and to vary considerably with the incubation time and slightly with the coexistence of an external surfactant. Excellent correlations were observed between the dechlorination rate and the relative abundance of Dehalogenimonas, Dechloromonas, and Geobacter, the dechlorination rate and the cathodic current density recorded from the chronoamperometry tests, and the dechlorination rate and the charge transfer resistance derived from the electrochemical impedance tests, with respect to the 120 day-operation. After day 120, PCB 61 was resistant to further appreciable reduction, but substantial hydrogen production was detected, and the bacterial community and electrochemical parameters observed on day 180 were not distinctly different from those on day 120.

摘要

施加电场刺激微生物还原脱氯多氯联苯 (PCBs) 代表了受 PCB 污染场地生物修复的一种很有前途的方法。本研究旨在展示基于沉积物的生物电化学反应器 (BER) 中生物阴极膜促进 PCB 61 的还原,更重要的是,从微生物和电化学角度特别是在时间依赖的方式下,对电极-微生物相互作用进行特征描述。与开路(无电刺激)相比,施加阴极电势(相对于 SHE 为-0.45 V)可显著提高 PCB 61 脱氯的速率和程度,并且添加外部表面活性剂进一步增加了脱氯程度,吐温 80 的效果比鼠李糖脂更为明显。生物膜的细菌组成和 BER 的生物电化学动力学是时间依赖的,并且随孵育时间变化很大,与外部表面活性剂的共存略有变化。在 120 天的运行过程中,脱氯速率与 Dehalogenimonas、Dechloromonas 和 Geobacter 的相对丰度之间存在极好的相关性,脱氯速率与恒电流计时安培测试记录的阴极电流密度之间存在极好的相关性,脱氯速率与电化学阻抗测试得出的电荷转移电阻之间存在极好的相关性。在第 120 天后,PCB 61 不再容易进一步脱氯,但检测到大量的氢气产生,第 180 天的细菌群落和电化学参数与第 120 天没有明显的区别。

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