Efficient degradation of 2,4,6-trichlorophenol using microbial fuel cell with MnFe2O4/PTFE@CF cathode

IF 9 1区 工程技术 Q1 ENGINEERING, CHEMICAL Separation and Purification Technology Pub Date : 2024-12-26 DOI:10.1016/j.seppur.2024.131308
Dong Yu , Qing Jiang , Tao Zhang , Hongqing Zhu , Hui Ma , Shengyan Pu
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Abstract

Chlorophenol contamination in groundwater is considered a significant environmental issue. The remediation of groundwater pollution using electrochemical catalytic technology is regarding as an economical and environmentally friendly method. This study developed a novel MnFe2O4/PTFE@CF electrode as a bioelectro-Fenton cathode for the degradation of 2,4,6-TCP. PTFE modification created a gas diffusion layer on the surface of the carbon felt current collector, enhancing the oxygen utilization rate and the performance of the two-electron reduction to generate H2O2 at the bioelectro-Fenton cathode. Additionally, the MnFe2O4 material, adhered to the carbon felt surface by PTFE, formed a bimetallic heterogeneous Fenton catalyst. Comparing the new MnFe2O4/PTFE@CF electrode with an unmodified CF electrode as the bioelectro-Fenton cathode for degrading 2,4,6-TCP, the heterogeneous system exhibited superior performance in terms of aeration rate, pH, and pollutant initial concentration. The MnFe2O4/PTFE@CF electrode showed degradation rates that were 27.81% and 46.5% higher than those of the individual iron and manganese oxide catalysts, respectively. After 70 h, the TOC mineralization rate reached 58.08%. Among the coexisting ions, Cl- promotes the degradation of pollutants, while SO42-、HCO3-和NO3- inhibit the degradation as their concentrations increase. Radical quenching experiments indicated that ·OH radicals produced from H2O2 playing a dominant role for the the degradation of 2,4,6-TCP. Specific degradation products were identified through GC–MS, and a reasonable degradation pathway was proposed based on these findings. After five cycles in the heterogeneous bioelectro-Fenton system, the degradation rate of 2,4,6-TCP remained over 70%, and less than 1% of iron and manganese ions leaching from the cathode was detected. In addition, the Microbial Fuel Cell with MnFe2O4/PTFE@CF Cathode was coupled with groundwater circulation well, and the remediation efficiency of 58.42% to 93.34% was achieved for 2,4,6-TCP in sandbox after 120 h.

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MnFe2O4/PTFE@CF阴极微生物燃料电池高效降解2,4,6-三氯苯酚
地下水中氯酚的污染被认为是一个重大的环境问题。利用电化学催化技术修复地下水污染是一种经济、环保的方法。本研究开发了一种新型的MnFe2O4/PTFE@CF电极作为降解2,4,6- tcp的生物电- fenton阴极。聚四氟乙烯改性在碳毡集流器表面形成气体扩散层,提高了氧利用率和生物电- fenton阴极双电子还原生成H2O2的性能。此外,将MnFe2O4材料通过PTFE粘附在碳毡表面,形成双金属非均相Fenton催化剂。将新制备的MnFe2O4/PTFE@CF电极与未修饰的CF电极作为降解2,4,6- tcp的生物电- fenton阴极进行比较,发现该非均相体系在曝气速率、pH值和污染物初始浓度方面表现出优越的性能。MnFe2O4/PTFE@CF电极的降解率分别比单独的铁氧化物和锰氧化物催化剂高27.81 %和46.5 %。70 h后TOC矿化率达到58.08 %。共存离子中Cl-对污染物的降解有促进作用,而SO42-、HCO3-和NO3-随着浓度的增加对污染物的降解有抑制作用。自由基猝灭实验表明,H2O2产生的·OH自由基对2,4,6- tcp的降解起主导作用。通过GC-MS鉴定了特定的降解产物,并在此基础上提出了合理的降解途径。在非均相生物电- fenton体系中循环5次后,2,4,6- tcp的降解率保持在70 %以上,阴极中铁和锰离子的浸出率低于1 %。此外,采用MnFe2O4/PTFE@CF阴极的微生物燃料电池与地下水循环耦合良好,对沙箱中2,4,6- tcp经过120 h的修复效率达到58.42 % ~ 93.34 %。
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来源期刊
Separation and Purification Technology
Separation and Purification Technology 工程技术-工程:化工
CiteScore
14.00
自引率
12.80%
发文量
2347
审稿时长
43 days
期刊介绍: Separation and Purification Technology is a premier journal committed to sharing innovative methods for separation and purification in chemical and environmental engineering, encompassing both homogeneous solutions and heterogeneous mixtures. Our scope includes the separation and/or purification of liquids, vapors, and gases, as well as carbon capture and separation techniques. However, it's important to note that methods solely intended for analytical purposes are not within the scope of the journal. Additionally, disciplines such as soil science, polymer science, and metallurgy fall outside the purview of Separation and Purification Technology. Join us in advancing the field of separation and purification methods for sustainable solutions in chemical and environmental engineering.
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