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在微生物燃料电池中,以电活性生物膜与N-MnO修饰的层状双氢氧化物作为阴极耦合降解甲砜霉素。

Degradation of thiamphenicol by electroactive biofilm coupled with N-MnO modified layer double hydroxides as cathode in microbial fuel cell.

作者信息

Chen Junfeng, Xu Yuling, Zhang Xinyi, Lan Feng, Cao Yuchen, Liu Yanyan, Wang Renjun, Yang Yuewei

机构信息

School of Life Sciences, Qufu Normal University, Qufu, 273165, PR China.

School of Life Sciences, Qufu Normal University, Qufu, 273165, PR China.

出版信息

J Environ Manage. 2025 Sep;391:126649. doi: 10.1016/j.jenvman.2025.126649. Epub 2025 Jul 19.

DOI:10.1016/j.jenvman.2025.126649
PMID:40684587
Abstract

N-doped MnO composite NiAl-Layer double hydroxides (N-MnO@NiAl-LDH) with a ping-pong chrysanthemum like structure was prepared by hydrothermal method as a cathode catalyst in microbial fuel cells (MFCs) in previous study, which demonstrating excellent catalytic performance. This study investigated the power generation performance and the degradation of thiamphenicol (TAP) in N-MnO@NiAl-LDH-cathode MFC. After the addition of TAP, the maximum power density generated by N-MnO@NiAl-LDH-cathode MFC was 537.83 mW/m, which was 5.1 times higher than control MFC. The degradation rate of TAP by N-MnO@NiAl-LDH-cathode was 81.62 %, which was 2.7 times higher than that of unmodified MFC, the degradation efficiency was significantly improved. Microorganisms were significantly affected by TAP, the abundance of electroactive bacteria (Pseudomonas) decreased, while bacteria related to the biodegradation of TAP (Sphingopyxis, Aridibacter, Norank_ Minicenantales, Petrimonas, etc.) were enriched. The modification of N-MnO@NiAl-LDH reduced the internal resistance of MFC and accelerated the electron transfer rate, the large specific surface area provided more active sites for electrons, allowing more electrons to be transferred to the cathode. Under the reduction effect of electrons, chlorine atoms of TAP were gradually removed. Meanwhile, a large number of degrading bacteria were attached to the cathode, the dechlorination products underwent C-C bond cleavage and benzene ring opening under the biodegradation of degrading bacteria. The combined effect of electron reduction and microbial oxidation promoted the efficient degradation of TAP.

摘要

在先前的研究中,通过水热法制备了具有乒乓菊状结构的氮掺杂MnO复合镍铝层状双氢氧化物(N-MnO@NiAl-LDH)作为微生物燃料电池(MFC)的阴极催化剂,其表现出优异的催化性能。本研究考察了N-MnO@NiAl-LDH阴极MFC的发电性能及对甲砜霉素(TAP)的降解情况。添加TAP后,N-MnO@NiAl-LDH阴极MFC产生的最大功率密度为537.83 mW/m²,比对照MFC高5.1倍。N-MnO@NiAl-LDH阴极对TAP的降解率为81.62%,比未改性MFC高2.7倍,降解效率显著提高。微生物受到TAP的显著影响,电活性细菌(假单胞菌属)的丰度降低,而与TAP生物降解相关的细菌(鞘氨醇单胞菌属、干旱杆菌属、诺卡氏菌属、Petrimonas等)则富集。N-MnO@NiAl-LDH的改性降低了MFC的内阻,加速了电子传递速率,大比表面积为电子提供了更多活性位点,使更多电子能够转移到阴极。在电子的还原作用下,TAP的氯原子逐渐被去除。同时,大量降解细菌附着在阴极上,脱氯产物在降解细菌的生物降解作用下发生C-C键断裂和苯环开环。电子还原和微生物氧化的协同作用促进了TAP的高效降解。

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