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Multiple electron transfer systems in oxygen reducing biocathodes revealed by different conditions of aeration/agitation

机译:曝气/搅动条件不同显示氧气还原生物阴极中的多个电子转移系统

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Oxygen reducing biocathodes were formed at -02 V/SCE (+ 0.04 V/SHE) from compost leachate. Depending on whether aeration was implemented or not, two different redox systems responsible for the electrocatalysis of oxygen reduction were evidenced. System I was observed at low potential (-0.03 V/SHE) on cyclic voltammetries (CVs). It appeared during the early formation of the biocathode (few hours) and resisted the hydrodynamic conditions induced by the aeration. System II was observed at higher potential on CV (+0.46 V/SHE); it required a longer lag time (up to 10 days) and quiescent conditions to produce an electrochemical signal. The hydrodynamic effects produced by the forced aeration led to its extinction. From their different behaviors and examples in the literature, system I was identified as being a membrane-bound cytochrome-related molecule, while system II was identified as a soluble redox mediator excreted by the biofilm. This study highlighted the importance of controlling the local hydrodynamics to design efficient oxygen reducing biocathodes able to operate at high potential. (C) 2016 Elsevier B.V. All rights reserved.
机译:从堆肥渗滤液中以-02 V / SCE(+ 0.04 V / SHE)形成了减少氧气的生物阴极。根据是否进行通气,证明了两个不同的氧化还原系统负责电催化还原氧气。在循环伏安法(CV)上以低电势(-0.03 V / SHE)观察到系统I。它出现在生物阴极的早期形成(几个小时)中,并且抵抗了通气引起的流体动力学条件。观察到系统II的CV电位较高(+0.46 V / SHE);它需要更长的延迟时间(最多10天)和静态条件才能产生电化学信号。强制曝气产生的水力效应导致其灭绝。从它们的不同行为和文献中的实例来看,系统I被确定为与膜结合的细胞色素相关分子,而系统II被确定为被生物膜排泄的可溶性氧化还原介体。这项研究强调了控制局部流体动力学以设计能够在高电势下运行的高效降氧生物阴极的重要性。 (C)2016 Elsevier B.V.保留所有权利。

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