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阴极析氢速率对 CO 生物电化学还原为乙酸盐的影响。

Effect of different hydrogen evolution rates at cathode on bioelectrochemical reduction of CO to acetate.

机构信息

Beijing Key Laboratory for Source Control Technology of Water Pollution, Engineering Research Center for Water Pollution Source Control and Eco-remediation, College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China.

School of Environmental Science & Engineering, Shandong Key Laboratory of Water Pollution Control and Resource Reuse, Environment Research Institute, Shandong University, Qingdao 266237, PR China.

出版信息

Sci Total Environ. 2024 Feb 25;913:169744. doi: 10.1016/j.scitotenv.2023.169744. Epub 2024 Jan 3.

Abstract

Microbial electrosynthesis (MES) offers a promising approach for converting CO into valuable chemicals such as acetate. However, the relative low conversion rate severely limits its practical application. This study investigated the impact of different hydrogen evolution rates on the conversion rate of CO to acetate in the MES system. Three potentials (-0.8 V, -0.9 V and -1.0 V) corresponding to various hydrogen evolution rates were set and analyzed, revealing an optimal hydrogen evolution rate, yielding a maximum acetate formation rate of 1410.9 mg/L and 73.5 % coulomb efficiency. The electrochemical findings revealed that an optimal hydrogen evolution rate facilitated the formation of an electroactive biofilm. The microbial community of the cathode biofilm highlighted key genera, including Clostridium and Acetobacterium, which played essential roles in electrosynthesis within the MES system. Notably, a low hydrogen evolution rate failed to provide sufficient energy for the electrochemical reduction of CO to acetate, while a high rate led to cathode alkalinization, impeding the reaction and causing significant energy wastage. Therefore, maintaining an appropriate hydrogen evolution rate is crucial for the development of mature electroactive biofilms and achieving optimal performance in the MES system.

摘要

微生物电解合成(MES)为将 CO 转化为有价值的化学物质(如乙酸盐)提供了一种很有前景的方法。然而,相对较低的转化率严重限制了其实际应用。本研究探讨了不同析氢速率对 MES 系统中 CO 转化为乙酸盐的转化率的影响。设置并分析了三个对应的电位(-0.8 V、-0.9 V 和-1.0 V),揭示了一个最佳的析氢速率,产生了 1410.9 mg/L 的最大乙酸盐生成速率和 73.5%的库仑效率。电化学研究结果表明,最佳的析氢速率有利于形成电活性生物膜。阴极生物膜中的微生物群落突出了关键属,包括梭菌属和乙酸菌属,它们在 MES 系统中的电合成中发挥了重要作用。值得注意的是,低析氢速率无法为 CO 电化学还原为乙酸盐提供足够的能量,而高速率则会导致阴极碱化,阻碍反应并造成大量能量浪费。因此,保持适当的析氢速率对于成熟电活性生物膜的发展和 MES 系统的最佳性能至关重要。

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