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基于电渗透的微生物燃料电池阴极液制备用于碳捕获。

Electro-osmotic-based catholyte production by Microbial Fuel Cells for carbon capture.

机构信息

Bristol BioEnergy Centre, Bristol Robotics Laboratory, Block T, UWE, Coldharbour Lane, Bristol BS16 1QY, UK.

Bristol BioEnergy Centre, Bristol Robotics Laboratory, Block T, UWE, Coldharbour Lane, Bristol BS16 1QY, UK; Biological, Biomedical and Analytical Sciences, UWE, Coldharbour Lane, Bristol BS16 1QY, UK.

出版信息

Water Res. 2015 Dec 1;86:108-15. doi: 10.1016/j.watres.2015.08.014. Epub 2015 Aug 12.

DOI:10.1016/j.watres.2015.08.014
PMID:26343045
Abstract

In Microbial Fuel Cells (MFCs), the recovery of water can be achieved with the help of both active (electro-osmosis), and passive (osmosis) transport pathways of electrolyte through the semi-permeable selective separator. The electrical current-dependent transport, results in cations and electro-osmotically dragged water molecules reaching the cathode. The present study reports on the production of catholyte on the surface of the cathode, which was achieved as a direct result of electricity generation using MFCs fed with wastewater, and employing Pt-free carbon based cathode electrodes. The highest pH levels (>13) of produced liquid were achieved by the MFCs with the activated carbon cathodes producing the highest power (309 μW). Caustic catholyte formation is presented in the context of beneficial cathode flooding and transport mechanisms, in an attempt to understand the effects of active and passive diffusion. Active transport was dominant under closed circuit conditions and showed a linear correlation with power performance, whereas osmotic (passive) transport was governing the passive flux of liquid in open circuit conditions. Caustic catholyte was mineralised to a mixture of carbonate and bicarbonate salts (trona) thus demonstrating an active carbon capture mechanism as a result of the MFC energy-generating performance. Carbon capture would be valuable for establishing a carbon negative economy and environmental sustainability of the wastewater treatment process.

摘要

在微生物燃料电池 (MFC) 中,通过半透选择性分离器中的电解质的主动(电渗析)和被动(渗透)传输途径可以实现水的回收。电流依赖性传输导致阳离子和电渗析拖曳的水分子到达阴极。本研究报告了在阴极表面上产生的阴极电解液,这是使用 MFC 从废水中发电并采用无 Pt 的碳基阴极电极直接实现的。用活性炭阴极产生的 MFC 实现了最高的 pH 值 (>13),产生的功率最高 (309 μW)。苛性阴极电解液的形成是在有益的阴极淹没和传输机制的背景下提出的,试图理解主动和被动扩散的影响。在闭路条件下,主动运输占主导地位,并且与功率性能呈线性相关,而在开路条件下,渗透压(被动)运输控制着液体的被动通量。苛性阴极电解液被矿化为碳酸盐和碳酸氢盐(天然碱)的混合物,因此证明了由于 MFC 发电性能而导致的活性炭捕获机制。碳捕获对于建立碳负经济和废水处理过程的环境可持续性将是有价值的。

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