Bioelectrosynthesis of renewable energy carriers from carbon dioxide

从二氧化碳生物电合成可再生能源载体

• 批准号: RGPIN-2020-06279
• 负责人: Tartakovsky, Boris
• 金额: $ 2.04万
• 依托单位: École Polytechnique de Montréal
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2022
• 资助国家: 加拿大
• 起止时间: 2022-01-01 至 2023-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=753758
• 关键词: Bioelectrosynthesis; renewable; energy; carriers; carbon

Microbial electrosynthesis (bioelectrosynthesis) of renewable fuels is an emerging research area, which attracts significant attention of researchers, as can be evidenced from the exponential growth in the number of publications dedicated to this area. In microbial electrosynthesis, electroactive microorganisms catalyze cathodic reactions (e.g. CO2 reduction) acting as biocatalysts. Importantly, electroactive microorganisms were also shown to interact with metal catalysts resulting in enhanced bioreactions rates. Several bioelectrochemical cathodic transformations were demonstrated, including CO2 conversion to CH4 (electromethanogenesis) and electrosynthesis of C2-C4 compounds such as acetate, ethanol, and butanol. Although our knowledge of direct and indirect electron transfer mechanisms at the anode of such bioelectrochemical systems as microbial fuel cells (MFCs) significantly advanced in recent years, much less is known about the electron transfer mechanisms at a biocathode. Also, very few existing studies are dedicated to biocathode modeling. All existing studies on electromethanogenesis and production of C2-C4 compounds from CO2 are limited to laboratory-scale proof-of-concept demonstrations. In particular, multiple electromethanogenesis studies showed either an incomplete conversion of CO2 or presence of H2 catalytically (or biocatalytically) produced at the cathode. The proposed research program seeks to advance the understanding of bioelectrochemical processes and commercialization of CO2 conversion to renewable energy carriers by applying a thorough system engineering approach, where experimental work is combined with modelling and operational optimization aimed at maximizing yields, reducing operational costs, and developing practical control algorithms for stable system operation. The following objectives will be pursued (i) Enhanced understanding of pathways and electron transfer mechanisms, and identification of electroactive microorganisms capable of CO2 reduction to CH4 and C2-C4 compounds; (ii) Development of a dynamic mathematical model capable of adequate description of the biocathode kinetics and electroactive biofilm formation; (iii) application of the mathematical model to operational optimization and real-time control of the bioelectrosynthesis process, including experimental validation of the proposed on-line process control algorithms.

可再生燃料的微生物电合成（bioelectrosynthesis）是一个新兴的研究领域，吸引了研究人员的极大关注，这可以从致力于该领域的出版物数量的指数增长中得到证明。在微生物电合成中，电活性微生物作为生物催化剂催化阴极反应（例如CO2还原）。重要的是，电活性微生物也显示出与金属催化剂相互作用，从而提高生物反应速率。几个生物电化学阴极转化，包括CO2转化为CH 4（电产甲烷）和C2-C4化合物，如乙酸，乙醇和丁醇的电合成。尽管近年来我们对微生物燃料电池（MFC）等生物电化学系统阳极处的直接和间接电子转移机制的认识有了显著的进步，但对生物阴极处的电子转移机制知之甚少。此外，很少有现有的研究致力于生物阴极建模。所有现有的研究电产甲烷和生产的C2-C4化合物从CO2是有限的实验室规模的概念验证演示。特别地，多个电产甲烷研究显示在阴极处催化（或生物催化）产生的CO2的不完全转化或H2的存在。 拟议的研究计划旨在通过应用彻底的系统工程方法，将实验工作与建模和操作优化相结合，旨在最大限度地提高产量，降低运营成本，并开发实用的控制算法，以稳定系统运行，从而促进对生物电化学过程和CO2转化为可再生能源载体的商业化的理解。将实现以下目标：（一）加强对途径和电子转移机制的理解，并鉴定能够将CO2还原为CH 4和C2-C4化合物的电活性微生物;（二）开发能够充分描述生物阴极动力学和电活性生物膜形成的动态数学模型;（iii）将数学模型应用于生物电合成过程的操作优化和实时控制，包括对所提出的在线过程控制算法的实验验证。