Lakshmi Pathi Thulluru, Anil Dhanda, Manikanta M. Doki, Makarand M. Ghangrekar and Shamik Chowdhury
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Additionally, key structural properties, such as elevated specific surface area, abundant surface functional groups, and the presence of nitrogen in the form of pyridinic and graphitic nitrogen, are primarily responsible for enhancing the organic product synthesis in MES. Furthermore, the hydrochar composite catalyzed MES resulted in an acetate production of 41.14 ± 5.03 mM L<small><sup>−1</sup></small>, which was nearly twice that of the uncatalyzed MES. Moreover, the current and carbon recovery efficiencies were found to be 52.44% and 45.44%, which were 1.47 and 2.44 times that of uncatalyzed MES. 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引用次数: 0
摘要
微生物电合成(MES)是一项先进的技术,可以将二氧化碳(CO2)隔离,以生产高价值的多碳有机化合物。然而,有限的有机生产速度是主要的瓶颈,限制了该技术的实际应用。为了克服这一挑战,本研究探索了污泥衍生的碳氢化合物作为阴极催化剂,以增强MES中的二氧化碳生物还原。以厌氧污泥(ANS)和明矾污泥(ALS)为原料合成的复合炭具有较高的极限电流密度和较低的电荷转移电阻等优异的电化学性能。此外,关键的结构特性,如提高的比表面积,丰富的表面官能团,以及氮以吡啶和石墨氮的形式存在,是提高MES中有机产物合成的主要原因。此外,烃类复合催化剂催化MES的乙酸产量为41.14±5.03 mM L−1,是未催化MES的近两倍。电回收率和碳回收率分别为52.44%和45.44%,分别是未催化MES的1.47倍和2.44倍。这些结果表明,污泥衍生的碳氢化合物有潜力作为一种有前途的阴极电催化剂,在MES中加强二氧化碳的生物还原。
Sludge-derived hydrochar as a potential electrocatalyst for improved CO2 reduction in microbial electrosynthesis†
Microbial electrosynthesis (MES) is a progressive technology that can sequester carbon dioxide (CO2) to produce high-value multi-carbon organic compounds. However, the limited organic production rate is the primary bottleneck, limiting the real-life application of this technology. To overcome this challenge, the present investigation explores sludge-derived hydrochar as a cathode catalyst to enhance CO2 bioreduction in MES. The hydrochar composite synthesized using anaerobic sludge (ANS) and alum sludge (ALS) exhibited excellent electrochemical properties with higher limiting current density and lower charge transfer resistance. Additionally, key structural properties, such as elevated specific surface area, abundant surface functional groups, and the presence of nitrogen in the form of pyridinic and graphitic nitrogen, are primarily responsible for enhancing the organic product synthesis in MES. Furthermore, the hydrochar composite catalyzed MES resulted in an acetate production of 41.14 ± 5.03 mM L−1, which was nearly twice that of the uncatalyzed MES. Moreover, the current and carbon recovery efficiencies were found to be 52.44% and 45.44%, which were 1.47 and 2.44 times that of uncatalyzed MES. These results demonstrate the potential of sludge-derived hydrochar as a promising cathode electrocatalyst for enhancing CO2 bioreduction in MES.