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Electrochemically enhanced microbial CO conversion to volatile fatty acids using neutral red as an electron mediator

Authors
Im, Chae HoKim, ChangmanSong, Young EunOh, Sang-EunJeon, Byong HunKim, Jung Rae
Issue Date
Jan-2018
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Carbon monoxide; Bioelectrochemical system; Neutral red; Electrosynthesis; Biological CO conversion; Reducing equivalent
Citation
CHEMOSPHERE, v.191, pp.166 - 173
Indexed
SCIE
SCOPUS
Journal Title
CHEMOSPHERE
Volume
191
Start Page
166
End Page
173
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150707
DOI
10.1016/j.chemosphere.2017.10.004
ISSN
0045-6535
Abstract
Conversion of Cl gas feedstock, including carbon monoxide (CO), into useful platform chemicals has attracted considerable interest in industrial biotechnology. Nevertheless, the low conversion yield and/or growth rate of CO-utilizing microbes make it difficult to develop a C1 gas biorefinery process. The WoodLjungdahl pathway which utilize CO is a pathway suffered from insufficient electron supply, in which the conversion can be increased further when an additional electron source like carbohydrate or hydrogen is provided. In this study, electrode-based electron transference using a bioelectrochemical system (BES) was examined to compensate for the insufficient reducing equivalent and increase the production of volatile fatty acids. The BES including neutral red (BES-NR), which facilitated electron transfer between bacteria and electrode, was compared with BES without neutral red and open circuit control. The coulombic efficiency based on the current input to the system and the electrons recovered into VFAs, was significantly higher in BES-NR than the control. These results suggest that the carbon electrode provides a platform to regulate the redox balance for improving the bioconversion of CO, and amending the conventional C1 gas fermentation.
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Jeon, Byong Hun
COLLEGE OF ENGINEERING (DEPARTMENT OF EARTH RESOURCES AND ENVIRONMENTAL ENGINEERING)
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