Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4364
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dc.contributor.authorRoy, Moumita-
dc.contributor.authorYadav, Ravineet-
dc.contributor.authorChiranjeevi, P.-
dc.contributor.authorPatil, Sunil A.-
dc.date.accessioned2023-08-05T06:26:29Z-
dc.date.available2023-08-05T06:26:29Z-
dc.date.issued2021-
dc.identifier.citationBioresource Technology, 320, 124289.en_US
dc.identifier.urihttps://doi.org/10.1016/j.biortech.2020.124289-
dc.identifier.urihttp://hdl.handle.net/123456789/4364-
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractThe present study aimed to demonstrate the utilization of unpurified industrial CO2 with low impurities for acetate production via microbial electrosynthesis (MES) for the first time. In MES experiments with CO2-rich brewery gas, the enriched mixed culture dominated by Acetobacterium produced 1.8 ± 0.2 g/L acetic acid at 0.26 ± 0.03 g/Lcatholyte/d rate and outperformed a pure culture of Clostridium ljungdahlii (1.1 ± 0.02 g/L; 0.138 ± 0.004 g/Lcatholyte/d). The electron recovery in acetic acid was also more for mixed culture (84 ± 13%) than C. ljungdahlii (42 ± 14%). Electrochemical analysis of biocathodes suggested the role of microbial biofilm in improved hydrogen electrocatalysis. In comparative gas fermentation tests, the mixed culture outperformed C. ljungdahlii and produced acetic acid at a similar level with both industrial and pure CO2 feedstocks. These results suggest the robustness and capability of the mixed microbial community for utilizing slightly impure industrial CO2 for bioproduction and presents a major advancement in MES technology.en_US
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.subjectCarbon capture and utilization (CCU)en_US
dc.subjectWood-Ljungdahl pathwayen_US
dc.subjectElectricity-driven bioproductionen_US
dc.subjectAcetic aciden_US
dc.subjectBioelectrochemical systemen_US
dc.titleDirect utilization of industrial carbon dioxide with low impurities for acetate production via microbial electrosynthesisen_US
dc.typeArticleen_US
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