H2 mediated mixed culture microbial electrosynthesis for high titer acetate production from CO2

IF 14 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Environmental Science and Ecotechnology Pub Date : 2023-09-28 DOI:10.1016/j.ese.2023.100324
Yanhong Bian , Aaron Leininger , Harold D. May , Zhiyong Jason Ren
{"title":"H2 mediated mixed culture microbial electrosynthesis for high titer acetate production from CO2","authors":"Yanhong Bian ,&nbsp;Aaron Leininger ,&nbsp;Harold D. May ,&nbsp;Zhiyong Jason Ren","doi":"10.1016/j.ese.2023.100324","DOIUrl":null,"url":null,"abstract":"<div><p>Microbial electrosynthesis (MES) converts CO<sub>2</sub> into value-added products such as volatile fatty acids (VFAs) with minimal energy use, but low production titer has limited scale-up and commercialization. Mediated electron transfer via H<sub>2</sub> on the MES cathode has shown a higher conversion rate than the direct biofilm-based approach, as it is tunable via cathode potential control and accelerates electrosynthesis from CO<sub>2</sub>. Here we report high acetate titers can be achieved via improved <em>in situ</em> H<sub>2</sub> supply by nickel foam decorated carbon felt cathode in mixed community MES systems. Acetate concentration of 12.5 g L<sup>−1</sup> was observed in 14 days with nickel-carbon cathode at a poised potential of −0.89 V (vs. standard hydrogen electrode, SHE), which was much higher than cathodes using stainless steel (5.2 g L<sup>−1</sup>) or carbon felt alone (1.7 g L<sup>−1</sup>) with the same projected surface area. A higher acetate concentration of 16.0 g L<sup>−1</sup> in the cathode was achieved over long-term operation for 32 days, but crossover was observed in batch operation, as additional acetate (5.8 g L<sup>−1</sup>) was also found in the abiotic anode chamber. We observed the low Faradaic efficiencies in acetate production, attributed to partial H<sub>2</sub> utilization for electrosynthesis. The selective acetate production with high titer demonstrated in this study shows the H<sub>2</sub>-mediated electron transfer with common cathode materials carries good promise in MES development.</p></div>","PeriodicalId":34434,"journal":{"name":"Environmental Science and Ecotechnology","volume":"19 ","pages":"Article 100324"},"PeriodicalIF":14.0000,"publicationDate":"2023-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science and Ecotechnology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666498423000893","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Microbial electrosynthesis (MES) converts CO2 into value-added products such as volatile fatty acids (VFAs) with minimal energy use, but low production titer has limited scale-up and commercialization. Mediated electron transfer via H2 on the MES cathode has shown a higher conversion rate than the direct biofilm-based approach, as it is tunable via cathode potential control and accelerates electrosynthesis from CO2. Here we report high acetate titers can be achieved via improved in situ H2 supply by nickel foam decorated carbon felt cathode in mixed community MES systems. Acetate concentration of 12.5 g L−1 was observed in 14 days with nickel-carbon cathode at a poised potential of −0.89 V (vs. standard hydrogen electrode, SHE), which was much higher than cathodes using stainless steel (5.2 g L−1) or carbon felt alone (1.7 g L−1) with the same projected surface area. A higher acetate concentration of 16.0 g L−1 in the cathode was achieved over long-term operation for 32 days, but crossover was observed in batch operation, as additional acetate (5.8 g L−1) was also found in the abiotic anode chamber. We observed the low Faradaic efficiencies in acetate production, attributed to partial H2 utilization for electrosynthesis. The selective acetate production with high titer demonstrated in this study shows the H2-mediated electron transfer with common cathode materials carries good promise in MES development.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
H2介导混合培养微生物电合成高滴度CO2醋酸盐
微生物电合成(MES)将CO2转化为增值产品,如挥发性脂肪酸(VFAs),能耗最低,但生产滴度低,限制了规模化和商业化。通过MES阴极上的H2介导的电子转移显示出比直接基于生物膜的方法更高的转化率,因为它可以通过阴极电势控制进行调节,并加速CO2的电合成。在这里,我们报道了在混合社区MES系统中,通过镍泡沫装饰碳毡阴极改善原位H2供应,可以实现高乙酸盐滴度。在镍-碳阴极处于−0.89 V(相对于标准氢电极,SHE)的稳定电位下的14天内,观察到乙酸盐浓度为12.5 g L−1,这远高于使用具有相同投影表面积的不锈钢(5.2 g L−2)或单独使用碳毡(1.7 g L−3)的阴极。在长达32天的长期操作中,阴极中的乙酸盐浓度达到了更高的16.0 g L−1,但在分批操作中观察到了交叉,因为在非生物阳极室中也发现了额外的乙酸盐(5.8 g L−2)。我们观察到乙酸盐生产中的法拉第效率较低,这归因于H2部分用于电合成。本研究中证明的具有高滴度的选择性乙酸盐生产表明,用普通阴极材料进行H2介导的电子转移在MES开发中具有良好的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
20.40
自引率
6.30%
发文量
11
审稿时长
18 days
期刊介绍: Environmental Science & Ecotechnology (ESE) is an international, open-access journal publishing original research in environmental science, engineering, ecotechnology, and related fields. Authors publishing in ESE can immediately, permanently, and freely share their work. They have license options and retain copyright. Published by Elsevier, ESE is co-organized by the Chinese Society for Environmental Sciences, Harbin Institute of Technology, and the Chinese Research Academy of Environmental Sciences, under the supervision of the China Association for Science and Technology.
期刊最新文献
Editorial Board Accelerating the establishment of a new science-policy panel to address the triple planetary crisis Rapid identification of antibiotic resistance gene hosts by prescreening ARG-like reads Enhanced removal of chiral emerging contaminants by an electroactive biofilter Mitigating household air pollution exposure through kitchen renovation
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1