TY - JOUR
T1 - Nickel-Coated ceramic hollow fiber cathode for fast enrichment of chemolithoautotrophs and efficient reduction of CO2 in microbial electrosynthesis
AU - Bian, Bin
AU - Singh, Yogesh Balwant
AU - Rabaey, Korneel
AU - Saikaly, Pascal
N1 - KAUST Repository Item: Exported on 2022-09-14
Acknowledged KAUST grant number(s): URF/1/2985-01-01
Acknowledgements: This work was supported by KAUST Competitive Research Grant (URF/1/2985-01-01). We appreciate the support from Dr. Narasimha Murthy Srivatsa Bettahalli, Dr. Yong Jin, Dr. Yuquan Li, Dr. Nimer Wehbe, and Mr. Ping Hu for material testing and characterization, and Heno Hwang, a scientific illustrator at KAUST, for his creation of Fig. 1.
PY - 2022/7/30
Y1 - 2022/7/30
N2 - Microbial electrosynthesis (MES) explores the potential of chemolithoautotrophs for the production of value-added products from CO2. However, the enrichment of chemolithoautotrophs on a cathode is relatively slow and the separation of the products is energy intensive. In this study, a novel and multifunctional cathode configuration, enabling the simultaneous enrichment of chemolithoautotrophs and separation of acetate from MES, was developed through one-step electroless nickel plating on ceramic hollow fiber (CHF) membrane. A thick layer of chemolithoautotrophs with 5.2 times higher cell density, which was dominated by Sporomusa (68 % of the total sequence reads in biocathode), was enriched on the membrane cathode surface through suspended biomass microfiltration compared to MES reactors operated without filtration. Simultaneously, >87 % of acetate (31 mM) per batch could be harvested after catholyte microfiltration. The Ni content was > 80 % on the CHF surface after long-term operation in the two-chamber MES system, which exhibited 78 % lower charge transfer resistance compared to three-chamber MES system (∼110 vs 510 Ω) for acetate separation/extraction. The ease of product separation in two-chamber MES systems and the fast establishment of chemolithoautotrophs on the cathode are a step forward in realizing MES systems as a promising platform for CO2 reduction and biochemical production in a circular carbon bioeconomy.
AB - Microbial electrosynthesis (MES) explores the potential of chemolithoautotrophs for the production of value-added products from CO2. However, the enrichment of chemolithoautotrophs on a cathode is relatively slow and the separation of the products is energy intensive. In this study, a novel and multifunctional cathode configuration, enabling the simultaneous enrichment of chemolithoautotrophs and separation of acetate from MES, was developed through one-step electroless nickel plating on ceramic hollow fiber (CHF) membrane. A thick layer of chemolithoautotrophs with 5.2 times higher cell density, which was dominated by Sporomusa (68 % of the total sequence reads in biocathode), was enriched on the membrane cathode surface through suspended biomass microfiltration compared to MES reactors operated without filtration. Simultaneously, >87 % of acetate (31 mM) per batch could be harvested after catholyte microfiltration. The Ni content was > 80 % on the CHF surface after long-term operation in the two-chamber MES system, which exhibited 78 % lower charge transfer resistance compared to three-chamber MES system (∼110 vs 510 Ω) for acetate separation/extraction. The ease of product separation in two-chamber MES systems and the fast establishment of chemolithoautotrophs on the cathode are a step forward in realizing MES systems as a promising platform for CO2 reduction and biochemical production in a circular carbon bioeconomy.
UR - http://hdl.handle.net/10754/680146
UR - https://linkinghub.elsevier.com/retrieve/pii/S1385894722037135
UR - http://www.scopus.com/inward/record.url?scp=85135135782&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2022.138230
DO - 10.1016/j.cej.2022.138230
M3 - Article
SN - 1385-8947
VL - 450
SP - 138230
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -