Three-dimensional macroporous structure and surface carbon-coating modification of stainless-steel anode boost bioelectrocatalytic performance

[Display omitted] •A novel stainless-steel based electrode was proposed for the scaling-up of BESs.•Surface carbon-coating modification greatly improved electrode’s biocompatibility.•Macroporous structure enabled well mass transfer through electrode.•Projected current density increased linearly with...

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Veröffentlicht in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2023-07, Vol.468, p.143682, Article 143682
Hauptverfasser: Liu, Cheng-Yan, Cheng, Hao-Yi, Zhai, Si-Yuan, Zeng, Ran, Zhang, De-Xin, Wang, Ai-Jie
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Sprache:eng
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Zusammenfassung:[Display omitted] •A novel stainless-steel based electrode was proposed for the scaling-up of BESs.•Surface carbon-coating modification greatly improved electrode’s biocompatibility.•Macroporous structure enabled well mass transfer through electrode.•Projected current density increased linearly with increase of electrode thickness. Bioelectrochemical systems (BESs) is a promising and sustainable technology for wastewater treatment, and the practical application of BESs generally requires scalable three-dimensional (3D) electrodes. In this study, we present a stainless-steel crochet mesh electrode (P-SS) with 3D macroporous structure, and modified by carbon coating through pyrolyzing residual lubricating oil in the mesh production process. The effect of 3D macroporous structure and surface carbon-coating modification on the improvement of electrode bioelectrocatalytic performance was investigated during the study. When the electrode was used as the anode in BESs reactors, a superior bioeletrocatalytic current was generated, reaching a maximum projected current density of 9.95 mA·cm−2 and achieving a highest geometric current density of 1.89 mA·cm−2 ever recorded. We found the 3D macroporous structure and surface carbon-coating modification enabled the electrode well mass transfer, excellent biocompatibility and fluent electron transport, finally boosted the superior bioeletrocatalytic performance. We also verified the electrode has a remarkable stackability as suggested by the bioelectrocatalytic current increasing linearly with the increase of electrode thickness. In addition, the acceptable capital cost (<6500 $·m−3), adequate mechanical strength and feasible industrial process of this novel electrode all indicate its great prospects for the scaling-up of BESs.
ISSN:1385-8947
DOI:10.1016/j.cej.2023.143682