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Article: Fabrication of a permeable SnO2-Sb reactive anodic filter for high-efficiency electrochemical oxidation of antibiotics in wastewater

TitleFabrication of a permeable SnO<inf>2</inf>-Sb reactive anodic filter for high-efficiency electrochemical oxidation of antibiotics in wastewater
Authors
Keywords3D porous electrode
Antibiotic wastewater
Ciprofloxacin
Electrochemical treatment
Flow through
Reactive filter
Issue Date2021
Citation
Environment International, 2021, v. 157, article no. 106827 How to Cite?
AbstractElectrochemical oxidation (ECO) is an appealing technology for treating emerging organic pollutants in wastewater. However, the conventional flow-by ECO process is expensive with a low energy efficiency owing to the limitations of mass transport of contaminants to the limited surface area of the anode. In this study, a novel freestanding porous and permeable SnO2-Sb anode was fabricated by one-step sintering using micrometer-sized (NH4)2CO3 grains as the pore-forming agents. This permeable SnO2-Sb anode without Ti substrate functioned as a reactive anodic filter (RAF) in an ECO cell to treat wastewater containing ciprofloxacin (CIP). Forcing the wastewater through the porous RAF depth-wise improved the mass transport and vastly enlarged the electroactive surface area. Compared with the conventional flow-by configuration, the flow-through RAF exhibited a 12-fold increase in the mass transfer rate constant (60.7 × 10−6 m s−1) and a 5-fold increase in the CIP degradation rate constant (0.077 min−1). At a cell potential of 4.0 V, more than 92% of the CIP was degraded in a single-pass operation at a filtration flux of 54 L m−2 h−1 and a short retention time of 1.7 min through the RAF. The robustness and stability of the RAF were demonstrated by its remarkable CIP degradation efficacy of 99% during 200 h of operation. The mechanism of CIP degradation was examined using probe molecules and density functional theory calculations and found to be a combined effect of direct electron transfer and oxidation by generated radicals ([rad]OH and SO4[rad]−). The great potential of RAF in flow-through ECO was further validated by its effective removal (>92%) of various organic pollutants in actual municipal wastewater at a low energy consumption of 0.33 kWh m−3. The RAF-based ECO process thus provides an advanced environmental technology for the oxidation of toxic and recalcitrant organic pollutants in wastewater treatment.
Persistent Identifierhttp://hdl.handle.net/10722/327349
ISSN
2023 Impact Factor: 10.3
2023 SCImago Journal Rankings: 3.015
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYang, Chao-
dc.contributor.authorFan, Yiang-
dc.contributor.authorShang, Shanshan-
dc.contributor.authorLi, Pu-
dc.contributor.authorLi, Xiao yan-
dc.date.accessioned2023-03-31T05:30:42Z-
dc.date.available2023-03-31T05:30:42Z-
dc.date.issued2021-
dc.identifier.citationEnvironment International, 2021, v. 157, article no. 106827-
dc.identifier.issn0160-4120-
dc.identifier.urihttp://hdl.handle.net/10722/327349-
dc.description.abstractElectrochemical oxidation (ECO) is an appealing technology for treating emerging organic pollutants in wastewater. However, the conventional flow-by ECO process is expensive with a low energy efficiency owing to the limitations of mass transport of contaminants to the limited surface area of the anode. In this study, a novel freestanding porous and permeable SnO2-Sb anode was fabricated by one-step sintering using micrometer-sized (NH4)2CO3 grains as the pore-forming agents. This permeable SnO2-Sb anode without Ti substrate functioned as a reactive anodic filter (RAF) in an ECO cell to treat wastewater containing ciprofloxacin (CIP). Forcing the wastewater through the porous RAF depth-wise improved the mass transport and vastly enlarged the electroactive surface area. Compared with the conventional flow-by configuration, the flow-through RAF exhibited a 12-fold increase in the mass transfer rate constant (60.7 × 10−6 m s−1) and a 5-fold increase in the CIP degradation rate constant (0.077 min−1). At a cell potential of 4.0 V, more than 92% of the CIP was degraded in a single-pass operation at a filtration flux of 54 L m−2 h−1 and a short retention time of 1.7 min through the RAF. The robustness and stability of the RAF were demonstrated by its remarkable CIP degradation efficacy of 99% during 200 h of operation. The mechanism of CIP degradation was examined using probe molecules and density functional theory calculations and found to be a combined effect of direct electron transfer and oxidation by generated radicals ([rad]OH and SO4[rad]−). The great potential of RAF in flow-through ECO was further validated by its effective removal (>92%) of various organic pollutants in actual municipal wastewater at a low energy consumption of 0.33 kWh m−3. The RAF-based ECO process thus provides an advanced environmental technology for the oxidation of toxic and recalcitrant organic pollutants in wastewater treatment.-
dc.languageeng-
dc.relation.ispartofEnvironment International-
dc.subject3D porous electrode-
dc.subjectAntibiotic wastewater-
dc.subjectCiprofloxacin-
dc.subjectElectrochemical treatment-
dc.subjectFlow through-
dc.subjectReactive filter-
dc.titleFabrication of a permeable SnO<inf>2</inf>-Sb reactive anodic filter for high-efficiency electrochemical oxidation of antibiotics in wastewater-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.envint.2021.106827-
dc.identifier.pmid34418849-
dc.identifier.scopuseid_2-s2.0-85112851414-
dc.identifier.volume157-
dc.identifier.spagearticle no. 106827-
dc.identifier.epagearticle no. 106827-
dc.identifier.eissn1873-6750-
dc.identifier.isiWOS:000704379000011-

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