Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.13091/1047
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dc.contributor.authorTutar Öksüz, Seçil-
dc.contributor.authorBeyenal, Haluk-
dc.date.accessioned2021-12-13T10:34:37Z-
dc.date.available2021-12-13T10:34:37Z-
dc.date.issued2021-
dc.identifier.issn2213-1388-
dc.identifier.issn2213-1396-
dc.identifier.urihttps://doi.org/10.1016/j.seta.2021.101507-
dc.identifier.urihttps://hdl.handle.net/20.500.13091/1047-
dc.description.abstractIn the past decade, bioelectrochemical systems (BESs) have been studied extensively for the generation of power and maximizing power densities. In recent years, it was noticed that BESs applications can critically improve wastewater treatment. Most of the previous BESs work has used varied reactor geometry and configuration, wastewater composition, electrolyte solution, and constant electrode size to maximize power generation. However, there is limited research investigating the influence of increased electrode size on the wastewater treatment process. We investigated the effect of increased electrode surface area on wastewater treatment effi-ciency and studied the mechanism of nitrogen removal. In this study, we developed a flow-through electrode in a 3-electrode bioelectrochemical reactor. The anodic biofilms were enriched on electrodes for one week. Following the anodic enrichment period, the reactor was operated in a semi-continuous mode with raw domestic waste-water. To investigate the wastewater treatment efficiency, the chemical oxygen demand (COD), total nitrogen (TN), ammonia (NH3-N), nitrite (NO2-N), and nitrate (NO3-N) concentrations were measured. We found that increased surface area of anode did not significantly contribute to COD removal rate, most likely indicating the limits of BES. On the other hand, the TN removal rate increased proportionally to the surface area of the anode in the BES. We also found that outlet NO3-N and NO2-N concentrations were 1.2 +/- 0.2 and 3.2 +/- 0.9 mg/L, respectively. Our results indicated that it is possible to remove COD and TN simultaneously. Analysis of the microbial community structure showed that nitrogen removal was dominated by sulfidogenesis, anodic ammonia oxidation, autotrophic and heterotrophic denitrification as well as reducing NO3-N to NO2-N using Geo-bacter species in our system.en_US
dc.description.sponsorshipOffice of Naval ResearchOffice of Naval Research [N000141512471]; US National Science Foundation award CBET [1706889]; Turkish Ministry of National Education Scholarshipsen_US
dc.description.sponsorshipThis research was supported by a grant from Office of Naval Research award number N000141512471 and US National Science Foundation award CBET #1706889. The authors acknowledge the staff at the Moscow Water Reclamation and Reuse Facility (Moscow, ID) for providing wastewater and mixed culture inoculum. We are grateful forthe help of Phuc Ha for the part of microbial community analysis. Secil Tutar Oksuz also acknowledges support from Turkish Ministry of Na-tional Education Scholarships.en_US
dc.language.isoenen_US
dc.publisherELSEVIERen_US
dc.relation.ispartofSUSTAINABLE ENERGY TECHNOLOGIES AND ASSESSMENTSen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnodic Biofilmen_US
dc.subject3-Electrode Setupen_US
dc.subjectCoden_US
dc.subjectTotal Nitrogenen_US
dc.subjectFlow Through Electrodeen_US
dc.subjectMicrobial Fuel-Cellsen_US
dc.subjectWaste-Water Treatmenten_US
dc.subjectBiological Phosphorus Removalen_US
dc.subjectAnodic Ammonia Oxidationen_US
dc.subjectElectricity Productionen_US
dc.subjectAnammoxen_US
dc.subjectPerformanceen_US
dc.subjectSystemsen_US
dc.subjectNitriteen_US
dc.subjectEnergyen_US
dc.titleEnhanced bioelectrochemical nitrogen removal in flow through electrodesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.seta.2021.101507-
dc.departmentKTÜNen_US
dc.identifier.volume47en_US
dc.identifier.wosWOS:000709249900008en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
item.openairetypeArticle-
item.languageiso639-1en-
item.grantfulltextembargo_20300101-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept02.06. Department of Environmental Engineering-
Appears in Collections:WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collections
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