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dc.contributor.authorLiu, Xun
dc.contributor.authorRehman, Danyal
dc.contributor.authorShu, Yufei
dc.contributor.authorLiu, Bei
dc.contributor.authorWang, Li
dc.contributor.authorLi, Li
dc.contributor.authorWang, Mengxia
dc.contributor.authorWang, Kunkun
dc.contributor.authorHan, Qi
dc.contributor.authorZang, Linlin
dc.contributor.authorLienhard, John H.
dc.contributor.authorWang, Zhongying
dc.date.accessioned2024-06-13T20:52:17Z
dc.date.available2024-06-13T20:52:17Z
dc.date.issued2024-02
dc.identifier.issn1385-8947
dc.identifier.urihttps://hdl.handle.net/1721.1/155273
dc.description.abstractSelective capacitive deionization (SCDI) is a promising process for preferentially removing specific ions from waters with complex compositions. The selectivity towards certain species in CDI is most frequently achieved through novel electrode materials with high affinities towards targeted species. In this study, we investigate the selective removal of fluoride ions from groundwater containing concentrated co-existing chloride ions. A carbon nanotube-CeO2 (CNT-CeO2) electrode is employed for the electro-sorption of fluoride ions. Our findings are compelling: when processing a mixed F−/Cl− solution comprising 10 mg/L F− and 100 mg/L Cl−, the CNT-CeO2 electrode is seen to reduce the concentration of F− ions to 1.5 mg/L in just 150 min, amounting to an 85 % F− removal efficiency, while the Cl− removal efficiency remains below 2 %. Importantly, this translates to a F−/Cl− separation factor of up to 4.16 when using the CeO2-based electrodes, which is 40 times higher than that achieved with conventional activated carbon (AC) electrodes. Furthermore, the energy consumption for treating actual groundwater using scaled-up equipment is impressively low at approximately 0.2 kWh/m3. The high affinity of CNT-CeO2 towards fluoride is attributed to the intercalation Faraday capacitance initiated by the reaction between F− with CeO2, as verified by the electrochemical quartz crystal microbalance (EQCM). Moreover, EQCM results show a substantial increase in both mass and current as the potential increased beyond 0.8 V vs Ag/AgCl, implying that the current surge is not a result of water splitting but rather the adsorption of F− onto the CNT-CeO2 electrode. The addition of CNTs substantially increases the conductivity of CeO2 electrodes and restricts the aggregation of CeO2, thereby accelerating ion diffusion and promoting selective adsorption characteristics. Importantly, our electro-driven approach demonstrates excellent adsorption–desorption over 20 cycles. This comprehensive study advances the technological development of selective CDI, while providing new insights for fluoride removal in groundwater.en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionof10.1016/j.cej.2024.149097en_US
dc.rightsCreative Commons Attribution-Noncommercial-ShareAlikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceAuthoren_US
dc.titleSelective fluoride removal from groundwater using CNT-CeO2 electrodes in capacitive deionization (CDI)en_US
dc.typeArticleen_US
dc.identifier.citationLiu, Xun, Rehman, Danyal, Shu, Yufei, Liu, Bei, Wang, Li et al. 2024. "Selective fluoride removal from groundwater using CNT-CeO2 electrodes in capacitive deionization (CDI)." Chemical Engineering Journal, 482.
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Center for Computational Science and Engineering
dc.relation.journalChemical Engineering Journalen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2024-06-13T20:45:33Z
dspace.orderedauthorsLiu, X; Rehman, D; Shu, Y; Liu, B; Wang, L; Li, L; Wang, M; Wang, K; Han, Q; Zang, L; Lienhard, JH; Wang, Zen_US
dspace.date.submission2024-06-13T20:45:38Z
mit.journal.volume482en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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