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Enhanced cesium adsorption and desorption mechanisms in ZnFe Prussian blue analogs: Structural transformation and reusability
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dc.contributor.author Eun, Semin -
dc.contributor.author Cho, Eunkyung -
dc.contributor.author Ryu, Jungho -
dc.contributor.author Kim, Hyuncheol -
dc.contributor.author Kim, Minsun -
dc.contributor.author Kim, Bokyung -
dc.contributor.author Kim, Soonhyun -
dc.date.accessioned 2025-01-22T15:40:15Z -
dc.date.available 2025-01-22T15:40:15Z -
dc.date.created 2025-01-22 -
dc.date.issued 2025-02 -
dc.identifier.issn 1385-8947 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/57661 -
dc.description.abstract The management of radioactive cesium (137Cs) is critical due to its long half-life, environmental persistence, and harmful effects on human health and ecosystems. Although Prussian blue analogs (PBAs) have gained attention for their potential in adsorption-based Cs+ removal, the structural changes that occur during adsorption and desorption cycling are poorly understood. This study investigates the synthesis of ZnFe-PBAs using various methodologies, including photochemical reduction and the use of different precursors and reducing agents, to achieve diverse oxidation states in their lattice structures. The photochemically synthesized ZnFe-PBAs exhibited significantly enhanced Cs+ adsorption capacities compared to those of conventional materials. Comprehensive characterization techniques, including X-ray diffraction, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy, were employed to assess the physicochemical properties of the ZnFe-PBAs and examine their structural changes during Cs+ adsorption and desorption. The results revealed that the ZnFe samples exhibited distinct structural transformations, with ZnFe-W showing rapid structural changes that facilitated rapid Cs+ adsorption and desorption. In contrast, ZnFe-Y maintained a stable cubic structure throughout the process. Adsorption isotherm and kinetic studies confirmed that ion exchange with K+ is the primary mechanism of Cs+ adsorption, and it was deduced that the desorption efficiency varied with the choice of desorption solution. This study highlights the importance of understanding structural changes during Cs+ removal and provides insights into designing more efficient and reusable adsorbents. These findings suggest that ZnFe-PBAs have strong potential for 137Cs removal in simulated nuclear waste environments and a promising strategy for radioactive contaminant management. © 2024 Elsevier B.V. -
dc.language English -
dc.publisher Elsevier -
dc.title Enhanced cesium adsorption and desorption mechanisms in ZnFe Prussian blue analogs: Structural transformation and reusability -
dc.type Article -
dc.identifier.doi 10.1016/j.cej.2024.159161 -
dc.identifier.wosid 001401522500001 -
dc.identifier.scopusid 2-s2.0-85214124562 -
dc.identifier.bibliographicCitation Eun, Semin. (2025-02). Enhanced cesium adsorption and desorption mechanisms in ZnFe Prussian blue analogs: Structural transformation and reusability. Chemical Engineering Journal, 505. doi: 10.1016/j.cej.2024.159161 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordAuthor ZnFe Prussian blue analog (ZnFe-PBA) -
dc.subject.keywordAuthor Cesium adsorption and desorption -
dc.subject.keywordAuthor Ion exchange mechanism -
dc.subject.keywordAuthor Structural transformation -
dc.subject.keywordAuthor Reusability -
dc.subject.keywordPlus RADIOACTIVE CESIUM -
dc.subject.keywordPlus SELECTIVE REMOVAL -
dc.subject.keywordPlus AMMONIUM MOLYBDOPHOSPHATE -
dc.subject.keywordPlus NUCLEAR-WASTE -
dc.subject.keywordPlus COMPOSITE -
dc.subject.keywordPlus EFFICIENT -
dc.subject.keywordPlus SEPARATION -
dc.subject.keywordPlus HYDROGEL -
dc.subject.keywordPlus CS(I) -
dc.subject.keywordPlus WATER -
dc.citation.title Chemical Engineering Journal -
dc.citation.volume 505 -
dc.description.journalRegisteredClass scie -
dc.relation.journalResearchArea Engineering -
dc.relation.journalWebOfScienceCategory Engineering, Environmental; Engineering, Chemical -
dc.type.docType Article -
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