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Effect of monovalent and divalent ion solutions as washing agents on the removal of Sr and Cs from soil near a nuclear power plant

DC Field Value Language
dc.contributor.authorSong, Hojae-
dc.contributor.authorChung, Hyeonyong-
dc.contributor.authorNam, Kyoungphile-
dc.date.accessioned2023-09-12T07:56:36Z-
dc.date.available2023-09-12T07:56:36Z-
dc.date.created2021-06-07-
dc.date.created2021-06-07-
dc.date.issued2021-06-
dc.identifier.citationJournal of Hazardous Materials, Vol.412, p. 125165-
dc.identifier.issn0304-3894-
dc.identifier.urihttps://hdl.handle.net/10371/195498-
dc.description.abstractSolutions of monovalent and divalent ions, including calcium, magnesium, ammonium, and potassium, were tested in the removal of Sr and Cs from soil near a nuclear power plant. The Ca2+ and K+ solutions exhibited removal efficiencies of 68.2% and 81.3% for Sr and Cs, respectively. This high performance was probably due to the physicochemical similarities between ?Ca and Sr? and ?K and Cs?. Alternatively, the Mg2+ and NH4+ solutions performed much worse, despite having the same valences as Ca2+ and K+, respectively. Ca2+ and K+ solutions could also simultaneously remove cationic toxic metals present with the nuclides, albeit much less efficiently (30?40%). For anionic metalloid As and anionic toxic metal Cr, the efficiency was even lower (< 20%). The fivestep sequential extraction experiment confirmed that all chemical forms of Sr and Cs, except the residual form, were extensively removed by the Ca2+ and K+ solutions, respectively. For comparison, widely used washing agents exhibited removal efficiencies of 25?30%. Notably, Fe2+ and Mn2+ ions were hardly detected in the Ca2+ solution, while their concentrations were much higher in the common washing agents, suggesting the involvement of an ion-exchange mechanism in Sr and Cs removal, rather than a Fe/Mn oxide dissolution mechanism.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleEffect of monovalent and divalent ion solutions as washing agents on the removal of Sr and Cs from soil near a nuclear power plant-
dc.typeArticle-
dc.identifier.doi10.1016/j.jhazmat.2021.125165-
dc.citation.journaltitleJournal of Hazardous Materials-
dc.identifier.wosid000649730300008-
dc.identifier.scopusid2-s2.0-85100302221-
dc.citation.startpage125165-
dc.citation.volume412-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorNam, Kyoungphile-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusSEQUENTIAL EXTRACTION-
dc.subject.keywordPlusHEAVY-METALS-
dc.subject.keywordPlusCONTAMINATED SOIL-
dc.subject.keywordPlusTRACE-ELEMENTS-
dc.subject.keywordPlusREMEDIATION-
dc.subject.keywordPlusSTRONTIUM-
dc.subject.keywordPlusCESIUM-
dc.subject.keywordPlusFRACTIONATION-
dc.subject.keywordPlusSPECIATION-
dc.subject.keywordPlusCADMIUM-
dc.subject.keywordAuthorSoil washing-
dc.subject.keywordAuthorPhysicochemical similarity-
dc.subject.keywordAuthorCalcium solution-
dc.subject.keywordAuthorPotassium solution-
dc.subject.keywordAuthorFive-step sequential extraction-
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