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dc.creatorRaičević, Slavica
dc.creatorWright, JV
dc.creatorVeljković, Veljko
dc.creatorConca, JL
dc.date.accessioned2018-03-01T19:45:48Z
dc.date.available2018-03-01T19:45:48Z
dc.date.issued2006
dc.identifier.issn0048-9697
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/2979
dc.description.abstractAddition of an amendment or reagent to soil/sediment is a technique that can decrease mobility and reduce bioavailability of uranium (U) and other heavy metals in the contaminated site. According to data from literature and results obtained in field studies, the general mineral class of apatites was selected as a most promising amendment for in situ immobilization/ remediation of U. In this work we presented theoretical assessment of stability of U(VI) in four apatite systems (hydroxyapatite (HAP), North Carolina Apatite (NCA), Lisina Apatite (LA), and Apatite H) in order to determine an optimal apatite soil amendment which could be used for in situ remediation of uranium. In this analysis we used a theoretical criterion which is based on calculation of the ion-ion interaction potential, representing the main term of the cohesive energy of the matrix/ pollutant system. The presented results of this analysis indicate (i) that the mechanism of immobilization of U by natural apatites depends on their chemical composition and (ii) that all analyzed apatites represent, from the point of view of stability, promising materials which could be used in field remediation of U-contaminated sites. (c) 2005 Elsevier B.V. All rights reserved.en
dc.rightsrestrictedAccessen
dc.sourceScience of the Total Environmenten
dc.subjecturaniumen
dc.subjectapatiteen
dc.subjectremediationen
dc.subjectcohesive energyen
dc.subjectstabilityen
dc.titleTheoretical stability assessment of uranyl phosphates and apatites: Selection of amendments for in situ remediation of uraniumen
dc.typearticleen
dcterms.abstractРаицевиц, С; Цонца, ЈЛ; Wригхт, ЈВ; Вељковић Вељко;
dc.citation.volume355
dc.citation.issue1-3
dc.citation.spage13
dc.citation.epage24
dc.identifier.wos000235508500002
dc.identifier.doi10.1016/j.scitotenv.2005.03.006
dc.citation.rankM21
dc.identifier.pmid15885755
dc.identifier.scopus2-s2.0-31344456969


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