化学
镅
镧系元素
锕系元素
十二烷
水溶液
无机化学
二乙烯三胺
钍
螯合作用
双水相体系
配合物的稳定常数
离解(化学)
核化学
离子
物理化学
铀
有机化学
冶金
材料科学
作者
A. Apichaibukol,Yuji Sasaki,Yasuji Morita
标识
DOI:10.1081/sei-200037727
摘要
Abstract For the separation of trivalent lanthanides [Ln(III)] and actinides[An(III)], the chelating agent, diethylenetriamine‐N,N,N′,N″,N″‐pentaacetic acid (DTPA), was used to decrease selectively the distribution ratios (D) of An(III) between TODGA/n‐dodecane and nitrate solution. The D values of An(III) and Ln(III) decrease with an increase of the pH of the aqueous phase. Their dependencies for light Ln(III) are different from those for medium and heavy Ln(III), which implies that the complexing ability of DTPA5− with Ln(III) is different from each other. The calculation of D values was performed using dissociation constants of H5DTPA and the formation constants of Ln–DTPA. Their results suggested the existence of Ln(III) ions without any complexation at the intermediate stage of the extraction reactions and demonstrated the curvilineal relation of D with pH in Ln–TODGA–DTPA extraction system. Americium(III) and Cm(III) form more stable 1:1 complex with DTPA5− and show lower D values than light Ln(III), it is expected to have a high separation against light Ln(III). The separation factors (SF), D Ln/D Am, and D Ln/D Cm, determined varied within the range of 1–60.
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