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Systematic Modifications of BTP-type Ligands and Effects on the Separation of Trivalent Lanthanides and Actinides

机译:BTP型配体的系统修饰及对三价镧系元素分离的影响

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In this study the separation of Am(III) from Eu(III) in nitric acid using two BTP-type N-donor ligands, 2,6-bis(6-ethyl-1,2- diazine-3-yl)pyridine (Et-BDP) and 2,6-bis(4-~npropyl-2,3,5,6-tetrazine-1 -yl)pyridine (~nPr-tetrazine) is presented. The extraction and separation properties of both ligands are tested by two phase liquid-liquid extraction at different acid concentrations. In contrast to ~nPr-BTP the bisdiazinyl ligand Et-BDP is prone to protonation at nitric acid concentrations of 0.2 M and higher. A separation factor of SF_(Am/Eu) ≈ 5 is obtained using Et-BDP as extracting ligand and with "Pr-tetrazine a SF_(Am/Eu) of 9.1 is realized. Hereby 2-bromodecanoic acid as lipophilic anion source is needed.
机译:在该研究中,使用两种BTP型N-供体配体,2,6-双(6-乙基-1,2-二氮杂-3-基)吡啶(1,2-二嗪-3-基)分离eu(iii)在硝酸中的eu(iii)分离&-BDP)和2,6-双(4-〜甲基-2,3,5,6-四嗪-1-基氮)吡啶(〜NPR-四嗪)。两个配体的提取和分离性能通过不同酸浓度的两相液 - 液萃取测试。与〜NPR-BTP相比,双二唑啉基配体ET-BDP在0.2μm和更高的硝酸浓度下容易产生质子化。使用ET-BDP获得SF_(AM / EU)≈5的分离因子作为提取配体,并实现了“Pr-四嗪A(AM / EA / EU)的9.1。因此,需要2-溴癸酸作为亲脂性阴离子来源。

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