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关于使用磷酸三正丁酯将硝酸溶液中的铀(VI)萃取到离子液体中的机理研究

Insights into the mechanism of extraction of uranium (VI) from nitric acid solution into an ionic liquid by using tri-n-butyl phosphate.

作者信息

Gaillard Dr Clotilde, Boltoeva Maria, Billard Isabelle, Georg Sylvia, Mazan Valérie, Ouadi Ali, Ternova Dariia, Hennig Christoph

机构信息

Institut de Physique Nucléaire de Lyon, Université de Lyon, CNRS-IN2P3, 69622 Villeurbanne cedex (France).

Université de Strasbourg, IPHC, 23 rue du Lœss, 67037 Strasbourg (France).

出版信息

Chemphyschem. 2015 Aug 24;16(12):2653-62. doi: 10.1002/cphc.201500283. Epub 2015 Jul 6.

Abstract

We present new results on the liquid-liquid extraction of uranium (VI) from a nitric acid aqueous phase into a tri-n-butyl phosphate/1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (TBP/[C4 mim][Tf2 N]) phase. The individual solubilities of the ionic-liquid ions in the upper part of the biphasic system are measured over the whole acidic range and as a function of the TBP concentration. New insights into the extraction mechanism are obtained through the in situ characterization of the extracted uranyl complexes by coupling UV/Vis and extended X-ray absorption fine structure (EXAFS) spectroscopy. We propose a chemical model to explain uranium (VI) extraction that describes the data through a fit of the uranyl distribution ratio DU . In this model, at low acid concentrations uranium (VI) is extracted as the cationic complex UO2 (TBP)2 , by an exchange with one proton and one C4 mim(+) . At high acid concentrations, the extraction proceeds through a cationic exchange between UO2 (NO3 )(HNO3 )(TBP)2 and one C4 mim(+) . As a consequence of this mechanism, the variation of DU as a function of TBP concentration depends on the C4 mim(+) concentration in the aqueous phase. This explains why noninteger values are often derived by analysis of DU versus [TBP] plots to determine the number of TBP molecules involved in the extraction of uranyl in an ionic-liquid phase.

摘要

我们展示了关于将硝酸水相中的铀(VI)液 - 液萃取到磷酸三正丁酯/1 - 丁基 - 3 - 甲基咪唑双(三氟甲基磺酰)亚胺(TBP/[C4mim][Tf2N])相中的新结果。在整个酸性范围内并作为TBP浓度的函数,测量了双相体系上部离子液体离子的各自溶解度。通过耦合紫外/可见光谱和扩展X射线吸收精细结构(EXAFS)光谱对萃取的铀酰配合物进行原位表征,获得了萃取机理的新见解。我们提出了一个化学模型来解释铀(VI)的萃取,该模型通过拟合铀酰分配比DU来描述数据。在这个模型中,在低酸浓度下,铀(VI)以阳离子配合物UO2(TBP)2的形式被萃取,通过与一个质子和一个C4mim(+)进行交换。在高酸浓度下,萃取通过UO2(NO3)(HNO3)(TBP)2与一个C4mim(+)之间的阳离子交换进行。由于这种机理,DU随TBP浓度的变化取决于水相中C4mim(+)的浓度。这解释了为什么在分析DU与[TBP]的关系图以确定离子液体相中参与铀酰萃取的TBP分子数时,常常会得出非整数值。

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