高选择性配体CyMe4BTBP和CyMe4BTPhen的γ辐射分解:辐射分解产物的定性和定量研究

Holger Schmidt , Andreas Wilden , Giuseppe Modolo , Dirk Bosbach , Beatrix Santiago-Schübel , Michelle Hupert , Jaroslav Švehla , Bohumir Grüner , Christian Ekberg
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引用次数: 15

摘要

在相同的实验条件下,γ -辐照在1 -辛醇中与硝酸溶液接触和不接触,获得了高选择性的氮给体CyMe4BTBP和CyMe4BTPhen。随后,进行溶剂萃取实验,以评估萃取剂对γ -辐射监测Am(III)和Eu(III)分布比的稳定性。一般情况下,两种分子的分布比随吸收剂量的增加而减小。此外,通过质谱分析和HPLC-DAD法测定辐照后配体浓度,探讨辐照降解机制。两种配体均随吸收剂量的增加呈指数下降,且CyMe4BTPhen的吸收速率较快。主要放射解产物表明,通过稀释剂放射解产生α-羟基辛基自由基,使一个或多个稀释剂分子(1 -辛醇)加入配体。在辐照过程中加入硝酸导致了系统的显著稳定,因为在整个检测剂量范围内,Am(III)和Eu(III)的提取没有显著变化。另一方面,剩余配体浓度的定量显示,浓度随着吸收剂量的增加而降低。因此,D值的稳定可以用1 -辛醇加成产物的形成来解释,这些产物也能够提取所研究的金属离子。
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Gamma Radiolysis of the Highly Selective Ligands CyMe4BTBP and CyMe4BTPhen: Qualitative and Quantitative Investigation of Radiolysis Products

The highly selective nitrogen donor ligands CyMe4BTBP and CyMe4BTPhen where γ–irradiated under identical experimental conditions in 1–octanol with and without contact to nitric acid solution. Subsequently, solvent extraction experiments were carried out to evaluate the stability of the extractants against γ–radiation monitoring Am(III) and Eu(III) distribution ratios. Generally, decreasing distribution ratios with increasing absorbed dose were detected for both molecules. Furthermore, qualitative mass spectrometric analyses were performed and ligand concentrations were determined by HPLC-DAD after irradiation to investigate the radiolysis mechanism. An exponential decrease with increasing absorbed dose was observed for both ligands with a faster rate for CyMe4BTPhen. Main radiolysis products indicated the addition of one or more diluent molecules (1–octanol) to the ligand via prior production of α-hydroxyoctyl radicals from diluent radiolysis. The addition of nitric acid during the irradiation lead to a remarkable stabilization of the system, as the extraction of Am(III) and Eu(III) did not change significantly over the whole examined dose range. Quantification of the remaining ligand concentration on the other hand showed decreasing concentrations with increasing absorbed dose. The stabilization of D values is therefore explained by the formation of 1–octanol addition products which are also able to extract the studied metal ions.

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