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新型基于[5]轮烷的吡啶甲酰胺配体对锕系(III)/镧系(III)的高效分离:合成、溶剂萃取和络合研究。

Highly efficient actinide(III)/lanthanide(III) separation by novel pillar[5]arene-based picolinamide ligands: A study on synthesis, solvent extraction and complexation.

机构信息

Key Laboratory of Radiation Physics and Technology of the Ministry of Education, Institute of Nuclear Science and Technology, College of Chemistry, Sichuan University, Chengdu 610064, China.

Radiochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085, India.

出版信息

J Hazard Mater. 2021 Mar 5;405:124214. doi: 10.1016/j.jhazmat.2020.124214. Epub 2020 Oct 8.

Abstract

Selective extraction of highly radiotoxic actinides(III) is an important and challenging task in nuclear wastewater treatment. Many proposed ligands containing S or P atoms have drawbacks including high reagent consumption and possible secondary pollution after incineration. The present work reports five novel pillar[5]arene-based extractants that are anchored with picolinamide substituents of different electronic nature by varying spacer. These ligands reveal highly efficient separation of actinides(III) over lanthanides(III). Specifically, almost all of these ligands could extract Am(III) over Eu(III) selectively at around pH 3.0 (SF>11) with fast extraction kinetics. Variation of the pyridine nitrogen basicity via changing para-substitution leads to an increase in the distribution ratios by a factor of over 300 times for Am(III) with an electron-withdrawing group compared to those with an electron donating group. Investigation of complexation mechanism by slope analysis, NMR, IR, EXAFS, and DFT techniques indicates that each ligand binds two metal ions by pyridine nitrogen and amide oxygen. Finally, these ligands do not show obvious decrease in both extraction and separation ability after being exposed to 250 kGy absorbed gamma radiation. These results demonstrate the potential application of pillar[5]arene-picolinamides for actinide(III) separation.

摘要

选择性萃取高放射性锕系元素(III)是核废水处理中的一项重要且具有挑战性的任务。许多含硫或磷原子的配体虽然被提出来了,但存在试剂消耗量大和焚烧后可能产生二次污染等缺点。本工作报道了五种新型的杯[5]芳烃基萃取剂,它们通过改变间隔基连接了不同电子性质的吡啶甲酰胺取代基。这些配体对锕系元素(III)和镧系元素(III)的分离具有很高的效率。具体来说,在 pH 值约为 3.0 时(SF>11),这些配体几乎都可以选择性地萃取 Am(III)而不是 Eu(III),且萃取动力学很快。通过改变对位取代基来改变吡啶氮的碱性,使得 Am(III)的分配比增加了 300 多倍,而对于带吸电子基团的取代基,分配比则增加了 300 多倍。通过斜率分析、NMR、IR、EXAFS 和 DFT 技术研究配合物的形成机制表明,每个配体通过吡啶氮和酰胺氧结合两个金属离子。最后,这些配体在暴露于 250 kGy 吸收伽马辐射后,其萃取和分离能力并没有明显下降。这些结果表明杯[5]芳烃-吡啶甲酰胺在锕系元素(III)分离方面具有潜在的应用。

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