Laboratory of Nuclear Energy Chemistry, Institute of High Energy Physics, Chinese Academy of Sciences , Beijing 100049, China.
Beijing Key Laboratory of Bioprocess, College of Life Science and Technology, Beijing University of Chemical Technology , Beijing 100029, China.
ACS Appl Mater Interfaces. 2017 Aug 2;9(30):25216-25224. doi: 10.1021/acsami.7b04192. Epub 2017 Jul 19.
Thorium separation has recently become a hot topic because of the potential application of thorium as a future nuclear fuel, while metal-organic framework (MOF) materials have received much attention in the separation field due to their unique properties. Herein, a highly porous and stable MOF, UiO-66, and its carboxyl derivatives (UiO-66-COOH and UiO-66-(COOH)) were synthesized and explored for the first time for Th(IV) capture from a weak acidic solution. Although the introduction of carboxyl groups into UiO-66 leads to an obvious decrease in the surface area and pore volume, the adsorbability toward Th(IV) is greatly enhanced. At pH = 3.0, the saturated sorption capacity for Th(IV) into UiO-66-(COOH) reached 350 mg/g, representing one of the largest values for Th(IV) capture by solid extraction. Moreover, the functionalized MOFs show fast sorption kinetics and desirable selectivity toward Th(IV) over a range of competing metal ions. A possible mechanism for the selective recognition of Th(IV) by these MOFs was explored on the basis of extended X-ray absorption fine structure and Fourier transform infrared analysis. It is concluded that UiO-66-COOH and UiO-66-(COOH) sorb Th(IV) through the coordination of carboxyl anions in the pores of the MOFs, whereas in the case of UiO-66, both the precipitation and the exchange with the organic solvent contribute to the Th(IV) uptake. This study contributes to the assessment of the feasibility of MOFs applied in actinides separation and better understanding of actinides sorption behavior in this kind of hybrid porous solid materials.
钍分离最近成为一个热门话题,因为钍作为未来核燃料的潜在应用,而金属-有机骨架(MOF)材料由于其独特的性质在分离领域受到了广泛关注。本文首次合成了高度多孔和稳定的 MOF UiO-66 及其羧基衍生物(UiO-66-COOH 和 UiO-66-(COOH)),并探索了它们从弱酸性溶液中捕获 Th(IV)的性能。尽管在 UiO-66 中引入羧基基团会导致比表面积和孔体积明显减少,但对 Th(IV)的吸附能力却大大增强。在 pH = 3.0 时,UiO-66-(COOH)对 Th(IV)的饱和吸附容量达到 350 mg/g,是固体萃取中对 Th(IV)捕获的最大值之一。此外,功能化 MOFs 对 Th(IV)表现出快速的吸附动力学和对一系列竞争金属离子的理想选择性。根据扩展 X 射线吸收精细结构和傅里叶变换红外分析,探讨了这些 MOFs 对 Th(IV)选择性识别的可能机制。结论是 UiO-66-COOH 和 UiO-66-(COOH)通过 MOFs 孔中羧基阴离子的配位来吸附 Th(IV),而对于 UiO-66,Th(IV)的摄取既包括沉淀,也包括与有机溶剂的交换。该研究有助于评估 MOFs 在锕系元素分离中的应用可行性,并更好地了解这类混合多孔固体材料中锕系元素的吸附行为。