Ioannidis Ioannis, Pashalidis Ioannis, Arkas Michael
Laboratory of Radioanalytical and Environmental Chemistry, Department of Chemistry, University of Cyprus, P.O. Box 20537, Cy-1678 Nicosia, Cyprus.
National Centre for Scientific Research "Demokritos", Institute of Nanoscience and Nanotechnology, 15310 Athens, Greece.
Gels. 2023 Aug 27;9(9):690. doi: 10.3390/gels9090690.
The binding of actinide ions (Am(III) and U(VI)) in aqueous solutions by hybrid silica-hyperbranched poly(ethylene imine) nanoparticles (NPs) and xerogels (XGs) has been studied by means of batch experiments at different pH values (4, 7, and 9) under ambient atmospheric conditions. Both materials present relatively high removal efficiency at pH 4 and pH 7 (>70%) for Am(III) and U(VI). The lower removal efficiency for the nanoparticles is basically associated with the compact structure of the nanoparticles and the lower permeability and access to active amine groups compared to xerogels, and the negative charge of the radionuclide species is formed under alkaline conditions (e.g., UO(CO) and Am(CO)). Generally, the adsorption process is relatively slow due to the very low radionuclide concentrations used in the study and is basically governed by the actinide diffusion from the aqueous phase to the solid surface. On the other hand, adsorption is favored with increasing temperature, assuming that the reaction is endothermic and entropy-driven, which is associated with increasing randomness at the solid-liquid interphase upon actinide adsorption. To the best of our knowledge, this is the first study on hybrid silica-hyperbranched poly(ethylene imine) nanoparticle and xerogel materials used as adsorbents for americium and uranium at ultra-trace levels. Compared to other adsorbent materials used for binding americium and uranium ions, both materials show far higher binding efficiency. Xerogels could remove both actinides even from seawater by almost 90%, whereas nanoparticles could remove uranium by 80% and americium by 70%. The above, along with their simple derivatization to increase the selectivity towards a specific radionuclide and their easy processing to be included in separation technologies, could make these materials attractive candidates for the treatment of radionuclide/actinide-contaminated water.
在环境大气条件下,通过批量实验研究了杂化二氧化硅-超支化聚(乙烯亚胺)纳米颗粒(NPs)和干凝胶(XGs)对水溶液中锕系元素离子(Am(III)和U(VI))的吸附。在pH值为4、7和9时,两种材料对Am(III)和U(VI)均表现出较高的去除效率(>70%)。纳米颗粒去除效率较低主要与纳米颗粒的致密结构、与干凝胶相比更低的渗透性以及活性胺基团的可及性有关,并且放射性核素物种的负电荷是在碱性条件下形成的(例如UO(CO)和Am(CO))。一般来说,由于研究中使用的放射性核素浓度极低,吸附过程相对较慢,并且基本上受锕系元素从水相扩散到固体表面的控制。另一方面,吸附作用随温度升高而增强,假设该反应是吸热且由熵驱动的,这与锕系元素吸附时固液界面处随机性增加有关。据我们所知,这是首次关于将杂化二氧化硅-超支化聚(乙烯亚胺)纳米颗粒和干凝胶材料用作超痕量镅和铀吸附剂的研究。与用于结合镅和铀离子的其他吸附剂材料相比,这两种材料均表现出高得多的结合效率。干凝胶甚至可以从海水中去除近90%的两种锕系元素,而纳米颗粒可以去除80%的铀和70%的镅。上述特性,连同它们通过简单衍生化提高对特定放射性核素的选择性以及易于加工以纳入分离技术的特点,可能使这些材料成为处理受放射性核素/锕系元素污染水的有吸引力的候选材料。