方解石
硅酸铝
沸石
铯
放射性废物
放射性核素
化学
化学工程
碱土金属
吸附
无机化学
碱金属
放射化学
材料科学
吸附
核化学
物理化学
有机化学
催化作用
物理
工程类
量子力学
作者
Anton Kasprzhitskii,Yakov Ermolov,Vasilii Mischinenko,Andrey Vasilchenko,E. A. Yatsenko,V. A. Smoliy
标识
DOI:10.3390/ijms242317023
摘要
Conditioning of radioactive waste generated from the operation of medical institutions, nuclear cycle facilities, and nuclear facilities is important for the safety of the environment. One of the most hazardous radionuclides is radioactive cesium. There is a need for more effective solutions to contain radionuclides, especially cesium (Cs+). Geopolymers are promising inorganic materials that can provide a large active surface area with adjustable porosity and binding capacity. The existence of nanosized zeolite-like structures in aluminosilicate gels was shown earlier. These structures are candidates for immobilizing radioactive cesium (Cs+). However, the mechanisms of their interactions with the aluminosilicate framework related to radionuclide immobilization have not been well studied. In this work, the influence of alkaline cations (Na+ or K+) and the aluminosilicate framework structure on the binding capacity and mechanism of interaction of geopolymers with Cs+ is explored in the example of a sodalite framework. The local structure of the water molecules and alkaline ions in the equilibrium state and its behavior when the Si/Al ratio was changed were studied by DFT.
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