1. First-Principles Insights into the Selective Separation of MoS42–and WO42–: Crucial Role of Hydration Structures
- Author
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Han, Mingjun, Fan, Dong, Zhang, Chenyang, Liu, Hengzhi, Pei, Yong, Li, Jie, Chen, Jianhua, Sun, Wei, and Zhao, Zhongwei
- Abstract
The selective separation of MoS42–and WO42–using quaternary ammonium salt through solvent extraction or ion exchange methods has been well-established in the metallurgical industry. However, the conventional electrostatic adsorption theory falls short in explaining the separation mechanism. Through first-principles density functional theory (DFT) calculations and newly self-developed deep potential molecular dynamics (DPMD) simulation method, our work first reveals that the disparity in hydration structures of MoS42–and WO42–plays a crucial role in their selective separation. It is proposed that MoS42–and WO42–anions undergo hydration to form [MoS4(H2O)n]2–and [WO4(H2O)n]2–, respectively, facilitated by hydrogen bond (H-bond) interactions. Emphasis is placed on the discrepancy between MoS42–and WO42–in hydration structures by the hydration energy, Hirshfeld charge, evaluation of weak interactions, hydration radius, hydration coordination number, and H-bonds distribution. MoS42–presents a larger first hydration radius and a lower first hydration coordination number due to weaker interactions with H2O, while WO42–is subjected to enhanced hydration shielding, resulting in MoS42–anions being more susceptible to be selectively separated by a quaternary ammonium salt. This insight paves the way for the selective separation of MoS42–and WO42–, further bridging the gap between theory and industry applications.
- Published
- 2024
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