Li Yan, Cheng Huaigang, He Yueyue, Zhao Jing
Institute of Resources and Environmental Engineering, School of Environment and Resources, Shanxi University, Taiyuan 030006, China.
Salt Lake Chemical Engineering Research Complex, Qinghai University, Xining 810016, China.
Molecules. 2025 Feb 7;30(4):776. doi: 10.3390/molecules30040776.
The magnesium impurities in lithium carbonate cannot be detected quickly in an aqueous environment. To solve this bottleneck problem, this study proposes a new method for the rapid detection of trace Mg in lithium carbonate using a water-soluble fluorescent probe. A water-soluble fluorescent probe A was obtained by introducing hydroxyl groups on a fluorescent oxazole ring. After modification, the hydrogen bonding between the probe and water molecules increased by more than 62 times. Consequently, the energy loss of outward transfer of the fluorescent probe increased, resulting in weak fluorescence in saline systems. Mg was captured by N on the oxazole ring and O on the phenolic hydroxyl group through a 1:1 coordination ratio within the probe structure. The hydrogen bonding attraction between the complex and water molecules increased 16 times. Additionally, the orbital energy gap was reduced from 2.817 to 0.383 eV. Meanwhile, the Mg impeded the phototropic electron transfer effect process, resulting in enhanced fluorescence and completing this process within 3 to 10 s, with a detection limit of 6.06 μmol/L. This method can promote the real-time and rapid quality control of Mg impurities in the refining and purification of lithium carbonate, as well as effectively reduce production costs.
碳酸锂中的镁杂质在水性环境中无法快速检测。为解决这一瓶颈问题,本研究提出一种使用水溶性荧光探针快速检测碳酸锂中痕量镁的新方法。通过在荧光恶唑环上引入羟基获得了水溶性荧光探针A。修饰后,探针与水分子之间的氢键增加了60多倍。因此,荧光探针向外转移的能量损失增加,导致在盐溶液体系中荧光减弱。在探针结构内,镁通过1:1的配位比被恶唑环上的氮和酚羟基上的氧捕获。配合物与水分子之间的氢键吸引力增加了16倍。此外,轨道能隙从2.817 eV降低到0.383 eV。同时,镁阻碍了光致电子转移效应过程,导致荧光增强,并在3至10秒内完成此过程,检测限为6.06 μmol/L。该方法可促进碳酸锂精炼和提纯过程中镁杂质的实时快速质量控制,并有效降低生产成本。