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Ion and water transport during lithium chloride concentration from aqueous organic solutions by electrodialysis

机译:通过电渗析从有机水溶液中浓缩氯化锂期间的离子和水传输

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摘要

The concentration of lithium chloride from aqueous organic solutions with different volume concentrations of N,N-dimethylacetamide (DMAA) was studied experimentally. An extended model of the limiting electrodialysis concentration of electrolytes from mixed media was developed. The model takes into account the osmotic and electroosmotic mechanisms of the transfer of water and organic solvent, as well as the electromigration and diffusion mechanisms of the salt transfer. Using the experimental data and the extended model, we evaluated the transport parameters of the MK-40/MA-40 membrane pair in aprotic solutions of variable compositions and studied how they changed with an increase in the volume fraction of DMAA in a mixed solution. The contribution of each of these mechanisms of ion and water transport to the electrodialysis concentration of electrolyte from aqueous and organic aqueous solutions was determined. Electroosmotic transfer was found to be the main mechanism of the solvent transfer that limits the stage of the electrodialysis concentration of the electrolyte from aqueous and organic aqueous solutions.
机译:实验研究了具有不同体积浓度的N,N-二甲基乙酰胺(DMAA)的有机水溶液中氯化锂的浓度。建立了混合介质中电解质极限电渗析浓度的扩展模型。该模型考虑了水和有机溶剂转移的渗透和电渗机制,以及盐转移的电迁移和扩散机制。使用实验数据和扩展模型,我们评估了MK-40 / MA-40膜对在可变组成的非质子溶液中的传输参数,并研究了它们在混合溶液中随DMAA体积分数的增加而变化的情况。确定了这些离子和水传输机制对来自水溶液和有机水溶液的电解质的电渗析浓度的贡献。发现电渗转移是溶剂转移的主要机理,其限制了来自水溶液和有机水溶液的电解质的电渗析浓度阶段。

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