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Stripping and recycling of metal ions in aqueous nitric acid solutions: Experimental and molecular dynamics insights

机译:硝酸水溶液中金属离子的剥离和再循环:实验和分子动力学见解

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摘要

Stripping of metal ions (i.e., Cs+ and Na+) in presence of ionophore such as dibenzo-18-crown-6, (DB18C6) from the ionic liquid phase to the aqueous nitric acid phase by molecular dynamics simulation is reported. The experimentally determined stripping percentages of Na+ (i.e., 43.4, 38.5, 34.4, and 31.9%) were found to be higher than the same for Cs+ (i.e., 32.6, 32.0, 31.3, and 30.2%). The nonbonded and the hydrogen bond energies between Na+ and water (i.e., -356.41 and -363.77 kcal/mol) were higher when compared with Cs+ (i.e., -212.43 and -221.04 kcal/mol). The spatial distribution functions further confirmed that the surfaces of Na+ were very closely distributed around the active sides of water whereas for Cs+, it was distributed very far from the water molecules. In the penultimate section, the effect of methanol to the aqueous phase was studied so as to enhance the extraction efficiency of the complex.
机译:据报道,通过分子动力学模拟,报道了通过分子动力学模拟在离子液相与离子液相中与离子液相的离子液相存在于离子液相中的金属离子(即,Cs +和Na +)。 发现Na +(即43.4,38.5,34.4和31.9%)的实验确定的剥离百分比高于Cs +(即32.6,32.0,31.3和30.2%)。 与Cs +(即-212.43和-221.04 kcal / mol)相比,Na +和水(即-356.41和-363.77kcal / mol)之间的非粘附和氢键合能较高。 空间分布功能进一步证实,对于Cs +,Na +的表面非常紧密地分布在水的活性侧,而其分布远离水分子。 在倒数二部分中,研究了甲醇对水相的影响,以提高复合物的提取效率。

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