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Binary mixtures of HMIMPF6 ionic liquid and n-butyl acetate cosolvent in the extraction of acetone from aqueous solutions

机译:Hmimpf6离子液体和乙酸正丁酯的二元混合物在水溶液中提取丙酮中的乙酸叔丁酯

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摘要

A remarkable disadvantage of pure ionic liquids, to be used as a solvent in different processes, is their high viscosity and density. Here, n-butyl acetate was used as a cosolvent in the liquid-liquid system of {water+acetone+1-hexyl-3-methylimidazolium hexafluorophosphate (HMIMPF6) ionic liquid}. Mixtures of the ionic liquid and the cosolvent were used as the organic phase to extract acetone from aqueous phase. A drastic decrease in viscosity and a significant decrease in density of the ionic liquid were achieved in the presence of cosolvent. Accordingly, the liquid-liquid equilibrium of different provided systems was studied under temperature of 298.2K and atmospheric pressure of 81.5kPa. Binary phase regions and corresponding tie-lines and binodal curves were obtained for ternary and quaternary systems. Results show the extension of the binodal solubility region as well as enhancements up to 41.8% in the acetone separation factor. The tie-line data consistency was confirmed by the Othmer-Tobias and the Hand equations. Moreover, the nonrandom two-liquid model of activity coefficient was applied satisfactorily to reproduce the equilibrium data with a root-mean-square deviation of only 1.95%.
机译:纯离子液体的显着缺点,用作不同方法的溶剂,是它们的高粘度和密度。这里,乙酸正丁酯用作液 - 液体体系中的溶剂液中的溶剂液体系统中的溶液体系六氟哌啶六氟磷酸盐(Hmimpf6)离子液体}。将离子液体和助溶剂的混合物用作从水相中提取丙酮的有机相。在共溶剂存在下,实现了离子液体密度的粘度急剧下降和显着降低。因此,在298.2K的温度下,在298.2k和81.5kpa的大气压下研究了不同提供的系统的液体 - 液平衡。为三元和四元系统获得二进制相区域和相应的扎带线和二合一曲线。结果表明二合一溶解度区域的延伸以及丙酮分离因子的增强率高达41.8%。通过othmer-tobias和手方程确认了连接线数据一致性。此外,令人满意地应用活性系数的非谐波二液模型,以再现具有1.95%的根均方偏差的平衡数据。

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