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A critical assessment of the mechanisms governing the formation of aqueous biphasic systems composed of protic ionic liquids and polyethylene glycol

机译:对控制由质子离子液体和聚乙二醇组成的水性双相体系形成机理的关键评估

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摘要

An extensive study on the formation of aqueous biphasic systems (ABS) using aqueous solutions of protic ionic liquids (PILs) and polyethylene glycol (PEG) was performed in order to understand the mechanisms underlying the phase separation. Aqueous solutions of PEG polymers with different molecular weights (600, 1000, 2000, and 3400 g mol−1) and several N-alkyl-, dialkyl-, and trialkyl-ammonium salts of acetate, propanoate, butanoate, hexanoate and octanoate were prepared and their ability to form ABS at several temperatures assessed. The ternary liquid–liquid phase diagrams were determined at several temperatures, as well as binary PIL (or salt)-PEG-1000 and salt-water solubility data to better clarify the mechanisms responsible for the phase separation. All data gathered indicate that the formation of PEG–PIL-based ABS is mainly governed by the PIL–PEG mutual interactions, where PILs with a higher solubility in the polymer exhibit a lower aptitude to form ABS displaying thus a smaller biphasic region, for which a direct correlation was identified. The effects of the molecular weight and temperature of the polymer were also addressed. The increase of the PEG hydrophobicity or molecular weight favours the phase separation, whereas the effect of temperature was found to be more complex and dependent on the nature of the PIL, with an increase or decrease of the biphasic regime with an increase in temperature.
机译:为了了解相分离的机理,对使用质子离子液体(PIL)和聚乙二醇(PEG)的水溶液形成双相水相(ABS)进行了广泛的研究。分子量分别为600、1000、2000和3400 g mol -1 的PEG聚合物的水溶液,以及乙酸盐,丙酸盐的几种N-烷基,二烷基和三烷基铵盐,制备丁酸酯,己酸酯和辛酸酯,并评估它们在几种温度下形成ABS的能力。在几个温度下确定了三元液相图,并确定了二元PIL(或盐)-PEG-1000和盐水溶解度数据,以更好地阐明造成相分离的机理。收集到的所有数据表明,基于PEG-PIL的ABS的形成主要受PIL-PEG相互作用的控制,其中在聚合物中具有较高溶解度的PIL显示形成ABS的能力较低,因此显示出较小的双相区域,为此,确定了直接相关性。还讨论了聚合物的分子量和温度的影响。 PEG疏水性或分子量的增加有利于相分离,而发现温度的影响更为复杂,并且取决于PIL的性质,随着温度的升高,双相态的增加或减少。

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