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Aqueous biphasic systems comprising copolymers and cholinium-based salts or ionic liquids: Insights on the mechanisms responsible for their creation

机译:包含共聚物和基于胆碱的盐或离子液体的水性双相体系:对其创作负责的机制见解

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Aqueous biphasic systems (ABS) formed by copolymers and ionic liquids (ILs) have demonstrated to be effective separation platforms, but there is still a gap on the complete understanding of the molecular-level mechanisms ruling the two-phase formation for this type of systems. This work addresses the determination of the liquid-liquid equilibrium of ABS composed of cholinium-based salts or cholinium-based ILs and the triblock copolymer Pluronic PE6200 (PL6200). It is demonstrated that PL6200 can form ABS with all investigated cholinium-based salts or ILs, contrarily to most poly(ethylene)glycol polymers, which is due to the presence of hydrophobic propylene oxide (PO) blocks. From the phase diagrams behavior and IL/salt anions properties, it is shown that the formation of ABS with cholinium-based salts is ruled by the anions polar surface and ability to be hydrated, whereas in systems comprising ILs van der Waals interactions between the copolymer and the IL cannot be discarded. The partition of a series of alkaloids in these systems, namely caffeine, nicotine, theophylline, and theobromine, was additionally appraised. It is shown that caffeine, theophylline, and theobromine preferentially migrate to the more hydrophobic PL6200-rich phase, and that their partition depends on the water content in the respective phase, being ruled by the phases' hydrophobicity. On the other hand, nicotine, with the most prominent hydrophobic character amongst the studied alkaloids, preferentially migrates to the salt- or ILrich phase, in which interactions occurring between this alkaloid and the IL/salt cannot be discarded. The ABS formed by cholinium dihydrogenphosphate is the most selective system identified to separate nicotine from the remaining alkaloids, giving some insights into their investigation as separation platforms for alkaloids from natural extracts.
机译:由共聚物和离子液体(ILS)形成的水性双相系统(ABS)已经证明是有效的分离平台,但是对分子水平机制的完全理解仍然存在差距,该类型的这种系统统治两相形成。该工作地解决了由基于硫氨酸的盐或基于胆管基ILS和三嵌段共聚物PLURONIC PE6200(PL6200)组成的ABS液 - 液平衡的测定。结果证明,PL6200可以形成含有所有研究的胆碱的盐或ILS,与大多数聚(乙烯)二醇聚合物相反,这是由于存在疏水环氧丙烷(PO)块的存在。从相位图行为和IL /盐阴离子特性,显示含有硫鎓基盐的ABS的形成由阴离子极性表面和被水合的能力统治,而在包含ILS范德华相互作用的系统中,共聚物之间的体系并且IL不能被丢弃。另外评估了这些系统中一系列生物碱的分区,即咖啡因,尼古丁,茶碱和甲霉素。结果表明,咖啡因,茶碱和神经甘氨酸优先迁移到富含疏水性PL6200的相位,并且它们的分区取决于各相中的水含量,通过阶段的疏水性训练。另一方面,尼古丁,在研究的生物碱中具有最突出的疏水性特性,优先迁移到盐或ilRICH期,其中不能丢弃在该生物碱和IL /盐之间发生的相互作用。由硫氨基磷酸硫铵形成的ABS是鉴定的最选择性的系统,鉴定为与剩余的生物碱分离尼古丁,对其进行一些洞察力作为来自天然提取物的生物碱的分离平台。

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