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对由质子离子液体和聚乙二醇组成的双水相体系形成机制的批判性评估。

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

作者信息

Cláudio Ana Filipa M, Pereira Jorge F B, McCrary Parker D, Freire Mara G, Coutinho João A P, Rogers Robin D

机构信息

CICECO - Aveiro Institute of Materials, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.

出版信息

Phys Chem Chem Phys. 2016 Nov 21;18(43):30009-30019. doi: 10.1039/c6cp06289j. Epub 2016 Oct 24.

DOI:10.1039/c6cp06289j
PMID:27774550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5325265/
Abstract

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) 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.

摘要

为了理解双相分离背后的机制,开展了一项关于使用质子离子液体(PILs)水溶液和聚乙二醇(PEG)形成双水相体系(ABS)的广泛研究。制备了具有不同分子量(600、1000、2000和3400 g/mol)的PEG聚合物水溶液以及几种乙酸盐、丙酸盐、丁酸盐、己酸盐和辛酸盐的N-烷基-、二烷基-和三烷基-铵盐,并评估了它们在几个温度下形成ABS的能力。测定了几个温度下的三元液-液相图,以及二元PIL(或盐)-PEG-1000和盐-水的溶解度数据,以更好地阐明导致相分离的机制。收集的所有数据表明,基于PEG-PIL的ABS的形成主要受PIL-PEG相互作用的控制,其中在聚合物中溶解度较高的PIL形成ABS的能力较低,因此双相区域较小,为此确定了直接相关性。还讨论了聚合物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,而温度的影响更为复杂,取决于PIL的性质,随着温度升高,双相区域可能增加或减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/0f8094b4a4bc/emss-71584-f008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/1171f9d206e8/emss-71584-f001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/f42eafd4e6b2/emss-71584-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/2a807e3fff56/emss-71584-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/341669075e3f/emss-71584-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/2498bb798434/emss-71584-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/59aab59cdeb2/emss-71584-f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/0f8094b4a4bc/emss-71584-f008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/1171f9d206e8/emss-71584-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/ee148deca928/emss-71584-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/f42eafd4e6b2/emss-71584-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/2a807e3fff56/emss-71584-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/341669075e3f/emss-71584-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/2498bb798434/emss-71584-f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/59aab59cdeb2/emss-71584-f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b0/5325265/0f8094b4a4bc/emss-71584-f008.jpg

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