Mechanisms of phase separation in temperature-responsive acidic aqueous biphasic systems

被引:27
|
作者
Schaeffer, Nicolas [1 ]
Perez-Sanchez, German [1 ]
Passos, Helena [1 ]
Gomes, Jose R. B. [1 ]
Papaiconomou, Nicolas [2 ]
Coutinho, Joao A. P. [1 ]
机构
[1] Univ Aveiro, Dept Chem, CICECO Aveiro Inst Mat, P-3810193 Aveiro, Portugal
[2] Univ Nice Sophia Antipolis, Dept Chem, 28 Ave Valrose, F-06103 Nice, France
关键词
COARSE-GRAINED MODEL; IONIC-LIQUID; WATER; SURFACTANTS; COACERVATION; TRANSITION; EXTRACTION; MIXTURES; MICELLES; BEHAVIOR;
D O I
10.1039/c8cp07750a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The temperature responsive solubility of ionic liquids with bulky' polar regions, such as tributyltetradecyl phosphonium chloride ([P-44414]Cl), in acidic aqueous solutions is elucidated through a combined experimental and computational approach. The temperature effect in the acidic aqueous biphasic system HCl/[P-44414]Cl/H2O was characterised in the range 273 K to 373 K and was found to significantly deviate from the corresponding aqueous biphasic system with NaCl. A new transferable coarse grained MARTINI model for [P-44414]Cl was developed, validated and applied to provide a molecular understanding of the experimental results. It is shown that the presence of large aliphatic moieties around the central phosphorus atoms of [P-44414]Cl results in a decrease in the electrostatic repulsion between the cationic moieties, leading the [P-44414](+) cation to present a behaviour conventionally associated with non-ionic surfactants. This difference in behaviour between HCl and NaCl was shown to result from the greater interaction of the hydronium cation with the micelle surface, thereby enhancing the [P-44414]Cl aggregation.
引用
收藏
页码:7462 / 7473
页数:12
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