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Evaluation of the impact of phosphate salts on the formation of ionic-liquid-based aqueous biphasic systems
被引:75
|作者:
Mourao, Teresa
[1
]
Claudio, Ana Filipa M.
[1
]
Boal-Palheiros, Isabel
[1
]
Freire, Mara G.
[1
]
Coutinho, Joao A. P.
[1
]
机构:
[1] Univ Aveiro, CICECO, Dept Quim, P-3810193 Aveiro, Portugal
关键词:
Aqueous biphasic system;
Ionic liquid;
Salting-out effect;
Phosphate salts;
pH effect;
MUTUAL SOLUBILITIES;
ACTIVITY-COEFFICIENTS;
POTASSIUM PHOSPHATE;
INFINITE DILUTION;
2-PHASE SYSTEMS;
HYDROGEN-BONDS;
CONTROLLED PH;
CATION-ANION;
AMINO-ACIDS;
WATER;
D O I:
10.1016/j.jct.2012.05.019
中图分类号:
O414.1 [热力学];
学科分类号:
摘要:
The present study aims at evaluating the capability of phosphate-based salts, whose anions can coexist in water depending on the media pH, to promote aqueous biphasic systems (ABS) formation with 1-butyl-3-methylimidazolium-based ionic liquids, as well as to infer on the influence of the ionic liquid anion in the overall process of liquid-liquid demixing. In this context, novel phase diagrams of ABS composed of several imidazolium-based ionic liquids and three phosphate salts and a mixture of salts (K3PO4, K2HPO4, K2HPO4 + KH2PO4, and KH2PO4) were determined by the cloud point titration method at 298 K and atmospheric pressure. The corresponding tie-line compositions, tie-line lengths, and pH values of the coexisting phases were also determined. The ionic liquids ability to promote ABS is related with the hydrogen-bond basicity of the composing anion - the lower it is the higher the ability of the ionic fluid to undergo liquid-liquid demixing. Moreover, similar patterns on the ionic liquids sequence were observed with the different phosphate salts. The phosphate anion charge plays a determinant role in the formation of ABS. The two-phase formation aptitude (with a similar ionic liquid) decreases in the rank: K3PO4 > K2HPO4 > K2HPO4 + KH2PO4 > KH2PO4. Yet, besides the charge of the phosphate anion, the pH and ionic strength of the aqueous media also influence the phase separation ability. (C) 2012 Elsevier Ltd. All rights reserved.
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页码:398 / 405
页数:8
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