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为了理解水相离子液体溶液中的盐析效应:汽液平衡、液液平衡、体积、压缩性和电导率行为。

Toward an understanding of the salting-out effects in aqueous ionic liquid solutions: vapor-liquid equilibria, liquid-liquid equilibria, volumetric, compressibility, and conductivity behavior.

机构信息

Department of Chemistry, University of Kurdistan, Sanandaj, Iran.

出版信息

J Phys Chem B. 2010 Dec 16;114(49):16528-41. doi: 10.1021/jp108609b. Epub 2010 Nov 16.

DOI:10.1021/jp108609b
PMID:21080679
Abstract

The action of particular electrolytes in altering the solution properties of ionic liquids is well documented, although the origin of this effect is not clearly defined. In order to clarify this point, the aim of this work is to obtain further evidence about the salting-out effect produced by the addition of different salts to aqueous solutions of water miscible ionic liquids by evaluating the effect of a large series of salts on the vapor-liquid equilibria, liquid-liquid phase diagram, volumetric, compressibility, and conductometric properties of ionic liquids 1-alkyl-3-methylimidazolium halide ([C(n)mim][X]). In the first part of this work, the experimental measurements of water activity at 298.15 and 308.15 K for aqueous binary and ternary solutions containing 1-alkyl-3-methylimidazolium bromide ([Rmim][Br], R = butyl (C(4)), heptyl (C(7)), and octyl (C(8))), sodium dihydrogen citrate (NaH(2)Cit), disodium hydrogen citrate (Na(2)HCit), and trisodium citrate (Na(3)Cit) are taken using both vapor pressure osmometry (VPO) and improved isopiestic methods. The effect of temperature, charge on the anion of sodium citrate salts, and alkyl chain length of ionic liquids on the vapor-liquid equilibria properties of the investigated systems are studied. The constant water activity lines of all the ternary systems show large negative deviation from the linear isopiestic relation (Zdanovskii-Stokes-Robinson rule) derived using the semi-ideal hydration model, and the vapor pressure depression for a ternary solution is much larger than the sum of those for the corresponding binary solutions with the same molality of the ternary solution. The results have been interpreted in terms of the solute-water and solute-solute interactions. In the second part of this work, the effects of the addition of (NH(4))(3)Cit, K(3)Cit, Na(3)Cit, (NH(4))(2)HPO(4), and (NH(4))(3)PO(4) on the liquid-liquid phase diagram, apparent molar volume, isentropic compressibility, and conductivity of aqueous solutions containing the model ionic liquid 1-butyl-3-methylimidazolium iodide, [C(4)mim][I], are investigated at different temperatures. It was found that there is a relation between the relative concentration of various salts to form two-phase systems with [C(4)mim][I] and apparent molar volume or isentropic compressibility of transfer of [C(4)mim][I] from water to aqueous solutions of the investigated salts.

摘要

特定电解质在改变离子液体溶液性质方面的作用已有大量文献记载,尽管这种效应的起源尚未明确界定。为了澄清这一点,本工作的目的是通过评估一系列盐对水混溶性离子液体 1-烷基-3-甲基咪唑卤化物([C(n)mim][X])的蒸气压平衡、液-液相图、体积、压缩性和电导率性质的影响,获得更多关于添加不同盐对水相离子液体产生盐析效应的证据。在本工作的第一部分,使用蒸汽压渗透压(VPO)和改进的等压法测量了 298.15 和 308.15 K 时含 1-烷基-3-甲基咪唑溴化物([Rmim][Br],R = 丁基 (C(4))、庚基 (C(7))和辛基 (C(8))、柠檬酸氢二钠 (NaH(2)Cit)、柠檬酸二氢钠 (Na(2)HCit)和柠檬酸三钠 (Na(3)Cit)的水合二元和三元溶液的水活度。研究了温度、柠檬酸氢二钠盐阴离子的电荷和离子液体的烷基链长对所研究体系蒸气压平衡性质的影响。所有三元体系的恒定水活度线都与根据半理想水合模型推导出的线性等压关系(Zdanovskii-Stokes-Robinson 规则)有很大的负偏差,并且三元溶液的蒸气压降低远大于相同摩尔质量的相应二元溶液的蒸气压降低之和。结果根据溶质-水和溶质-溶质相互作用进行了解释。在本工作的第二部分,研究了 (NH(4))(3)Cit、K(3)Cit、Na(3)Cit、(NH(4))(2)HPO(4)和 (NH(4))(3)PO(4)的加入对模型离子液体 1-丁基-3-甲基咪唑碘化物 [C(4)mim][I]在不同温度下的液-液相图、表观摩尔体积、等熵压缩性和电导率的影响。结果发现,各种盐的相对浓度与 [C(4)mim][I]形成两相体系以及 [C(4)mim][I]从水向所研究盐的水溶液的转移的表观摩尔体积或等熵压缩性之间存在关系。

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