Mechanisms ruling the partition of solutes in ionic-liquid-based aqueous biphasic systems - the multiple effects of ionic liquids

被引:14
|
作者
Passos, Helena [1 ]
Dinis, Teresa B. V. [1 ]
Capela, Emanuel V. [1 ]
Quental, Maria V. [1 ]
Gomes, Joana [1 ]
Resende, Judite [1 ]
Madeira, Pedro P. [1 ]
Freire, Mara G. [1 ]
Coutinho, Joao A. P. [1 ]
机构
[1] Univ Aveiro, Dept Chem, CICECO Aveiro Inst Mat, P-3810193 Aveiro, Portugal
基金
欧洲研究理事会;
关键词
SOLVATOCHROMIC COMPARISON METHOD; SOLVATION ENERGY RELATIONSHIP; HYDROGEN-BOND ACIDITY; 2-PHASE SYSTEMS; SOLVENT PROPERTIES; RELATIVE HYDROPHOBICITY; METHYLENE GROUP; EXTENDED SCALE; PEG-SALT; EXTRACTION;
D O I
10.1039/c8cp00383a
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
In the past decade, the remarkable potential of ionic-liquid-based aqueous biphasic systems (IL-based ABSs) to extract and purify a large range of valued-added biocompounds has been demonstrated. However, the translation of lab-scale experiments to an industrial scale has been precluded by a poor understanding of the molecular-level mechanisms ruling the separation or partition of target compounds between the coexisting phases. To overcome this limitation, we carried out a systematic evaluation of specific interactions, induced by ILs and several salts used as phase-forming components, and their impact on the partition of several solutes in IL-based ABSs. To this end, the physicochemical characterization of ABSs composed of imidazolium-based ILs, three salts (Na2SO4, K2CO3 and K3C6H5O7) and water was performed. The ability of the coexisting phases to participate in different solute-solvent interactions (where solvent corresponds to each ABS phase) was estimated based on the Gibbs free energy of transfer of a methylene group between the phases in equilibrium, G(CH2), and on the Kamlet-Taft parameters - dipolarity/polarizability (*), hydrogen-bonding donor acidity () and hydrogen-bonding acceptor basicity () - of the coexisting phases. Relationships between the partition coefficients, the phase properties expressed as Kamlet-Taft parameters and COSMO-RS descriptors were established, highlighting the ability of ILs to establish specific interactions with given solutes. The assembled results clearly support the idea that the partition of solutes in IL-based ABSs is due to multiple effects resulting from both global solute-solvent and specific solute-IL interactions. Solute-IL specific interactions are often dominant in IL-based ABSs, explaining the higher partition coefficients, extraction efficiencies and selectivities observed with these systems when compared to more traditional ones majorly composed of polymers.
引用
收藏
页码:8411 / 8422
页数:12
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