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308.15 K
JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2021 · IF 2.694

Pseudoternary Systems of Deep Eutectic Solvents + tert-Butanol + Water at T = 288.15 K, 298.15 K, and 308.15 K: Liquid–Liquid Equilibrium and Ability for Syringic Acid/Eugenol Separation

Kangling Yin,Li Chen,Feng Liu,Taotao Fan,Zongcheng Yan

Aiming at developing more biocompatible and economic separation platforms, aqueous biphasic systems (ABS) composed of deep eutectic solvents (DES) and tert-butanol were proposed for the first time. The effects of key factors such as the hydrogen-bond donor (HBD) properties and temperature on the phase-forming ability of DES/tert-butanol ABS were investigated. Meanwhile, syringic acid and eugenol mixtures were selected as model biomolecules to evaluate the efficiency of DES/tert-butanol ABS to use as liquid–liquid extraction systems. The results indicated that DES components migrated preferentially to the bottom phase while tert-butanol was concentrated in the top phase. The more hydrophilic HBD or lower temperature was responsible for greater efficiency to induce the formation of DES/tert-butanol ABS. The reason for phase separation was the incompatibility of the hydrogen-bond acceptor (HBA) and HBD with tert-butanol in aqueous solution, where the higher hydrophilic HBD enriched favorably in the lower phase, allowing for the formation of the DES/tert-butanol ABS. The selective separation of syringic acid and eugenol was a consequence of the HBD characters, temperature, and tie-lines length of the ABS, and they could be greatly separated by using the ABS composed of betaine-xylitol (DES) and tert-butanol at 298.15 K. The highest extraction efficiency of syringic acid and eugenol was 91.64 and 97.62%, respectively. Further, syringic acid and eugenol as well as DES can be recovered and reused by using water as the antisolvent and the vacuum distillation method. This study may be expected to lay a solid foundation for the expansion of DES-based ABS and selective separation of similar biomolecules.

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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2022 · IF 3.119

Measurements of Solid–Liquid Equilibria in Quaternary System LiBr–MgBr2–KBr–H2O and Its Two Ternary Systems (LiBr–MgBr2–H2O and MgBr2–KBr–H2O) at 288.15 and 308.15 K

Guopeng Chen,Junsheng Yuan,Zilong Liu,Ming Lei,Bin Li

The solid–liquid equilibria in the LiBr–MgBr2–KBr–H2O system was measured, along with its two subsystems, LiBr–MgBr2–H2O and MgBr2–KBr–H2O, at 308.15 and 288.15 K using the isothermal dissolution equilibrium method. The stable phase diagrams of the three systems at 308.15 and 288.15 K were plotted. For the ternary LiBr–MgBr2–H2O system, two univariant curves, one ternary invariant point, and two crystallization fields, the fields being MgBr2·6H2O and LiBr·2H2O, were identified. The ternary system MgBr2–KBr–H2O contained three univariant curves, two ternary invariant points, and three crystallization fields corresponding to KBr, KBr·MgBr2·6H2O, and MgBr2·6H2O. From the stable phase diagram of the quaternary system, five univariant curves, four crystallization fields, and two invariant points were observed. The corresponding solids of the four crystallization fields were KBr, LiBr·2H2O, KBr·MgBr2·6H2O, and MgBr2·6H2O. The quaternary phase diagrams at 288.15 and 308.15 K had similar shapes, and the shapes of each crystallization field were identical. The crystallization field of KBr was larger than the other crystallization fields. With an increase in temperature, the crystallization field of KBr became smaller and that of LiBr became larger.

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