Liquid-liquid extraction of phenolic compounds from aqueous solution using hydrophobic deep eutectic solvents

被引:30
作者
Cable, Pierre-Alann [1 ]
Le Brech, Yann [1 ]
Mutelet, Fabrice [1 ]
机构
[1] Univ Lorraine, Ecole Natl Super Ind Chim, CNRS, Lab React & Genie Procedes,UMR 7274, 1 Rue Grandville, F-54000 Nancy, France
关键词
Ternary phase diagrams; Liquid-liquid extraction; Phenolic compounds; Hydrophobic deep eutectic solvents; COSMO; -RS; IONIC LIQUIDS; PYROLYSIS OIL; SEPARATION; WATER; SOLUBILITY; EQUILIBRIA; TEMPERATURE; MIXTURES; TERNARY; SYSTEMS;
D O I
10.1016/j.molliq.2022.120266
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
This work evaluates the efficiency of extracting phenolic compounds (phenol, guaiacol, eugenol and pyro-catechol) from aqueous solution using Hydrophobic Deep Eutectic Solvents (HDESs). Four solvents were selected by screening HDESs database using the predictive model COSMO-RS (Conductor like Screening Model for Real Solvent): menthol: dodecanoic acid [2:1], decanoic acid: dodecanoic acid [2:1], octanoic acid: menthol [2:1] and thymol: menthol [1:1]. Experimental liquid-liquid equilibria of ternary systems {water - HDESs - phenolic compounds} measured at 298.15 K under atmospheric pressure were used to determine the distribution coefficient and selectivity values. Experimental data were used to determine the interaction parameters of the thermodynamic Non-Random Two-Liquid model (NRTL). NRTL model represents with good accuracy experimental data. COSMO-RS model predicts well the ternary systems containing phenolic compounds except those containing pyrocatechol. Finally, extraction of the four phe-nolic compounds from synthetic oil and kinetics study were performed. The extraction process using HDES: octanoic acid: menthol [2:1] exhibits the highest efficiency and more than 85 % of phenolic com-pounds are extracted after 5 min.(c) 2022 Published by Elsevier B.V.
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页数:9
相关论文
共 71 条
[21]   Separation characteristics of biomass pyrolysis oil in molecular distillation [J].
Guo, Zuogang ;
Wang, Shurong ;
Gu, Yueling ;
Xu, Guohui ;
Li, Xin ;
Luo, Zhongyang .
SEPARATION AND PURIFICATION TECHNOLOGY, 2010, 76 (01) :52-57
[22]   Dineric distribution [J].
Hand, DB .
JOURNAL OF PHYSICAL CHEMISTRY, 1930, 34 (09) :1961-2000
[23]   Increasing the efficiency of fast pyrolysis process through sugar yield maximization and separation from aqueous fraction bio-oil [J].
Hassan, El Barbary ;
Abou-Yousef, Hussein ;
Steele, Phillip .
FUEL PROCESSING TECHNOLOGY, 2013, 110 :65-72
[24]   The mutual solubility of liquids III The mutual solubility of phenol and water IV The mutual solubility of normal butyl alcohol and water [J].
Hill, AE ;
Malisoff, WM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1926, 48 (01) :918-927
[25]  
Holladay J.E., 2007, Top Value-Added Chemicals from Biomass-Volume II-Results of Screening for Potential Candidates from Biorefinery Lignin, DOI [10.2172/921839, DOI 10.2172/921839]
[26]   Room temperature ionic liquids as novel media for 'clean' liquid-liquid extraction [J].
Huddleston, JG ;
Willauer, HD ;
Swatloski, RP ;
Visser, AE ;
Rogers, RD .
CHEMICAL COMMUNICATIONS, 1998, (16) :1765-1766
[27]   Synthesis and characterization of green menthol-based low transition temperature mixture with tunable thermophysical properties as hydrophobic low viscosity solvent [J].
Hussin, Siti Amira Mat ;
Varanusupakul, Pakorn ;
Shahabuddin, Syed ;
Hui, Boon Yih ;
Mohamad, Sharifah .
JOURNAL OF MOLECULAR LIQUIDS, 2020, 308
[28]   Anti-dermaptophyte activity of phenolic compounds in "Mokusaku-Eki" [J].
Ikegami, F ;
Sekine, T ;
Fujii, Y .
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 1998, 118 (01) :27-A4
[29]  
Iwata T., 2000, ULLMANNS ENCY IND CH
[30]   Liquid-liquid and liquid-solid equilibria of systems containing water and selected chlorophenols [J].
Jaoui, M ;
Luszczyk, M ;
Rogalski, M .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1999, 44 (06) :1269-1272