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Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes

The solubility of β-cyclodextrin (β-CD) in ionic liquids (ILs) and the activity coefficients at infinite dilution ( [Formula: see text]) of more than 20 solutes (alkanes, aromatic hydrocarbons, alcohols) were measured in four chosen ionic liquids, their mixtures with β-CD, and in the β-CD at high te...

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Autores principales: Rogalski, Marek, Modaressi, Ali, Magri, Pierre, Mutelet, Fabrice, Grydziuszko, Aleksandra, Wlazło, Michał, Domańska, Urszula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759929/
https://www.ncbi.nlm.nih.gov/pubmed/23945559
http://dx.doi.org/10.3390/ijms140816638
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author Rogalski, Marek
Modaressi, Ali
Magri, Pierre
Mutelet, Fabrice
Grydziuszko, Aleksandra
Wlazło, Michał
Domańska, Urszula
author_facet Rogalski, Marek
Modaressi, Ali
Magri, Pierre
Mutelet, Fabrice
Grydziuszko, Aleksandra
Wlazło, Michał
Domańska, Urszula
author_sort Rogalski, Marek
collection PubMed
description The solubility of β-cyclodextrin (β-CD) in ionic liquids (ILs) and the activity coefficients at infinite dilution ( [Formula: see text]) of more than 20 solutes (alkanes, aromatic hydrocarbons, alcohols) were measured in four chosen ionic liquids, their mixtures with β-CD, and in the β-CD at high temperatures from 338 to 398 K using the inverse gas chromatography. The intermolecular interactions, inclusion complexes and the possible increasing of the solubility of β-CD in water using the IL are presented. The solubility of β-CD in ten chosen hydrophobic ILs at the temperature T = 423 K was detected. The solid-liquid phase diagrams (SLE) of {IL (1) + β-CD (2)} binary systems at the high mole fraction of the IL were measured for three systems (1-ethyl-3-methylimidazolium chloride, [EMIM][Cl], 1-ethyl-3-methylimidazolium bromide, [EMIM][Br]; and for 1-butyl-3-methylimidazolium chloride, [BMIM][Cl]). The eutectic points were determined at the high IL concentration for all binary systems. The intermolecular interaction and the possibility of inclusion complexes of the IL and/or solvents with β-CD were discussed. The infrared spectroscopy, IR was used for the description of the intermolecular interactions in the (β-CD + IL) systems. It was shown via the activity coefficients at infinite dilution results that the inclusion complexes are dependent on the temperature. The addition of β-CD to the IL does not improve the selectivity of the separation of the aliphatics from aromatics.
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spelling pubmed-37599292013-09-03 Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes Rogalski, Marek Modaressi, Ali Magri, Pierre Mutelet, Fabrice Grydziuszko, Aleksandra Wlazło, Michał Domańska, Urszula Int J Mol Sci Article The solubility of β-cyclodextrin (β-CD) in ionic liquids (ILs) and the activity coefficients at infinite dilution ( [Formula: see text]) of more than 20 solutes (alkanes, aromatic hydrocarbons, alcohols) were measured in four chosen ionic liquids, their mixtures with β-CD, and in the β-CD at high temperatures from 338 to 398 K using the inverse gas chromatography. The intermolecular interactions, inclusion complexes and the possible increasing of the solubility of β-CD in water using the IL are presented. The solubility of β-CD in ten chosen hydrophobic ILs at the temperature T = 423 K was detected. The solid-liquid phase diagrams (SLE) of {IL (1) + β-CD (2)} binary systems at the high mole fraction of the IL were measured for three systems (1-ethyl-3-methylimidazolium chloride, [EMIM][Cl], 1-ethyl-3-methylimidazolium bromide, [EMIM][Br]; and for 1-butyl-3-methylimidazolium chloride, [BMIM][Cl]). The eutectic points were determined at the high IL concentration for all binary systems. The intermolecular interaction and the possibility of inclusion complexes of the IL and/or solvents with β-CD were discussed. The infrared spectroscopy, IR was used for the description of the intermolecular interactions in the (β-CD + IL) systems. It was shown via the activity coefficients at infinite dilution results that the inclusion complexes are dependent on the temperature. The addition of β-CD to the IL does not improve the selectivity of the separation of the aliphatics from aromatics. MDPI 2013-08-13 /pmc/articles/PMC3759929/ /pubmed/23945559 http://dx.doi.org/10.3390/ijms140816638 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Rogalski, Marek
Modaressi, Ali
Magri, Pierre
Mutelet, Fabrice
Grydziuszko, Aleksandra
Wlazło, Michał
Domańska, Urszula
Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes
title Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes
title_full Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes
title_fullStr Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes
title_full_unstemmed Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes
title_short Physico-Chemical Properties and Phase Behavior of the Ionic Liquid-β-Cyclodextrin Complexes
title_sort physico-chemical properties and phase behavior of the ionic liquid-β-cyclodextrin complexes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759929/
https://www.ncbi.nlm.nih.gov/pubmed/23945559
http://dx.doi.org/10.3390/ijms140816638
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