Design and characterization of novel hydrophobic eutectic solvents based on metal-extracting ligands

IF 5.3 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Liquids Pub Date : 2025-03-11 DOI:10.1016/j.molliq.2025.127332
B. Bernicot , G. Arrachart , S. Dourdain , N. Schaeffer , G. Teixeira , S. Pellet-Rostaing
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Abstract

In the search for efficient and sustainable liquid–liquid extraction systems, some examples of hydrophobic deep eutectic solvents (HDES) recently emerged as promising alternatives due to their lower volatility, higher stability and extraction performances compared to conventional systems with organic diluents. However, the novelty of HDES has so far limited their study to a small number of systems, precluding further optimization and a deeper understanding. In the present study, we propose the design and full characterization of new non-ionic HDES using a combined experimental and simulation-based approach. These HDES are formulated with extractant molecules that are well known in the field of hydrometallurgy. Specifically, neutral extractants never explored in HDES, such as Tributyl phosphate (TBP), N,N′-dimethyl,N,N′-dioctylhexylethoxymalonamide (DMDOHEMA) or N,N,N′,N′ tetraoctyl diglycolamide (TODGA), were selected as Hydrogen Bond Acceptors (HBA), and associated with decanoic acid (DecA), as a Hydrogen Bond Donor (HBD). A detailed characterization study, using complementary techniques such as FT-IR spectroscopy, small angle X-rays scattering (SAXS) and molecular dynamics (MD), allowed us to elucidate the structural features and intermolecular interactions governing HDES formation. FT-IR and MD revealed quantitatively how the solvent properties are related to hydrogen bond interactions. MD results were successfully exploited to reproduce the experimental SAXS signals, which allowed for the accurate interpretation of the HDES structure. A physicochemical characterization study was further applied to demonstrate the possible application of these HDES as media for liquid–liquid extraction.

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基于金属萃取配体的新型疏水共晶溶剂的设计与表征
在寻找高效、可持续的液-液萃取系统的过程中,最近出现了一些疏水性深共晶溶剂(HDES)的例子,它们与使用有机稀释剂的传统系统相比,挥发性更低、稳定性更高、萃取性能更好,因此成为很有前途的替代品。然而,由于 HDES 的新颖性,迄今为止对其的研究仅限于少数体系,无法对其进行进一步优化和深入了解。在本研究中,我们采用实验和模拟相结合的方法,对新型非离子 HDES 进行了设计和全面表征。这些 HDES 是用湿法冶金领域众所周知的萃取剂分子配制的。特别是在 HDES 中从未使用过的中性萃取剂,如磷酸三丁酯(TBP)、N,N′-二甲基、N,N′-二辛基己基乙氧基丙二酰胺(DMDOHEMA)或 N,N、N′,N′ 四辛基二甘醇酰胺 (TODGA) 被选为氢键受体 (HBA),与癸酸 (DecA) 联用则被选为氢键供体 (HBD)。利用傅立叶变换红外光谱、小角 X 射线散射(SAXS)和分子动力学(MD)等互补技术进行的详细表征研究,使我们得以阐明 HDES 的结构特征和分子间相互作用。傅立叶变换红外光谱和分子动力学定量揭示了溶剂特性与氢键相互作用的关系。利用 MD 结果成功地再现了 SAXS 的实验信号,从而准确地解释了 HDES 的结构。理化特性研究进一步证明了将这些 HDES 用作液-液萃取介质的可能性。
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来源期刊
Journal of Molecular Liquids
Journal of Molecular Liquids 化学-物理:原子、分子和化学物理
CiteScore
10.30
自引率
16.70%
发文量
2597
审稿时长
78 days
期刊介绍: The journal includes papers in the following areas: – Simple organic liquids and mixtures – Ionic liquids – Surfactant solutions (including micelles and vesicles) and liquid interfaces – Colloidal solutions and nanoparticles – Thermotropic and lyotropic liquid crystals – Ferrofluids – Water, aqueous solutions and other hydrogen-bonded liquids – Lubricants, polymer solutions and melts – Molten metals and salts – Phase transitions and critical phenomena in liquids and confined fluids – Self assembly in complex liquids.– Biomolecules in solution The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include: – Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.) – Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.) – Light scattering (Rayleigh, Brillouin, PCS, etc.) – Dielectric relaxation – X-ray and neutron scattering and diffraction. Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.
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