Percevault Lucie, Jani Aicha, Sohier Thibaut, Noirez Laurence, Paquin Ludovic, Gauffre Fabienne, Morineau Denis
Institute of Chemical Sciences of Rennes, CNRS-University of Rennes 1, UMR 6226, Rennes F-35042, France.
Institute of Physics of Rennes, CNRS-University of Rennes 1, UMR 6251, Rennes F-35042, France.
J Phys Chem B. 2020 Oct 15;124(41):9126-9135. doi: 10.1021/acs.jpcb.0c06317. Epub 2020 Oct 6.
We have performed small-angle neutron scattering in a momentum transfer range (0.05 < < 0.5 Å) to study long-range order and concentration fluctuations in deep eutectic solvents (DESs) and their aqueous solutions. Ethaline (choline chloride/ethylene glycol), glycerol/lactic acid, and menthol/decanoic acid mixtures were selected to illustrate individually the case of ionic, nonionic, and hydrophobic mixtures. Carefully designed isotopic labeling was used to emphasize selectively the spatial correlations between the different solvent components. For ethaline DESs and their aqueous solutions, a weak low- peak observed only for certain compositions and some partial structure factors revealed the mesoscopic segregation of ethylene glycol molecules that do not participate in the solvation of ionic units, either because they are in excess with respect to the eutectic stoichiometry (1:4 neat ethaline) or substituted by water (4-ethaline and higher aqueous dilutions). For the nonionic hydrophilic solutions, such a mesoscopic segregation was not observed. This indicates that the better balanced interactions between the three nonionic H-bonded components (water, lactic acid, and glycerol) favor homogeneous mixing. For the hydrophobic DESs, we observed an excess of coherent scattering intensity centered at = 0, which could be reproduced by a model of noninteracting spherical domains. Local concentration fluctuations are not excluded either. However, unlike liquid mixtures with a tendency to demix, we have found no evidence of expansion of domains with different compositions to a large scale.
我们在动量转移范围(0.05<q<0.5 Å)内进行了小角中子散射,以研究深共晶溶剂(DESs)及其水溶液中的长程有序和浓度涨落。选择乙酰胺(氯化胆碱/乙二醇)、甘油/乳酸和薄荷醇/癸酸混合物分别来说明离子型、非离子型和疏水型混合物的情况。使用精心设计的同位素标记来选择性地强调不同溶剂组分之间的空间相关性。对于乙酰胺DESs及其水溶液,仅在某些组成下观察到一个微弱的低q峰,并且一些部分结构因子揭示了未参与离子单元溶剂化的乙二醇分子的介观偏析,这要么是因为它们相对于共晶化学计量比(纯乙酰胺为1:4)过量,要么被水取代(4-乙酰胺及更高的水稀释液)。对于非离子型亲水溶液,未观察到这种介观偏析。这表明三种非离子氢键结合组分(水、乳酸和甘油)之间更好平衡的相互作用有利于均匀混合。对于疏水DESs,我们观察到在q = 0处有过量的相干散射强度,这可以用非相互作用球形域模型来再现。局部浓度涨落也未被排除。然而,与有相分离倾向的液体混合物不同,我们没有发现不同组成的域大规模扩展的证据。