Deep eutectic solvents on a tightrope: balancing the entropy and enthalpy of mixing†

IF 3.4 3区 化学 Q2 Chemistry Faraday Discussions Pub Date : 2024-03-18 DOI:10.1039/D4FD00048J
Adriaan van den Bruinhorst, Chiara Corsini, Guillaume Depraetère, Nithavong Cam, Agílio Pádua and Margarida Costa Gomes
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Abstract

The large melting point depressions characterising deep eutectic solvents (DESs) are related to negative deviations from ideal mixing behaviour characterised by the excess Gibbs energy. Favourable excess Gibbs energies result from a balance between the excess entropy and enthalpy of mixing, which was experimentally determined for three choline chloride (ChCl) based mixtures using calorimetry. While the excess Gibbs energy of H2O + ChCl is enthalpy dominated, those of ethylene glycol (EG) + ChCl and 1,3-propanediol + ChCl are entropy dominated. Molecular dynamics simulations using polarisable force-fields show intermolecular hydrogen bonds between DES constituents for H2O + ChCl and EG + ChCl. Hence, inter-species hydrogen bonding does not guarantee enthalpy-dominated melting point depressions. We suggest future research to focus on tuning the entropy–enthalpy balance via the chemical nature of the DES constituents.

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走钢丝的深共晶溶剂:平衡混合的熵和焓
深共晶溶剂(DES)的熔点降低与以过剩吉布斯能为特征的理想混合行为的负偏差有关。有利的过剩吉布斯能来自过剩熵和混合焓之间的平衡,我们使用量热计对三种氯化胆碱(ChCl)基混合物进行了实验测定。H2O + ChCl 的过剩吉布斯能以焓为主,而乙二醇 (EG) + ChCl 和 1,3-丙二醇 + ChCl 的过剩吉布斯能以熵为主。使用可极化力场进行的分子动力学模拟显示,H2O + ChCl 和 EG + ChCl 的 DES 成分之间存在分子间氢键。因此,物种间氢键并不能保证以焓为主的熔点下降。我们建议今后的研究重点是通过 DES 成分的化学性质来调整熵焓平衡。
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Faraday Discussions
Faraday Discussions CHEMISTRY, PHYSICAL-
CiteScore
4.90
自引率
0.00%
发文量
259
审稿时长
2.8 months
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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Back cover List of participants Poster list Correction: Challenges with relativistic GW calculations in solids and molecules List of participants
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