基于氟化胆碱的深共晶溶剂的非同寻常的水合特性。

IF 2.9 2区 化学 Q3 CHEMISTRY, PHYSICAL
Ibrahim Alfurayj, Desiree Mae Prado, Ross Clark Prado, Anna Cristina Samia and Clemens Burda*, 
{"title":"基于氟化胆碱的深共晶溶剂的非同寻常的水合特性。","authors":"Ibrahim Alfurayj,&nbsp;Desiree Mae Prado,&nbsp;Ross Clark Prado,&nbsp;Anna Cristina Samia and Clemens Burda*,&nbsp;","doi":"10.1021/acs.jpcb.3c07625","DOIUrl":null,"url":null,"abstract":"<p >The hydration properties of the fluoride-based deep eutectic solvent ethalineF [a solution of choline fluoride in ethylene glycol (EG) at a 1:2 molar ratio] are studied and compared to the most common deep eutectic solvent ethaline (the solution of choline chloride in EG at 1:2 molar ratio). The densities of the deep eutectic solvent (DES) based on choline fluoride in EG (ethalineF) and its mixtures with water as cosolvent are measured over the temperature range of 298–323 K. The excess properties, including excess molar volumes, excess partial molar volumes, and viscosity deviations from ideal behavior, are calculated for ethalineF/water and ethaline/water mixtures and compared. The experimental excess molar volumes and viscosity deviations of the studied pseudobinary mixtures are fitted using the Redlich–Kister (R–K) equation. The results of the R–K model successfully reproduced the experimentally calculated values with minimal standard deviations. All excess molar volumes and viscosity deviations had negative values, indicating stronger solvation interactions between the mixture components than between each pure DES or water. The excess partial molar volumes show that water molecules are preferentially solvated by the DES environment. We show that the disruption of the DES interactions (primarily OH...halide interactions) by high mole fractions of water is related to the peak ionic conductivity. The stark differences in hydration behavior between fluoride- and chloride-based ethaline are analyzed and discussed.</p>","PeriodicalId":60,"journal":{"name":"The Journal of Physical Chemistry B","volume":"128 11","pages":"2762–2772"},"PeriodicalIF":2.9000,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unusual Hydration Properties of Choline Fluoride-Based Deep Eutectic Solvents\",\"authors\":\"Ibrahim Alfurayj,&nbsp;Desiree Mae Prado,&nbsp;Ross Clark Prado,&nbsp;Anna Cristina Samia and Clemens Burda*,&nbsp;\",\"doi\":\"10.1021/acs.jpcb.3c07625\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The hydration properties of the fluoride-based deep eutectic solvent ethalineF [a solution of choline fluoride in ethylene glycol (EG) at a 1:2 molar ratio] are studied and compared to the most common deep eutectic solvent ethaline (the solution of choline chloride in EG at 1:2 molar ratio). The densities of the deep eutectic solvent (DES) based on choline fluoride in EG (ethalineF) and its mixtures with water as cosolvent are measured over the temperature range of 298–323 K. The excess properties, including excess molar volumes, excess partial molar volumes, and viscosity deviations from ideal behavior, are calculated for ethalineF/water and ethaline/water mixtures and compared. The experimental excess molar volumes and viscosity deviations of the studied pseudobinary mixtures are fitted using the Redlich–Kister (R–K) equation. The results of the R–K model successfully reproduced the experimentally calculated values with minimal standard deviations. All excess molar volumes and viscosity deviations had negative values, indicating stronger solvation interactions between the mixture components than between each pure DES or water. The excess partial molar volumes show that water molecules are preferentially solvated by the DES environment. We show that the disruption of the DES interactions (primarily OH...halide interactions) by high mole fractions of water is related to the peak ionic conductivity. The stark differences in hydration behavior between fluoride- and chloride-based ethaline are analyzed and discussed.</p>\",\"PeriodicalId\":60,\"journal\":{\"name\":\"The Journal of Physical Chemistry B\",\"volume\":\"128 11\",\"pages\":\"2762–2772\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-03-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Physical Chemistry B\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jpcb.3c07625\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry B","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpcb.3c07625","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

研究了氟化物深共晶溶剂 ethalineF [氟化胆碱在乙二醇(EG)中的溶液,摩尔比为 1:2]的水合特性,并将其与最常见的深共晶溶剂 ethaline(氯化胆碱在 EG 中的溶液,摩尔比为 1:2)进行了比较。在 298-323 K 的温度范围内测量了基于 EG 中氟化胆碱的深共晶溶剂(DES)(乙碱 F)及其与水作为共溶剂的混合物的密度,计算并比较了乙碱 F/水和乙碱/水混合物的过剩特性,包括过剩摩尔体积、过剩部分摩尔体积和与理想行为的粘度偏差。所研究的假二元混合物的实验过剩摩尔体积和粘度偏差采用 Redlich-Kister (R-K) 方程进行拟合。R-K 模型的结果以最小的标准偏差成功地再现了实验计算值。所有过剩摩尔体积和粘度偏差均为负值,表明混合物成分之间的溶解相互作用比每种纯 DES 或水之间的作用更强。过剩部分摩尔体积表明,水分子优先被 DES 环境溶解。我们的研究表明,高分子分数的水对 DES 相互作用(主要是 OH...halide 相互作用)的破坏与离子电导率峰值有关。我们还分析并讨论了氟基和氯基乙碱液在水合行为上的明显差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unusual Hydration Properties of Choline Fluoride-Based Deep Eutectic Solvents

Unusual Hydration Properties of Choline Fluoride-Based Deep Eutectic Solvents

Unusual Hydration Properties of Choline Fluoride-Based Deep Eutectic Solvents

The hydration properties of the fluoride-based deep eutectic solvent ethalineF [a solution of choline fluoride in ethylene glycol (EG) at a 1:2 molar ratio] are studied and compared to the most common deep eutectic solvent ethaline (the solution of choline chloride in EG at 1:2 molar ratio). The densities of the deep eutectic solvent (DES) based on choline fluoride in EG (ethalineF) and its mixtures with water as cosolvent are measured over the temperature range of 298–323 K. The excess properties, including excess molar volumes, excess partial molar volumes, and viscosity deviations from ideal behavior, are calculated for ethalineF/water and ethaline/water mixtures and compared. The experimental excess molar volumes and viscosity deviations of the studied pseudobinary mixtures are fitted using the Redlich–Kister (R–K) equation. The results of the R–K model successfully reproduced the experimentally calculated values with minimal standard deviations. All excess molar volumes and viscosity deviations had negative values, indicating stronger solvation interactions between the mixture components than between each pure DES or water. The excess partial molar volumes show that water molecules are preferentially solvated by the DES environment. We show that the disruption of the DES interactions (primarily OH...halide interactions) by high mole fractions of water is related to the peak ionic conductivity. The stark differences in hydration behavior between fluoride- and chloride-based ethaline are analyzed and discussed.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.80
自引率
9.10%
发文量
965
审稿时长
1.6 months
期刊介绍: An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信