Effect of ion structure on the physicochemical properties and gas absorption of surface active ionic liquids

Jocasta Ávila, Daniel Lozano-Martín, Mirella Simões Santos, Yunxiao Zhang, Hua Li, Agilio Pádua, Rob Atkin, Margarida Costa Gomes
{"title":"Effect of ion structure on the physicochemical properties and gas absorption of surface active ionic liquids","authors":"Jocasta Ávila, Daniel Lozano-Martín, Mirella Simões Santos, Yunxiao Zhang, Hua Li, Agilio Pádua, Rob Atkin, Margarida Costa Gomes","doi":"arxiv-2409.11853","DOIUrl":null,"url":null,"abstract":"Surface active ionic liquids (SAILs) combine useful characteristics of both\nionic liquids (ILs) and surfactants, hence are promising candidates for a wide\nrange of applications. However, the effect of SAIL ionic structures on their\nphysicochemical properties remains unclear, which limits their uptake. To\naddress this knowledge gap, in this work we investigated the density,\nviscosity, surface tension, and corresponding critical micelle concentration in\nwater, as well as gas absorption of SAILs with a variety of cation and anion\nstructures. SAILs containing anions with linear alkyl chains have smaller molar\nvolumes than those with branched alkyl chains, because linear alkyl chains are\ninterdigitated to a greater extent, leading to more compact packing. This\ninterdigitation also results in SAILs being about two orders of magnitude more\nviscous than comparable conventional ILs. SAILs at the liquid-air interface\norient alkyl chains towards the air, leading to low surface tensions closer to\nn-alkanes than conventional ILs. Critical temperatures of about 900 K could be\nestimated for all SAILs from their surface tensions. When dissolved in water,\nSAILs adsorb at the liquid-air interface and lower the surface tension, like\nconventional surfactants in water, after which micelles form. Molecular\nsimulations show that the micelles are spherical and that lower critical\nmicelle concentrations correspond to the formation of aggregates with a larger\nnumber of ion pairs. $\\mathrm{CO_{2}}$ and $\\mathrm{N_{2}}$ absorption\ncapacities are examined and we conclude that ionic liquids with larger\nnon-polar domains absorb larger quantities of both gases.","PeriodicalId":501304,"journal":{"name":"arXiv - PHYS - Chemical Physics","volume":"49 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Chemical Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.11853","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Surface active ionic liquids (SAILs) combine useful characteristics of both ionic liquids (ILs) and surfactants, hence are promising candidates for a wide range of applications. However, the effect of SAIL ionic structures on their physicochemical properties remains unclear, which limits their uptake. To address this knowledge gap, in this work we investigated the density, viscosity, surface tension, and corresponding critical micelle concentration in water, as well as gas absorption of SAILs with a variety of cation and anion structures. SAILs containing anions with linear alkyl chains have smaller molar volumes than those with branched alkyl chains, because linear alkyl chains are interdigitated to a greater extent, leading to more compact packing. This interdigitation also results in SAILs being about two orders of magnitude more viscous than comparable conventional ILs. SAILs at the liquid-air interface orient alkyl chains towards the air, leading to low surface tensions closer to n-alkanes than conventional ILs. Critical temperatures of about 900 K could be estimated for all SAILs from their surface tensions. When dissolved in water, SAILs adsorb at the liquid-air interface and lower the surface tension, like conventional surfactants in water, after which micelles form. Molecular simulations show that the micelles are spherical and that lower critical micelle concentrations correspond to the formation of aggregates with a larger number of ion pairs. $\mathrm{CO_{2}}$ and $\mathrm{N_{2}}$ absorption capacities are examined and we conclude that ionic liquids with larger non-polar domains absorb larger quantities of both gases.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
离子结构对表面活性离子液体理化性质和气体吸收的影响
表面活性离子液体(SAILs)结合了双离子液体(ILs)和表面活性剂的有用特性,因此有望得到更广泛的应用。然而,SAIL 离子结构对其物理化学性质的影响仍不清楚,这限制了它们的应用。为了填补这一知识空白,我们在这项工作中研究了具有各种阳离子和阴离子结构的 SAIL 在水中的密度、粘度、表面张力和相应的临界胶束浓度,以及气体吸收情况。含有线性烷基链阴离子的 SAIL 的摩尔体积小于含有支链烷基链的 SAIL,这是因为线性烷基链在更大程度上发生了交错,从而导致了更紧凑的堆积。这种交错也导致 SAIL 的粘度比同类传统 IL 高出两个数量级。处于液气界面的 SAIL 会将烷基链导向空气,从而导致与传统 IL 相比,SAIL 与烷烃的表面张力较低。根据其表面张力,可以估算出所有 SAIL 的临界温度约为 900 K。当溶解在水中时,SAILs 会吸附在液气界面并降低表面张力,就像传统表面活性剂在水中一样,然后形成胶束。分子模拟显示,胶束呈球形,临界胶束浓度越低,形成的离子对数量越多。我们研究了 $\mathrm{CO_{2}}$ 和 $\mathrm{N_{2}}$ 的吸收能力,并得出结论:具有较大非极性结构域的离子液体能吸收更多的这两种气体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Phase-cycling and double-quantum two-dimensional electronic spectroscopy using a common-path birefringent interferometer Developing Orbital-Dependent Corrections for the Non-Additive Kinetic Energy in Subsystem Density Functional Theory Thermodynamics of mixtures with strongly negative deviations from Raoult's law. XV. Permittivities and refractive indices for 1-alkanol + n-hexylamine systems at (293.15-303.15) K. Application of the Kirkwood-Fröhlich model Mutual neutralization of C$_{60}^+$ and C$_{60}^-$ ions: Excitation energies and state-selective rate coefficients All-in-one foundational models learning across quantum chemical levels
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1