Role of isomers and steric hindrance in the micellization of carboxylated carbosilane surfactants

IF 1.6 4区 工程技术 Q3 CHEMISTRY, APPLIED
Tianquan Wu, Hailong Liu, Jinglin Tan
{"title":"Role of isomers and steric hindrance in the micellization of carboxylated carbosilane surfactants","authors":"Tianquan Wu,&nbsp;Hailong Liu,&nbsp;Jinglin Tan","doi":"10.1002/jsde.12744","DOIUrl":null,"url":null,"abstract":"<p>A series of carboxylated carbosilane surfactants with methyl, ethyl, branching CH<sub>3</sub><span></span>, phenyl, and cyclohexyl (Me-Si<sub>2</sub>C-COONa, Et-Si<sub>2</sub>C-COONa, Si<sub>2</sub>C-La-COONa, Ph-Si<sub>2</sub>C-COONa, and Cy-Si<sub>2</sub>C-COONa) were prepared. The effect of isomer and steric hindrance on their micellization in aqueous solution was investigated by surface tension, conductivity, transmission electron microscopy (TEM) and dynamic light scattering (DLS). Si<sub>2</sub>C-La-COONa with branching CH<sub>3</sub><span></span> shows a lower γ<sub>CMC</sub> value and higher the CMC value compared with Et-Si<sub>2</sub>C-COONa. Cy-Si<sub>2</sub>C-COONa with cyclohexyl (41.6 mN m<sup>−1</sup>) and Ph-Si<sub>2</sub>C-COONa with phenyl (43.9 mN m<sup>−1</sup>) have larger γ<sub>CMC</sub> values due to the distinct steric hindrance and hydrophobicity. In aqueous solution, the aggregation behavior of Si<sub>2</sub>C-La-COONa, Cy-Si<sub>2</sub>C-COONa, and Ph-Si<sub>2</sub>C-COONa is enthalpy-driven. However, the micellization process of Me-Si<sub>2</sub>C-COONa and Et-Si<sub>2</sub>C-COONa is governed by the enthalpy-driven at high temperature and entropy-driven at low temperature. DLS and TEM results indicate that the carboxylated carbosilane surfactants can self-assemble into aggregate with hydrodynamic diameters of 50–400 nm.</p>","PeriodicalId":17083,"journal":{"name":"Journal of Surfactants and Detergents","volume":"27 4","pages":"535-545"},"PeriodicalIF":1.6000,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Surfactants and Detergents","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jsde.12744","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

A series of carboxylated carbosilane surfactants with methyl, ethyl, branching CH3, phenyl, and cyclohexyl (Me-Si2C-COONa, Et-Si2C-COONa, Si2C-La-COONa, Ph-Si2C-COONa, and Cy-Si2C-COONa) were prepared. The effect of isomer and steric hindrance on their micellization in aqueous solution was investigated by surface tension, conductivity, transmission electron microscopy (TEM) and dynamic light scattering (DLS). Si2C-La-COONa with branching CH3 shows a lower γCMC value and higher the CMC value compared with Et-Si2C-COONa. Cy-Si2C-COONa with cyclohexyl (41.6 mN m−1) and Ph-Si2C-COONa with phenyl (43.9 mN m−1) have larger γCMC values due to the distinct steric hindrance and hydrophobicity. In aqueous solution, the aggregation behavior of Si2C-La-COONa, Cy-Si2C-COONa, and Ph-Si2C-COONa is enthalpy-driven. However, the micellization process of Me-Si2C-COONa and Et-Si2C-COONa is governed by the enthalpy-driven at high temperature and entropy-driven at low temperature. DLS and TEM results indicate that the carboxylated carbosilane surfactants can self-assemble into aggregate with hydrodynamic diameters of 50–400 nm.

异构体和立体阻碍在羧基碳硅烷表面活性剂胶束化中的作用
制备了一系列具有甲基、乙基、分支 CH3、苯基和环己基的羧基碳硅烷表面活性剂(Me-Si2C-COONa、Et-Si2C-COONa、Si2C-La-COONa、Ph-Si2C-COONa 和 Cy-Si2C-COONa)。通过表面张力、电导率、透射电子显微镜(TEM)和动态光散射(DLS)研究了异构体和立体阻碍对它们在水溶液中胶束化的影响。与 Et-Si2C-COONa 相比,具有支化 CH3 的 Si2C-La-COONa 的 γCMC 值更低,CMC 值更高。环己基的 Cy-Si2C-COONa (41.6 mN m-1)和苯基的 Ph-Si2C-COONa (43.9 mN m-1)由于具有明显的立体阻碍和疏水性,γCMC 值较大。在水溶液中,Si2C-La-COONa、Cy-Si2C-COONa 和 Ph-Si2C-COONa 的聚集行为是焓驱动的。然而,Me-Si2C-COONa 和 Et-Si2C-COONa 的胶束化过程在高温下受焓驱动,在低温下受熵驱动。DLS 和 TEM 结果表明,羧基碳硅烷表面活性剂可自组装成水动力直径为 50-400 nm 的聚集体。
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 求助全文
来源期刊
Journal of Surfactants and Detergents
Journal of Surfactants and Detergents 工程技术-工程:化工
CiteScore
3.80
自引率
6.20%
发文量
68
审稿时长
4 months
期刊介绍: Journal of Surfactants and Detergents, a journal of the American Oil Chemists’ Society (AOCS) publishes scientific contributions in the surfactants and detergents area. This includes the basic and applied science of petrochemical and oleochemical surfactants, the development and performance of surfactants in all applications, as well as the development and manufacture of detergent ingredients and their formulation into finished products.
×
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:481959085
Book学术官方微信