Assembling Xanthan Gum at the Air–Water Interface and Disentangling It with Ionic Liquids

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Nancy Jaglan, Gunjan Sharma, Prashant Hitaishi, Rajendra P. Giri, Nicolas Hayen, Bridget M. Murphy and Sajal K. Ghosh*, 
{"title":"Assembling Xanthan Gum at the Air–Water Interface and Disentangling It with Ionic Liquids","authors":"Nancy Jaglan,&nbsp;Gunjan Sharma,&nbsp;Prashant Hitaishi,&nbsp;Rajendra P. Giri,&nbsp;Nicolas Hayen,&nbsp;Bridget M. Murphy and Sajal K. Ghosh*,&nbsp;","doi":"10.1021/acs.langmuir.4c0474310.1021/acs.langmuir.4c04743","DOIUrl":null,"url":null,"abstract":"<p >Xanthan gum is a biopolymer used in a wide range of products in the food and cosmetic industries. As ionic liquids (ILs) have emerged as antimicrobial molecules, they can be used as preservatives for this polymer. Hence, it is important to understand the interaction of ionic liquids with Xanthan gum. In this investigation, polymer self-assembly at the air–water interface has been studied in the presence of ionic liquids floating at the air–water interface. From the surface pressure–area isotherm, it is shown that the electrostatic interaction drives the polymer to the interface, resulting in a viscoelastic film. In-plane dilation rheology has determined the storage and loss moduli of the film, which are found to depend on the concentration of the polymer dissolved in the water subphase. Additionally, a synchrotron-based X-ray reflectivity study has produced the electron density profile across the interface, depicting the structure of the film and suggesting that the negatively charged side groups of Xanthan gum attach to the positively charged headgroup of ionic liquids. This assembly drives the polymer to disentangle, which has been further verified in an aqueous solution of the polymer showing a non-newtonian shear-thinning behavior. The storage and loss moduli curves show two crossover frequencies, manifesting an elastic plateau width that decreases in the presence of IL in the solution. This, in turn, is a signature of the disentangling effect of the IL.</p>","PeriodicalId":50,"journal":{"name":"Langmuir","volume":"41 13","pages":"8535–8544 8535–8544"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Langmuir","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.langmuir.4c04743","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Xanthan gum is a biopolymer used in a wide range of products in the food and cosmetic industries. As ionic liquids (ILs) have emerged as antimicrobial molecules, they can be used as preservatives for this polymer. Hence, it is important to understand the interaction of ionic liquids with Xanthan gum. In this investigation, polymer self-assembly at the air–water interface has been studied in the presence of ionic liquids floating at the air–water interface. From the surface pressure–area isotherm, it is shown that the electrostatic interaction drives the polymer to the interface, resulting in a viscoelastic film. In-plane dilation rheology has determined the storage and loss moduli of the film, which are found to depend on the concentration of the polymer dissolved in the water subphase. Additionally, a synchrotron-based X-ray reflectivity study has produced the electron density profile across the interface, depicting the structure of the film and suggesting that the negatively charged side groups of Xanthan gum attach to the positively charged headgroup of ionic liquids. This assembly drives the polymer to disentangle, which has been further verified in an aqueous solution of the polymer showing a non-newtonian shear-thinning behavior. The storage and loss moduli curves show two crossover frequencies, manifesting an elastic plateau width that decreases in the presence of IL in the solution. This, in turn, is a signature of the disentangling effect of the IL.

Abstract Image

在空气-水界面组装黄原胶并与离子液体解结
黄原胶是一种生物聚合物,广泛用于食品和化妆品行业的产品中。随着离子液体(ILs)作为抗菌分子的出现,它们可以用作这种聚合物的防腐剂。因此,了解离子液体与黄原胶的相互作用是很重要的。本研究研究了离子液体漂浮在空气-水界面时聚合物在空气-水界面的自组装。从表面压力-面积等温线可以看出,静电相互作用驱使聚合物靠近界面,形成粘弹性膜。平面内膨胀流变学决定了薄膜的储存和损失模量,这取决于溶解在水亚相中的聚合物的浓度。此外,一项基于同步加速器的x射线反射率研究得出了界面上的电子密度分布图,描绘了薄膜的结构,并表明黄原胶的负电荷侧基与离子液体的正电荷头基相连。这种组合驱动聚合物解缠,这在聚合物的水溶液中得到进一步验证,显示出非牛顿剪切减薄行为。存储和损耗模量曲线显示两个交叉频率,在溶液中存在IL时表现出弹性平台宽度减小。反过来,这是IL解纠缠效应的标志。
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
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
×
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