Self-Consistent Field Analysis of Segregative Aqueous Dextran-Polyethylene Glycol Solutions: (2) Adsorption and Wetting.

IF 2.9 2区 化学 Q3 CHEMISTRY, PHYSICAL
F A M Leermakers, L Ruiz-Martínez, S D Stoyanov, J van der Gucht
{"title":"Self-Consistent Field Analysis of Segregative Aqueous Dextran-Polyethylene Glycol Solutions: (2) Adsorption and Wetting.","authors":"F A M Leermakers, L Ruiz-Martínez, S D Stoyanov, J van der Gucht","doi":"10.1021/acs.jpcb.5c04279","DOIUrl":null,"url":null,"abstract":"<p><p>Aqueous two-phase systems (ATPS), with dextran-water-poly(ethylene glycol) (PEG) as the main example, are water-continuous polymer segregated systems. How such ATPS behaves near solid interfaces is studied using the Scheutjens Fleer self-consistent field (SF-SCF) theory. We have analyzed the adsorption isotherms of the minority (wetting) component PEG at either a fixed solvent- or a fixed dextran bulk volume fraction and focused on wetting and polymer displacement transitions. When the driving force for segregative phase behavior is sufficiently strong (repulsive interactions between dextran and PEG: the major driving force), a jump-like transition displacing adsorbed dextran by PEG may take the form of a prewetting transition when the PEG-rich phase wets the surface. Interestingly, the first-order displacement transition manifests as a pure surface phase transition at supercritical conditions. This explains why the wetting transition is robust first order. Only when the segregative phase behavior is triggered by a solvent quality disparity (minor driving force), one may find isotherms with two consecutive transitions, that is, a smooth displacement transition followed by a jump-like prewetting transition. Explained by the low interfacial tension between the PEG-rich and dextran-rich phases, the parameter window for partial wetting is small. Remarkably, for an experimentally realistic ATPS and carefully tuned adsorption parameters, it is possible that upon a change of the solvent content there is a sequence of two wetting transitions (going from partial wet to wet and back to partial wet) followed by a drying transition.</p>","PeriodicalId":60,"journal":{"name":"The Journal of Physical Chemistry B","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-10-13","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://doi.org/10.1021/acs.jpcb.5c04279","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

Abstract

Aqueous two-phase systems (ATPS), with dextran-water-poly(ethylene glycol) (PEG) as the main example, are water-continuous polymer segregated systems. How such ATPS behaves near solid interfaces is studied using the Scheutjens Fleer self-consistent field (SF-SCF) theory. We have analyzed the adsorption isotherms of the minority (wetting) component PEG at either a fixed solvent- or a fixed dextran bulk volume fraction and focused on wetting and polymer displacement transitions. When the driving force for segregative phase behavior is sufficiently strong (repulsive interactions between dextran and PEG: the major driving force), a jump-like transition displacing adsorbed dextran by PEG may take the form of a prewetting transition when the PEG-rich phase wets the surface. Interestingly, the first-order displacement transition manifests as a pure surface phase transition at supercritical conditions. This explains why the wetting transition is robust first order. Only when the segregative phase behavior is triggered by a solvent quality disparity (minor driving force), one may find isotherms with two consecutive transitions, that is, a smooth displacement transition followed by a jump-like prewetting transition. Explained by the low interfacial tension between the PEG-rich and dextran-rich phases, the parameter window for partial wetting is small. Remarkably, for an experimentally realistic ATPS and carefully tuned adsorption parameters, it is possible that upon a change of the solvent content there is a sequence of two wetting transitions (going from partial wet to wet and back to partial wet) followed by a drying transition.

分离性葡聚糖-聚乙二醇水溶液的自一致场分析:(2)吸附和润湿。
以葡聚糖-水-聚乙二醇(PEG)为主要例子的水两相体系(ATPS)是水连续聚合物分离体系。利用Scheutjens Fleer自洽场(SF-SCF)理论研究了这种ATPS在固体界面附近的行为。我们分析了少数(润湿)组分PEG在固定溶剂或固定葡聚糖体积分数下的吸附等温线,并重点研究了润湿和聚合物位移转变。当分离相行为的驱动力足够强时(葡聚糖和PEG之间的排斥相互作用是主要驱动力),当富含PEG的相润湿表面时,取代被PEG吸附的葡聚糖的跳变转变可能以预润湿转变的形式出现。有趣的是,一阶位移相变在超临界条件下表现为纯表面相变。这就解释了为什么润湿转变是一阶的。只有当分离相行为由溶剂质量差异(次要驱动力)触发时,人们才会发现等温线有两个连续的转变,即平滑的位移转变和跳变的预润湿转变。由于富聚乙二醇相和富葡聚糖相之间的界面张力较低,部分润湿的参数窗口较小。值得注意的是,对于实验上真实的ATPS和精心调整的吸附参数,在溶剂含量的变化后,可能存在两个润湿转变序列(从部分湿到湿,再回到部分湿),然后是干燥转变。
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
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