Pattern Formation in Evaporating Polymer Solutions─Interplay between Dewetting and Decomposition

Pankaj Mahawar, M. Praveena, Shreyanil Bhuyan, Dipin S. Pillai and Sivasurender Chandran*, 
{"title":"Pattern Formation in Evaporating Polymer Solutions─Interplay between Dewetting and Decomposition","authors":"Pankaj Mahawar,&nbsp;M. Praveena,&nbsp;Shreyanil Bhuyan,&nbsp;Dipin S. Pillai and Sivasurender Chandran*,&nbsp;","doi":"10.1021/acspolymersau.4c0001810.1021/acspolymersau.4c00018","DOIUrl":null,"url":null,"abstract":"<p >Pattern formation during solution evaporation is common in several industrial settings and involves a complex interplay of multiple processes, including wetting/dewetting, diffusion, and rheological characteristics of the solution. Monitoring the emergence of patterns during evaporation under controlled conditions may allow deconvolution of different processes and, in turn, improve our understanding of this common yet complex phenomenon. Here, we probe the importance of initial conditions, defined by the solution concentration <i>c</i><sub>0</sub>, on the pattern formation in evaporating polymer solutions on the air–water interface. Intriguingly, the initial decrease in the lateral length scale (ξ), characterizing the patterns, takes an upturn at higher concentrations, revealing reentrant behavior. We employ a gradient dynamics model consisting of coupled evolution equations for the film height and the polymer fraction in the solution. Our simulations capture two different length scales revealing the reasons underlying the re-entrant behavior of ξ(<i>c</i><sub>0</sub>). While the long-range destabilizing interactions between suspension and water result in the dewetting of thin film solutions, the phase separation between the polymer and solvent occurs at shorter length scales. Our results demonstrate the importance of initial concentration on pattern formation and, thereby, on the resultant properties of thin polymer films.</p>","PeriodicalId":72049,"journal":{"name":"ACS polymers Au","volume":"4 4","pages":"302–310 302–310"},"PeriodicalIF":4.7000,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acspolymersau.4c00018","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS polymers Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acspolymersau.4c00018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

Pattern formation during solution evaporation is common in several industrial settings and involves a complex interplay of multiple processes, including wetting/dewetting, diffusion, and rheological characteristics of the solution. Monitoring the emergence of patterns during evaporation under controlled conditions may allow deconvolution of different processes and, in turn, improve our understanding of this common yet complex phenomenon. Here, we probe the importance of initial conditions, defined by the solution concentration c0, on the pattern formation in evaporating polymer solutions on the air–water interface. Intriguingly, the initial decrease in the lateral length scale (ξ), characterizing the patterns, takes an upturn at higher concentrations, revealing reentrant behavior. We employ a gradient dynamics model consisting of coupled evolution equations for the film height and the polymer fraction in the solution. Our simulations capture two different length scales revealing the reasons underlying the re-entrant behavior of ξ(c0). While the long-range destabilizing interactions between suspension and water result in the dewetting of thin film solutions, the phase separation between the polymer and solvent occurs at shorter length scales. Our results demonstrate the importance of initial concentration on pattern formation and, thereby, on the resultant properties of thin polymer films.

Abstract Image

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
蒸发聚合物溶液中的图案形成--渗湿与分解之间的相互作用
溶液蒸发过程中的图案形成在一些工业环境中很常见,涉及多个过程的复杂相互作用,包括溶液的润湿/脱湿、扩散和流变特性。在受控条件下监测蒸发过程中出现的模式,可以对不同过程进行解构,进而加深我们对这一常见而复杂现象的理解。在此,我们探究了初始条件(由溶液浓度 c0 定义)对空气-水界面上蒸发聚合物溶液中图案形成的重要性。耐人寻味的是,作为图案特征的横向长度尺度(ξ)的初始下降在浓度较高时出现了上扬,揭示了重入行为。我们采用的梯度动力学模型由薄膜高度和溶液中聚合物比例的耦合演化方程组成。我们的模拟捕捉了两种不同的长度尺度,揭示了ξ(c0)重入行为的内在原因。悬浮液与水之间的长程不稳定相互作用导致了薄膜溶液的脱水,而聚合物与溶剂之间的相分离则发生在较短的长度尺度上。我们的研究结果表明了初始浓度对图案形成的重要性,以及由此对聚合物薄膜最终特性的影响。
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
CiteScore
2.50
自引率
0.00%
发文量
0
期刊最新文献
Issue Editorial Masthead Issue Publication Information Design of Highly Conductive PILs by Simple Modification of Poly(epichlorohydrin-co-ethylene oxide) with Monosubstituted Imidazoles Issue Publication Information Issue Editorial Masthead
×
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