Architectural influence of polymer brush-modified tri-compartmental anisotropic particles in stabilizing pickering emulsion

IF 4.5 2区 化学 Q2 POLYMER SCIENCE Polymer Pub Date : 2025-04-17 Epub Date: 2025-03-04 DOI:10.1016/j.polymer.2025.128222
Subhashree Subhasmita Pradhan , Ashank Upadhyay , Samiksha Shrivastava , Awaneesh Singh , Sampa Saha
{"title":"Architectural influence of polymer brush-modified tri-compartmental anisotropic particles in stabilizing pickering emulsion","authors":"Subhashree Subhasmita Pradhan ,&nbsp;Ashank Upadhyay ,&nbsp;Samiksha Shrivastava ,&nbsp;Awaneesh Singh ,&nbsp;Sampa Saha","doi":"10.1016/j.polymer.2025.128222","DOIUrl":null,"url":null,"abstract":"<div><div>We aimed to create tri-compartmental polymeric particles (TPs), with selective areas conjugated with hydrophilic patches, to produce an array of amphiphilic particles with various architectures. Briefly, the electrohydrodynamic co-jetting technique (EHDC) was employed to produce 4 sets of TPs comprising PLA (polylactide) in one/two compartments and a blend of PLA and a macro-initiator at a ratio of 90/10 in other compartments (s). Upon grafting a hydrophilic polymer brush (poly(2-dimethyl amino ethyl methacrylate) (polyDMAEMA)) onto the surface of macroinitiator (10 wt%) containing compartment using Surface Initiated Atom Transfer Radical Polymerization (SIATRP), particles were expected to become amphiphilic. By locating the macroinitiator in various compartments (TBP 1–4), an array of amphiphilic particles with various architectures was created. This study allowed us to produce a repertoire of anisotropic particles with varying amphiphilicity for investigating their role as Pickering emulsion stabilizers beyond Janus geometry. The relative performance of the brush-modified TPs (TBPs) in stabilizing octanol/water-based emulsion was explained with the aid of their HLB balance, interfacial tension, location of the macroinitiator, and the macroinitiator content/grafting density. The particles having a maximum area of hydrophilic lobes confined to one hemisphere were found to prolong the emulsion stability for the maximum time (∼8 days), thus considered the most efficient one. In addition to polyDMAEMA, strongly hydrophilic poly(ethylene glycol methyl ether methacrylate) (polyEGMA) brushes were also grafted onto TPs to enhance their hydrophilicity, which ultimately yielded an emulsion with prolonged stability (∼11 days).</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"324 ","pages":"Article 128222"},"PeriodicalIF":4.5000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032386125002083","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/4 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

We aimed to create tri-compartmental polymeric particles (TPs), with selective areas conjugated with hydrophilic patches, to produce an array of amphiphilic particles with various architectures. Briefly, the electrohydrodynamic co-jetting technique (EHDC) was employed to produce 4 sets of TPs comprising PLA (polylactide) in one/two compartments and a blend of PLA and a macro-initiator at a ratio of 90/10 in other compartments (s). Upon grafting a hydrophilic polymer brush (poly(2-dimethyl amino ethyl methacrylate) (polyDMAEMA)) onto the surface of macroinitiator (10 wt%) containing compartment using Surface Initiated Atom Transfer Radical Polymerization (SIATRP), particles were expected to become amphiphilic. By locating the macroinitiator in various compartments (TBP 1–4), an array of amphiphilic particles with various architectures was created. This study allowed us to produce a repertoire of anisotropic particles with varying amphiphilicity for investigating their role as Pickering emulsion stabilizers beyond Janus geometry. The relative performance of the brush-modified TPs (TBPs) in stabilizing octanol/water-based emulsion was explained with the aid of their HLB balance, interfacial tension, location of the macroinitiator, and the macroinitiator content/grafting density. The particles having a maximum area of hydrophilic lobes confined to one hemisphere were found to prolong the emulsion stability for the maximum time (∼8 days), thus considered the most efficient one. In addition to polyDMAEMA, strongly hydrophilic poly(ethylene glycol methyl ether methacrylate) (polyEGMA) brushes were also grafted onto TPs to enhance their hydrophilicity, which ultimately yielded an emulsion with prolonged stability (∼11 days).

Abstract Image

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
聚合物刷改性三室各向异性颗粒对酸洗乳稳定性的影响
我们的目标是创建三室室聚合物颗粒(TPs),具有选择性区域与亲水性斑块共轭,以生产具有不同结构的两亲性颗粒阵列。简单地说,采用电流体动力共喷射技术(EHDC)在一个/两个隔间中生产了4组TPs,其中包括PLA(聚乳酸),在其他隔间中以90/10的比例混合PLA和宏观引发剂。在使用表面引发原子转移自由基聚合(SIATRP)将亲水性聚合物刷(聚(2-二甲基氨基乙基甲基丙烯酸酯)(polyDMAEMA)接枝到含有大引发剂(10 wt%)的隔间表面上,粒子被认为是两亲性的。通过将宏观引发剂定位在不同的隔室中(TBP 1-4),可以创建具有不同结构的两亲性颗粒阵列。这项研究使我们能够产生一系列具有不同两亲性的各向异性颗粒,以研究它们在Janus几何结构之外作为皮克林乳液稳定剂的作用。从HLB平衡、界面张力、引发剂位置、引发剂含量/接枝密度等方面分析了电刷改性TPs (TBPs)稳定辛醇/水基乳液的相对性能。具有最大亲水性裂片面积的颗粒被发现局限于一个半球,可以延长乳液稳定性的时间最长(~ 8天),因此被认为是最有效的。除了聚dmaema外,还将强亲水性聚乙二醇甲基丙烯酸甲醚(polyethylene glycol methyl ether methacrylate,简称polyethylene ma)刷子接枝到TPs上,以增强其亲水性,最终得到具有较长稳定性(~ 11天)的乳液。
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
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
期刊最新文献
Ionic versus steric: Regulating charge transport in D–A–D polymers for tailored electrochromic and capacitive behaviors Salt distribution and microphase separation behavior of lithium salt-doped block copolymers containing poly(ethylene oxide) and polyzwitterion Ionic liquid-mediated impedance modulation for enhanced actuation performance in iPVCG stacked actuators Enhanced electrical and corrosion-resistant behavior of graphene-reinforced PTFE composites via solid state synthesis Development of polyetheramine-loaded calcium polyacrylate self-healing microcapsules for anti-corrosion coatings on low-carbon steel in marine environments
×
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:604180095
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