IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2025-02-12 DOI:10.1021/acs.macromol.4c03034
Bin Zhao, Michael T. Kelly, Sachini H. Dayarathne, Shichen Yu, Kingsley O. Ojima, Christopher Y. Li
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摘要

通过利用可改变形状的分子瓶(MBB)的大尺寸和可调节的两亲性,我们发现具有异接枝聚(环氧乙烷)(PEO)和聚(2-(N,N-二乙氨基)乙基甲基丙烯酸酯)(PDEAEMA)侧链的分子瓶(MBB-OE)是一种高效的pH值响应型乳化剂,可产生高度稳定的乳液,并可被外部刺激破坏。由于 PDEAEMA 在碱性水中不溶解,MBB-OE 在酸性溶液中呈蠕虫状,并随着 pH 值的升高而塌缩成球状。在涡旋作用下,即使只使用 0.0068% 的 MBB-OE,甲苯与 pH 值为 9.5 的缓冲液的混合物也能形成质量比≥0.8:1.0 的油包水(w/o)乳液。涡旋使球状刷子展开并吸附在界面上,重新配置成 Janus 蠕虫状结构,PEO 和 PDEAEMA 分别伸入水相和甲苯相。PEO 和 PDEAEMA 在两相之间的分配以及溶剂蒸发过程中乳液液滴界面起皱的观察结果都证明了这一点。将 pH 值调至 4.0 后,乳状液很容易被破坏;将 pH 值调至 9.5 后,乳状液通过涡旋重新形成;乳状液的形成和破坏可重复多次。有趣的是,当甲苯与水的质量比≤0.6:1.0 时,水包油(o/w)乳液形成,并在 pH 值由盐酸变为 4.0 后保持稳定,这可能是因为 H+ 无法穿过界面。然而,二氧化碳气泡会破坏乳液。这项工作展示了可改变形状的 MBB 作为刺激响应型乳化剂的潜力,为利用 MBB 的大尺寸、独特特性和响应性设计先进的乳化剂提供了机会。
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pH-Responsive Shape-Changing Molecular Bottlebrush Emulsifier
By utilizing the large size and the tunable amphiphilicity of shape-changing molecular bottlebrushes (MBBs), we show that MBBs with heterografted poly(ethylene oxide) (PEO) and poly(2-(N,N-diethylamino)ethyl methacrylate) (PDEAEMA) side chains (MBB-OE) are an efficient and pH-responsive emulsifier, producing highly stable emulsions that can be disrupted by external stimuli. MBB-OE was wormlike in acidic solution and collapsed into a globular shape with increasing pH due to the insolubility of PDEAEMA in basic water. Upon vortexing, water-in-oil (w/o) emulsions were formed from the mixtures of toluene and a pH 9.5 buffer with mass ratios ≥0.8:1.0, even using only 0.0068% MBB-OE. Vortexing caused the globular brushes to unfold and adsorb at the interface, reconfiguring into a Janus wormlike structure with PEO and PDEAEMA extending into the aqueous and toluene phase, respectively. This is supported by the observations of the partitioning of PEO and PDEAEMA between the two phases and the interfacial wrinkling of emulsion droplets during solvent evaporation. The emulsions were readily disrupted by changing the pH to 4.0 and reformed by vortexing after increasing the pH to 9.5; the emulsion formation and breaking can be repeated multiple times. Interestingly, oil-in-water (o/w) emulsions were formed at the toluene-to-water mass ratio ≤0.6:1.0 and remained stable after the pH was changed to 4.0 by HCl, likely because H+ was unable to cross the interface. However, bubbling with CO2 disrupted the emulsions. This work demonstrates the potential of shape-changing MBBs as stimuli-responsive emulsifiers, opening up opportunities for designing advanced emulsifiers by leveraging the large size, unique characteristics, and responsiveness of MBBs.
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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