Dual Macroscale Wrinkling Mechanisms for Complex Surface Patterning in Photopolymer Resins

IF 4.4 2区 化学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Sabrina J. Curley,  and , Caroline R. Szczepanski*, 
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引用次数: 0

Abstract

Hierarchical and topographical surface structures are abundant in nature, from the beetle carapace to plant leaves. The interactions between hierarchically structured, natural surfaces and water continue to inspire researchers; these natural designs have been translated to engineering strategies for antifogging coatings and membrane filtration processes. In this work, photoinduced phase separation (PIPS) is utilized to generate naturally inspired hierarchical topographical features on polymer surfaces in a single-step procedure. These complex designs are accessible when a polymer coating undergoes PIPS since both the classic surface wrinkling phenomenon, facilitated by oxygen quenching of radicals, as well as additional patterning from the phase-separated morphology yield topographies on multiple length scales. We demonstrate this patterning in a photopolymerizable resin system composed of acrylonitrile and 1,6-hexanediol diacrylate (co)monomers with poly(methyl methacrylate) as an inert polymer additive. A wide range of surface features arise from this resin system, which were characterized via imaging and optical profilometry. Furthermore, the topographies that formed were mapped to resin formulation parameters (e.g., cross-linking fraction, inert polymer loading) and experimental conditions (e.g., UV intensity). Our analysis highlights how diffusional constraints vary based on cross-link density and thus impact the scale and quality of topography that forms during polymerization. Increased cross-linker loading results in a kinetically trapped system, where the rapid network formation inhibits surface relaxations. Conversely, with decreased cross-linking, mechanical gradients due to radical quenching can evolve, and when PIPS arises simultaneously multiple scales of patterning form on a single surface, spanning from the micro to macroscale. By linking the observed kinetics with the final surface morphologies, we detail how PIPS can be utilized in tandem with traditional wrinkling to tailor hierarchical surface morphologies in rapid, ambient photopolymerizations for the facile production of tunable coating topographies.

光聚合物树脂复杂表面图案的双宏观起皱机制
从甲虫的甲壳到植物的叶片,层次和地形表面结构在自然界中比比皆是。分层结构的自然表面与水之间的相互作用不断激发着研究人员的灵感;这些自然设计已转化为防雾涂层和膜过滤过程的工程策略。在这项研究中,利用光诱导相分离(PIPS)技术,只需一步就能在聚合物表面生成受自然启发的分层地形特征。当聚合物涂层经过 PIPS 处理后,就可以获得这些复杂的设计,因为通过氧淬灭自由基而产生的典型表面起皱现象,以及相分离形态产生的额外图案,都会产生多种长度尺度的拓扑结构。我们在由丙烯腈和 1,6-己二醇二丙烯酸酯(共)单体组成的可光聚合树脂体系中,以聚甲基丙烯酸甲酯作为惰性聚合物添加剂,展示了这种图案化现象。这种树脂体系具有多种表面特征,可通过成像和光学轮廓仪对其进行表征。此外,形成的形貌还与树脂配方参数(如交联部分、惰性聚合物负载)和实验条件(如紫外线强度)相关联。我们的分析强调了扩散限制如何根据交联密度而变化,从而影响聚合过程中形成的形貌的规模和质量。增加交联剂的负载会形成一个动力学受困系统,在该系统中,快速的网络形成会抑制表面松弛。相反,当交联度降低时,由于自由基淬火会产生机械梯度,当 PIPS 同时出现时,会在单个表面上形成从微观到宏观的多尺度图案。通过将观察到的动力学与最终的表面形态联系起来,我们详细介绍了如何利用 PIPS 与传统的起皱技术相结合,在快速、常温光聚合反应中定制分层表面形态,从而方便地生产出可调整的涂层形貌。
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来源期刊
CiteScore
7.20
自引率
6.00%
发文量
810
期刊介绍: ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.
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