Force-Responsive Polyethylene with Quantifiable Visualized Color Changing

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Yanlin Zong, Yixin Zhang* and Zhongbao Jian*, 
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引用次数: 0

Abstract

Mechanochromic polymeric materials have enormous potential applications in stress-sensing and damage detection. These types of polymers including poly(methyl acrylate), poly(methyl methacrylate), poly(urethane), and poly(ε-caprolactone) have been achieved through various methods, such as postfunctional reaction, free radical polymerization, polycondensation, and ring-opening polymerization. However, coordination polymerization to incorporate mechanochromophores into semicrystalline polyethylene, an extremely important and common plastic, is rare. Herein, we report functionalized polyethylene materials via coordination copolymerization of ethylene and a well-designed comonomer C4-ABF containing the mechanochromic group catalyzed by phosphine–sulfonate palladium catalysts and the following cross-linking reaction. These copolymer materials exhibit a visible color change under force stimulus, transferring the force signal to the color signal. The red–green–blue (RGB) color analysis method is adapted to investigate the relationship between stress–strain and color change. It is noted that the blue channel intensity has a positive correlation with Hencky stress.

Abstract Image

Abstract Image

可量化可视变色的力响应聚乙烯
机械变色聚合物材料在应力传感和损伤检测方面具有巨大的应用潜力。这类聚合物包括聚(丙烯酸甲酯)、聚(甲基丙烯酸甲酯)、聚(氨基甲酸乙酯)和聚(ε-己内酯),已通过后功能反应、自由基聚合、缩聚和开环聚合等多种方法实现。然而,将机械色团配位聚合到半结晶聚乙烯(一种极其重要和常见的塑料)中的方法却很少见。在此,我们报告了在膦磺酸钯催化剂的催化下,乙烯与一种精心设计的含有机械色基的共聚单体 C4-ABF 进行配位共聚,并在随后发生交联反应,从而得到的功能化聚乙烯材料。这些共聚物材料在力的刺激下呈现出可见的颜色变化,将力信号转变为颜色信号。红-绿-蓝(RGB)色彩分析方法适用于研究应力-应变与颜色变化之间的关系。结果表明,蓝色通道强度与 Hencky 应力呈正相关。
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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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