甲基丙烯酸甲酯本体聚合过程中富聚合相与富单体相界面形成的超声检测

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Naoki Mori, Akikazu Matsumoto, Yasuhito Suzuki
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引用次数: 0

摘要

聚合物材料对于广泛的应用是必不可少的;然而,理解和控制它们的反应性处理,特别是在后期阶段,仍然具有挑战性。本体自由基聚合法聚合甲基丙烯酸甲酯(MMA)的一个显著现象是特罗姆斯多夫效应;这种效应使反应速率迅速加快,其机理仍有争议。在这项研究中,我们通过超声波监测、温度跟踪和视频记录来研究MMA聚合。这种方法可以观察到富聚合物相的形成和聚合前沿的传播。与MMA均相聚合的假设相反,我们的结果揭示了其从液体到玻璃态转变过程中的宏观非均质性。聚合过程根据其对超声波传播的响应可分为六个不同的阶段。这些结果从根本上增强了我们对本体聚合的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasonic Detection of the Interface Formation between the Polymer-Rich and Monomer-Rich Phases during Bulk Polymerization of Methyl Methacrylate

Ultrasonic Detection of the Interface Formation between the Polymer-Rich and Monomer-Rich Phases during Bulk Polymerization of Methyl Methacrylate
Polymeric materials are essential for a wide range of applications; however, understanding and controlling their reactive processing, especially in the later stages, remains challenging. One notable phenomenon in the polymerization of methyl methacrylate (MMA) via bulk radical polymerization is the Trommsdorff effect; this effect causes a rapid acceleration in the reaction rate, and its mechanism remains debatable. In this study, we investigated MMA polymerization by integrating ultrasonic monitoring, temperature tracking, and video recording. This approach enabled the observation of the formation of a polymer-rich phase and the propagation of the polymerization front. Contrary to the assumption that MMA undergoes homogeneous polymerization, our results revealed macroscopic heterogeneity during its transition from the liquid to the glassy state. The polymerization process can be categorized into six distinct stages based on its response to ultrasonic propagation. These results fundamentally enhance our understanding of bulk polymerization.
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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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