通过与硫基离子聚合物原位构建分层配位复合物来增韧橡胶

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2024-10-16 DOI:10.1021/acs.macromol.4c01907
Senmao Yu, Zhenghai Tang, Dong Wang, Baochun Guo, Liqun Zhang
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引用次数: 0

摘要

在聚合物中加入能量消耗单元是提高韧性的有效方法;然而,最先进的方法通常涉及复杂的化学操作和多步骤过程。在本文中,我们报告了一种全新的丁苯橡胶(SBR)增韧方法,即通过加入硫基离聚物来构建分层配位复合物。具体来说,我们通过硫辛酸与硫的共聚,然后引入氯化铁,合成了含有多硫化物骨架和羧酸铁络合物的离子聚合物 P(TA-S)/Fe。由于 P(TA-S)/Fe 中的多硫化物片段与丁苯橡胶发生反应,P(TA-S)/Fe 的加入使丁苯橡胶发生化学交联,并将羧酸铁络合物接枝到丁苯橡胶链上。接枝的羧酸铁络合物在丁苯橡胶中聚集并形成相分离结构,这提供了一种多级能量耗散机制,从而使丁苯橡胶的极限强度、模量和断裂韧性得到增强。
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Toughening Rubber by In Situ Construction of Hierarchical Coordination Complexes with a Sulfur-Based Ionomer
Programming energy-dissipating units into polymers is an effective method to improve the toughness; however, the state-of-art approaches usually involve complicated chemistry manipulation and multistep process. In this contribution, we report a brand-new way to toughen styrene–butadiene rubber (SBR) by incorporating a sulfur-based ionomer to construct hierarchical coordination complexes. Specifically, the ionomer P(TA-S)/Fe containing polysulfide backbones and iron–carboxylate complexes was synthesized through the copolymerization of thioctic acid and sulfur, followed by introducing ferric chloride. Due to the reaction between polysulfide fragments in P(TA-S)/Fe and SBR, the incorporation of P(TA-S)/Fe enabled the chemical cross-linking of SBR and grafting of iron–carboxylate complexes onto SBR chains. The grafted iron–carboxylate complexes aggregated and formed a phase separate structure within SBR, which provided a multilevel energy-dissipating mechanism and consequently led to an integration of enhanced ultimate strength, modulus, and fracture toughness of SBR.
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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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