具有动态氢和亚胺键的无异氰酸酯生物基聚脲Vitrimers的设计,提供环境自修复,再加工和回收特性

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Bao Ding, Nadège Follain, Nasreddine Kébir
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引用次数: 0

摘要

以氨基端非异氰酸酯聚脲低聚物(NIPUrea)、对苯二甲酸乙二醛和三(2-氨基乙基)胺为原料,以不同的当量比例反应制备了一系列动态氢键与亚胺键结合的玻璃聚合体。采用环境友好和可持续的方法制备了不同分子量的NIPUrea低聚物,这意味着transsurethane缩聚技术。所制备的玻璃体具有不同的交联密度,Tg值在20℃左右,热稳定性超过300℃。材料具有较高的机械强度和塑性,杨氏模量为1.7 ~ 26.4 MPa,断裂应力为7.9 ~ 12.9 MPa,断裂伸长率为147 ~ 517%。除了在酸性THF/水溶液中发生不可逆降解和增溶外,它们表现出良好的耐溶剂性。大多数制备的材料在室温下具有优异的自愈效率(93 ~ 107%),热压后具有良好的再加工性和可回收性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design of Isocyanate-Free Biobased Polyurea Vitrimers with Dynamic Hydrogen and Imine Bonds, Offering Ambient Self-Healing, Reprocessing, and Recycling Properties

Design of Isocyanate-Free Biobased Polyurea Vitrimers with Dynamic Hydrogen and Imine Bonds, Offering Ambient Self-Healing, Reprocessing, and Recycling Properties
A series of vitrimers combining dynamic hydrogen and imine bonds was prepared by a reaction between amine-terminated nonisocyanate polyurea oligomers (NIPUrea), terephthalaldehyde, and tris(2-aminoethyl)amine at various equivalent ratios. NIPUrea oligomers of different molecular weights were prepared using an environmentally friendly and sustainable approach, implying transurethane polycondensation technology. The vitrimers prepared possessed different cross-linking densities and exhibited Tg values of around 20 °C, as well as thermal stabilities exceeding 300 °C. They displayed high and tunable mechanical strength and ductility, with Young’s modulus from 1.7 to 26.4 MPa, breaking stress from 7.9 to 12.9 MPa and elongation at break from 147 to 517%. They revealed good solvent resistance except in acidic THF/water solutions, in which they underwent irreversible degradation and solubilization. Most of the materials prepared exhibited excellent self-healing efficiency at room temperature (93 to 107%) and good reprocessability and recyclability after hot pressing.
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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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