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氮配位硼氧杂环戊烷实现了在温和条件下可修复和可回收的机械坚固的超分子热固性塑料的制备。

Nitrogen-Coordinated Boroxines Enable the Fabrication of Mechanically Robust Supramolecular Thermosets Capable of Healing and Recycling under Mild Conditions.

机构信息

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry , Jilin University , Changchun 130012 , P. R. China.

出版信息

ACS Appl Mater Interfaces. 2019 Mar 6;11(9):9478-9486. doi: 10.1021/acsami.9b00006. Epub 2019 Feb 25.

Abstract

The fabrication of mechanically robust polymeric materials capable of self-healing and recycling remains challenging because the mobility of polymer chains in such polymers is very limited. In this work, mechanically robust supramolecular thermosets capable of healing physical damages and recycling under mild conditions are fabricated by trimerization of bi-( ortho-aminomethyl-phenylboronic acid)- and tri-( ortho-aminomethyl-phenylboronic acid)-terminated poly(propylene glycol) oligomers (denoted as Bi-PBA-PPG and Tri-PBA-PPG, respectively). The resultant supramolecular thermosets are cross-linked by dynamic covalent bonds of nitrogen-coordinated boroxines. The mechanical properties of the supramolecular thermosets can be systematically tailored by varying the ratios between Tri-PBA-PPG and Bi-PBA-PPG, which changes the cross-linking density of nitrogen-coordinated boroxines and the topology of the supramolecular thermosets. The mechanically strongest supramolecular thermosets with a molar ratio of Tri-PBA-PPG to Bi-PBA-PPG being 1:2 have a glass transition temperature of ∼36 °C, a tensile strength of ∼31.96 MPa, and a Young's modulus of ∼298.5 MPa. The high reversibility of nitrogen-coordinated boroxines and the flexibility of poly(propylene glycol) chains enable the supramolecular thermosets with the strongest mechanical strength to be highly efficiently healed at 55 °C and recycled under a pressure of 4 MPa at 60 °C to regain their original mechanical strength and integrity.

摘要

制造具有机械强度、能够自我修复和回收的聚合物材料仍然具有挑战性,因为这些聚合物中聚合物链的迁移率非常有限。在这项工作中,通过双-(邻-氨甲基-苯硼酸)-和三-(邻-氨甲基-苯硼酸)-封端的聚(丙二醇)低聚物(分别表示为 Bi-PBA-PPG 和 Tri-PBA-PPG)的三聚反应,制造了能够在温和条件下修复物理损伤和回收的机械强度高的超分子热固性材料。所得的超分子热固性材料通过氮配位的硼酸酯的动态共价键交联。通过改变 Tri-PBA-PPG 和 Bi-PBA-PPG 的比例,可以系统地调整超分子热固性材料的机械性能,从而改变氮配位的硼酸酯的交联密度和超分子热固性材料的拓扑结构。具有摩尔比为 Tri-PBA-PPG 与 Bi-PBA-PPG 为 1:2 的超分子热固性材料具有最高的机械强度,玻璃化转变温度约为 36°C,拉伸强度约为 31.96 MPa,杨氏模量约为 298.5 MPa。氮配位的硼酸酯的高可逆性和聚(丙二醇)链的柔韧性使得具有最强机械强度的超分子热固性材料能够在 55°C 下进行高效修复,并在 60°C 下 4 MPa 的压力下进行回收,从而恢复其原始的机械强度和完整性。

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