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ACS Applied Materials & Interfaces · 2020 · IF 8.758

Water-Enabled Room-Temperature Self-Healing and Recyclable Polyurea Materials with Super-Strong Strength, Toughness, and Large Stretchability

Zhen Shi,Jing Kang,Ling Zhang

The synthesis of polymeric materials that simultaneously possess multiple excellent mechanical properties and high-efficient self-healability at room temperature is always a huge challenge. Here, we report the synthesis of a transparent polyurea material that can self-heal at room temperature with the aid of water and, meanwhile, has multiple remarkable mechanical performances, including super-high strength, excellent toughness, and large stretchability. Thanks to the synergistic enhancement of both dynamic imine bonds and hierarchical hydrogen bonds within the networks, the resulting polyureas have a world-record tensile strength of 41.2 MPa when compared with other polyurethanes that can self-heal at room temperature and, at the same time, a large breaking strain of 823.0% and a superior toughness of 127.2 MJ/m3. Besides the influence of imine bonds, the mechanical properties of the polyureas are also strongly related to the density and strength of the hierarchical hydrogen bonds within the polyurea networks, and these two factors could be finely controlled by adjusting the mass ratio of the soft segments with different chain lengths and the types of diisocyanates used for polyurea synthesis, respectively. More importantly, the highly dynamic characteristic of both imine bonds and hierarchical hydrogen bonds within the polyureas endows the materials with repeated water-enabled room-temperature self-healing capacity with a high healing efficiency of 92.2%. Moreover, the polyureas can also be recycled or remolded under mild conditions by the hot-pressing or dissolution/casting process. The synthesized polyureas also show great potential in damping applications with a loss factor larger than 0.3 over the temperature range from 12 to 75 °C. It is believed that polyureas with super-high and well-tunable mechanical properties and high-efficient room-temperature self-healing ability have great potential to substitute traditional irreparable polymers in diverse practical applications.

CAS / MDL: 4098-71-9
研究领域: 材料科学 · 化学工程
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2023 · IF 4.2

Mechanically Robust and Self-Healable Polyureas Based on Multiple Dynamic Bonds

Yujia Hao,Guangming Zhu,Ben Li

The synthesis of polymeric materials that simultaneously possess multiple outstanding mechanical properties and self-healability is always a great challenge. Herein, we report the synthesis of a robust and self-healing polyurea material, which contains a dual metal coordination structure of Zn(II)-urea and Zn(II)-diamidepyridine as well as dense hydrogen bonds. Due to the synergistic enhancement of dynamic coordination bonds and hydrogen bonds in the supramolecular network, the obtained polyurea materials possess a combination of excellent mechanical properties and high-efficiency self-healing properties, which are adjustable by varying the content of Zn(II) ions. The optimal PU-L/Zn-3 sample has a tensile strength of ∼22.82 MPa, while the elongation at break is ∼1312% and the toughness is ∼222.68 MJ/m3. In addition, the fully cut sample exhibits a high healing efficiency of 95.7% based on toughness after treatment at 50 °C for 4 h. Multi-dynamic cross-linked polymers might provide a new way to obtain robust self-healing materials for protection materials and wearable electronics.

研究领域: 材料科学 · 化学工程
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2019 ·Vol. 57 ·期 13 ·1460-1466 · IF 2.591

Aromatic amine-terminated polysulfide oligomer: Synthesis and application in self-healable polyurea

Wentong Gao,Jianwei Xu,Pengfei Zuo,Hao Dong,Yiwu Quan,Pengshan Chang

The dynamic chemistry of disulfide bonds has emerged as one of the most powerful tools used for the fabrication of organic compounds and self-healing materials. In this article, a novel aromatic amine-terminated polysulfide oligomer is first synthesized from thiol-terminated polysulfide oligomer and bis(4-aminophenyl) disulfide via disulfide metathesis mechanism. The resulting oligomer is confirmed by FTIR and 1 H NMR spectra and then successfully applied in constructing self-healable polyurea material (A-LP23-I), which combines the advantages of higher strength of polyureas and excellent self-healing ability of polysulfide-based materials. After subjecting to a temperature of 75 °C for 48 h, both the tensile strength and ultimate elongation of A-LP23-I restore to more than 90% of the original values (3.32 MPa and 396%). This study demonstrates a novel strategy for synthesizing aromatic amine-terminated oligomer. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1460–1466

CAS / MDL: 68-12-2 109-99-9
研究领域: 材料科学 · 有机化学
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