Transparent, self-recoverable, highly tough, puncture and tear resistant polyurethane supramolecular elastomer with fast self-healing capacity via "hard-soft" hard domain design.

The integration of superior mechanical properties and fast healing efficiency for self-healing polyurethane supramolecular elastomers is challenging due to the confliction between high chain mobility for healing and high chain rigidity for mechanical properties. Herein, a strategy to design a "hard-soft" hard domain by the cooperation of quadruple hydrogen bonds (HBs) in the mainchain as restriction units and single HBs in the side chain as diffusion units is reported. The resulting transparent supramolecular elastomer exhibited fast self-recoverability, good puncture resistance and superior mechanical properties with a tensile strength of 20.5 MPa, an extensibility of 2043.7%, a toughness of 146.1 MJ m-3 and a tear resistance of 13.8 kJ m-2. Moreover, the fast self-healing capacity (healing efficiency > 82% within 3 h under moderate condition) was realized due to the soft effects of weak HBs in the side chain on the strong HBs in the mainchain. Taking advantage of the merits of the supramolecular elastomer, a flexible sensor was simply fabricated, which showed good self-repairable and stable sensing properties. Thus, the elastomer has great potential in the field of flexible electronics and wearable devices.

Designing a Polymer-Based Hybrid with Simultaneously Improved Mechanical and Damping Properties via a Multilayer Structure Construction: Structure Evolution and a Damping Mechanism.

Though hindered phenol/polymer-based hybrid damping materials, with an excellent loss factor, attract more and more attention, the significantly decreased mechanical property and the narrow damping temperature range limit the application of such promising materials. To solve the problems, a polyurethane (hindered phenol)/polyvinyl acetate multilayer system with varied layer numbers was prepared in this study. The multilayer microstructures were first verified through the scanning electron microscopy. A subsequent molecular dynamics simulation revealed the promoted diffusion of polyurethane (hindered phenol) and polyvinyl acetate layers, the compact chain packing of the polyurethane (hindered phenol) layer, the extended chain packing of the polyvinyl acetate layer, the intermolecular hydrogen bonds among the three components and the enhanced interface interactions between the two layers in a quantitative manner. Further the mechanical and dynamic mechanical analysis detected the successful preparation of the multilayer hybrids with simultaneously improved mechanical and damping properties. Then, by a combination of molecular dynamics simulation and experiment, the relationship between the structure evolution and the properties of the multilayer hybrids was established, which was expected to have some guiding significance for industrial production.

Towards a Stable and High-Performance Hindered Phenol/Polymer-Based Damping Material Through Structure Optimization and Damping Mechanism Revelation.

Although hindered phenol/polymer-based hybrid damping materials, with excellent damping performance, attract more and more attention, the poor stability of hindered phenol limits the application of such promising materials. To solve this problem, a linear hindered phenol with amorphous state and low polarity was synthesized and related polyurethane-based hybrid materials were prepared in this study. The structure and state of the hindered phenol were confirmed by nuclear magnetic resonance spectrum, Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). The existence of intermolecular hydrogen bonds (HBs) between hindered phenol and polyurethane was confirmed by FT-IR, and the amorphous state of the hybrids was confirmed by XRD. Moreover, by a combination of molecular dynamics simulation and dynamic mechanical analysis, the relationship between the structure optimization of the hindered phenol and the high damping performance of the hybrids was quantitatively revealed. By constructing the synthetic hindered phenol, the intramolecular HBs between hindered phenols were restricted, while the strength and concentration of the intermolecular HBs increased by increasing the amount of hindered phenol. Thus, intermolecular interactions were enhanced, which lead to the compact chain packing of polyurethane, extended chain packing of hindered phenol, and good dispersion of hindered phenol in polyurethane. Therefore, the stability of the hindered phenol and the damping properties of the hybrids were both improved. The experiment results are expected to provide some useful information for the design and fabrication of high-performance polymeric damping materials.