To adapt to the complex application of polyurethane bearings, it is feasible to improve the tribological performance of single polyurethane-based friction materials through the synergistic effect produced by multi-component-lubricating fillers. In this context, rather than using tungsten disulfide (WS₂), which has demonstrated excellent self-lubricating performance as a lubricating oil additive, this paper proposes that WS₂ and single-walled carbon nanotubes (SWNTs) can be designed for addition into a polyether 4,4′-diphenylmethane diisocyanate (MDI) polyurethane matrix as self-lubricating fillers so as to explore the synergistic effect of micro- and nano-lubricating fillers on the tribological performance of polyurethane matrix materials. Through a series of characterizations and tests, it was found that the dispersion of two-component-lubricating additives in a polyurethane matrix is improved when the ratio of WS₂ to SWNTs is roughly 2:1. In this case, the tribological performance of polyurethane matrix composites is more satisfactory than at other ratios. In addition, compared with the blank sample, the tribological performance of the synergistically modified polyurethane composites under dry friction is more significantly improved with the increase in contact load, while there is no significant improvement under water lubrication. Aside from contributing to the idea of exploring the synergistic effect of WS₂ and other micro or nanofillers, this method also opens up the possibility of practically applying WS₂ in the field of friction.

Film-forming resins, as carriers of antifouling coatings, play an essential role in the functional performance of coatings. With the gradual promotion of coatings in the field of marine antifouling, the preparation of film-forming resins containing hydrophilic chain segments is urgently needed to give full play to the functional and time-sensitive performance of antifouling coatings. In this paper, the single-ended isocyanate group (NCO) polyurethane (PU) prepolymer with hydrophilic chain segments was prepared and grafted onto an epoxy resin (EP) molecular chain to obtain the PU/EP grafted blend. Successful preparation of the PU/EP grafted blends was confirmed by infrared spectrum analysis. Simultaneously, the grafted blend was cured, and its hydrophilicity and mechanical properties were also tested. The results demonstrate that the grafted method can effectively improve the hydrophilicity of the film-forming resin while maintaining its mechanical properties. It can be concluded from the hydrophilic and mechanical properties of the materials that the comprehensive properties of PU/EP grafted blends are the best when the PU content is between 40% and 50%. The hanging plate test showed that the antifouling effect of the antifouling coating prepared by hydrophilic modified PU/EP film-forming resin was better than that of the traditional antifouling coating under the experimental conditions.

Polyurethane dielectric elastomer (PUDE) is considered a potential underwater flexible actuator material due to its excellent designability and environmental tolerance at the molecular level. Currently, the application of the polyurethane elastomer as an actuating material is constrained by such problems as the conflict between various properties such as dielectric properties and modulus and the low level of dielectric sensitivity. This is a common challenge facing polyurethane dielectric research related to the uneven distribution of dielectric fillers in the matrix. Besides, another challenge for the academic circles is the easy agglomeration of micro and nanofillers. Given the above-mentioned background of the application and technical problems, the coaxial electrospinning technology is proposed in this paper. The polyurethane fiber network is constructed with the preferred hydrolysis resistant polyether-Diphenylmethane diisocyanate (MDI) thermoplastic polyurethane elastomer as the matrix material. Dispersed by ultrasound, the micro nano dielectric filler is integrated into polyurethane fiber through the coaxial dual-channel design. Additionally, directional constraint molding is conducted to improve the agglomeration of small-scale particles induced by the loss of mechanical energy in traditional blending. After characterization, the distribution of BaTiO₃ particles in the fiber bundle is relatively uniform. Compared to the polyurethane dielectric composites prepared by traditional blending (BaTiO₃-Dielectric Elastomer, BaTiO₃-DE), the dielectric sensitivity factor of the polyurethane composite fiber membrane (BaTiO₃-Dielectric Elastomer Membrane, BaTiO₃-DEM) is enhanced by over 25%; the electrostrictive strain of BaTiO₃-DEM is boosted by least 10%.

Polyurethane dielectric elastomer (PUDE), a typical representative of emerging intelligent materials, has advantages, such as good elasticity and flexibility, fast response speed, high electromechanical conversion efficiency, and strong environmental tolerance. It has promising applications in underwater bionic actuators, but its electromechanical properties should be improved further. In this context, the design of polyethylene glycol (PEG) single-walled carbon nanotube (SWNTs) dielectric microcapsules was adopted to balance the problem of contradictions, which conventional dielectric modification methods face between comprehensive properties (e.g., dielectric properties and modulus). Moreover, the dielectric microcapsule was evenly filled into the polyurethane fiber by coaxial spinning technology to enhance the actuation performance and instability of the electrical breakdown threshold of conventional polyurethane dielectric modification. It was revealed that the dielectric microcapsules were oriented in the polyurethane fiber, and the actuation performance of the composite fiber membrane was significantly better than that of the polyurethane fiber membrane filled with SWNTs, thus confirming that the filling design of the dielectric microcapsules in polyurethane fiber could have certain technical advantages. On that basis, this study provides a novel idea for the dielectric modification of polyurethane.