The limitations of hydrophilicity, strength, antibacterial activity adsorption performance of the biobased and biocompatible polymer materials, such as polyhydroxyalkanoates (PHAs), significantly restrict their wider applications especially in medical areas. In this paper, a novel composite membrane with high antibacterial activity and platelet adsorption performance was prepared based on graphene oxide (GO), MXene and 3-hydroxybutyrate-co-hydroxyvalerate (PHBV), which are medium-chain-length-copolymers of PHA. The GO/MXene nanosheets can uniformly inset on the surface of PHBV fibre and give the PHBV—GO/MXene composite membranes superior hydrophilicity due to the presence of hydroxyl groups and terminal oxygen on the surface of nanosheets, which further provides the functional site for the free radical polymerization of ester bonds between GO/MXene and PHBV. As a result, the tensile strength, platelet adsorption, and blood coagulation time of the PHBV—GO/MXene composite membranes were remarkably increased compared with those of the pure PHBV membranes. The antibacterial rate of the PHBV—GO/MXene composite membranes against gram-positive and gram-negative bacteria can reach 97% due to the antibacterial nature of MXene. The improved strength, hydrophilicity, antibacterial activity and platelet adsorption performance suggest that PHBV—GO/MXene composite membranes might be ideal candidates for multifunctional materials for haemostatic applications.

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The characteristic transition from ferroelectric (FE) to ergodic relaxor (ER) state in (Bi0.5Na0.5)TiO3 (BNT) based lead-free ceramics provides an efficient approach to bring a highly ordered phase back to a disordered one. It would be rational to utilize this transition to improve relevant non-piezoelectric properties based on domain decomposition. In this work, different La contents were introduced to 0.93(Bi0.5Na0.5)TiO3-0.07Ba(Ti0.945Zr0.055)O3 ceramics (BNT-BZT-xLa) to induce evolution of ergodic degree. The results reveal that with increasing La content, both the FE-ER transition temperature TF-R and depolarization temperature Td shift towards room temperature, implying a deepened ergodic degree. By modulation of ergodic degree, thermally stimulated depolarization current experiment shows a higher current density peak, and corresponding pyroelectric coefficient increases from 2.46 to 2.81 μC/(cm2∙°C) at Td. For refrigeration, the indirect measurement demonstrates the ΔT maximum increases from 1.1 K to 1.4 K, indicating an enhanced electrocaloric effect. Moreover, the optimized energy storage effect is observed after La doping. With appearance of “slimmer” P-E loops, both calculated recoverable energy storage density Wrec and storage efficiency η increase to 0.23 J/cm3 and 22.8%, respectively. These results denote La doping conduces to the improvement of non-piezoelectric properties of BNT-based ceramics in a certain range. Therefore, La doping should be an adopted modification strategy for lead-free ceramics used in areas like refrigerator and pulse capacitors.

In the present research, the carbon fiber reinforced thermoplastic (CFRTP) was laser joined with the Al alloy whose joining interface was pretreated by laser micro-texturing, anodizing, and hybrid of laser micro-texturing and anodizing. The surface morphology of the pretreated Al joining interface and bonding strength of the corresponding Al/CFRTP butt joint were investigated. The results show that the laser micro-texturing has fabricated the micro-pit or micro-furrow in the Al joining interface. With the increasing of laser scanning times, the size of the micro-pit or micro-furrow decreases, when the laser scanning distance is constant. The bonding strength of the Al/CFRTP butt joint with Al joining interface pretreated by micro-texturing fluctuates with the increasing of laser scanning distance and times, reaching the maximum value of 20 MPa at laser scanning distance of 0.1 mm and 1 time. The anodizing pretreatment has formed the Al2O3 oxide layer on the Al joining interface. The Al/CFRTP butt joint with Al joining interface pretreated by anodizing obtains the maximum bonding strength of 11 MPa at anodizing time of 10 min. The hybrid pretreatment of micro-texturing and subsequent anodizing fabricates the regular grid structure with smooth micro-furrow and micro-pit, while the hybrid pretreatment of anodizing and subsequent micro-texturing fabricates the Al joining interface with explosive micro-pit and micro-furrow. The bonding strength of the Al/CFRTP butt joint with hybrid-pretreated Al joining interface is relative better than that of the Al/CFRTP butt joint with anodizing-pretreated Al joining interface but almost lower than that of the Al/CFRTP butt joint with micro-texturing pretreated Al joining interface. Such results should be attributed to the surface morphology of the Al joining interface.

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In this article, the elastocaloric effect of a commercial superelastic NiTi shape memory alloy (SMA) tube (with an outer diameter of 5 mm and wall thickness of 1 mm) to be applied in a compressive cooler was measured and analyzed. The elastocaloric effect of the tube was measured vs the applied strain and strain rate. The largest temperature changes of 21 K during loading and 16 K during unloading were measured at an applied strain of 3.30% and strain rate of 0.33 s−1. In the fatigue testing of the sample, only 0.20% of the residual strain accumulated after a runout of 1 × 106 sinusoidal force-controlled loading–unloading cycles at a maximum compressive stress of 1100 MPa and frequency of 20 Hz. Numerical results of the cooling characteristics of a compressive device using a single NiTi tube with the above-mentioned cross section and an aspect ratio of 60:1 as the refrigerant showed that the device could produce a total cooling power of up to 20 W and a coefficient of performance of up to 6.5. The results of this article demonstrate that superelastic NiTi SMA tubes of suitable wall thickness and aspect ratios are good candidates to be applied in a compressive elastocaloric cooler.

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Depolarization behavior is one of the main shortcomings of (Bi0.5Na0.5)TiO3-based ceramics. Considering the undesirable efficiency of traditional modification methods, in this paper a series of 0–3 type ceramic composites 0.85(Bi0.5Na0.5)TiO3-0.11(Bi0.5K0.5)TiO3-0.04BaTiO3-x mol% ZnO (BNKT-BT-xZnO)) were synthesized by introducing ZnO nanoparticles. The results of the X-ray diffraction pattern (XRD) and energy dispersive spectroscopy (EDS) demonstrate that the majority of ZnO nanoparticles grow together to form enrichment regions, and the other Zn2+ ions diffuse into the matrix after sintering. With ZnO incorporated, the ferroelectric–ergodic relaxor transition temperature, TF-R, and depolarization temperature, Td, increase to above 120 °C and 110 °C, respectively. The research on temperature-dependent P–E loops verifies an attenuated ergodic degree induced by ZnO incorporation. For this reason, piezoelectric properties can be well-maintained below 110 °C. The electron backscatter diffraction (EBSD) was employed to investigate the stress effect. Orientation maps reveal the random orientation of all grains, excluding the impact of texture on depolarization. The local misorientation image shows that more pronounced strain appears near the boundaries, implying stress is more concentrated there. This phenomenon supports the hypothesis that potential stress suppresses depolarization. These results demonstrate that the depolarization behavior is significantly improved by the introduction of ZnO. The composites BNKT-BT-xZnO are promising candidates of lead-free ceramics for practical application in the future.