Polyacrylonitrile‐carbon Nanotube‐polyacrylonitrile: A Versatile Robust Platform for Flexible Multifunctional Electronic Devices in Medical Applications

Flexible multifunctional electronic devices are of high interest for a wide range of applications including thermal therapy and respiratory devices in medical treatment, safety equipment, and structural health monitoring systems. This paper reports a scalable and efficient strategy of manufacturing a polyacrylonitrile‐carbon nanotube‐polyacrylonitrile (PAN‐CNT‐PAN) robust flexible platform for multifunctional electronic devices including flexible heaters, temperature sensors, and flexible thermal flow sensors. The key advantages of this platform include low cost, porosity, mechanical robustness, and electrical stability under mechanical bending, enabling the development of fast‐response flexible heaters with a response time of ≈1.5 s and relaxation time of ≈1.7 s. The temperature‐sensing functionality is also investigated with a range of temperature coefficient of resistances from ?650 to ?900 ppm K^?1. A flexible hot‐film sensing concept is successfully demonstrated using PAN‐CNT‐PAN with a high sensitivity of 340 mV (m s^?1)^?1. The sensitivity enhancement of 50% W^?1 is also observed with increasing supply power. The low cost, porosity, versatile, and robust properties of the proposed platform will enable the development of multifunctional electronic devices for numerous applications such as flexible thermal management, temperature stabilization in industrial processing, temperature sensing, and flexible/wearable devices for human healthcare applications.     

Model simplification and optimization of a passive wind turbine generator

In this paper, the design of a “low cost full passive structure” of wind turbine system without active electronic part (power and control) is investigated. The efficiency of such device can be obtained only if the design parameters are mutually adapted through an optimization design approach. For this purpose, sizing and simulating models are developed to characterize the behavior and the efficiency of the wind turbine system. A model simplification approach is presented, allowing the reduction of computational times and the investigation of multiple Pareto-optimal solutions with a multiobjective genetic algorithm. Results show that the optimized wind turbine configurations are capable of matching very closely the behavior of active wind turbine systems which operate at optimal wind powers by using a MPPT control device.     

Enhancement in High-Field J c Properties and the Flux Pinning Mechanism of MgB2 Thin Films on Crystalline SiC Buffer Layers

We have studied the influence of crystalline SiC buffer layers on the critical current density and on the flux pinning mechanism in MgB₂ thin films. Crystalline SiC buffer layers were deposited on the Al₂O₃ (0001) substrates by using a pulsed laser deposition method, and then MgB₂ thin films were grown on the SiC-buffered layer by using a hybrid physical-chemical vapor deposition technique. MgB₂ thin films with crystalline SiC-buffered layers showed a significant critical current density’s enhancement in the high magnetic field region. An uncommon plateau-like behavior was also observed when the normalized flux pinning force density was scaled with the reduced magnetic field. Based on the analyses of the scaling behavior of the flux pinning force, grain boundary pinning is likely to be a dominant pinning mechanism in the SiC-buffered MgB₂ thin films.     

Effect of trace Na additions on the hydriding kinetics of hypo-eutectic Mg–Ni alloys

Mg–Ni alloys are among the most promising candidates for solid-state hydrogen storage systems. This paper reveals the effect of Na doping in accelerating initial hydrogen uptake in Mg–Ni alloys using in-situ Synchrotron X-ray powder diffraction. A minimum concentration of approximately 0.2 wt.% Na must be achieved for the alloys to show reasonably fast hydriding kinetics. Surface analysis shows that a Na-modified Mg–Ni surface facilitates the chemisorption and dissociation of hydrogen molecules in the early stage of hydriding as evidenced by a rapid formation of the saturated hydrogen solid solution Mg₂NiH_0.3 from the original Mg₂Ni. The subsequent hydrogen absorption is based on a mechanism of nucleation and growth of MgH₂ where a high density of dislocations develops ahead of the growing hydride-metal interface.     

Development and long-term in vivo evaluation of a biodegradable urethane-doped polyester elastomer

We have recently reported upon the development of crosslinked urethane-doped polyester (CUPE) network elastomers, which was motivated by the desire to overcome the drawbacks presented by crosslinked network polyesters and biodegradable polyurethanes for soft tissue engineering applications. Although the effect of the isocyanate content and post-polymerization conditions on the material structure-property relationship was examined in detail, the ability of the diol component to modulate the material properties was only studied briefly. Herein, we present a detailed report on the development of CUPE polymers synthesized using diols 4, 6, 8, 10, or 12 methylene units in length in order to investigate what role the diol component plays on the resulting material's physical properties, and assess their long-term biological performance in vivo. An increase in the diol length was shown to affect the physical properties of the CUPE polymers primarily through lowered polymeric crosslinking densities and elevated material hydrophobicity. The use of longer chain diols resulted in CUPE polymers with increased molecular weights resulting in higher tensile strength and elasticity, while also increasing the material hydrophobicity to lower bulk swelling and prolong the polymer degradation rates. Although the number of methylene units largely affected the physical properties of CUPE, the choice of diol did not affect the overall polymer cell/tissue-compatibility both in vitro and in vivo. In conclusion, we have established the diol component as an important parameter in controlling the structure-property relationship of the polymer in addition to diisocyanate concentration and post-polymerization conditions. Expanding the family of CUPE polymers increases the choices of biodegradable elastomers for tissue engineering applications.