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.     

Magnetoelectric sensor for microtesla magnetic-fields based on (Fe80Co20)78Si12B10/PZT laminates

The magnetoelectric sensor based on (Fe₈₀Co₂₀)₇₈Si₁₂B₁₀/PZT laminates is designed, fabricated and characterized for determining dc and ac magnetic-field strengths as well as field orientations. At low dc magnetic-fields, a ME-voltage response (dV_ME/dH) as high as 2 mV/Oe is achieved. The linear relation V_ME(h_ac) with a slope of dV_ME/dh_ac of 17 mV/Oe shows a great ability to self-powered detecting low ac magnetic-fields. The field orientation can be detected by using the sinusoidal dependence of the magnetoelectric voltage. The sensor is promising not only for microtesla magnetic-field sensing but also for magnetic biosensor applications.     

Are disulphide bonds formed during acid gelation of preheated milk?

The role of thiol/disulphide exchanges during acid gelation of preheated milk was studied with milk samples with or without N‐ethylmaleimide (NEM), a thiol‐blocking agent, and acidified to pH 4 by the addition of glucono‐delta‐lactone at 20 °C. Active or total thiol groups, particle size with light scattering measurements in a dissociating solvent or by SDS‐agarose electrophoresis were determined on acidified milk samples. Diffusing wave spectroscopy and rheology in low strain were applied during acidification of sample, while rheology in large strain was applied on final acid gels. The only effect of the presence of NEM was a reduced firmness of acid gels as measured at large strain and a reduced tendency to form large aggregates at pH<5.5. In conclusions, thiol/disulphide exchanges during acidification of milk played only a minor role in the building of acid gel networks from heated milk.     

Visualizing chemical compositions and kinetics of sol-gel by near-infrared multispectral imaging technique

Kinetics of sol-gel formation were studied using the recently developed near-infrared (NIR) multispectral imaging instrument. This imaging spectrometer possesses all the advantages of conventional spectrometers. It also has additional features that NIR spectrometers cannot offer, namely, its ability to provide kinetic information at different positions within a sample. The high spatial resolution and sensitivity of the InSb camera make it possible for the imaging spectrometer to determine the kinetic from data recorded by a single pixel. Kinetics of sol-gel reactions, determined by this multispectral imaging instrument, show that the initial hydrolysis of the TEOS, MTES, or a mixture of these two alkoxysilanes is relatively inhomogeneous. The inhomogeneity is dependent on the number of pixels used to calculate the spectrum for each spot. Data calculated from a single pixel provide the largest inhomogeneity. No inhomogeneity was observed when an average of a large number of pixels (e.g., 10 x 10) is used for calculation. The inhomogeneities observed for TEOS sol-gels are different from those for the MTES sol-gels, and those for sol-gels prepared from a mixture of TEOS and MTES are relatively larger and more similar to those of the MTES sol-gels. A variety of reasons might account for the observed inhomogeneities including differences in the structure of the TEOS sol-gels and MTES sol-gels and the inability of the TEOS to mix well with MTES with the latter being more hydrophobic.     

Determination of binding constants of cyclodextrins in room-temperature ionic liquids by near-infrared spectrometry

Near-infrared spectrometry has been successfully used to determine association binding constants between phenol and alpha-, beta- and gamma-cyclodextrin (CD) in [butylmethylimidazolium][chloride] room-temperature ionic liquid (RTIL). It was found that adding CD into the RTIL solution of phenol resulted in an enhancement in the absorption coefficient of the stretching overtone of the aromatic C-H groups. However, the enhancement induced by CDs in RTIL is much lower (order of magnitude) than those corresponding in D20. The binding constants in RTIL are also much lower than those in D2O ((11 +/- 2), (16 +/- 2), and (40 +/- 6) M(-1) for phenol and alpha-, beta- and gamma-CD, respectively, as compared to 87 and 214 M(-1) for a- and beta-CD in D2O). The results obtained seem to suggest that in ionic liquid, the main interaction between phenol and CDs may not be inclusion complex formation but rather external adsorption. A variety of reasons may be responsible for relatively weaker interactions and lower binding constants in the ionic liquid, including differences in the polarity and viscosity of RTIL and D20. However, the main reason may be due to the possibility that the 1-butyl-3-methylimidazolium cation of the ionic liquid may form inclusion complexes with CDs either through its imidazolium moiety or its butyl group. Such complex formation would prevent phenol from being included in the cavity of the CDs.