Press molding of a Si–HDPE hybrid lens substrate and evaluation of its infrared optical properties

A hybrid structure of single-crystal silicon (Si) and high-density polyethylene (HDPE) was developed as a new substrate for infrared lenses by using precision press molding. A thin HDPE film was used to laminate a silicon wafer and their interface was directly bonded by the silane cross-link. The HDPE film is easy to be hot-embossed to form three-dimensional surface microstructures and the silicon wafer provides a high stiffness for the hybrid substrate. The infrared (IR) optical properties of the hybrid substrate were examined by two kinds of measurements, transmittance and image sharpness. Interestingly, the transmittance measurement result shows that the IR transmittance of the hybrid substrate is higher than that of Si itself in some region of wavelength. The imaging test result shows that the hybrid substrate is capable to produce similar image quality as Si itself. These results strongly demonstrate that the developed Si–HDPE hybrid substrate is a promising alternative substrate material for IR lens.     

Hydrogen-storage properties of MgH2–10Ni–2NaAlH4–2Ti prepared by reactive mechanical grinding

A sample of 86 wt% MgH₂–10 wt% Ni–2 wt% NaAlH₄–2 wt% Ti (named MgH₂–10Ni–2NaAlH₄–2Ti) was prepared by reactive mechanical grinding. Activation of the sample was not required at 573 K. At the first hydriding–dehydriding cycle (n = 1), the sample absorbed more than 5 wt% H at 573 K under 12 bar H₂ for 60 min. The hydriding rate increased as the temperature increased from 423 K to 553 K. MgH₂–10Ni–2NaAlH₄–2Ti showed quite high hydridng rates at relatively low temperatures of 423 K and 473 K under 12 bar H₂, absorbing 4.02 wt% H for 60 min at 473 K.     

Heterostructured dysprosium vanadate – ZnO for photo-electrocatalytic and self-cleaning applications

In this article, we report fabrication of 5 wt% of Dy as DyVO₄ supported ZnO by template-free hydrothermal-thermal decomposition method and its photocatalytic activity towards degradation of azo dyes Rhodamine-B (Rh-B) and Trypan Blue (TB) in solar light, Electrocatalytic activity in methanol oxidation and Self-cleaning properties. The as prepared DyVO₄-ZnO was characterized by surface analytical and spectroscopic techniques. The results suggested that Dysprosium vanadate doping on ZnO has increased its photocatalytic efficiency with high reusability. DyVO₄-ZnO exhibits higher electrocatalytic activity than prepared ZnO for methanol electrooxidation in alkaline medium, revealing its promising potential as the anode in direct methanol fuel cells. Hydrophobicity of ZnO increases by doping of DyVO_4.     

Electrochemical study on new polymer composite for zinc corrosion protection

Galvanostatic electrodeposition mode was employed for the synthesis of new polyaniline and polypyrrole-based composite coatings (PANI/PPY) onto pure zinc electrode. Potentiodynamic polarization, open circuit potential measurements and Electrochemical Impedance Spectroscopy (EIS) were employed to assess the ability of these composite coatings to provide an effective barrier to corrosion in chloride environment. Fourier Transform Infrared (FTIR) spectroscopy and Scanning Electron Microscopy (SEM) observations were employed to characterize the structure and morphology of the modified electrodes. The coatings deposited galvanostatically at lower current density showed the best quality in terms of protection ability towards aggressive medium. It was found that the new PANI/PPY composite coatings had significantly better properties than single polymer coatings regarding the corrosion protection.     

Controllable ZnO nanostructures evolution via synergistic pulsed laser ablation and hydrothermal methods

We report the morphology-controlled ZnO nanostructures (ZNSs) evolution synthesized via a novel and facile technique at different growth times, where the pulse laser ablation in liquid (PLAL) is creatively combined with hydrothermal (H) method (hereafter called PLAL-H technique). Four types of ZNSs with varying sizes and shapes such as tapers, multipods, flowers, and hollow flowers are produced on Si substrate via PLAL-H technique. Furthermore, multipod- and flower-like ZNSs are grown using direct hydrothermal method to compare them with the one obtained via synergistic effects of PLAL-H method. This catalyst-free fabrication method is not only cost-effective but greatly useful for the rapid production of different quality of ZNSs at low temperature. ZNSs synthesized under prolonged growth time (60 min) exhibited structural deformation. Growth technique and time dependent morphology, structure, composition, and optical properties of these as-grown ZNSs are characterized using FESEM, X-ray diffraction, FTIR, photoluminescence, and UV–vis measurements. Synthesized ZNSs revealed excellent crystallinity and growth process dependent variation in the physical and optical features. The ZNSs growth mechanism is understood. Excellent features of the results demonstrate that this synergized new growth technique may constitute a basis for modifying the morphology, sizes, and optical properties of ZNSs in a controllable manner useful for diverse applications.     

Integrated Ni/Nb2O5 nanocatalytic agent dose for improving the hydrogenation/dehydrogenation kinetics of reacted ball milled MgH2 powders

Reactive ball milling (RBM) technique was employed to synthesize ultrafine powders of MgH₂, using high energy ball mill operated at room temperature under 50 bar of a hydrogen gas atmosphere. The MgH₂ powders obtained after 200 h of continuous RBM time composed of β and γ phases. The powders possessed nanocrystalline characteristics with an average grain of about 10 nm in diameter. The time required for complete hydrogen absorption and desorption measured at 250 °C was 500 s and 2500 s, respectively. In order to improve the hydrogenation/dehydrogenation kinetics of as synthesized MgH₂ powders, three different types of nanocatalysts (metallic Ni, Nb₂O₅ and (Ni)_x/(Nb₂O₅)_y) were utilized with different weight percentages and independently ball milled with the MgH₂ powders for 50 h under 50 bar of a hydrogen gas atmosphere. The results showed that the prepared nanocomposite MgH₂/5Ni/5Nb₂O₅ powders possessed superior hydrogenation/dehydrogenation characteristics, indexed by low values of activation energy for β-phase (68 kJ/mol) and γ-phase (74 kJ/mol). This nanocomposite system showed excellent hydrogenation/dehydrogenization behavior, indexed by the short time required to uptake (41 s) and release (121 s) of 5 wt% H₂ at 250 °C. At this temperature the synthesized nanocomposite powders possessed excellent absorption/desorption cyclability of 180 complete cycles. No serious degradation on the hydrogen storage capacity could be detected and the system exhibited nearly constant absorption and desorption values of +5.46 and −5.46 wt% H₂, respectively.     

Fatigue behaviour of nanoclay reinforced epoxy resin composites

Nanoparticle filling is a feasible way to increase the mechanical properties of polymer matrices. Abundant research work has been published in the last number of years concerning the enhancement of the mechanical properties of nanoparticle filled polymers, but only a reduced number of studies have been done focusing on the fatigue behaviour. This work analyses the influence of nanoclay reinforcement and water presence on the fatigue behaviour of epoxy matrices. The nanoparticles were dispersed into the epoxy resin using a direct mixing method. The dispersion and exfoliation of nanoparticles was characterised by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Fatigue strength decreased with the nanoclay incorporation into the matrix. Fatigue life of nanoclay filled composites was significantly reduced by the notch effect and by the immersion in water.     

Control of microstructural heterogeneities in carbon nanotube foams

Arrays of aligned carbon nanotubes (CNTs) under compression are known to exhibit a dissipative hysteretic response similar to classical foams. Here, we control the microstructure of the arrays during synthesis using a variable supply of carbon source and catalyst. We control CNT alignment and density along the array height, creating bands of high- and low-density regions. We study the dynamic response of these materials and show the ability to tailor the location and extent of strain localization under compression. We show that the synthesis procedures described herein allow for construction of CNT arrays with improved protection and energy dissipation in impact tests.