The advanced development of biocomposites made of biodegradable polymers and natural fibers has initiated great interest because the resultant polymer will degrade absolutely and will not emit toxic substances. Among the biodegradable polymers, the poly(butylene succinate) and poly(lactic acid) have diverse commercial applications and the natural fiber such as wood flour is renewable and cheaper alternative to synthetic fiber. The properties of the composite made of poly(butylene succinate)/poly(lactic acid) blend and wood flour are not compatible due to the poor wettability and interfacial adhesion. Therefore, in the study presented, the Fusabond MB 100 D has been used to improve the interfacial bonding between poly(butylene succinate)/poly(lactic acid) blend and the dispersed wood flour. The results reveal that the addition of FB not only increases the tensile strength but also improves the impact strength of poly(butylene succinate)/poly(lactic acid)wood flour composite under high dynamic loading. Moreover, when Fusabond MB 100 D is added as a coupling agent to the poly(butylene succinate)/poly(lactic acid)wood flour composite results of X-ray photo spectroscopy, fracture surface morphology and dynamical mechanical property indicate the interaction between the poly(butylene succinate)/poly(lactic acid) blend with the wood flour.

One of the ideal energy carriers for the future is hydrogen. It has a high energy density and is a source of clean energy. A crucial step in the development of the hydrogen economy is the safety and affordable storage of a large amount of hydrogen. Thus, owing to its large storage capacity, good reversibility, and low cost, Magnesium hydride (MgH₂) was taken into consideration. Unfortunately, MgH₂ has a high desorption temperature and slow ab/desorption kinetics. Using the ball milling technique, adding cobalt lanthanum oxide (LaCoO₃) to MgH₂ improves its hydrogen storage performance. The results show that adding 10 wt.% LaCoO₃ relatively lowers the starting hydrogen release, compared with pure MgH₂ and milled MgH₂. On the other hand, faster ab/desorption after the introduction of 10 wt.% LaCoO₃ could be observed when compared with milled MgH₂ under the same circumstances. Besides this, the apparent activation energy for MgH₂–10 wt.% LaCoO₃ was greatly reduced when compared with that of milled MgH₂. From the X-ray diffraction analysis, it could be shown that in-situ forms of MgO, CoO, and La₂O_3, produced from the reactions between MgH₂ and LaCoO₃, play a vital role in enhancing the properties of hydrogen storage of MgH₂.

The spray drying technique is suitable for different kinds of liquid dispersions and can be easily optimized to produce solid particles with tailored properties. The spray drying technique is a complex process. As an example, it is difficult to track drying kinetics, shape, and morphological changes on the scale of a single droplet. To better understand the effect of drying process variables on dried particle formation, it is useful to observe the drying of single droplets. Fundamental processes, such as mass and heat transfer, can then be easily monitored and compared with theoretical models. Acoustic levitation enables droplet/particle suspension in the air without any mechanical contact. Experiments in the acoustic levitator can be used to mimic the drying process in the spray dryer. The drying kinetics of single droplets of PEG6000 into solid particles was studied. Droplets with an initial polymer concentration (PEG6000 aqueous solution of 5%, 10%, and 15% (w/w)) were investigated at different gas drying temperatures. The size of the droplet, moisture content, and the shape evolution of the droplet/particle during the drying process were studied. The experimental drying curves were compared with the Reaction Engineering Approach (REA). The REA models were shown to provide a very good agreement for drying behavior, with a relative error of about ±3% between the initial and predicted droplet mass. This model can be implemented into the large-scale modeling of spray drying using Computational Fluid Dynamics (CFD).

Radiative cooling is a new large-scale cooling technology with the promise of lowering costs and decreasing global warning. Currently, daytime radiative cooling is achieved via the application of reflective metal layers and complicated multilayer structures, limiting its application on a massive scale. In our research, we explored and tested the daytime subambient cooling effect with the help of single-layer films consisting of BaSO₄, TiO₂, and BaSO₄/TiO₂ microparticles embedded in PVDF/PTFE polymers. The film, consisting of BaSO₄/TiO₂ microparticles, offers a low solar absorbance and high atmospheric window emissivity. The solar reflectance is enhanced by micropores in the PVDF/PTFE polymers, without any significant influence on the thermal emissivity. The BaSO₄/TiO₂/PVDF/PTFE microparticle film attains 0.97 solar reflectance and 0.95 high sky-window emissivity when the broadly distributed pore size reaches 180 nm. Our field test demonstrated that the single-layer BaSO₄/TiO₂/PVDF/PTFE microparticle film achieved a temperature 5.2 °C below the ambient temperature and accomplished a cooling power of 74 W/m². Also, the results show that, when the humidity rises from 33% to 38% at 12:30 pm, it hinders the cooling of the body surface and lowers the cooling effect to 8%.