Zinc–air batteries are promising candidates as stationary power sources because of their high specific energy density, high volumetric energy density, environmental friendliness, and low cost. The oxygen-related reactions at the air electrode are kinetically slow; thus, the air electrode integrated with an oxygen electrocatalyst is the most critical component, and inevitably determines the performance of a Zn–air battery. The aim of this paper was to document progress in researching bifunctional catalysts for Zn–air batteries. The catalysts are divided into several categories: noble metal, metal nanoparticle (single and bimetallic), multicomponent nanoparticle, metal chalcogenide, metal oxide, layered double hydroxide, and non-metal materials. Finally, the battery performance is compared and discussed.

As most plastic materials disintegrate without being properly reused after they are discarded, this present study developed a novel thermoplastic elastomer (TPE) using recycled high-density polyethylene (rHDPE) and natural rubber (NR) with kenaf fibre as a sustainable filler. Apart from being used as filler, this present study aimed to examine the use of kenaf fibre as a natural anti-degradant as well. The results indicated that the tensile strength of the samples was found to have significantly decreased after 6 months of natural weathering and had decreased by a further 30% after 12 months due to the chain scission of the polymeric backbones and the degradation of the kenaf fibre. However, the composites that contained kenaf fibre significantly retained their properties post-natural weathering. In terms of tensile strength and elongation at the break, the addition of only 10 phr of kenaf increased the retention properties by 25% and 5%, respectively. This is noteworthy as kenaf fibre also contains a certain amount of natural anti-degradants. Therefore, as the kenaf fibre improves the weather resistance of composites, plastic manufacturers could use it as either a filler or a natural anti-degradant.

Cardanol-furfurylamine benzoxazine (CFB) is a bio-based resin thanks to cardanol as a by-product of cashew nut shell liquid. Polybenzoxanize obtained from CFB exhibited high thermal stability, however, it requires a high thermal curing temperature. This research was aimed to reduce the curing temperature of CFB by blending it and diphenolic acid-aniline benzoxazine (DAB). The blend molar ratio of CFB:DAB was 4:1. Under thermal curing, carboxyl group in DAB was degraded and accelerated ring-opening polymerization of CFB/DAB blend so that no catalyst was used. Different curing temperatures of CFB/DAB blend was investigated. Results from fourier transform infrared (FTIR) and differential scanning calorimetry (DSC) proved that the ring-opening initiated at 115.2 °C for DAB, 141.6 °C for blend and 206.2 °C for CFB. It proved that CfB/DAB blend could start thermal curing at an obvious lower temperature. Moreover, polybenzoxazine synthesized from CFB/DAB blend exhibited good thermal stability compared to DAB-polybenzoxazine and obtained higher char yields compared to CFB-polybenzoxazine.

The growing demand for electronic storage devices with faster charging rates, higher energy capacities, and longer cycle lives has led to significant advancements in supercapacitor technology. These devices typically utilize high-surface-area carbon-based materials as electrodes, which provide excellent power densities and cycling stability. However, challenges such as inadequate electrolyte interaction, hydrophobicity that impedes ion transport, and high manufacturing costs restrict their effectiveness. This study aims to enhance carbon-based materials by grafting polymer chains onto their surfaces for supercapacitor applications. A simple solution plasma process (SPP), followed by heating, prepared the polymer-grafted carbon materials. Carbon nanoparticles were synthesized from benzene through plasma discharge in liquid under ambient conditions, forming free radical sites on the carbon surface. Subsequently, benzene molecules were grafted onto the surface via radical polymerization during heating. We investigated the structural and morphological properties of the synthesized materials using scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), and Raman spectroscopy. Additionally, N₂ absorption–desorption isotherms were measured, pore structure was analyzed with the Dubinin–Astakhov (DA) average pore size model, and specific surface area was determined using the Brunauer–Emmett–Teller (BET) equation for all synthesized samples. The results indicated that the grafting process was influenced by heating time and drying temperature. Furthermore, the electrical properties of the samples were evaluated using cyclic voltammetry (CV), which demonstrated enhancements in both areal capacitance and cycling stability for the polybenzene-grafted carbon compared to the non-grafted variant. This research illustrates that polymer grafting can effectively improve the performance and stability of carbon-based materials for supercapacitor applications. Future work will aim to optimize these materials for broader applications.