A solar photovoltaic (PV) system produces electrical energy from solar energy. This green, sustainable system has low energy conversion efficiency due to the rise in PV temperature throughout the day. In order to keep the temperature of the panels close to ambient, this study examines the usage of hydrated salt (HS36) as a Phase Change Material (PCM) for PV cooling. The primary goal of this experimental study is to cool the PV panel by introducing PCM behind the PV system (PV-PCM), thus increasing its performance. An energy and exergy performance assessment was carried out on PV and PV-PCM systems. The result indicates that placing a PCM over the back of the solar panel’s back reduced the operational temperature by 25.4% and increased the panel’s electrical efficiency by 17.5%. PV-PCM systems’ maximum exergy efficiency increased by 12.57%, and their exergy destruction ratio decreased by 12.49%. The proposed PV-PCM system with HS36 PCM increased the PV panel performance and can be deployed in the PV system.

Apart from the widely discussed pineapple leaf fibers, normally referred to as PALF, fibers from other parts of the plant also exist, particularly those in the fruit crown, which are known as pineapple crown leaf fibers (PCLF). In this work, PCLF were characterized using thermogravimetric analysis (TGA), Fourier transform IR spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The results indicated that the properties of PCLF do not greatly differ from those observed for PALF. In particular, a cellulose content of over 67% was observed, with approximately 76% crystallinity. The main degradation phenomena of the fibers took place between 230 and 380 °C, peaking at 324 °C, which is in line with observations in other fibers which have similar cellulose and crystalline contents. There was 13.4% residue at 680 °C. Bare mechanical retting of PCLF, although not allowing a full and thorough degumming, which would only be achieved through more aggressive chemical treatment, enabled aspect ratios of over 10³ to be obtained. This indicates some potential for their application as short fibers in composites. In this respect, the considerable roughness of PCLF when compared to other leaf-extracted fibers, and in particular when compared to PALF, could suggest an ability to obtain a sufficiently sound fiber–matrix interface.

The contribution of natural lignocellulosic fibers to the reduction in wear damage in polymer resins is of interest, especially when two of these fibers can combine their respective effects. Wear properties of hybrid kenaf/banana epoxy composites have been investigated using three different total amount of fibers, 20, 30 and 40 wt.%, at loading forces up to 30 N and to sliding distances of up to 75 m. This demonstrated that the introduction of the highest level of fibers proved the most suitable for consistency of results and containment of wear with increasing load, as was also found from the morphological evaluation of wear degradation using scanning electron microscopy (SEM). Subsequently, tensile, flexural and impact properties of as-received and post-water-saturation hybrid composites were examined. The tests revealed a limited reduction in tensile and flexural strength, not exceeding 10% of the initial values, which were very high compared to similar materials, almost reaching 140 MPa for tensile strength and exceeding 170 MPa for flexural strength. In contrast, a higher standard deviation of values was found for impact strength, although the decrease in average values was only slightly above 10%. The results suggest the availability of these hybrids for wear-resisting applications in high-moisture environments, and the even more limited water absorption conferred by banana fibers added to kenaf ones.

In recent years, there has been growing interest in utilizing bark fibers as reinforcements for polymer composites. This study focused on the characterization of epoxy composites reinforced with Acacia caesia bark (ACB) fibers, considering their mechanical, morphological, and thermal properties. Various amounts of ACB fibers with three different lengths (10, 20, and 30 mm) were incorporated into the composites, ranging from 10 to 35 wt.% in 5% increments. This resulted in 18 sample categories, which were compared to neat epoxy samples. The findings demonstrated that the introduction of ACB fibers, even at the highest fiber content, led to improved mechanical performance. However, a transition in fiber length from 20 to 30 mm exhibited conflicting effects on the composite, likely due to the tendency of bark fibers to bend and split into fibrils during loading. Regarding thermal degradation, the advantages over neat epoxy were evident, particularly for 20 mm fibers, suggesting enhanced interfacial bonding between the matrix and the reinforcement. The epoxy adequately protected the bark fibers, enabling the composite to withstand degradation at temperatures comparable to pure resin, with minimal structural damage below 320 °C.

New fibers extracted from plant barks are a recent subject of investigation as possible fillers for polymer composites. In this work, Grewia Monticola Sond (GMS) fibers have been characterized from a morphological, chemical, and thermal point of view. This involved using a number of techniques, including Fourier infrared spectroscopy (FTIR), X-ray diffraction (×RD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), atomic force microscopy (AFM), and ¹³C nuclear magnetic resonance (NMR). Results indicated that GMS fibers have relatively high cellulose (55%), with 33.5% crystallinity index and a crystallite size of 4.89 nm, and lower hemicellulose (14%) and lignin (15%) contents. The fibers showed cellulose degradation onset at around 324°C, while kinetic activation energy (74.18 kJ/mol) is quite low. The roughness of the fibers was in the range expected for similar natural fibers, and they may be considered silky according to their kurtosis values. As for possible application in composites, they would definitely withstand process temperatures with thermoplastics. However, their not very high crystallinity and low crystallite size might suggest a limited strength, to be verified in future after optimizing GMS fiber extraction from bark.