Per and polyfluoroalkyl substances (PFAS) have been extensively employed in a broad range of manufacturing and consumer goods due to their highly persistent nature. PFAS exposure is recognized to pose serious health hazards; therefore, addressing PFAS pollution in water has become a top priority for public health and environmental protection organizations. This review article focuses on the efficiency of different removal techniques (activated carbon, biochar, ion exchange resin, membrane filtration, reverse osmosis, metal-organic frameworks, foam fractionation, ozone fractionation, and destruction techniques) for eliminating different types of short- and long-chain PFAS from water. Hydrophobicity and electrostatic interactions are revealed to be the primary mechanisms for the elimination of PFAS. The efficiency of all techniques to eradicate short-chain PFAS is comparatively lower compared to long-chain PFAS. The destruction techniques are the most efficient but have some drawbacks, including the formation of PFAS precursors and high operational costs. According to the findings from the study, it is anticipated that combined methods will be required to effectively remediate PFAS-contaminated water.

This research explores the enhancement of bio-oil quality through upgrading with the magnetic bimetallic oxide (CuO-Fe₃O₄) catalysts supported on activated rice straw biochar (AcB). These catalysts were employed in a supercritical ethanol-based upgrading process. Various characterization techniques, including elemental analysis, Fourier transform infrared (FTIR), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) analysis, thermogravimetric analysis (TGA), and scanning electron microscopy (SEM), were utilized to characterize the prepared catalysts. This study revealed significant improvements in the physical characteristics and chemical composition of the bio-oil, with an increase in the heating value (HHV) from 21.3 to 32.1 MJ/kg. Esterification and transesterification were identified as key reactions contributing to this improvement. Notably, the pH of bio-oil increased from 4.3 (raw bio-oil) to 5.63 (after upgrading), signifying reduced acidity. The analysis of the bio-oil’s chemical composition highlighted a decrease in oxygen content and an increase in carbon and hydrogen content. At the optimum conditions, the application of supercritical ethanol proved to be an efficient method for enhancing the bio-oil’s properties. A crucial transformation occurred during the upgrading process and more than 90% of carboxylic acids were converted into esters, primarily ethyl acetate at the optimal conditions. This study has demonstrated the effective enhancement of raw bio-oil from rice straw through the utilization of carbon-based bimetallic oxide catalysts in a supercritical upgrading procedure.

Bio-oil produced via fast pyrolysis, irrespective of the biomass source, faces several limitations, such as high water content, significant oxygenated compound concentration (35–40 wt.%), a low heating value (13–20 MJ/kg), and poor miscibility with fossil fuels. These inherent drawbacks hinder the bio-oil’s desirable properties and usability, highlighting the necessity for advanced processing techniques to overcome these challenges and improve the bio-oil’s overall quality and applicability in energy and industrial sectors. To address the limitations of bio-oil, a magnetic bimetallic oxide catalyst supported on activated rice straw biochar (ZrO₂-Fe₃O₄/AcB), which has not been previously employed for this purpose, was developed and characterized for upgrading rice straw bio-oil in supercritical butanol via esterification. Furthermore, the silica in the biochar, combined with the Lewis acid sites provided by ZrO₂ and Fe₃O₄, offers Brønsted acid sites. This synergistic combination enhances the bio-oil’s quality by facilitating esterification, deoxygenation, and mild hydrogenation, thereby reducing oxygen content and increasing carbon and hydrogen levels. The effects of variables, including time, temperature, and catalyst load, were optimized using response surface methodology (RSM). The optimal reaction conditions were determined using a three-factor, one-response, and three-level Box-Behnken design (BBD). The ANOVA results at a 95% confidence level indicate that the results are statistically significant due to a high Fisher’s test (F-value = 37.07) and a low probability (p-value = 0.001). The minimal difference between the predicted R² and adjusted R² for the ester yield (0.0092) suggests a better fit. The results confirm that the optimal reaction conditions are a catalyst concentration of 1.8 g, a reaction time of 2 h, and a reaction temperature of 300 °C. Additionally, the catalyst can be easily recycled for four reaction cycles. Moreover, the catalyst demonstrated remarkable reusability, maintaining its activity through four consecutive reaction cycles. Its magnetic properties allow for easy separation from the reaction mixture using an external magnet.