Efficient and excellent nanoparticles are required for the degradation of organic dyes in photocatalysis. In this study, silver–manganese oxide nanoparticles (Ag-Mn-NPs) were synthesized through a wet chemical precipitation method and characterized as an advanced catalyst that has enhanced photocatalytic activity under sunlight irradiation. The nanoparticles were characterized using scanning electron microscopy (SEM), XRD, UV–vis light spectra, and energy-dispersive X-ray (EDX) spectroscopy, revealing their spherical and agglomerated form. The EDX spectra confirmed the composition of the nanoparticles, indicating their presence in oxide form. These bimetallic oxide nanoparticles were employed as photocatalysts for the degradation of malachite green (MG) dye under sunlight irradiation in an aqueous medium. The study investigated the effects of various parameters, such as irradiation time, catalyst dosage, recovered catalyst dosage, dye concentration, and pH, on the dye’s photodegradation. The results showed that Ag-Mn oxide nanoparticles exhibited high photocatalytic activity, degrading 92% of the dye in 100 min. A longer irradiation time led to increased dye degradation. Moreover, a higher catalyst dosage resulted in a higher dye degradation percentage, with 91% degradation achieved using 0.0017 g of the photocatalyst in 60 min. Increasing the pH of the medium also enhanced the dye degradation, with 99% degradation achieved at pH 10 in 60 min. However, the photodegradation rate decreased with increasing dye concentration. The Ag-Mn oxide nanoparticles demonstrate excellent potential as a reliable visible-light-responsive photocatalyst for the efficient degradation of organic pollutants in wastewater treatment.

In order to satisfy the increasing need for renewable chemicals and fuels, it is important to replace petroleum-based products with alternative feedstocks. Lignocellulosic biomass is considered to be the most capable alternative source for producing sustainable biofuels. Catalytic co-pyrolysis (CCP) is a process that involves simultaneously pyrolyzing biomass and plastics to produce a combination of liquid and gaseous products, such as bio-oil and syngas. Catalysts are used to raise the reaction degree and the selectivity of the co-pyrolysis process, with the choice of catalyst dependent on the physico-chemical features of the feedstock. Catalytic pyrolysis is a useful method for producing high-quality biofuels directly from biomass, although it typically yields a modest amount of aromatic hydrocarbons (HCs) and a large amount of coke, even with highly effective catalysts. Adding a co-reactant high in hydrogen to the CCP process can significantly increase the yield of aromatics while reducing coke formation. The use of CCP can help to address the environmental issues related to waste plastic disposal and improve energy security. This review article thoroughly discusses the process and mechanism of catalytic co-pyrolysis, the influence of plastics on the process, and how the addition of plastics can improve the quality and output of bio-oil while reducing the production of oxygenated compounds and coke. The importance of various catalysts (such as biochar, activated carbon, and acid and base catalysts) in improving the production and quality of obtained products is also compared and discussed.