The constant search for the proper management of non-degradable waste in conjunction with the circular economy makes the thermal pyrolysis of plastics an important technique for obtaining products with industrial interest. The present study aims to produce pyrolytic oil from thermoplastics and their different mixtures in order to determine the best performance between these and different mixtures, as well as to characterize the liquid fraction obtained to analyze its use based on said properties. This was carried out in a batch type reactor at a temperature of 400 °C for both individual plastics and their mixtures, from which the yields of the different fractions are obtained. The liquid fraction of interest is characterized by gas chromatography and its properties are characterized by ASTM standards. The product of the pyrolysis of mixtures of 75% polystyrene and 25% polypropylene presents a yield of 82%, being the highest, with a viscosity of 1.12 cSt and a calorific power of 42.5 MJ/kg, which has a composition of compounds of carbon chains ranging between C6 and C20, for which it is proposed as a good additive agent to conventional fuels for industrial use.

Currently, the pyrolysis process is an important technology for the final treatment of plastic waste worldwide. For this reason, knowing in detail the chemical process and the thermodynamics that accompany cracking reactions is of utmost importance. The present study aims to determine the thermodynamic parameters of the degradation process of conventional thermoplastics (polystyrene (PS), polyethylene terephthalate (PET), high-density polyethylene (HDPE), polypropylene (PP) and polyvinyl chloride (PVC)) from the study of their chemical kinetics by thermogravimetric analysis (TG). Non-isothermal thermogravimetry was performed at three heating rates from room temperature to 550 °C with an inert nitrogen atmosphere with a flow of 20 mL min⁻¹. Once the TG data is obtained, an analysis is carried out with the isoconversional models of Friedman (FR), Kissinger–Akahira–Sunose (KAS), and Flynn–Wall–Ozawa (FWO) in order to determine the one that best fits the experimental data, and with this, the calculation of the activation energy and the pre-exponential factor is performed. The validation of the model was carried out using the correlation factor, determining that the KAS model is the one that best adjusts for the post-consumer thermoplastic degradation process at the three heating rates. With the use of the kinetic parameters, the variation of the Gibbs free energy is determined in each of the cases, where it is necessary that for structures containing aromatic groups a lower energy is presented, which implies a relative ease of degradation compared to the linear structures.

This study aimed at preparing three types of biochar derived from rice husk via pyrolysis, including unactivated biochar, biochar chemically activated after with H₃PO₄, and biochar impregnated with γ-Fe₂O₃ nanoparticles. These materials were subsequently characterized using Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) analysis, which revealed favorable textural properties, such as an increased surface area and porosity, as well as the presence of functional groups that facilitate the adsorption of methylene blue and malachite green in aqueous solutions. Several factors that affect the adsorption capacity, including the type of material, pH effect, and adsorbent dosage, were evaluated and optimized. The adsorption behavior was analyzed using isotherm and kinetic models to better understand the mechanisms involved. Under optimal conditions, biochar@γ-Fe₂O₃ NPs emerged as the most effective material due to its high surface area, functionalized surface, and magnetic properties, allowing easy water recovery without the need for complex instrumentation. Among the kinetic models evaluated, the pseudo-second-order model exhibited the highest linear regression coefficient (R² = 0.99), supporting a chemisorption process driven by strong interactions and stable chemical bond formation between the adsorbate and the adsorbent, while equilibrium data fit well with the Sips isotherm model, indicating a combination of monolayer and multilayer adsorption mechanisms. This magnetic biochar achieved removal efficiencies of 97% for methylene blue and 95% for malachite green, demonstrating a high performance and reusability over four cycles. Moreover, a possible adsorption mechanism of MB on the magnetic biochar was proposed to explain the interaction between the dye and the adsorbent surface. Thus, this work demonstrates that magnetic biochar is a sustainable and cost-effective adsorbent for wastewater treatment, integrating circular economy principles by transforming rice husk into a high-value material. The incorporation of γ-Fe₂O₃ nanoparticles enhances adsorption while enabling magnetic recovery, providing an eco-friendly and scalable solution for dye removal.

Currently, catalytic pyrolysis has become a versatile and highly useful technology in the treatment of different plastic wastes. Thus, the development of selective catalysts to carry out cracking reactions and obtain a greater fraction of the desired products is essential. This study focuses on the synthesis of monometallic (Ni) and bimetallic (Ni-Zn) catalysts supported on ZSM-5 zeolite using an impregnation and co-impregnation method, respectively. The obtained catalysts were characterized by FTIR spectroscopy, N₂ adsorption/desorption measurements, scanning electron microscopy (SEM) and energy dispersive X-Ray spectroscopy (EDS), temperature programmed NH₃ desorption (TPD-NH₃) and thermogravimetric analysis (TGA). In this way, a mixture of polystyrene and polypropylene recycled with a catalyst/plastic waste ratio of 1:500 was used for pyrolysis tests. The best results were obtained using the Ni-Zn/ZSM-5 catalyst, which included better impregnation, increased surface acidity, decreased dispersion and a shorter reaction time in the catalytic pyrolysis process. Under the optimized conditions, catalytic pyrolysis showed an excellent performance to generate hydrocarbons of greater industrial interest.

The environmental pressure to reduce the use of fossil fuels such as gasoline generates the need to search for new fuels that have similar characteristics to conventional fuels. In this sense, the objective of the present study is the use of commercial gasoline in mixtures with pyrolytic oil from plastic waste and the addition of γ-Fe₂O₃ nanoparticles (NPs) in a spark ignition engine to analyze both the power generated in a real engine and the emissions resulting from the combustion process. The pyrolytic oil used was obtained from thermal pyrolysis at low temperatures (450 °C) of a mixture composed of 75% polystyrene (PS) and 25% polypropylene (PP), which was mixed with 87 octane commercial gasoline in 2% and 5% by volume and 40 mg of γ-Fe₂O₃ NPs. A standard sample was proposed, which was only gasoline, one mixture of gasoline with bio-oil, and a gasoline, bio-oil, and NPs mixture. The bio-oil produced from the pyrolysis of PS and PP enhances the octane number of the fuel and improves the engine’s power performance at low revolutions. In contrast, the addition of iron NPs significantly improves gaseous emissions with a reduction in emissions of CO (carbon monoxide), NOx (nitrogen oxide), and HCs (hydrocarbons) due to its advantages, which include its catalytic effect, presence of active oxygen, and its large surface area.