Recently, the pyrolysis process has been adapted as a sustainable strategy to convert metallized food packaging plastics waste (MFPW) into energy products (paraffin wax, biogas, and carbon black particles) and to recover aluminum. Usually, catalysts are used in pyrolysis treatment to refine pyrolysis products and to increase their yield. In order to study the effect of a catalyst on the formulated volatile products, this work aims to study the pyrolysis behavior of MFPW in presence of catalyst, using TG-FTIR-GC–MS system. The pyrolysis experiments were conducted with ZSM-5 Zeolite catalyst with different concentrations (10, 30, and 50 wt.%) at different heating rates (5, 10, 15, 20, 25, and 30 °C/min). In addition, TG-FTIR system and GC-MS unit were used to observe and analyze the thermal and chemical degradation of the obtained volatile compounds at maximum decomposition peaks. In addition, the kinetic results of catalytic pyrolysis of ZSM-5/MFPW samples matched when model-free methods, a distributed activation energy model (DAEM), and an independent parallel reaction kinetic model (IPR) were used. The TGA-DTG results showed that addition of a catalyst did not have a significant effect on the features of the TGA-DTG curves with similar weight loss of 87–90 wt.% (without taking the weight of the catalyst into account). Meanwhile, FTIR results manifested strong presence of methane and high-intensity functional group of carboxylic acid residues, especially at high concentration of ZSM-5 and high heating rates. Likewise, GC-MS measurements showed that Benzene, Toluene, Hexane, p-Xylene, etc. compounds (main flammable liquid compounds in petroleum oil) generated catalysts exceeding 50%. Finally, pyrolysis kinetics showed that the whole activation energies of catalytic pyrolysis process of MFPW were estimated at 289 kJ/mol and 110, 350, and 174 kJ/mol for ZSM-5/MFPW samples (10, 30, and 50 wt.%, respectively), whereas DAEM and IPR approaches succeeded to simulate TGA and DTG profiles with deviations below <1.

Due to the increasing demand for glass fibre-reinforced epoxy resin composites (GFRC), huge amounts of GFRC waste are produced annually in different sizes and shapes, which may affect its thermal and chemical decomposition using pyrolysis technology. In this context, this research aims to study the effect of mechanical pre-treatment on the pyrolysis behaviour of GFRC and its pyrolysis kinetic. The experiments were started with the fabrication of GFRC panels using the vacuum-assisted resin transfer method followed by crushing the prepared panels using ball milling, thus preparing the milled GFRC with uniform shape and size. The elemental, proximate, and morphology properties of the panels and milled GFRC were studied. The thermal and chemical decomposition of the milled GFRC was studied using thermogravimetric coupled with Fourier-transform infrared spectroscopy (TG-FTIR) at different heating rates. Meanwhile, the volatile products were examined using TG coupled with gas chromatography–mass spectrometry (GC-MS). The TG-FTIR and TG-GC-MS experiments were performed separately. Linear (Kissinger–Akahira–Sunose (KAS), Flynn–Wall–Ozawa (FWO), and Friedman) and nonlinear (Vyazovkin and Cai) isoconversional methods were used to determine the pyrolysis kinetic of the milled GFRC based on thermogravimetry and differential thermal gravimetry (TG/DTG). In addition, the TG/DTG data of the milled GFRC were fitting using the distributed activation energy model and the independent parallel reactions kinetic model. The TG results showed that GFRC can decompose in three stages, and the main decomposition is located in the range 256–500 °C. On the other hand, aromatic benzene and a C-H bond were the major functional groups in the released volatile components in FTIR spectra, while phenol (27%), phenol,4-(1-methylethyl) (40%), and p-isopropenylphenol (34%) were the major compounds in GC-MS analysis. Whereas, the kinetic results showed that both isoconversional methods can be used to determine activation energies, which were estimated 165 KJ/mol (KAS), 193 KJ/mol (FWO), 180 KJ/mol (Friedman), 177 KJ/mol (Vyazovkin), and 174 KJ/mol (Cai).

This research aims to maximize polyethylene terephthalate (PET) nonwoven fabric waste and make it as a new source for benzoic acid extraction using a pyrolysis process. The treatment was performed using a thermogravimetric analyzer (TGA) and released products were characterized using FTIR spectroscopy and gas chromatography–mass spectrometry (GC–MS). The pyrolysis kinetic and thermodynamic behavior of PET fabric was also studied and simulated using different linear and nonlinear models. The results show that the PET fabric is very rich in volatile matter (80 wt.%) and can completely degrade under 490 °C with a weight loss of 84%. Meanwhile, the generated vapor was rich in the carbonylic C=O functional group (FTIR), and the GC–MS analysis concluded that benzoic acid was the major compound with an abundance of 75% that was achieved at the lowest heating rate (5 °C/min). The linear kinetic results showed that PET samples had an activation energy in the ranges of 193–256 kJ/mol (linear models) and ~161 kJ/mol (nonlinear models). The thermodynamic parameters, including enthalpy, Gibbs free energy, and entropy, were estimated in the ranges of 149–250 kJ/mol, 153–232 kJ/mol, and 256–356 J/mol K, respectively. Accordingly, pyrolysis treatment can be used to extract benzoic acid from PET fabric waste with a 134% increase in the benzoic acid abundance that can be recovered from PET bottle plastic waste.

The depletion and usage of fossil fuels causes environmental issues and alternative fuels and technologies are urgently required. Therefore, thermal arc water vapor plasma for a fast and robust waste/biomass treatment is an alternative to the syngas method. Waste cooking oil (WCO) can be used as an alternative potential feedstock for syngas production. The goal of this experimental study was to conduct experiments gasifying waste cooking oil to syngas. The WCO was characterized in order to examine its properties and composition in the conversion process. The WCO gasification system was quantified in terms of the produced gas concentration, the H₂/CO ratio, the lower heating value (LHV), the carbon conversion efficiency (CCE), the energy conversion efficiency (ECE), the specific energy requirements (SER), and the tar content in the syngas. The best gasification process efficiency was obtained at the gasifying agent-to-feedstock (S/WCO) ratio of 2.33. At this ratio, the highest concentration of hydrogen and carbon monoxide, the H₂/CO ratio, the LHV, the CCE, the ECE, the SER, and the tar content were 47.9%, 22.42%, 2.14, 12.7 MJ/Nm³, 41.3% 85.42%, 196.2 kJ/mol (or 1.8 kWh/kg), and 0.18 g/Nm³, respectively. As a general conclusion, it can be stated that the thermal arc-plasma method used in this study can be effectively used for waste cooking oil gasification to high quality syngas with a rather low content of tars.

Modern day industries are highly focused on the development of bio-inspired hybrid natural fiber composites for lightweight biosensor chips, automobile, and microfluidic applications. In the present research, the mechanical properties and morphological characteristics of alkaline (NaOH)-treated hemp, flax, noil hemp, and noil flax fiber-reinforced ecopoxy biocomposites were investigated. The samples were fabricated by employing the hand layup technique followed by the compression molding process. A total of two sets of composites with various weight fractions were fabricated. The samples were tested for mechanical properties such as flexural strength, interlaminar shear strength, moisture absorption, and contact angle measurement. The treated fibers were analyzed by using an optical microscope and Fourier transform infrared spectrometer (FTIR). The morphological characteristics, such as porosity and fracture mechanisms, were investigated by using scanning electron microscopy and SEM−EDX spectroscopy. The results revealed that the flexural properties of hybrid composites vary from 22.62 MPa to 30.04 MPa for hemp and flax fibers and 21.86 MPa to 24.70 MPa for noil fibers, whereas in individual fiber composites, the strength varies from 17.11 MPa to 21.54 MPa for hemp and flax fibers and 15.83 MPa to 18.79 MPa for noil fibers. A similar trend was observed in interlaminar shear properties in both cases. From moisture analysis, the rate of absorption is increased with time up to 144 h and remains constant in both cases. The moisture gain was observed more in individual composites than hybrid composites in both cases. Hence, the impact of hybridization was observed clearly in both cases. Also, hybrid composites showed improved properties compared to individual fiber composites.