Catalytic flash pyrolysis for recovery of gasoline-range hydrocarbons from electric cable residue using a low-cost natural catalyst: An analytical Py-GC/MS study.

This investigation's novelty and objective reside in exploring catalytic flash pyrolysis of cross-linked polyethylene (XLPE) plastic residue in the presence of kaolin, with the perspective of achieving sustainable production of gasoline-range hydrocarbons. Through proximate analysis, thermogravimetric analysis, and heating value determination, this study also assessed the energy-related characteristics of cross-linked polyethylene plastic residue, revealing its potential as an energy source (44.58 MJ kg-1) and suitable raw material for pyrolysis due to its low ash content and high volatile matter content. To understand the performance as a low-cost catalyst in the flash pyrolysis of cross-linked polyethylene plastic residue, natural kaolin was subjected to characterization through thermogravimetric analysis, X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray fluorescence (XRF). Cross-linked polyethylene plastic residue was subjected to thermal and catalytic pyrolysis in an analytical microreactor coupled to gas chromatography-mass spectrometry (Py-GC/MS system), operating at 500 °C, to characterize the distribution and composition of volatile reaction products. The application of kaolin as a catalyst resulted in a decline of the relative concentration of hydrocarbons in the diesel range (C8-C24) from approximately 87 % to 28 %, and a reduction in lubricating oils (C14-C50) from about 70 % to 13 %, while concomitantly increasing the relative concentration of lighter hydrocarbons in the gasoline range (C8-C12) from around 28 % to 87 %. Therefore, catalytic flash pyrolysis offers the potential for converting this plastic waste into a new and abundant chemical source of gasoline-range hydrocarbons. This process can be deemed viable and sustainable for managing and valorizing cross-linked polyethylene plastic residue.

Catalytic flash pyrolysis of Scenedesmus sp. post-extraction residue using low-cost HZSM-5 catalyst with the perspective to produce renewable aromatic hydrocarbons.

Recovering renewable chemicals from de-fatted microalgal residue derived from lipid extraction within the algal-derived biofuel sector is crucial, given the rising significance of microalgal-derived biodiesel as a potential substitute for petroleum-based liquid fuels. As a circular economy strategy, effective valorization of de-fatted biomass significantly improves the energetic and economic facets of establishing a sustainable algal-derived biofuel industry. In this scenario, this study investigates flash catalytic pyrolysis as a sustainable pathway for valorizing Scenedesmus sp. post-extraction residue (SPR), potentially yielding a bio-oil enriched with upgraded characteristics, especially renewable aromatic hydrocarbons. In the scope of this study, volatile products from catalytic and non-catalytic flash pyrolysis were characterized using a micro-furnace type temperature programmable pyrolyzer coupled with gas chromatographic separation and mass spectrometry detection (Py-GC/MS). Flash pyrolysis of SPR resulted in volatile products with elevated oxygen and nitrogen compounds with concentrations of 46.4% and 26.4%, respectively. In contrast, flash pyrolysis of lyophilized microalgal biomass resulted in lower concentrations of these compounds, with 40.9% oxygen and 17.3% nitrogen. Upgrading volatile pyrolysis products from SPR led to volatile products comprised of only hydrocarbons, while completely removing oxygen and nitrogen-containing compounds. This was achieved by utilizing a low-cost HZSM-5 catalyst within a catalytic bed at 500 °C. Catalytic experiments also indicate the potential conversion of SPR into a bio-oil rich in monocyclic aromatic hydrocarbons, primarily BETX, with toluene comprising over one-third of its composition, thus presenting a sustainable pathway for producing an aromatic hydrocarbon-rich bio-oil derived from SPR. Another significant finding was that 97.8% of the hydrocarbon fraction fell within the gasoline range (C5-C12), and 35.5% fell within the jet fuel range (C8-C16). Thus, flash catalytic pyrolysis of SPR exhibits significant promise for application in drop-in biofuel production, including green gasoline and bio-jet fuel, aligning with the principles of the circular economy, green chemistry, and bio-refinery.

A novel intensified approach for treating produced water from oil extraction using a multi-tube type falling-film distillation column equipped with a biphasic thermosiphon: a promising feasibility study.

This study has the novel aim of experimentally examining the efficiency of a pilot-scale treatment plant, composed of a multi-tube type falling-film distillation column equipped with a biphasic thermosiphon, for treating a real sample of high-salinity produced water (electrical conductivity of 20,700 µS cm-1). It investigates the influence of operational parameters, including feed temperature and steam chamber temperature of the biphasic thermosiphon, on distillate flow rate and reduction of conductivity. All experimental conditions tested achieved a reduction greater than 98% in terms of electrical conductivity. The production of treated water increased with increasing feed temperature; the flow rate increased from 20.8 L h-1 to 28.2 L h-1 as the feed temperature was increased from 80 °C to 90 °C, when the steam chamber temperature was fixed at 119 °C. Within the temperature range of the steam chamber, the specific energy consumption during the treatment process, with respect to the biphasic thermosiphon, remained practically unchanged between 0.58 kWh L-1 and 0.60 kWh L-1, when the feed temperature was 90 °C. The results proved the potential of the falling-film distillation technology assisted by heat pipes to be a promising proposal for removing salinity from produced water from oil extraction operations.

Effect of compacting conditions on the viscoelastic properties of banana leaf waste and briquette quality.

This study evaluated the effects of the temperature and pressure used when compacting banana leaves on viscoelastic properties and briquette quality. Banana leaves with 12.4% of humidity were milled at two ranges of average particle size. The briquetting was carried out in a cylinder-piston device coupled to a universal mechanical test machine, under different compacting temperatures (30 and 120 °C) and pressures (20, 40 and 60 MPa). Several parameters, including compacting module, porosity index, final density, critical density, compacting energy, compression ratio, higher heating value, and energy density, were investigated. The banana leaf particles smaller than 1.7 mm performed better during compaction, with low compacting resistance. Temperature showed less influence on final density than pressure. The increase of pressure contributed to decreasing the compacting module and to achieving denser briquettes. It was not necessary to apply high temperature to obtain briquettes with high final density and energy density. The optimum briquetting process parameters identified can be used to produce briquettes from banana leaves at an industrial scale with an extruder. Briquetting adds value to banana leaf waste and reduces environmental pollution.

Upgrading of banana leaf waste to produce solid biofuel by torrefaction: physicochemical properties, combustion behaviors, and potential emissions.

This study is the first report that focuses on investigating the effects of torrefaction on the bioenergy-related properties, combustion behavior, and potential emissions of banana leaf waste (BLW). Experiments were first conducted in a bench-scale fixed-bed reactor operating at light (220 °C), mild (250 °C), and severe (280 °C) torrefaction conditions to torrefy the raw BLW. Torrefaction pretreatments reduced the weight of the raw BLW by about 60%, but the resulting solid biofuel can preserve up to 77% of the energy content of the raw biomass. It was found that torrefied BLW contains more concentrated fixed carbon than the raw BLW, volatile matter content of up to 59.8 wt.%, and a higher HHV of up to 20.7 MJ kg-1 with higher concentrations of carbon, nitrogen, and ash. Bulk density increased 13.0% over the raw BLW, and the torrefied BLW became a solid biofuel with 51.5% greater energy density under the severe torrefaction condition. The upgrading of BLW by torrefaction enhanced its combustion performance in terms of comprehensive combustion, ignition, burnout, and flammability indices. Compared with commercial hard coal, BLW torrefied at the mild condition (250 °C) had lower potential emissions per unit of energy, 25.3% less CO2 emission, 3.1% less CO emission, 96.4% less SO2 emission, and 18.4% less dust emission, except for NOX emission. This study conclusively indicates that BLW after torrefaction has enhanced bioenergy-related properties, improved combustion performance, and reduced emissions potential, proving to be a promising method for its valorization.

Bioenergy potential of red macroalgae Gelidium floridanum by pyrolysis: Evaluation of kinetic triplet and thermodynamics parameters.

The aim of this study was to investigate the bioenergy potential of red macroalgae GF by evaluating its biofuel physicochemical characteristics, and conducting a kinetic study and thermodynamic analysis of pyrolysis for the first time. The thermal decomposition study was performed at low heating rates (5, 10, 20 and 30 °C min-1) under N2 atmosphere. The thermal behavior of GF pyrolysis indicated the presence of three different decomposition stages, which are associated with different components in its structure and consequently influence the kinetic and thermodynamic parameters. The kinetic triplet obtained for GF provided a suitable description of experimental thermal behavior. The thermodynamic parameters demonstrated that GF is as a new promising feedstock for bioenergy and presented a similar potential to well-known bioenergy feedstock.

Pyrolysis kinetic evaluation by single-step for waste wood from reforestation.

The objective of this study was to evaluate the kinetic parameters of pyrolysis of waste wood from reforestation: Eucalyptus benthamii (EB), Eucalyptus dunnii (ED) and Pinus elliottii (PN). The kinetic study was performed using the Friedman, Flynn-Wall-Ozawa (FWO), Kissinger-Akahira-Sunose (KAS), Starink, and Vyazovkin methods from the experimental data at four heating rates (5, 10, 20 and 30 °C min-1). The Friedman method presented higher activation energy values (Ea) when compared to the other methods (EaEB = 142.98 kJ mol-1, EaED = 147.71 kJ mol-1, EaPN = 155.46 kJ mol-1). The KAS, Starink and Vyazovkin methods resulted in approximate values of activation energy (EaEB = 132.83-133.31 kJ mol-1, EaED = 137.51-137.98 kJ mol-1, EaPN = 145.24-145.70 kJ mol-1) due to the approximation equations with lowest relative errors. The simulation of curves using the kinetic parameters obtained with the Vyazovkin method showed that the decomposition process of EB and ED occurs as a multi-step process resulting in an unsatisfactory result for the simulation. On the other hand, for PN a satisfactory fit to the experimental data was obtained, which demonstrates its suitability for application to the modeling of thermochemical systems.

Combustion of pistachio shell: physicochemical characterization and evaluation of kinetic parameters.

The study of different renewable energy sources has been intensifying due to the current climate changes; therefore, the present work had the objective to characterize physicochemically the pistachio shell waste and evaluate kinetic parameters of its combustion. The pistachio shell was characterized through proximate analysis, ultimate analysis, SEM, and FTIR. The thermal and kinetic behaviors were evaluated by a thermogravimetric analyzer under oxidant atmosphere between room temperature and 1000 °C, in which the process was performed in three different heating rates (20, 30, and 40 °C min-1). The combustion of the pistachio shell presented two regions in the derivative thermogravimetric curves, where the first represents the devolatilization of volatile matter compounds and the second one is associated to the biochar oxidation. These zones were considered for the evaluation of the kinetic parameters E a , A, and f(α) by the modified method of Coats-Redfern, compensation effect, and master plot, respectively. The kinetic parameters for zone 1 were E a1 = 84.11 kJ mol-1, A 1 = 6.39 × 106 min-1, and f(α)1 = 3(1 - α)2/3, while for zone 2, the kinetic parameters were E a2 = 37.47 kJ mol-1, A 2 = 57.14 min-1, and f(α)2 = 2(1 - α)1/2.