Search Results (177)

Biochar is a carbon-rich material produced through the pyrolysis of agricultural waste. It effectively enhances the physical, chemical, and biological properties of salinity-affected soils. Chickpea (Cicer arietinum L.) is the world’s third most important legume crop, currently cultivated in over 50 countries. However, no study has yet established recommended biochar application rates for this crop under saline soil conditions. Therefore, this study aimed to assess the chemical properties of a clay soil following the application of varying rates of biochar and NaCl, and to evaluate their subsequent effects on the growth and yield of Cicer arietinum L. To evaluate the effect of biochar, a completely randomized experimental design with ten replicates was implemented. The biochar was produced from corncobs (Zea mays) and applied at two rates (1.5% and 3%). Soil salinity levels were classified into three groups: non-saline (S1 = 1.2 dS·m⁻¹), low/moderate salinity (S2 = 4.2 dS·m⁻¹), and moderate salinity (S3 = 5.6 dS·m⁻¹). The treatments were placed in pots for 100 days. The results demonstrated that biochar applications at 1.5% and 3% rates improved both soil chemical properties (pH, EC, SAR, and ESP) and the growth of C. arietinum across all evaluated treatments. The 3% biochar treatment showed superior effects compared to the 1.5% application. Therefore, biochar application in C. arietinum production emerges as an effective agronomic strategy to mitigate abiotic stress while simultaneously enhancing crop productivity and sustainability. Full article

A novel externally heated retort for Jimsar oil shale resources is proposed, and the symmetrical mathematical model of the transport process in the retort is established through intensively studying the mechanisms of shale gas flows, heat transfer, and pyrolysis reactions in the retort. The descriptions of axial and radial movements and temperature of oil shale and gases, and the distribution of pyrolysis reaction and yielding of gaseous products and semi-coke in various regions of the retort are simulated. The results show that oil shale can pyrolyze gradually from the region near the wall to the core region of the retorting chamber and pyrolyze completely at the bottom of the retorting zone through receiving the heat flux transferring from the combustion channels. The final pyrolysis temperature of oil shale is 821.05 K, and the outlet temperature of semi-coke cooled by cold recycled gas is 676.35 K, which are in agreement with the design requirements. In total, 75 toil shales can be retorted in one retorting chamber per day, and the productivity of the retort can be increased by increasing the number of retorting chambers. The fuel self-sufficiency rate of this externally heated oil shale retort can reach 82.83%. Full article

This study investigates hazardous emissions from foundry binder systems, comparing organic resins (phenolic urethane, furan, and alkaline-phenolic) and clay-bonded green sand with inorganic alternatives (sodium silicate and geopolymer). The research was conducted at the Fundaciόn Azterlan pilot plant (Spain), involving controlled chamber tests for the production of 60 kg iron alloy castings in 110 kg sand molds. The molds were evaluated under two configurations: homogeneous systems, where both mold and cores were manufactured using the same binder (five trials), and heterogeneous systems, where different binders were used for mold and cores (four trials). Each mold was placed in a metallic box fitted with a lid and an integrated gas extraction duct. The lid remained open during pouring and was closed immediately afterward to enable efficient evacuation of casting gases through the extraction system. Although the box was not completely airtight, it was designed to direct most exhaust gases through the duct. Along the extraction system line, different sampling instruments were strategically located for the precise measurement of contaminants: volatile organic compounds (VOCs), polycyclic aromatic hydrocarbons (PAHs), phenol, multiple forms of particulate matter (including crystalline silica content), and gases produced during pyrolysis. Across the nine trials, inorganic binders demonstrated significant reductions in gas emissions and priority pollutants, achieving decreases of over 90% in BTEX compounds (benzene, toluene, ethylbenzene, and xylene) and over 94% in PAHs compared to organic systems. Gas emissions were also substantially reduced, with CO emissions lowered by over 30%, NO_x by more than 98%, and SO₂ by over 75%. Conducted under the Greencasting LIFE project (LIFE 21 ENV/FI/101074439), this work provides empirical evidence supporting sodium silicate and geopolymer binders as viable, sustainable solutions for minimizing occupational and ecological risks in metal casting processes. Full article

To investigate the combustion characteristics of moxa under a nitrogen atmosphere, this study employed an integrated approach combining experimental and theoretical analysis. Twelve moxa floss samples with different leaf-to-floss ratios, geographical origins, and storage durations were selected for thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR) of their carbonized products in nitrogen environment. Through TG-DTG analysis, the thermal degradation patterns of the twelve moxa floss samples under nitrogen atmosphere were systematically examined to elucidate their pyrolysis behaviors, with particular emphasis on the influence of pyrolysis temperature and leaf-to-floss ratio on combustion characteristics. The pyrolysis process occurred in three distinct stages, with the most significant mass loss (120–430 °C) observed in the second stage. Higher leaf–fiber ratios and longer storage years were found to promote more complete pyrolysis. Kinetic analysis was performed to fit thermogravimetric data, establishing a reaction kinetic model for moxa pyrolysis. Results indicated that samples with higher leaf–fiber ratios required greater activation energy, while storage duration showed negligible impact. Notably, Nanyang moxa demanded higher pyrolysis energy than Qichun moxa. FTIR analysis identified the primary components of carbonized products as water, ester compounds, flavonoids, and cellulose. These findings suggest that moxa carbonization products retain chemical reactivity, demonstrating potential applications in adsorption and catalysis processes. Full article

The Central Depression of the Junggar Basin relies heavily on Permian lacustrine mudstone for deep-seated hydrocarbon sealing. This research investigated how the fluorescence parameters of caprock samples responded to the leakage of palaeo-oil zones based on measurements from SEM, Rock-Eval, and X-ray diffraction analysis. First, two sets of control experiments were conducted to establish the proper grain-size range of 100–140 mesh for testing caprock samples in the research area using quantitative fluorescence technology. Subsequently, based on the examination of the rock pyrolysis parameters and the fluorescence parameters against TOC values, the conjecture was formed that the quantitative fluorescence technology test results were mostly unaffected by the primary hydrocarbons. Lastly, four fluorescence parameters were used to assess seal integrity: quantitative grain fluorescence intensity of the extract (QGF E intensity, the meaning of QGF is the same in this study), QGF spectral peaks (QGF λmax), the ratio of QGF intensity to fluorescence intensity at 300 nm on the QGF spectrum (QGF index), and total scanning fluorescence spectral ratio R₁ (TSF R₁). The Permian caprock can effectively seal hydrocarbons as evidenced by the decrease of QGF E intensity and QGF index values with depth. When hydraulic fracturing causes caprock failure, it can lead to complete leakage of hydrocarbons from the palaeo-oil zones. As the depth becomes shallower, the QGF E intensity value increases, the QGF index value decreases. Due to the differences in the migration pathways of hydrocarbons in the caprock, those leaked from the Permian palaeo-oil zone into the well PD1 caprock are mainly condensate and light–normal crude oil, while the hydrocarbons from the Carboniferous palaeo-oil zone into the well MS1 caprock consist predominantly of light–normal crude oil and medium–heavy crude oil. Full article

This study describes the step-by-step development of a simplified system which can be implemented in industrial facilities with the help of their own surplus of plastic waste, mainly packaging waste, to reach a level of energy autonomy or semi-autonomy. This waste is converted to about 57,500 L of synthetic pyrolysis oil, which can then be used to power industries, being fed into a Combined Heat and Power system. To achieve this goal, the design has hydrocarbon stability at elevated temperature and restricted oxygen exposure, so that they can be converted to new products. Pyrolysis is a key process which causes thermo-chemical changes—ignition and vaporization. The research outlines the complete process of creating a basic small-scale pyrolysis system which industrial facilities can use to generate energy from their plastic waste. The proposed unit processes 360 tons of plastic waste yearly to produce 160 tons of synthetic pyrolysis oil which enables the generation of 500 MWh of electricity and 60 MWh of heat. The total investment cost is estimated at EUR 41,000, with potential annual revenue of up to EUR 45,000 via net metering. The conceptual design proves both environmental and economic viability by providing a workable method for decentralized waste-to-energy solutions for Small and Medium-sized Enterprises. Full article

To address the issues of poor Co²⁺ regeneration and limited interfacial electron transfer in heterogeneous catalytic systems, this study proposes the synthesis of highly efficient and stable Co₃O₄/ZnO composites through the pyrolysis–oxidation reaction of Co/Zn MOFs for the degradation of rhodamine B (RhB) using activated peroxymonosulfate (PMS). The results confirmed that the catalyst exhibited a high electron transfer capacity, and the synergistic effect between the bimetals enhanced the reversible redox cycle of Co³⁺/Co²⁺. Under optimal conditions, complete removal of RhB was achieved in just 6 min using the Co₃O₄/ZnO composite, which demonstrated excellent stability after five cycles. Furthermore, the catalyst exhibited a high degradation efficiency in real water samples with a total organic carbon (TOC) removal rate of approximately 65% after 60 min. The electrochemical measurements, identification of active species, and X-ray photoelectron spectroscopy (XPS) analysis revealed that non-radicals (¹O₂ and direct charge transfer) played a major role in the degradation of RhB. Finally, the potential mechanisms and degradation pathways for RhB degradation using this catalyst were systematically investigated. This study opens new avenues for the development of efficient and stable PMS catalysts, and provides insights into the preparation of other emerging metal oxides. Full article

The carbon isotopic behavior of hopane compounds during thermal maturation remains ambiguous due to limitations in current detection techniques. In this study, a low-maturity lacustrine shale sample was pyrolyzed in a hydrous semi-open pyrolysis system. The hopane compounds from the artificially matured samples (R_o = 0.72–1.28%) have been separated and enriched for the test of their carbon isotopes (δ¹³C). The results show that thermal maturity can somewhat affect the carbon isotopes of monomeric hopane compounds, with a maximum difference value over 21‰. However, thermal maturity has different effects on the δ¹³C values for different monomeric hopane compounds. For example, the carbon isotopic values of 22S-homohopane at different thermal stages can vary up to 21‰, while only 3‰ for C₂₉βα. In addition, the carbon isotopes of different monomeric hopane compounds show distinct evolution trends. For C₂₉αβ and C₂₉ Ts, their carbon isotopes first become slightly heavier and then become lighter, reaching the lightest value at 350 °C. When the pyrolysis temperature continues to increase, the δ¹³C values become heavier and finally become lighter. However, the δ¹³C values of Ts, Tm, 22S-homohopane, and 22R-homohopane show a completely reversed trend. They initially become slightly lighter and then become heavier, reaching the maximum value at 350 °C. When the pyrolysis temperature continues to increase, the δ¹³C values become lighter and finally become heavier. Meanwhile, the carbon isotopes of C₂₉βα, C₃₀αβ, C₃₀βα, and non-hopane gammacerane almost remain constant at different thermal stages. When the carbon isotopes of hopane compounds are used in the studies of oil–source correlation, it is prudent to consider the effects of thermal maturity on these values. Full article

Due to the increasing volumes of plastic waste generated from electric and electronic devices, research has focused on the investigation of recycling methods for their safe handling. Pyrolysis converts plastics from waste electric and electronic equipment (WEEE) into valuable products (pyrolysis oil). Nevertheless, the frequent presence of flame retardants, mainly brominated flame retardants (BFR), hinders pyrolysis’s wide application, since hazardous compounds may be produced, limiting the use of pyrolysis oils. Taking the aforementioned into account, this work focuses on the recycling, via pyrolysis, of various plastic samples gathered from WEEE, to explore the valuable products that are formed. Specifically, 14 plastic samples were collected, including parts of computer peripheral equipment, remote controls, telephones and other household appliances. Considering the difficulties when BFRs are present, the study went one step further, applying XRF analysis to identify their possible presence, and then Soxhlet extraction as an environmentally friendly method for the debromination of the samples. Based on the XRF results, it was found that 23% of the samples contained bromine. After each Soxhlet extraction, bromine was reduced, achieving a complete removal in the case of a remote control sample and when butanol was the solvent. Thermal pyrolysis led to the formation of valuable products, including the monomer styrene and other secondary useful compounds, such as alpha-methylstyrene. The FTIR results, in combination with the pyrolysis products, enabled the identification of the polymers present in the samples. Most of them were ABS or HIPS, while only three samples were PC. Full article

The article reviews the literature on the potential utilization of decommissioned wind turbine blade waste (WTBW) in construction materials, including geopolymers, which are rarely discussed. The review indicates that only the mechanical processing of WTBW creates prerequisites for its possible use as fillers in construction materials; however, adjustments to the composition of binding materials are necessary. Wind turbine blades (WTBs) are usually made from strong and durable composite materials, thus posing serious recycling and environmental challenges. Thermal process methods are promising approaches for recovering glass fibers from thermosets of WTBW through pyrolysis or converting WTBW into fibers via plasma processing. Preliminary durability studies of such recovered and recycled glass fibers have demonstrated their potential application in geopolymers or cement-based materials. Implementing these technologies would expand the waste management system, completing recycling and reuse solutions. To successfully adopt more environmentally friendly solutions, further development of geopolymer production processes and sustainable fiber recovery is recommended. Full article

Pyrolysis presents a promising solution for the complete purification and recycling of waste salt. However, the presence of organic pollutants in waste salts significantly hinders their practical application, owing to their diverse sources and strong resistance to degradation. This study developed predictive models for the removal of organic pollutants from waste salt using three machine learning techniques: Random Forest (RF), Support Vector Machine, and Artificial Neural Network. The models were evaluated based on the total organic carbon (TOC) removal rate and the mass loss rate, with the RF model demonstrating high accuracy, achieving R² values of 0.97 and 0.99, respectively. Feature engineering revealed that the contribution of salt components was minimal, rendering them redundant. Feature importance analysis identified temperature as the most critical factor for TOC removal, while moisture content and carbon and nitrogen content were key determinants of mass loss. Partial dependence plots further elucidated the individual and interactive effects of these variables. The model was validated using both the literature data and laboratory experiments, and a user interface was developed using the Python GUI library. This study provides novel insights into the pyrolysis process of waste salt and establishes a foundation for optimizing its application. Full article

In this paper, a series of graded Al-based composites, including Al@AP, Al@AP/BM−52, and Al@AP/BPE−1735, have been prepared by spray drying technology. The thermal decomposition characteristics, kinetic parameters of the decomposition reaction, and Pyro-GC/MS products were comprehensively investigated. The results showed that two inhibitors, BM−52 and BPE−1735, had a significant effect on the thermal decomposition of AP. The addition of BM−52 conspicuously enhanced the thermal interaction, resulting in a more complete decomposition reaction of AP. Meanwhile, the incorporation of BPE−1735 significantly enhanced the heat releases of AP, leading to a significant enhancement in the energetic performance during the decomposition process of AP. BM−52 and BPE1735 inhibit AP decomposition as evidenced by higher activation energies for thermal decomposition and altered physical models of decomposition. Pyro-GC/MS results reveal that the fundamental pathway of Al@AP thermal decomposition remains unaltered by BM−52. However, the proportion of oxygen-containing compound products is moderately reduced. In contrast, for Al@AP/BPE−1735, in addition to the same products as those from Al@AP pyrolysis, new pyrolysis peaks emerge. It is implied that specific chemical reactions or interactions are triggered during the thermal decomposition process, thereby resulting in the formation of distinct chemical species. Full article

PFASs, or per- and polyfluoroalkyl substances, comprise a diverse group of synthetic chemicals known for their widespread use, persistence, and potential environmental and health risks. The sonolytic treatment of PFASs is one of the technologies with the ability to complete destruction without harmful byproducts. This study aims to provide a theoretical explanation for the sonolytic treatment of PFAS. Combining insights from molecular dynamics simulations with experimental data, the influence of chain length and functional headgroups on the PFAS destruction mechanism was investigated. The findings revealed that the impact on functional head groups and chain length on PFAS degradation via sonolysis treatment is complex and multifaceted. The preliminary degradation step is attributed to be headgroup cleavage, while differences in degradation rates between perfluorocarboxylic acids (PFCAs) and perfluorosulfonic acids (PFSAs) are primarily influenced by adsorption at the air–water interface of micro/nanobubbles created by ultrasound and dictated by compound hydrophobicity characteristics. Moreover, longer-chain PFAS compounds tend to degrade faster than shorter-chain counterparts due to their enhanced hydrophobic characteristics, facilitating adsorption and subsequent mineralization. The sonolytic environment significantly influences PFAS degradation, with aqueous sonolysis proving the most effective compared to dry pyrolysis or thermal combustion, highlighting the importance of considering environmental factors in remediation strategies. These insights provide valuable guidance for designing effective PFAS remediation strategies, emphasizing the need to consider molecular structure and environmental conditions. Further research and technological innovation are essential for developing sustainable approaches to mitigate PFAS pollution’s adverse impacts on human health and the environment. Full article

EFB is a biomass waste primarily generated in Southeast Asia, and its pyrolysis enables both waste management and conversion into valuable products. In pyrolysis, the heating rate is a crucial factor; however, studies on its influence on EFB are extremely limited. This study investigates the pyrolysis characteristics of EFB by analyzing product properties based on reaction temperature and heating rate. TGA showed that the thermal decomposition of EFB begins at approximately 210 °C and is largely complete by 400 °C. Furthermore, kinetic analysis using TGA data, applying both differential and integral methods, revealed distinct trends. Through pyrolysis experiments using a fixed-bed reactor, the yield analysis of products under varying reaction temperatures and heating rates demonstrated that higher temperatures promote pyrolysis, leading to a decrease in biochar yield and an increase in gas product yield. For liquid products, a higher heating rate suppressed secondary reactions and led to an increase in the yield of the aqueous phase. Gas product characterization revealed that CO and CO₂ formation began simultaneously at approximately 270 °C. GC-MS analysis of the liquid products recovered under different pyrolysis conditions showed that most compounds contained oxygen, originating from hemicellulose, cellulose, and lignin. Additionally, FT-IR analysis of the biochar confirmed that oxygen-containing functional groups decomposed as pyrolysis progressed, and the presence of turbostratic carbon and crystallinity influenced by trace inorganic elements was identified. Full article

Incineration remains Europe’s main practice for plastic packaging waste treatment, primarily due to the limitations of mechanical recycling technology. Consequently, research and development of more sustainable and flexible approaches are of high importance. Thermochemical conversion of polypropylene, polystyrene, and municipal plastic packaging mix via high-temperature flash pyrolysis (1000 °C/s) is studied in this research, focusing on the kinetics and yields of the devolatilisation stage. The primary stage results in the formation of volatile organic compounds considered intermediate products for carbon black production. The experiments were conducted in a pressurised wire mesh reactor, investigating the influence of temperature (600–1200 °C), residence time (0.5–10 s), and pressure (1–25 bar). The positive effect of temperature on the volatile yield was observed up to 2–5 s. The devolatilisation stage was completed within a maximum of 5 s at temperatures ranging from 800 to 1200 °C. The pressure was determined to be a kinetically limiting factor of the process to up to 800 °C, and the effect was not present at ≥1000 °C. Raman spectroscopy measurements revealed that pyrolytic carbon deposited on the post-experimental meshes is structurally similar to the industrially produced carbon black. The kinetic data and developed model can be further applied in the upscale reactor design. Full article