Search Results (551)

The accumulation of plastic waste has become a significant environmental challenge, stimulating the development of efficient recycling technologies capable of converting polymers into valuable products. In this study, polypropylene wastes were thermocatalytically converted into liquid hydrocarbons using three naturally occurring types of clay as catalysts, namely, kaolin, illite, and bentonite. The obtained liquid products were investigated using one- and two-dimensional NMR spectroscopy, including 1H, 13C, and COSY techniques. Quantitative evaluation of hydrocarbon group composition was performed using established NMR correlations to determine the content of paraffins, olefins and aromatic compounds as well as fuel-related parameters. The results demonstrated that paraffins were the predominant constituents in all pyrolysis oils, accounting for more than 70 vol.%, while olefins and aromatics were present in smaller amounts. Although all catalysts promoted the formation of liquid mixtures of hydrocarbon, noticeable differences in product composition were observed. Oil obtained over illite exhibited increased aromaticity and lower olefin content, whereas kaolin produced a product characterized by the highest isoparaffin index and estimated research octane number. The findings indicate that variations in catalysts influence the characteristics of polypropylene-derived oils and may be used to tailor products’ properties for their utilization as fuel additives or petrochemical feedstocks. Full article

Compost maturity screening supports safe land application and organic waste recycling, but germination index (GI) assays are not always available for rapid process assessment. This study performed a secondary GI-based maturity classification reconstruction using a published Nature Food composting dataset. From this source, 184 observations from 24 manure-based composting batch trajectories across five feedstock domains were retained when GI and routine physicochemical variables were available. GI values were converted into three maturity stages and a binary mature/non-mature endpoint, while the GI itself was excluded from model inputs. Logistic regression, random forest, and extra trees models were evaluated under random split, batch-aware group split, and leave-one-feedstock-domain-out validation. Random and group splits showed stronger apparent performance than cross-feedstock validation, indicating sensitivity to feedstock-domain transfer. In binary classification, the area under the receiver operating characteristic curve (ROC-AUC) remained relatively high in several model–domain combinations, whereas mature-class F1 declined, revealing a discrimination decision gap under default thresholds. Training-domain threshold calibration partially improved mature-class detection without using the held-out feedstock domain for threshold selection. These results support feedstock-aware validation and calibrated decision thresholds for sustainable compost maturity screening. Full article

Environmental sustainability of natural and synthetic fibers used in textiles and composites depends on their impacts throughout production, use, and end-of-life (EoL) stages. Natural fibers are renewable and biodegradable but may require substantial water and agricultural inputs, whereas synthetic fibers contribute to fossil resource depletion, microplastic pollution, and persistent waste generation. Natural fibers are often regarded as more sustainable alternatives to synthetic fiber; however, evidence from a life cycle assessment (LCA) reveals a more nuanced reality. As demand for fiber-based materials increases across textile and composite applications, a deeper understanding of the environmental implications of both natural and synthetic options becomes essential. This review compares these fiber categories from a life cycle perspective, examining carbon footprint, energy demands, resource consumption, and EoL pathways. Natural fibers such as cotton, flax, jute, hemp, sisal, banana, coir, and emerging plant-based alternatives offer advantages including biodegradability and carbon sequestration during cultivation. Nevertheless, agricultural practices and subsequent industrial processing require substantial land, water, and chemical inputs. Synthetic fibers, predominantly derived from fossil resources, provide a long service life and consistent performance but are associated with high greenhouse gas (GHG) emissions, dependence on non-renewable feedstocks, microplastic pollution, and broader environmental impacts. By presenting a comprehensive life cycle-based comparison, this review identifies the conditions under which each fiber type may offer environmental benefits, supporting informed material selection for sustainable development. Full article

Small-scale biogas systems in developing regions are predominantly mono-digestion systems utilizing livestock manure as the primary feedstock. However, crop residues such as wheat straw offer significant potential for improving feedstock diversity and biogas production when applied in anaerobic co-digestion systems. Due to the recalcitrant nature of lignocellulosic biomass, pretreatment is required to enhance substrate degradability and methane production. In this study, the performance of integrated pretreatment and anaerobic co-digestion of cattle manure and wheat straw was evaluated using the modified ADM1_R3 model. Simulations were conducted under varying feedstock mixing ratios (0 to 100%wt wheat straw), pretreatment intensities (carbohydrate degradability levels of 50%, 67%, and 75%), organic loading rates (1 to 4 kgVSm⁻³day⁻¹), and digester volumes (2, 4, and 6 m³). The results showed that increasing the wheat straw fractions improved biogas production, although with a slight reduction in methane. Pretreatment further enhanced overall process performance, with biogas production enhancement of between 40% and 56% across the different mixing ratios and degradability increase from 50 to 75%, while higher loading rates combined with higher pretreatment intensities increased the risk of process instability. The findings demonstrate the feasibility of this innovative approach of flexible small-scale co-digestion systems supported by appropriate pretreatment strategies. This study advances the application of anaerobic digestion modelling to small-scale biogas systems by providing an integrated framework for evaluating the effects of operational and design parameters on technical performance. Full article

The growing volume of crustacean shell waste generated during seafood processing poses a serious environmental problem. However, this type of biowaste remains underutilized, despite being a promising renewable raw material for the production of functional carbon materials. This study aims to investigate how synthesis parameters influence the formation of a hierarchical porous structure in shrimp shell-based carbon materials and to optimize these parameters to improve CO₂ adsorption efficiency. Under optimal carbonization conditions (holding time: 2 h; temperature: 650 °C) and activation conditions (holding time: 2 h; temperature: 750 °C) with activator-to-carbon weight ratios (A/C) of 1/1, 2/1 and 4/1, the resulting porous carbon samples exhibited relatively high S_BET values (1175, 2708 and 3052 m²/g, respectively) and V_T (0.70, 1.55 and 2.60 cm³/g, respectively), as well as different pore size distributions. Notably, the resulting carbon materials demonstrated exceptional CO₂ adsorption performance at 298 K, reaching a maximum adsorption capacity of 40.03 mmol/g at 40 bar for sample SS_652_41752, 15.12 mmol/g at 15 bar for SS_652_21752, and 3.41 mmol/g at 1 bar for SS_652_11752. These values rank among the highest ever reported for biomass-derived porous carbon materials. The adsorption behavior of the most efficient sorbent, SS_652_41752, was further analyzed using Langmuir and Freundlich isotherm models over the temperature range of 298–318 K and at pressures up to 40 bar, and the isosteric heats of adsorption were calculated to elucidate adsorbent–adsorbate interactions. It was found that the differential molar isosteric heat of CO₂ adsorption decreased from approximately 20 to approximately 17 kJ/mol with increasing adsorption uptake, confirming the physisorption nature of the process. These results demonstrate that crustacean shell waste is a promising feedstock for producing carbon materials with tailored properties and significant potential for CO₂ adsorption applications. Full article

This study provides the main performance estimates for new concepts, using flexible gasification operation modes, adaptable to prevailing market conditions, for the production of bio-synthetic natural gas (bio-SNG) and biochar from biogenic residues and waste, such as bark, straw, and Solid Recovered Fuel (SRF). Dedicated integrated process models were developed in Aspen Plus based on and validated against data from experimental campaigns in a gasification and gas cleaning pilot plant. Simulation runs show that the proposed concepts convert biomass to bio-SNG 10% more efficiently than the reference case, mainly due to the considerably reduced oxygen demand at the Autothermal Reformer (ATR) enabled by the improved catalyst. The co-production mode schemes showed promising results in terms of overall plant efficiency, at 76.5–78.2%, and total carbon utilisation, at 41–55.3%. The hybrid cases require an electrolyser with a power capacity almost 70% of the biomass thermal input to the gasifier, resulting in a total electricity consumption of up to 0.769 kWhe/kWh of biofuel. In return, they achieve over 50% utilisation of the carbon contained in the feedstock for biofuel production and a 70.1–76.5% total plant energy efficiency. Efficient biofuel and biochar production unlock negative emission potential, further strengthening the value of these flexible concepts. Full article

Driven by the increasing demand for renewable energy integration and low-carbon transformation in the chemical industry, the production of green hydrogen from renewable electricity for subsequent ammonia synthesis has emerged as an important route for green ammonia production. However, the process still relies on the high-pressure Haber–Bosch synthesis loop, typically operating at 200–300 bar, where multi-stage compression, recycle gas treatment, and low-temperature condensation separation strongly influence energy consumption and feedstock utilization. In this study, a steady-state Aspen Plus (V15) model integrating an Alkaline Water Electrolysis Unit (AWE), cryogenic air separation for nitrogen production, and an ammonia synthesis loop was established for a liquid ammonia plant with an annual capacity of approximately 600,000 t. Under base-case conditions, the specific energy consumption of liquid ammonia production was 10.28 kWh/kg-NH₃, while the hydrogen and nitrogen elemental utilization rates reached 87.73% and 88.92%, respectively, both higher than those of conventional coal- and natural gas-based ammonia routes. Increasing the compression stages from 2 to 5 reduced the fresh syngas compression work by 6.69%, although the energy-saving benefit became marginal beyond four stages. A purge ratio of 1–2% achieved a reasonable balance between recycle compression work and hydrogen/nitrogen purge loss, while the preferred condensation temperature range for improved NH₃ recovery was −20 °C to −25 °C. Full article

Due to the rapid development of the textile industry and increased consumption of various textiles composed of both synthetic and natural fibers, large amounts of textile waste are produced, leading to environmental and economic problems on a global scale. Turning textile waste into carbon materials that can be used in a broad range of applications has become a viable solution to address this challenge in terms of sustainability and value generation. Natural and synthetic textile fibers have distinctive molecular structures with relatively high carbon content and variable chemical functionality; therefore, they have been identified as highly promising precursors for fabricating carbon materials with various electrochemical and environmental applications. At the same time, the properties of carbonized and activated textile fibers are strongly dependent on the molecular transformations taking place during thermal treatment and functionalization of textile fibers. This review will provide a comprehensive overview of the molecular evolution of natural and synthetic textile fibers during carbonization and activation processes in terms of dehydration, depolymerization, aromatization, heteroatom preservation, and graphitization mechanisms. The effect of precursor chemical composition, pyrolysis conditions, activation process, and heteroatom incorporation on the structure of carbonized and activated textile fibers and their physical and electrochemical properties will be analyzed. Particular emphasis is placed on electrochemical applications, including capacitive deionization, supercapacitors, electrocatalysis, and emerging smart electrochemical textile systems, highlighting how molecular transformation, pore engineering, and surface chemistry govern charge storage, ion adsorption, and catalytic behavior. In addition, major characterization techniques such as Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area analysis will be reviewed and discussed in relation to understanding the interdependence between molecular structure and material properties. Finally, recent issues related to feedstock heterogeneity, scalability, energy efficiency, and sustainability of processing are highlighted, and future perspectives on multifunctional carbon structures and circular utilization of textile waste are discussed. Full article

Biochar has emerged as one of the most promising nature-based strategies for improving soil quality, enhancing crop productivity and supporting climate-smart agriculture. However, the agronomic performance of biochar remains highly variable because its effects are governed by complex interactions among feedstock characteristics, pyrolysis conditions, soil properties and management practices. This review synthesizes recent advances in biochar research (2019–2026), examining how production variables determine biochar physicochemical properties and how these properties subsequently influence soil functioning, plant performance and long-term agricultural sustainability. The review integrates evidence on feedstock selection, pyrolysis technologies, biochar modification strategies and the relationships between biochar properties and soil physical, chemical and biological processes. Particular attention is given to crop productivity, nutrient use efficiency, stress mitigation, contaminant immobilization, greenhouse gas mitigation and long-term soil resilience. Across the literature, the most consistent agronomic benefits were observed when biochar was applied to degraded or resource-limited soils and integrated with complementary management practices, whereas responses were often limited under fertile soils, low application rates or short experimental periods. Rather than identifying a universally superior biochar, the evidence indicates that agronomic performance depends on matching biochar characteristics to specific production objectives and environmental conditions. Based on these findings, this review proposes a transition from generalized biochar application towards optimized deployment strategies supported by standardized characterization, long-term multi-site validation and integrated environmental and economic assessments. This synthesis provides a comprehensive framework for guiding future research and facilitating the effective implementation of biochar within sustainable and regenerative agricultural systems. Full article

Food waste has emerged as one of the most pressing global sustainability challenges because of its environmental, economic, and social implications. Nearly one-third of the food produced worldwide is lost or wasted each year, contributing to greenhouse gas emissions, depletion of natural resources, and increasing food insecurity. Advances in circular bioeconomy concepts and sustainable processing technologies have transformed food waste from an environmental liability into a valuable feedstock for producing biofuels, bioplastics, bioactive compounds, functional ingredients, prebiotics, and other high-value products. This review critically examines current strategies for converting food waste into value-added products, including green extraction technologies and biochemical, thermochemical, enzymatic, and microbial approaches. Attention is given to major agri-food by-products, such as fruit pomace, vegetable residues, oilseed meals, dairy by-products, and agro-industrial wastes. Emerging developments involving biorefinery concepts, artificial intelligence, digital biorefineries, synthetic biology, and carbon-neutral production systems are also discussed. Furthermore, the review highlights recent applications of waste-derived fibers, antioxidants, and polyphenols in functional foods, especially bakery products. Finally, key challenges related to feedstock heterogeneity, process scalability, regulatory frameworks, economic feasibility, and sustainability assessment are critically analyzed together with future research directions supporting the transition toward resilient circular bioeconomy systems. Full article

Growing environmental concerns over petroleum-based plastics have increased interest in sustainable and biodegradable alternatives such as polyhydroxybutyrate (PHB). PHB is a naturally produced biopolymer synthesized by microorganisms and is widely recognized for its biodegradability, biocompatibility, renewability, and thermoplastic properties. Despite these advantages, PHB use remains limited by brittleness, high crystallinity, low thermal stability, a narrow processing window, and high production costs. This review discusses the production, properties, biodegradation behavior, and applications of PHB, with a focus on strategies to improve its performance. Modification approaches, including copolymerization, polymer blending, filler reinforcement, plasticization, and hybrid composite formulation, are critically reviewed to evaluate their effects on the thermal, mechanical, and processing behavior of PHB-based materials. The review also highlights recent developments in additive manufacturing, particularly fused deposition modeling/fused filament fabrication (FDM/FFF) for the extrusion of biodegradable PHB composite filaments. In addition, the biodegradation of PHB under various environmental conditions, including soil, compost, freshwater, marine, aerobic, and anaerobic environments, are discussed. Current challenges, research gaps, commercialization barriers, and future opportunities related to sustainable feedstocks, advanced composites, additive manufacturing, and circular economy integration are addressed. Overall, PHB shows strong potential as a sustainable alternative for packaging, biomedical, agricultural, and three-dimensional (3D) printing applications. Full article

The instability of marine low-sulfur fuel oil caused by asphaltene precipitation poses significant operational challenges in the shipping industry. This study systematically investigates the dispersing effects of biodiesel derived from three different feedstocks—palm oil, waste cooking oil (WCO), and microalgae oil—and their individual fatty acid methyl ester components on asphaltenes extracted from VLSFO. Biodiesel was selected as a dispersant due to its renewable nature, polar ester functional groups, and variable unsaturation levels, which enable favorable interactions with asphaltene molecules through hydrogen bonding and π-π stacking. Using UV–Visible spectrophotometry, the dispersion performance was quantitatively evaluated under various conditions including dispersant concentration, temperature, storage time, and molecular structural characteristics. The results demonstrate that microalgae oil biodiesel exhibits the most superior asphaltene dispersion capability among the three biodiesels, with a dispersion improvement index of 35% at 12 g/L, compared to 28% and 22% for waste cooking and palm oil biodiesels. Optimal performance is achieved at 80 °C, where the asphaltene concentration increases by 68% relative to the control, and remains stable within the first 10 days of storage but deteriorates significantly after 30 days due to oxidative degradation. Among individual FAME components, the dispersion effectiveness increases with alkyl chain length from C10 to C20, with the latter reaching a 30% improvement index. Functional group polarity plays a critical role, with carboxylic acid exhibiting a 45% improvement at 14 g/L, substantially outperforming alcohol at 32% and ester at 28%. The degree of unsaturation further enhances dispersion, as the improvement index rises progressively from 20% for saturated methyl stearate to 42% for tri-unsaturated methyl linolenate, representing a 2.1-fold increase. Dynamic light scattering (DLS) measurements confirm that biodiesel addition reduces asphaltene particle size from the micrometer range of 2 to 5 μm down to submicron levels of 200 to 500 nm, while microscopic observations reveal inhibited aggregation. These findings provide theoretical foundations for biodiesel application in marine fuel systems. Full article

Associated gas in the Permian Basin is a methane-rich but spatially fragmented and intermittently available feedstock. Methane pyrolysis can convert hydrocarbons to hydrogen and solid carbon without forming process CO₂ in the reactor, but its practical value depends on the captured-gas capacity factor, feed composition, high-temperature heat supply, product purification, continuous carbon withdrawal, carbon offtake, and transparent greenhouse-gas accounting. This study presents an implemented screening model for a modular 1 million standard cubic feet per day (MMSCFD) Permian associated-gas unit. A representative Permian composition is evaluated with hydrocarbon cracking stoichiometry, catalytic and thermal conversion envelopes, a net hydrogen recovery assumption, an energy-duty allocation, a levelized-cost model, and a well-to-gate carbon-intensity model. The catalytic base case produces 3.78 t/d of saleable H₂ after 90% pressure-swing adsorption (PSA) recovery and 14.27 t/d of solid carbon; the thermal near-complete conversion bound produces 4.31 t/d of saleable H₂ and 16.15 t/d of solid carbon. At a 0.85 capacity factor, $10 million installed capital expenditure (CAPEX), 8% real discount rate, 20-year life, 10 kWh per kg H₂ energy intensity, and $0.06 per kWh electricity, the deterministic plant-gate levelized cost of hydrogen (LCOH) is $1.81 per kg H₂ at zero carbon value and $1.05 per kg H₂ at a net realized carbon value of $0.20 per kg C. Monte Carlo analysis over capacity factor, CAPEX, energy intensity, electricity price, carbon value, feed/capture cost, and yield uncertainty gives levelized cost of hydrogen values at the 10th, 50th, and 90th percentiles (P10/P50/P90) of $1.32/$1.91/$2.57 per kg H₂. The corresponding screening carbon-intensity distribution is 2.34/4.11/5.89 kg carbon dioxide equivalent (CO₂e) per kg H₂, dominated by electricity carbon intensity and upstream methane loss. Geothermal or waste-heat preheat is treated quantitatively as a partial offset to low- and mid-temperature duties, not as a replacement for high-grade 900–1200 °C trim heat. The pathway is benchmarked against steam methane reforming, autothermal reforming with carbon capture and storage, electrolysis, small-scale liquefied natural gas, and gas-to-liquids conversion. Reported LCOH values are plant-gate production costs; separate hydrogen-logistics and negative-carbon-value stress tests identify conditions under which remote delivery or carbon disposal can erode the apparent economic advantage. Full article

The role of internal combustion engines in future transport systems is expected to remain central, particularly in hard-to-abate sectors such as heavy-duty road transport and maritime applications. However, their decarbonization requires the adoption of low-carbon and renewable fuels. This review examines hydrogen, methane-based fuels, methanol, and ethanol for internal combustion engine applications using a pathway-based approach that integrates life-cycle assessment, technology readiness level, commercial readiness level, and engine-related considerations. The reviewed literature shows that the environmental performance of these fuels varies strongly depending on feedstock, production pathway, process configuration, and energy source. From a Well-to-Tank perspective, hydrogen pathways exhibit particularly large variability, ranging from around 3 gCO₂eq/MJ for wind-based electrolysis to around 230 g CO₂eq/MJ for coal gasification. Methane-based fuels range from around 16 gCO₂eq/MJ for fossil compressed and liquefied natural gas to negative values for waste- and manure-based biomethane. Methanol and ethanol also show substantial variability, with renewable, waste-derived, and bio-based pathways generally offering substantially lower life-cycle greenhouse gas (GHG) emissions than fossil-based routes. In the use phase, Tank-to-Wheel analysis shows that energy demand remains relatively similar across fuels, while differences in direct emissions are mainly related to fuel carbon content and other GHG species such as ${\mathrm{CH}}_4$ or ${\mathrm{H}}_2$ slip and combustion-related species such as ${\mathrm{N}}_2\mathrm{O}$. The Well-to-Wheel comparison for heavy-duty applications highlights that upstream fuel production pathways strongly influence overall performance, while use-phase contributions play a secondary role and mainly affect the final ranking when upstream emissions are comparable. Overall, the review shows that pathway selection is more influential than fuel identity itself, highlighting that effective decarbonization strategies should focus on pathway design and upstream fuel production rather than on fuel categories alone, and that renewable and bio-based pathways offer the greatest potential for achieving very low or near-zero life-cycle GHG emissions in internal combustion engine applications. Full article

Cellulose nanofibers (CNFs) have significant potential in composites as additives to improve mechanical properties, melt rheology, and more. However, agglomeration of CNFs is a key challenge in composite melt processing as obtaining nano-level dispersion of CNFs often requires cost- and energy-intensive processes (e.g., solvent exchange or freeze drying) due to the strong hornification tendencies of CNF. Herein, we avoid these challenges by using a natural fiber carrier method to integrate CNF into thermoplastic composites. Fibers are co-dried to create a hybrid fiber feedstock for compounding in which natural fibers are decorated with dispersed nanofibers. The hybridized fibers result in up to a 24% increase in tensile strength and up to a 35% increase in Young’s modulus compared to composites only containing natural fibers. The lignocellulosic nanofibers are found to outperform their purely cellulosic counterpart, which is theorized to be due to either an increased propensity for fibrillation of the lignocellulosic fibers or the increased hydrophobicity of the fibers due to the presence of lignin. Surface analysis of fiber feedstocks, via streaming potential measurements and dynamic light scattering (DLS), confirmed a significant change in the feedstock hydrophobicity before and after hybridization. While mild additions of CNF (1 wt.% on the macroscale fiber) do not impact the composite melt viscosity, the viscosity is found to increase at higher CNF loadings (5 wt.% on the macroscale fiber), indicating its utility as a rheology modifier. Lastly, use of these materials as novel feedstocks for medium-scale additive manufacturing in high-fidelity part production was demonstrated. Full article