Search Results (102)

The accelerating generation of waste streams is observed globally. Spanning lignocellulosic biomass, plastic waste, sewage sludge, and industrial residues, this review presents both an urgent management challenge and a compelling materials opportunity. Carbon materials derived from these waste streams offer a sustainable route to functional carbons applicable in electrochemical energy storage, adsorption, heterogeneous catalysis, and high-temperature applications. Yet their rational design remains constrained by incomplete understanding of the relationships between feedstock composition, processing pathway, structural characteristics, and functional performance. This review provides an integrated analysis of waste-derived carbon materials from processing pathways to structure–property–function relationships. The principal feedstock categories are examined for their compositional characteristics and implications for carbon yield and structure. Five primary processing routes are assessed. The five routes examined are pyrolysis, hydrothermal carbonisation, physical and chemical activation, and microwave-assisted processing. They are assessed comparatively with emphasis on structural outcomes and governing parameters. The resulting structural characteristics are discussed. These are morphology, hierarchical pore architecture, surface chemistry, heteroatom doping, and crystallinity. They are discussed alongside their characterisation methods and known limitations as performance predictors. Structure–property relationships are examined quantitatively. Heteroatom-doped hierarchical porous carbons achieve 612 F/g specific capacitance. Turbostratic hard carbons deliver 450 mAh/g sodium storage with over 90% retention. Hierarchical porous carbons demonstrate CO₂ uptake of 5.0 mmol/g and dye adsorption exceeding 9000 mg/g under optimised laboratory conditions; these values reflect individual studies and are not directly comparable across systems. Biomass-derived sulfonated carbon catalysts sustain biodiesel yields above 90% over multiple cycles. Challenges of feedstock variability, process scalability, environmental compliance, and economic feasibility are addressed, and machine learning-guided design, standardised characterisation methodology, and circular economy policy frameworks are identified as key enablers for translating laboratory performance into industrial reality. Full article

Effective management of organic wastes is essential for green and low-carbon development. Conventional technologies, including incineration, pyrolysis, hydrothermal carbonization (HTC), gasification, anaerobic digestion (AD), and composting, have supported waste reduction and basic resource recovery, but they remain limited in high-efficiency conversion and high-value utilization. This review comparatively evaluates these conventional routes together with advanced and intensified technologies, including microwave-assisted pyrolysis (MAP), plasma treatment, supercritical water gasification (SCWG), and flash joule heating (FJH), with emphasis on suitable feedstocks, performance characteristics, application boundaries, and integration potential. In general, wastes with high moisture content are more suitable for HTC, AD, and SCWG, whereas relatively dry wastes and wastes with high carbon content are more suitable for pyrolysis, gasification, plasma treatment, and FJH upgrading. The review also discusses representative integrated pathways, such as HTC-SCWG, pyrolysis and plasma coupling, AD and gasification coupling, and pyrolysis and FJH coupling, which may improve carbon conversion, broaden product portfolios, and reduce residual pollutants. However, large-scale implementation is still constrained by feedstock heterogeneity, heat and mass transfer limitations, catalyst deactivation, reactor corrosion, and system cost. Overall, no single technology is universally optimal; technology selection should depend on feedstock properties, moisture content, and target products. Full article

Microwave-assisted pyrolysis (MAP) has emerged as a revolutionary technology for converting solid waste into high-value hydrocarbons. However, conventional pyrolysis and traditional single-function catalysts often face an inevitable “performance trade-off” involving severe mass transfer resistance, poor microwave absorption, and rapid coking. This review systematically summarizes the recent evolution of catalyst design toward advanced multi-site composites. It highlights the synergistic mechanisms of integrating microwave-responsive cores, hierarchical pore networks, and metal-acid bifunctional sites to achieve ultrafast localized heat transfer, targeted bond cleavage, and in-situ coking suppression. Furthermore, this paper critically examines current bottlenecks in scaling MAP to industrial levels. To address these challenges, we discuss emerging solutions, including hydrogen-enriched co-pyrolysis, non-destructive in-situ regeneration, and the integration of machine learning frameworks for intelligent process optimization. Full article

This research systematically investigated the catalytic pyrolysis of Arab Heavy (AH) and Arab Light (AL) crude oils using NiO supported on Al₂O₃ or ZSM-5 in a microwave-assisted reactor, with particular emphasis on hydrogen (H₂) generation and value-added chemicals. To understand how both the catalyst and feedstock affect reaction products, gas and liquid products as well as catalyst activity were carefully examined. The production of H₂ and olefins was significantly enhanced by the NiO/Al₂O₃ catalyst, especially when using AL crude. This is most likely due to favorable metal-support interactions that increase the dehydrogenation activity. However, when paired with lighter feedstock, NiO/ZSM-5 greatly increased paraffin production and encouraged light alkane synthesis in both phases. GC-MS and FTIR spectroscopy confirmed that NiO/Al₂O₃ produced liquid products richer in aromatics while also containing a significant fraction of paraffins. Remarkably, the AL over NiO/Al₂O₃ combination showed very little liquid recovery, indicating that gas generation was higher in these reaction conditions. These results showed how H₂ selectivity and hydrocarbon routes in NiO/ZSM-5 and NiO/Al₂O₃ are controlled by various microwave-catalyst interactions. This work further highlights the importance of matching catalyst properties with feedstock type to control product selectivity, with NiO/Al₂O₃ showing particular promise for H₂-focused applications. Full article

The co-pyrolysis of Chlorella vulgaris (CV) and Eucalyptus branches (EP) offers a promising strategy to enhance bio-oil yield, improve resource utilization efficiency, and alleviate environmental pressures. In this study, the microwave-assisted co-pyrolysis of CV and EP at a mass ratio of 2:1 was investigated, focusing on the catalytic performance of Ni-X (X = Mg, Cu, Fe) bimetallic modified HZSM-5 zeolites. The effects of these catalysts on pyrolysis characteristics, product distribution, and bio-oil composition were systematically evaluated. Experimental results showed that the 15% Ni-Cu/HZSM-5 catalyst exhibited the best catalytic performance, achieving the highest bio-oil yield of 16.83%; it also elevated the R_m to 0.0687 wt.%/s and reduced T_s to 2084 s. Composition analysis revealed that Ni-Cu/HZSM-5 significantly promoted the formation of hydrocarbons, increasing their relative content from 11.59% (C2E1 Group) to 28.92%, while effectively suppressing the formation of nitrogen-containing compounds, reducing their content by 5.05%. Based on these results, a possible reaction pathway is proposed in which the Ni-Cu/HZSM-5 catalyst may enhance heteroatom removal through hydrodeoxygenation (HDO) at the Ni-Cu sites, followed by cracking and aromatization at the HZSM-5 acid sites. This effect may be complemented by preferential adsorption of oxygenated intermediates over nitrogen-containing species, which could help suppress the formation of nitrogenous heterocycles. This work provides theoretical guidance for the application of bimetallic zeolite catalysts in microalgae/lignocellulose co-pyrolysis, alongside a viable pathway for valorizing Eucalyptus by-products to produce high-quality bio-oil. Full article

Thermochemical/catalytic co-processing of biomass and solid wastes is a promising route for waste valorization, low-carbon energy recovery, and the co-production of fuels, chemicals, and carbon materials. Conventional pathways, including pyrolysis, gasification, liquefaction, and carbonization, provide the basic framework for mixed-feed conversion. Emerging routes, such as flash Joule heating, microwave-assisted conversion, plasma processing, supercritical water treatment, solar-driven systems, and machine-learning-assisted optimization, further expand opportunities for process intensification and selective upgrading. Owing to feedstock complementarity, including hydrogen donation from plastics, catalytic effects of ash minerals, and interactions among reactive intermediates, co-processing can enhance deoxygenation, hydrogen generation, aromatization, and carbon utilization. Major challenges remain, however, including feedstock heterogeneity, reactor scale-up, catalyst stability, and the limited transferability of laboratory-scale synergy to realistic waste streams. Future progress should therefore focus on continuous validation, mechanistic clarification, and integrated techno-economic, life-cycle, and data-driven assessments. Full article

This review critically evaluates current PA6 recycling technologies, with a specific focus on caprolactam-oriented chemical recycling pathways, including hydrolysis, pyrolysis, glycolysis, ammonolysis, hydrothermal treatment, ionic-liquid-assisted depolymerization, and microwave-assisted processes. Reported caprolactam yields vary significantly depending on reaction conditions and catalyst systems, ranging from below 60 wt% in conventional hydrolysis to above 90 wt% under optimized catalytic, hydrothermal, or microwave-assisted conditions. Among these approaches, microwave-assisted hydrolysis and catalytic depolymerization have emerged as particularly promising, offering substantially reduced reaction times (minutes rather than hours), improved energy efficiency, and high monomer selectivity at moderate temperatures (typically 200–350 °C). This review integrates kinetic modeling approaches, analytical methods for monitoring depolymerization, and downstream separation considerations that govern monomer purity and recyclability. Key challenges, including energy demand, feedstock contamination, scalability, and economic competitiveness, are critically discussed in relation to industrial implementation. Overall, hydrolysis-based and microwave-assisted chemical recycling routes are the most viable pathways for closed-loop recycling of PA6. Future progress will rely on integrated reaction–separation–repolymerization designs, catalyst optimization, and process intensification to enable sustainable and industrially relevant PA6 circularity. Full article

Non-recyclable plastic waste (PSW) and residual lignocellulosic biomass (WP) represent abundant yet underused resources whose conversion can generate renewable fuels with synergistic benefits. While conventional pyrolysis remains limited by slow heat transfer and poor adaptability to heterogeneous feeds, microwave-assisted pyrolysis (MAP) offers faster volumetric heating and improved syngas quality, though it is still largely confined to the laboratory scale due to limited understanding of feedstock interactions and process behaviour. In this context, the present work provides a laboratory-scale experimental investigation of the MAP co-pyrolysis of PSW/WP blends, focusing on gas yield and syngas quality, and complements the experimental analysis with a preliminary scale-up assessment for a continuous microwave reactor. The results reveal clear synergistic effects, with gas yields exceeding those predicted by linear mixing. A 70/30 wt% PSW/WP blend produced a hydrogen-rich syngas with H₂ concentrations of approximately 42 vol% and an H₂/CO ratio of 2–3. Compared to conventional pyrolysis under analogous conditions, MAP increased hydrogen content by around 35% and reduced CO₂ concentrations by up to 40%, resulting in a cleaner and more energy-dense gas. Overall, the findings highlight the strong potential of MAP for the valorization of mixed plastic–biomass wastes. Full article

Background/Objectives: The recent increase in antidepressant consumption, particularly venlafaxine, combined with the limited effectiveness of conventional wastewater treatment processes, has led to rising environmental concentrations. Adsorption methods have emerged as effective strategies for removing persistent pharmaceuticals without generating harmful by-products. This study aimed to develop and assess two activated carbons (ACs) derived from spent brewery grains as an efficient material for venlafaxine removal from wastewater. Methods: Two pyrolysis methods, conventional and microwave-assisted, were evaluated to assess their influence on the adsorption properties. The materials were characterized through nitrogen physisorption and scanning electron microscopy to evaluate surface area (S_BET), porosity, and morphology. Their adsorption properties were examined through batch adsorption experiments to analyze kinetic and equilibrium behavior, and the efficacy was evaluated in both ultrapure water and real wastewater. Results: The obtained AC exhibited high porosity, with the S_BET ranging from 1080 to 1197 m² g⁻¹. Kinetic studies indicated that adsorption followed a pseudo-second-order model, achieving equilibrium within 2 h. The equilibrium data were optimally described by the Langmuir isotherm, indicating monolayer adsorption, with the maximum adsorption capacity of microwave-assisted AC reaching 74 ± 6 mg g⁻¹. Microwave-assisted AC has shown higher efficiency than conventionally produced AC, demonstrating that this pyrolysis technique can produce materials with enhanced adsorption properties. Conclusions: This study evidences that microwave-assisted pyrolysis of an abundant agro-industrial residue yields high-performance materials capable of efficiently removing an antidepressant, included in the revised Urban Wastewater Treatment Directive, from complex effluents even at low doses, highlighting a sustainable route to mitigate pharmaceutical contamination in aquatic environments. Full article

Organic residues from households and food-service facilities, such as orange peels, spent coffee grounds, banana peels and potato skins, represent abundant biomass resources that can release undesirable compounds during degradation. Their conversion into carbonized materials through thermochemical processes offers a sustainable route for waste valorization. In this study, residues were characterized by proximate and elemental analyses, density, porosity, and calorific value. Valorization was performed using microwave-assisted pyrolysis and two hydrothermal carbonization (HTC) routes. Pyrolysis experiments were conducted at 450, 600 and 800 W with residence times of 20–70 min. Conventional HTC was carried out at 180, 200 and 220 °C for 20 h, while autoclave HTC was performed at 134 °C for 2 and 4 h. The resulting biochars and hydrochars were evaluated for their physicochemical and energetic properties and ANOVA was applied to assess the influence of operating conditions. Conventional HTC at higher temperatures produced the highest calorific values, whereas microwave-assisted pyrolysis at 800 W provided competitive HHVs with high solid yields. Autoclave HTC enhanced solid retention and carbon preservation. Among the investigated residues, spent coffee grounds exhibited the most favorable solid-phase energetic performance. These findings demonstrate that thermochemical conversion enables the transformation of common residues into carbon-rich materials with physicochemical and energetic properties relevant for comparative assessment and future application-oriented studies. It should be noted that conventional hydrothermal carbonization experiments were conducted using pre-dried biomass, which represents a methodological limitation of the comparative assessment. Full article

Bismuth-based semiconductors have emerged as a promising class of visible-light-responsive photo(electro)catalysts for environmental remediation owing to their tunable electronic structures, moderate band gaps, and relatively low toxicity. The stereochemically active Bi³⁺ 6s² lone pair and strong Bi–O orbital hybridization tailor valence-band states, enabling enhanced utilization of the solar spectrum and favorable charge-carrier dynamics. In addition, layered, perovskite-like, and aurivillius-type crystal frameworks generate internal electric fields that are advantageous for photoelectrochemical (PEC) operation. This review critically examines advances from 2015 to 2025 in the design, synthesis, modification, and environmental applications of bismuth-based photo(electro)catalysts, with particular emphasis on PEC systems for pollutant degradation. Major material families, including bismuth oxides, oxyhalides, oxychalcogenides, chalcogenides, perovskite-like oxides, and complex metal oxides, are discussed in relation to their structure–property–performance relationships. Key synthesis strategies, such as solid-state, sol–gel, hydro/solvothermal, microwave-assisted, spray pyrolysis, and electrodeposition methods, are compared with respect to morphology control, defect chemistry, and electrode integration. Performance-enhancing approaches, including elemental doping, oxygen-vacancy engineering, and the rational design of type-II, p–n, Z-scheme, and S-scheme heterojunctions, are critically assessed. Practical considerations related to stability, scalability, and techno-economic constraints are highlighted. Finally, current challenges and future directions toward durable and application-ready bismuth-based PEC technologies are outlined. Full article

Current agriculture faces the challenge of producing sufficient food from diminishing land resources, due to deteriorating soil quality and accelerated population growth. Numerous studies have demonstrated that biochar/hydrochar can serve as efficient soil amendments by improving soil fertility and enhancing crop productivity. Various food wastes are promising raw materials for biochar/hydrochar production due to their abundant organic matter. Recently, thermochemical techniques such as pyrolysis, hydrothermal carbonization (HTC), and microwave-assisted pyrolysis (MAP) have been widely proposed for converting food waste into biochar/hydrochar for soil amendment. However, the composition of food waste is complex and the parameters for its thermal treatment are highly variable, leading to uncertainties in the performance of the derived biochar/hydrochar for soil applications. This study aims to establish a structure–activity relationship linking food waste carbonization technology, the properties of the obtained biochar/hydrochar, and its functions as a soil amendment. Furthermore, the detailed mechanisms by which biochar improves plant growth or poses potential ecological risks to agricultural land are discussed. This review is intended to provide a guideline for the large-scale application of food waste-derived char for soil amendment. Full article

The growing volume of decommissioned wind turbine blades, primarily made of glass fibre-reinforced polymers (GFRP), poses major recycling challenges. This study explores a microwave (MW)-assisted thermochemical recycling to recover high-quality fibres from GFRP waste. Two routes were evaluated: (i) a dry route using direct MW heating, and (ii) a semi-wet route involving solvent pre-swelling followed by microwave pyrolysis. The dry route suffered from poor heating due to GFRP’s inherently low dielectric loss, whereas the semi-wet route enabled more effective resin degradation. Five swelling agents were tested: acetic acid (AcOH), hydrogen peroxide (H₂O₂), an AcOH/H₂O₂ mixture, dimethylformamide (DMF), and dimethyl sulfoxide (DMSO). Among these, DMSO achieved 92% resin removal in 9 min at 350 °C. Recycled fibres retained 1.48 ± 0.41 GPa strength (81% of virgin). Gas chromatography–mass spectrometry (GC–MS) analysis of pyrolysis oils revealed predominantly phenolic products with limited bisphenol A (BPA) retention. To demonstrate practical relevance, the semi-wet method was applied to real wind blade waste, where recovered fibres retained 72% of their tensile strength versus virgin fibres. These results indicate that the process remains effective for industrially aged GFRP. This study confirms the feasibility of MW-based semi-wet recycling and offers insights to support future process refinement, which will ultimately contribute to more sustainable end-of-life solutions for GFRP waste. Full article

Fiber-reinforced polymer composites (FRPCs) are increasingly used in construction due to their high performance and low environmental footprint. However, their widespread adoption has raised concerns over end-of-life management, particularly under European regulations mandating high recycling rates for construction and demolition waste (CDW). This study evaluates different systems for the chemical recycling of FRPCs through microwave (MW)-assisted solvolysis using green solvents, including deep eutectic solvents (DESs) and biobased acetic acid. The process targets thermoset resin depolymerization while preserving fiber integrity, operating at reduced temperatures (≤230 °C) and lower energy demand than conventional techniques, such as pyrolysis. A systematic experimental design was applied to CDW-derived polyester composites and extended to industrial epoxy and vinyl ester composites. Among the tested solvents, glacial acetic acid + ZnCl₂ (5 wt.%), achieved the highest degradation efficiency, exceeding 94% in small-scale trials and maintaining over 78% upon upscaling. Recovered fibers showed moderate property retention, with tensile strength and elongation losses of ~30% and ~45% for infusion-based epoxy composites, while those from pultrusion-based epoxy composites exhibited 16–19% and retained similar properties to the virgin material, respectively. The method facilitates fiber recovery with limited degradation and aligns with circular economy principles through solvent reuse and minimizing environmental impact. Full article

Plastic pyrolysis can not only effectively solve the environmental pollution caused by the large use of plastics products but also can produce valuable chemical products to alleviate the energy shortage problem. Firstly, this study designs a microwave pyrolysis device for polypropylene plastic based on a symmetrical circular waveguide slot radiation structure. The microwave energy is fed in through the bottom symmetrical circular waveguide port, transmitted to the slot array unit after passing through the horn amplification structure, and then uniformly radiated into the polypropylene plastic. Secondly, the finite element method is employed to conduct multi-physics field coupling calculations for the electromagnetic field, temperature field, chemical reaction field, mass transfer field of concentrated substances, and fluid field involved in the microwave pyrolysis process. Finally, to improve the efficiency of microwave pyrolysis, the wave-absorbing material SiC is introduced to investigate the effects of different doping methods and doping mass ratios m_SiC:m_PP on pyrolysis temperature distribution uniformity, pyrolysis gas yield (Y_G), energy consumption (Q), gas composition, and higher heating value (HHV). The results indicate that optimal pyrolysis performance is achieved when the microwave power is 1000 W, the pyrolysis time is 9.2 min, SiC is uniformly doped and the mass ratio is m_SiC:m_PP = 3:1. The COV of temperature is a mere 0.0004, the Y_G reaches 75.15 wt.%, and Q is 0.15 kWh, the HHV is up to 85.32 MJ/Nm³, and the percentages of C₃H₆ and CH₄ are relatively high at 72% and 11.4%. These findings confirm the designed microwave pyrolysis device can achieve uniform and high-efficiency pyrolysis capability for polypropylene plastic. Full article