Search Results (656)

The intensification of shrimp aquaculture is crucial for global food security, but poses significant environmental challenges. This review critically assesses the strengths and bottlenecks of two main treatment paradigms: in situ systems, chiefly biofloc technology (BFT), and advanced ex situ systems, such as recirculating aquaculture systems (RASs), constructed wetlands (CWs), and membrane bioreactors (MBRs). Although BFT enables nutrient recycling, it suffers from nitrate accumulation and a high energy demand. Likewise, ex situ technologies can achieve a high treatment efficiency, but contend with high costs, large footprints, or membrane fouling. In this review, we propose the strategic integration of microalgae, representing a universal and synergistic solution for overcoming these disparate bottlenecks. We dissect how a microalgal co-culture can simultaneously remove nitrate and reduce the aeration costs in BFT systems. Furthermore, we explore how microalgae-based units can serve as efficient polishing steps for RASs, enhance the performance of CWs, and mitigate fouling in MBRs. This review delves into the fundamental mechanisms of the microalgal–bacterial symbiosis that underpins these enhancements. Finally, we highlight the valorization of the resulting algal biomass as a high-value aquafeed ingredient, which can transform waste management into a value-creation opportunity. This review aims to provide a comprehensive roadmap for developing next-generation, microalgae-enhanced aquaculture systems. Full article

Spent coffee grounds (SCG) are an abundant, carbon-rich residue that can be valorized through thermochemical conversion into biochar. Conventional CO₂ activation is typically performed in a two-step process, which is time- and energy-consuming. This study aims to evaluate whether a one-step CO₂-assisted pyrolysis can produce biochar with comparable or enhanced structural and textural properties while simplifying the process. We compare a two-step pyrolysis process followed by CO₂ activation with a one-step CO₂-assisted route for producing biochar from SCG. CO₂ treatment markedly increases surface area (from 9.8 m²∙g⁻¹ to 550.6–671.0 m²∙g⁻¹) and pore volume. FTIR and Boehm titration indicate depletion of oxygenated surface groups, while N₂ adsorption–desorption analyses and SEM reveal a more uniform micro/mesoporous texture for the one-step sample. Although fixed carbon decreases due to gasification, the one-step route delivers superior textural properties in a single thermal stage, reducing energy demand. These results highlight one-step CO₂-assisted pyrolysis as an efficient, scalable option for producing high-porosity biochar from coffee waste. Full article

This study demonstrates a sustainable, integrated pathway for valorizing carrot processing by-products through solvent-free lycopene recovery. The approach combines optimized infrared dehydration with ultrasound-assisted extraction using edible oils. Drying kinetics were modeled at multiple temperatures, with the Midilli model providing the best fit (R² > 0.99), enabling accurate prediction of moisture content removal while preserving bioactive compounds. Optimization via Box–Behnken design identified efficient extraction conditions (49.7–60 °C, 10 mL/g, 60 min), achieving lycopene equivalent (LE) yields of 3.07 to 5.00 mg/kg oil. Sunflower and blended oils showed comparable performance under maximum sonication power (240 W), with strong agreement between predicted and experimental yields. The process generated two valuable outputs: a functional lycopene-enriched oil and an exhausted carrot powder co-product, the latter retaining its crude fiber content despite other compositional changes. This research presents a scalable, green methodology that aligns with circular economy principles, transforming agro-industrial waste into functional food ingredients without organic solvents. Thus, the developed approach establishes a transferable model for the sustainable valorization of carotenoid-rich residues, contributing directly to greener food production systems. By providing a practical technological framework to convert waste into wealth, this work supports the fundamental transition toward a circular bioeconomy. Full article

Valorizing coconut shell waste as a renewable lignocellulosic precursor offers a sustainable route to produce high-performance activated carbons for wastewater treatment. In this study, coconut shells were transformed into activated carbons through physical activation (air, CO₂, steam) and chemical activation (H₃PO₄, ZnCl₂, KOH), allowing direct comparison of how each method influences porosity and surface chemistry. Among the physically activated samples, steam activation produced the best material, A-ST, with S_BET = 738 m² g⁻¹, V_mi = 0.38 cm³ g⁻¹ and V_me = 0.07 cm³ g⁻¹. KOH activation yielded the top-performing carbon, A-KOH, achieving S_BET = 1600 m² g⁻¹, V_mi = 0.74 cm³ g⁻¹, and V_me = 0.22 cm³ g⁻¹. Adsorption tests with methylene blue, methyl orange, and orange G showed a clear link between physicochemical features and dye uptake. A-ST and A-KOH exhibited the highest capacities due to their wide micro–mesoporosity and favorable surface charge at the adsorption pH. In both cases, methylene blue was most strongly retained, confirming that large aromatic cations benefit from π–π interactions with graphene-like layers and easy micropore access. Overall, the results demonstrate that coconut-shell valorization is maximized when activation enhances both porosity and surface chemistry, enabling the production of tailored sorbents for the efficient removal of organic contaminants. Full article

Marine by-products represent an important source of bioactive lipids with potential applications in nutraceuticals and functional foods. This study provides a biochemical and lipidomic characterization of oils derived from sardine, monkfish, grey mullet roe, squid, and anchovy by-products, assessing how the extraction method influences their lipid and antioxidant profiles. Fatty acids were quantified by GC-FID, antioxidant compounds by HPLC-DAD, and untargeted lipidomics by TIMS-HRMS. A total of 228 lipid species were identified, predominantly triglycerides (TGs) and diglycerides (DGs), accounting for approximately 69% of the annotated lipidome. Grey mullet roe oils exhibited the highest levels of long-chain PUFAs (EPA, DHA) and antioxidants (α-tocopherol 205–469 mg/Kg, lutein 10–125 mg/Kg, and squalene 1004–6049 mg/Kg), whereas squid oils showed high n-3/n-6 proportions. The extraction method strongly affected lipid integrity. Supercritical CO₂ extraction with ethanol (SFE–SE) preserved the greatest proportion of PUFA-rich TGs, yielding ~27–28 g EPA + DHA per 100 g oil, while wet reduction and mechanical pressing produced lower PUFA levels (~22 g/100 g) and increased hydrolysis/oxidation-associated lipids. PCA and PLS-DA revealed clear clustering driven by species and extraction class, with PUFA-containing TGs and DGs identified as major discriminating lipids. These results highlight the critical role of extraction conditions in determining the nutritional and functional value of marine oils and support the valorization of marine by-products in high-value applications. Full article

The hydrogenation of the biomass platform compound, ethyl levulinate, for the synthesis of γ-valerolactone represents a highly promising pathway for biomass valorization. Transition metal phosphates are extensively utilized in biomass hydrogenation reactions due to their Brønsted and Lewis acid sites. In this study, we synthesized a series of transition metal (Ni, Co, and NiCo) phosphide catalysts using the liquid phase method. We investigated the effects of metal species and initial Co/Ni molar ratios on catalytic activity in hydrogenation of ethyl levulinate and optimized the reaction conditions. The NiCoP-1.00 sample, prepared with a Co/Ni molar ratio of 1, demonstrated high efficacy in the hydrogenation of ethyl levulinate to γ-valerolactone, achieving excellent selectivity (97.9%) under optimized conditions. Experimental findings indicate that the synergistic interaction between Ni and Co facilitates the hydrogenation of the intermediate ethyl 4-hydroxypentanoate to γ-valerolactone while inhibiting excessive hydrogenation. The catalytic performance of the NiCoP-1.00 catalyst remained stable over five recycling runs. Full article

Fungi have emerged as versatile biotechnological platforms for addressing environmental challenges with potential co-benefits for human health. Among them, Pleurotus ostreatus stands out for its ligninolytic enzyme systems (notably laccases), capacity to valorize lignocellulosic residues, and ability to form functional mycelial materials. We conducted an evidence-mapped review, based on a bibliometric analysis of the Scopus corpus (2001–2025; 2085 records), to characterize research fronts and practical opportunities in environmental remediation and sustainable bioprocesses involving P. ostreatus. The mapped literature shows sustained growth and global engagement, with prominent themes in: (a) oxidative transformation of phenolic compounds, dyes and polycyclic aromatic hydrocarbons; (b) biodegradation/bioconversion of agro-industrial residues into value-added products; and (c) development of bio-based materials and processes aligned with the circular bioeconomy. We synthesize how these strands translate to real-world contexts, reducing contaminant loads, closing nutrient loops, and enabling low-cost processes that may indirectly reduce exposure-related risks. Key translational gaps persist: standardization of environmental endpoints, scale-up from laboratory to field, performance in complex matrices, life-cycle impacts and cost, ecotoxicological safety, and long-term monitoring. A practical agenda was proposed that prioritizes field-scale demonstrations with harmonized protocols, integration of life-cycle assessment and cost metrics, data sharing, and One Health frameworks linking environmental gains with plausible health co-benefits. In conclusion, P. ostreatus is a tractable platform organism for sustainable remediation and bio-manufacturing. This evidence map clarifies where the field is mature and where focused effort can accelerate the impact of future research. Full article

The present study investigates the potential of poplar (Populus spp.) biomass from phytoremediation plantations as a feedstock for downdraft fixed bed gasification. The biomass was characterized in terms of moisture, ash content, elemental composition (C, H, N, O), and calorific values (HHV and LHV), confirming its suitability for thermochemical conversion. Gasification tests yielded a volumetric syngas production of 1.79 Nm³ kg⁻¹ biomass with an average composition of H₂ 14.58 vol%, CO 16.68 vol%, and CH₄ 4.74 vol%, demonstrating energy content appropriate for both thermal and chemical applications. Alkali and alkaline earth metals (AAEM), particularly Ca (273 mg kg⁻¹) and Mg (731 mg kg⁻¹), naturally present enhanced tar reforming and promoted reactive gas formation, whereas heavy metals such as Cd (0.27 mg kg⁻¹), Pb (0.02 mg kg⁻¹), and Bi (0.01 mg kg⁻¹) were detected only in trace amounts, posing minimal environmental risk. The results indicate that poplar pruning residues from phytoremediation sites can be a renewable and sustainable energy resource, transforming a waste stream into a process input. In this perspective, the integration of soil remediation with syngas production constitutes a tangible model of circular economy, based on the efficient use of resources through the synergy between environmental remediation and the valorization and sustainable management of marginal biomass—i.e., pruning residues—generating environmental, energetic, and economic benefits along the entire value chain. Full article

This study investigates the oxidative steam reforming (OSR) of simulated bio-oil aqueous fractions using Co/CeO₂-SBA-15 catalysts. Five representative compounds—methanol, acetic acid, hydroxyacetone, phenol, and furfural—were evaluated to assess their reactivity for hydrogen production. Aliphatic compounds achieved nearly complete conversion and stable hydrogen yields, while aromatic structures led to lower conversion and higher coke formation. Furfural exhibited higher reactivity than phenol due to its furan ring and aldehyde group. Catalysts with 10 and 20 wt.% Ce showed similar activity, but Co/20CeO₂-SBA-15 presented lower hydrogen yield. For this reason, next experiments of OSR of model compound mixtures were carried out only with Co/10CeO₂-SBA-15. To approach real bio-oil complexity, ternary and quinary mixtures were tested. High conversion and hydrogen yield were maintained over 50 h when the ternary mixture (methanol, hydroxyacetone, and acetic acid) was fed. When the quinary mixture was used as feedstock, which includes furfural and phenol, lower conversions were obtained for these compounds compared to aliphatic ones, although conversions remained above 80% after 50 h (88.9% for furfural and 82.6% for phenol). These results highlight Co/10CeO₂-SBA-15 as a viable catalyst for bio-oil aqueous fraction valorization under OSR conditions. Full article

This study presents a systematic approach for converting low-grade carbon derived from mining waste into functional carbon–zeolite composites with enhanced adsorption performance. To promote carbon deposition within and around zeolite frameworks, four industrially relevant zeolites, including zeolite socony mobil-5 (ZSM-5), Faujasite-type zeolite (Zeolite-Y), beta zeolite (Zeolite-β), and mordenite (MOR), were mechanically mixed with low-grade carbon under controlled stirring conditions (24 h at 250 rpm) and subsequently pyrolyzed at 800 °C. These treatments enabled a detailed assessment of structural stability and carbon–zeolite interactions. Scanning electron microscopy revealed pronounced modifications in surface morphology and carbon distribution after carbon treatment, while X-ray diffraction confirmed that the crystalline zeolite frameworks remained structurally intact despite the deposition of amorphous carbon. The adsorption performance of the resulting composites was evaluated through CO₂ adsorption measurements under controlled temperature and pressure conditions, demonstrating a clear enhancement relative to the pristine zeolites. Overall, this work highlights an effective strategy for valorizing low-grade carbon waste into high-performance carbon–zeolite hybrid adsorbents and provides new mechanistic insights into framework stability, selective atom removal, and carbon–zeolite interactions in high-temperature and acidic environments. Full article

The global floriculture industry generates massive organic residues that pose environmental risks but offer untapped bioenergy potential. This review evaluates the feasibility of valorizing flower waste through anaerobic digestion (AD) by synthesizing experimental data on substrate characterization, pretreatment efficacy, and reactor performance. Results indicate that biochemical methane potentials (BMP) vary significantly, ranging from 89 to 412 mL_CH4·g⁻¹_VS, depending on plant species and tissue composition. Major bottlenecks include high lignocellulosic recalcitrance (lignin content up to 0.28 g·g⁻¹_TS) and the presence of inhibitory phenolic compounds. Analysis reveals that while alkaline pretreatments effectively disrupt lignocellulosic structures, co-digestion strategies are essential to mitigate inhibition and balance nutrient ratios. However, current research is predominantly limited to laboratory-scale batch assays, leaving a critical knowledge gap regarding long-term process stability and inhibition dynamics in continuous systems. To transform this laboratory concept into a scalable technology, future efforts must focus on pilot-scale continuous reactor trials, standardized testing protocols, and comprehensive techno-economic and life cycle assessments. Full article

Plastic streams dominated by polyethylene (PE) including PE HD/MD (High Density/Medium Density) and PE LD/LLD (Low Density/Linear Low Density), polypropylene (PP), and polyvinyl chloride (PVC) across Europe demand a design framework that links synthesis with end of life reactivity, supporting circular economic goals and European Union waste management targets. This work integrates polymerization derived chain architecture and depolymerization mechanisms to guide selective valorization of commercial plastic wastes in the European context. Catalytic topologies such as Bronsted or Lewis acidity, framework aluminum siting, micro and mesoporosity, initiators, and strategies for process termination are evaluated under relevant variables including temperature, heating rate, vapor residence time, and pressure as encountered in industrial practice throughout Europe. The analysis demonstrates that polymer chain architecture constrains reaction pathways and attainable product profiles, while additives, catalyst residues, and contaminants in real waste streams can shift radical populations and observed selectivity under otherwise similar operating windows. For example, strong Bronsted acidity and shape selective micropores favor the formation of C₂ to C₄ olefins and Benzene, Toluene, and Xylene (BTX) aromatics, while weaker acidity and hierarchical porosity help preserve chain length, resulting in paraffinic oils and waxes. Increasing mesopore content shortens contact times and limits undesired secondary cracking. The use of suitable initiators lowers the energy threshold and broadens processing options, whereas diffusion management and surface passivation help reduce catalyst deactivation. In the case of PVC, continuous hydrogen chloride removal and the use of basic or redox co catalysts or ionic liquids reduce the dehydrochlorination temperature and improve fraction purity. Staged dechlorination followed by subsequent residue cracking is essential to obtain high quality output and prevent the release of harmful by products within European Union approved processes. Framing process design as a sequence that connects chain architecture, degradation chemistry, and operating windows supports mechanistically informed selection of catalysts, severity, and residence time, while recognizing that reported selectivity varies strongly with reactor configuration and feed heterogeneity and that focused comparative studies are required to validate quantitative structure to selectivity links. In European post consumer sorting chains, PS and PC are frequently handled as separate fractions or appear in residues with distinct processing routes, therefore they are not included in the polymer set analyzed here. Polystyrene and polycarbonate are outside the scope of this review because they are commonly handled as separate fractions and are typically optimized toward different product slates than the gas, oil, and wax focused pathways emphasized here. Full article

This work investigated the effects of gamma irradiation on the adsorption capacities of rice husk (RH) for the removal of Cu²⁺, Cr³⁺, and Zn²⁺ ions from aqueous solutions, with potential applications in wastewater remediation. RH samples were gamma-irradiated at doses up to 40 kGy and characterized using SEM-EDS, XRF, FTIR, XRD, and BET analyses. While morphological and textural changes remained subtle, FTIR and SEM-EDS confirmed the formation and intensification of oxygen-containing functional groups, including –OH, –COOH, and C=O, as well as increased exposure of silica (Si–O) on the surfaces, which substantially enhanced surface reactivity of RH toward metal ions. Batch adsorption experiments revealed that 40-kGy irradiated RH samples (RH-40) exhibited the highest removal efficiencies compared to non-irradiated and lower-dose samples (RH-0, RH-10, RH-20, and RH-30), specifically with improvements of 415% for Cu²⁺, 502% for Cr³⁺, and 663% for Zn²⁺ compared to RH-0, determined at the initial concentration of 10 mg/L. Kinetic studies also showed rapid adsorption within the first 10–15 min, dominated initially by boundary-layer diffusion, followed by chemisorption-driven equilibrium behavior. The pseudo-second-order (PSO) model provided an excellent fit for all metals (R² = 0.999), indicating maximum model-predicted kinetic capacities of 555.56 mg/g (Cu²⁺), 769.23 mg/g (Cr³⁺), and 434.78 mg/g (Zn²⁺). Langmuir isotherms also fitted well (R² = 0.941–0.995), with predicted monolayer capacities of 535.33 mg/g (Cu²⁺), 491.64 mg/g (Cr³⁺), and 318.88 mg/g (Zn²⁺). Freundlich modeling further indicated favorable heterogeneous adsorption, with K_F values of 42.614 (Zn²⁺), 20.443 (Cr³⁺), and 16.524 (Cu²⁺) and heterogeneity factors (n) greater than 1 for all metals. These overall results suggested that gamma irradiation substantially enhanced RH functionality that enabled fast and high-capacity heavy-metal adsorption through surface oxidation and carbon valorization. Gamma-irradiated RH, therefore, represented a promising, low-cost, and environmentally friendly biosorbent for wastewater treatment applications. Full article

The valorization of agro-industrial waste could be a strategy to improve organic waste management. The production of activated carbon (AC) is a path to use for this waste, with the aim of reducing its negative effects. AC is characterized by a high internal surface area, chemical stability, and oxygen-containing functional groups in its structure. This work is focused on the valorization of agro-industrial waste such as pineapple peel and coconut shells. These are made up of sucrose, glucose, fructose, and other essential nutrients, as well as cellulose, hemicellulose, and lignin. Activated Carbon was obtained with slow pyrolysis at 400 °C, for 4 h in a stainless-steel tubular reactor with physical activation. The obtained samples were analyzed using SEM, TGA, FTIR, and BET to verify the morphology, thermal degradation, functional groups and pores ratio of the AC, highlighting the presence of materials pore >10 µm. The TGA residual materials gave 16.3% of pineapple peel AC ashes and 0.2% of coconut AC. A C=C, C-H_X, CO, and OH stretching were observed in 400–4000 cm⁻¹. The peak intensity decreased once the biodiesel was treated with AC, because the traces of water and functional groups interacted actively, resulting a high content of bases. Activated carbon was used for dry cleaning of the obtained biodiesel from residual oil, which was effective in reducing pH and moisture levels in the biodiesel samples. Pore distribution was determined by BET, 5.6 nm for pineapple peel and 39.8243 nm for coconut shells. The obtained activated carbon offers a sustainable alternative to traditional carbon sources and contributes to the circular economy by recycling waste biomass. Full article

CO₂ valorization from real feedstocks through CH₄ tri-reforming (CH₄-TR), combining steam reforming (SR), dry reforming (DR), and partial oxidation (CPO) of methane in a single process, is a desirable strategy for greenhouse gas mitigation and syngas (CO + H₂) production. NiCo/γ−Al₂O₃ catalysts prepared by impregnation at different relative metal contents (Ni₅₀Co₅₀ and Ni₃₀Co₇₀) were investigated for CH₄-TR in a fixed-bed reactor under conventional heating and characterized by XRD, FESEM, and Raman spectroscopy after catalytic runs. This study focused on the role of the Ni/Co ratio and feed composition on selectivity for CO₂ valorization, syngas yield, and deactivation resistance. Both the catalysts showed high activity, with a superior performance of Ni₅₀Co₅₀ confirming Ni metal species as the active sites. While in DR, a slow deactivation occurred due to coke deposition, in CH₄-TR, the addition of small O₂ and/or H₂O amounts stabilized activity and selectivity due to surface carbon removal. Large O₂ and H₂O amounts strongly inhibited CO₂ conversion due to competition with CPO and SR, in the order CPO ≥ DR > SR. Interestingly, the stoichiometric CH₄-to-oxidants ratio favored the DR pathway, giving very high CO₂ conversion. Modulating CH₄ addition into real flue mixtures renders CH₄-TR on NiCo/γ-Al₂O₃ catalysts a favorable strategy for effective valorization of CO₂ industrial or biomass-derived streams. Full article