Search Results (1,004)

Water contamination by synthetic dyes such as malachite green (MG) remains a significant environmental and public health challenge due to their high toxicity, chemical stability, and resistance to biodegradation. In this study, a CaO-CuFe₂O₄ composite was synthesized through a sustainable route using eggshells and orange peel as agro-industrial waste precursors. Comprehensive structural, spectroscopic and microscopic analyses confirmed the coexistence of a predominant CaO-based phase with spinel CuFe₂O₄, together with nanometric features, satisfactory elemental dispersion and practical magnetic recoverability. Under the experimental conditions employed, the composite exhibited high adsorption performance towards MG, reaching an equilibrium capacity of 2288.4 mg g⁻¹ and 99.98% decolorization within 60 min. The kinetics were better described by the pseudo-second-order model, while the equilibrium behavior was more satisfactorily fitted by the Langmuir isotherm than by the Freundlich model. Thermodynamic analysis indicated that the adsorption process was favorable over the temperature range studied and became more pronounced at higher temperature. The results suggest that the adsorption behavior arises from the combined influence of surface chemistry, calcium-derived basic sites, ferrite-associated metal centers and interfacial accessibility, rather than from surface area alone. In addition, the material could be readily separated from aqueous solution using an external magnetic field, highlighting its practical post-treatment recoverability. Overall, this work demonstrates a viable waste valorization strategy for the development of a magnetically recoverable CaO-CuFe₂O₄ adsorbent for cationic dye removal. Beyond the specific case of MG, the study underscores the potential of agro-waste-derived hybrid oxides as application-relevant materials for water remediation. Full article

Amid growing environmental concerns regarding the use of non-biodegradable plastic packaging and its potential emerging contaminants, such as microplastics, currently among the most pressing global challenges, researchers in the food sector are increasingly pursuing sustainable alternatives. In this context, various organic sources have been explored for the development of innovative biocompatible films. These films exhibit properties such as low water vapor permeability, transparency, and biodegradability, and have recently gained active functionalities. These enable the extension of the shelf life of packaged foods by controlling microbial activity and oxidative degradation. Lipid-based compounds derived from animal and plant sources—including phospholipids, essential oils, free fatty acids, and saturated and polyunsaturated fatty acids—have proven highly effective when incorporated into films, leading to significant physicochemical, mechanical, and microbiological improvements in both the films and the packaged products. Owing to their high hydrophobic capacity, these lipids markedly reduce water vapor permeability, which is crucial for extending the shelf life of high-moisture foods. Studies have shown that the incorporation of lipid compounds can increase film tensile strength by up to 37% and enhance antioxidant activity by over 75%. Moreover, many of these compounds exhibit antibacterial and antimicrobial activities, becoming active on the surface of food in contact. However, many bioactive compounds have poor dispersion in aqueous solutions, limiting their effectiveness in the final product. When encapsulated with the aid of a lipid fraction, the bioavailability of these compounds is improved, and their release can be effectively controlled. This review aims to consolidate recent research on the production of biopolymer films incorporating various types of lipid compounds, highlighting their enhancements and potential applications in active food packaging systems. Full article

The prolonged use of traditional polyethylene mulch (PM) films has resulted in significant environmental issues, such as soil residues and white pollution, which pose challenges to sustainable agriculture. The transition from PM to fully biodegradable mulch (BDM) films has emerged as a prominent trend in contemporary farming practices. This study investigates the effects of various colors of biodegradable mulches on watermelon production and quality, with a particular emphasis on BDM in comparison to conventional PM. Within the 0.2–15.3 µm wavelength range, transparent variants demonstrate high light transmission, while the silver–black treatment exhibits greater reflectivity. The silver–black surface effectively reduces evaporation, maintaining soil water content 5–8% higher than that of PM. However, its thermal profile reveals periodic temperature increases similar to those observed with PM. The results indicate that BDM silver–black enhances biomass, root N and P levels, and leaf NPK retention compared to PM. Notably, among the BDM treatments, silver–black yielded the highest average fruit weight and width (7.68 kg, 22.83 cm), although these differences were not statistically significant when compared to PM. Additionally, it produced the highest soluble solids content (13.2 °Brix) at a significance level of p < 0.05 relative to PM. This finding suggests an enhancement in the soil’s capacity to retain moisture and its nutrient availability, thereby fostering plant growth. All treatments proved profitable and economically viable; however, the total inputs and outputs associated with BDM silver–black and CK-PM transparent yielded a satisfactory profit, ranging from $1937 to $2503 per hectare. These results advocate for the utilization of sensor-embedded mulch films and the silver–black color to optimize water and nutrient utilization, thereby promoting sustainable watermelon cultivation. Full article

This research focuses on developing bioplastic films using agrifood industrial waste, which included starch from avocado seed, cellulose from cornstalk, carrot and beet peel, and pulp from a food company in México. The films were produced with a matrix of gelatin and glycerol, and different formulations of starch and cellulose. The films were characterized and tested as wrappers of Manchego cheese. The films containing starch are transparent; films with cellulose showed opacity and paper-like structure. Films containing starch–cornstalk cellulose showed the highest hydrophobic properties. In turn, films with carrot cellulose had the highest plastic properties with high elongation capacity and the lowest Young modules; films with starch and other celluloses showed the opposite data. The highest thermal capacity was observed in films containing cellulose from cornstalks and beet waste. In turn, the highest temperatures of transition, crystallization, and melting were registered in films containing starch. Films with starch and cellulose served well as wrappers of Manchego cheese, conserving 92% of the weight of cheese after 21 days of storage at 4 °C. All films were biodegradable in compost after 10 days, and they were degradable by physicochemical factors after 40 days. Full article

Sustainable fertilizer technologies are essential to address nutrient losses, environmental pollution, and inefficiencies associated with conventional urea application. In this study, humic acid–functionalized starch (St–HA) gel coatings were developed and optimized via a Wurster fluidized-bed system to produce controlled-release urea granules, with an additional carnauba wax outer layer to further extend nutrient release duration. The coating formulation was synthesized through in situ crosslinking of tapioca starch with humic acid using N,N′-methylenebisacrylamide and potassium persulfate, yielding a cohesive film. A central composite rotatable design (CCRD) was employed to investigate the influence of atomizing air pressure, fluidizing air flow rate, fluidized-bed temperature, and spray rate on coating performance. Comprehensive characterization; including FTIR, XRD, rheological analysis, thermogravimetric studies, water retention, biodegradability, and surface abrasion, confirmed chemical crosslinking, structural stability, and mechanical robustness of the coatings. Nitrogen release analysis in both water and soil demonstrated a substantial extension of release longevity from less than 2 days (uncoated) to 18–20 days for St–HA-coated urea, and up to 28 days with the additional wax coating. Coated granules exhibited low abrasion (8–24%), high water-retention capacity, and 68% biodegradation in 60 days, ensuring environmental compatibility. The findings establish St–HA/wax hybrid coatings as a viable, eco-friendly strategy for controlled-release fertilizers, integrating renewable feedstocks with scalable industrial processing for precision nutrient management. Full article

The development of sustainable packaging materials with advanced functional properties is a key priority for the food industry. In this study, chitosan (CS)-based nanocomposite films incorporating titanium dioxide (TiO₂), zinc oxide (ZnO), hybrid ZnO_TiO₂ nanoparticles, lignin (LG), and nanolignin (nLG) were synthesized and comprehensively characterized. Structural analyses (FTIR, XRD, SEM) confirmed strong intermolecular interactions and homogeneous nanoparticle dispersion, particularly for TiO₂ and low ZnO concentrations. Mechanical testing showed that TiO₂ and ZnO significantly enhanced tensile strength (up to fourfold) and elongation at break. Among the prepared nanocomposite films, CS-TiO₂ films at 2 wt% exhibited the best balance of mechanical performance and antioxidant activity. Subsequent incorporation of LG and especially nLG into the CS-TiO₂ matrix further enhanced flexibility and toughness, antioxidant efficiency, and radical-scavenging activity above 90%, and improved UV-shielding capacity by reducing light transmittance. Moreover, antibacterial testing against Escherichia coli demonstrated that CS/TiO₂/nLG films achieved the highest reduction (~46%), attributed to synergistic electrostatic, oxidative, and phenolic mechanisms. Overall, CS/TiO₂/nLG nanocomposites emerge as multifunctional, biodegradable films with significant potential for next-generation active food packaging applications. Full article

Biopolymers such as chitosan are considered important candidates for water purification due to their non-toxicity, biodegradability, natural origin, biocompatibility, and potential for modification to provide additional capabilities, such as incorporating nanomaterials for magnetism to enable rapid separation or adding functional groups to enhance selectivity towards target adsorbates. This study investigated adsorption of Co (II), traced by Co-60 radionuclide, systematically evaluated in natural aquatic matrices selected according to water body type: seawater (Baltic Sea) and freshwater systems further distinguished as lentic (Lake Balsys) and lotic (Neris River) environments, using synthesized magnetite–chitosan nanocomposites (MCNs) with varying loadings of Fe₃O₄ (10–30 wt. %) nanoparticles providing different levels of magnetization. Comprehensive characterization (TEM, FTIR, AFM, XRD, and Mössbauer spectroscopy) confirmed successful integration of magnetite nanoparticles within the chitosan matrix and reproducible structural properties. An optimal magnetization of 11 emu/g was achieved at 20 wt. % Fe₃O₄, enabling rapid magnetic separation within <1 min without compromising sorption capacity. Adsorption isotherm models were applied to investigate the adsorption parameters, and sorption kinetics were studied, yielding a maximum adsorption capacity of 14.93 mg/g for MCN-10 in seawater and 11.95 mg/g for MCN-20 in freshwater with observed equilibrium within 120 min. These promising results indicate that the MCN is a suitable nanocomposite for the removal of Co (II) ions and the Co-60 radionuclide from aquatic media. Full article

Background/Objectives: Achieving effective hemostasis is a vital step in wound healing, particularly in cases of severe bleeding caused by surgical procedures or trauma. This study focuses on the development of chitosan-based dressings enriched with Heparin (hep)-loaded poly(butylene succinate) (PBSu) nanoparticles to combine hemostatic and anticoagulant properties. Methods: Chitosan, a biocompatible and biodegradable carbohydrate with inherent antibacterial and hemostatic properties, was chemically modified with 2-(N-morpholino)ethanesulfonic acid (MES) and 2-acrylamido-2-methylpropane sulfonic acid (AMPS) to enhance its swelling ability and hemostatic activity. PBSu nanoparticles were synthesized using an oil-in-water emulsification method and loaded with Hep to achieve controlled anticoagulant release. The dressings of the modified chitosan derivatives with the nanoparticles which were systematically characterized for morphology, chemical structure, swelling ability, loading capacity, and Hep release kinetics. Results: This dual-function system is designed to decouple local surface hemostasis from thrombotic processes: the chitosan matrix provides rapid topical hemostasis, while controlled heparin release from the nanoparticles aims to modulate excessive fibrin deposition, support microvascular perfusion, and exploit the pro-healing benefits of low-dose heparin reported in advanced wound dressings, particularly in high-risk or thrombotic-prone patients. In vitro and in vivo studies demonstrated their potential for promoting rapid hemostasis. Conclusions: These findings suggest that the integration of modified chitosan and Hep-loaded nanoparticles is a promising strategy for advancing wound care and hemostatic technologies. Full article

Over the past few decades, ionic liquids (ILs) have gained attention as electrolytes, although concerns about their environmental persistence and toxicity challenge their status as green solvents. In this framework, choline chloride (ChCl) offers a more sustainable alternative due to its low toxicity, biodegradability, and cost-effectiveness. Although ChCl has a high melting point, its combination with hydrogen bond donor compounds (HBDs) can result in liquid mixtures at much lower temperatures, known as deep eutectic solvents (DESs). This study presents a comparative evaluation of three ChCl-based DESs, glyceline, ethaline, and reline (obtained from mixtures of ChCl and glycerol, ethylene glycol, and urea), with a focus specifically on their potential as electrolyte candidates for supercapacitors. Using differential scanning calorimetry (DSC), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and nuclear magnetic resonance (NMR), we assess their thermal, electrochemical, and structural properties. All DESs displayed amorphous behavior and a strong tendency to remain liquid even at very low temperatures. Among them, ethaline showed the most promising electrochemical performance, exhibiting the lowest resistivity and the highest capacity. Full article

Composite superabsorbents (C-SAPs) that combine synthetic and polysaccharide components hold great promise for sustainable agriculture. They improve water management and enable the controlled release of agrochemicals. However, increasing the polysaccharide content to enhance biodegradability often reduces water absorption capacity. In this study, we explore plasticization with succinic acid esters as a strategy to overcome this limitation. Our goal is to establish structure–property relationships between plasticizer architecture and C-SAP performance. A series of carboxymethyl cellulose-based superabsorbents was synthesized via radical copolymerization. They were then plasticized with 5 wt.% of dibutyl succinate, di-sec-butyl succinate, or di-iso-butyl succinate. The resulting materials were characterized using FTIR spectroscopy, differential scanning calorimetry, rheological tests, swelling kinetics, and phytotoxicity assays against oilseed radish and common oat. Increased plasticizer branching and molecular volume enhanced polymer network elasticity, lowered the glass transition temperature (by up to 6 °C), and increased the equilibrium swelling ratio by up to 64% compared to the unplasticized C-SAP (661 ± 17 vs. 402 ± 10 g/g). All plasticized C-SAPs retained more than 80% of their initial swelling capacity over five swelling–deswelling cycles across pH 3.0–9.2. They also showed no phytotoxicity at agriculturally relevant concentrations. These findings demonstrate that molecular engineering of plasticizer architecture enables simultaneous optimization of water absorption and environmental safety in C-SAPs for agricultural use. Full article

Water contamination by heavy metals remains a major global challenge, requiring efficient, sustainable, and low-cost remediation materials. Chitosan and cellulose are recognized as effective biosorbents due to their high affinity toward metal ions, biodegradability, and availability. However, their individual limitations motivate the design of composite with enhanced properties. In this study, chitosan/cellulose composite hydrogel beads crosslinked with glutaraldehyde (CHB-CF-GLA) were synthesized and evaluated for Cu(II) removal under batch and dynamic conditions. The composite was characterized by FESEM-EDS, ATR-FTIR, XRD, swelling analysis, and determination of pH_pzc to elucidate its structural and physicochemical features. Batch experiments optimized pH, initial Cu(II) concentration, and adsorption capacity, while non-linear kinetic and isotherm models described the adsorption mechanism. The adsorbent exhibited good stability and reusability over multiple cycles. Fixed-bed column studies demonstrated that increasing bed height prolonged breakthrough and exhaustion times, while higher influent concentrations and flow rates led to earlier column saturation. The experimental breakthrough curves were well described by the Thomas and Yoon–Nelson models, whereas the Adams–Bohart model showed limited applicability. COMSOL Multiphysics 3.5 simulations validated the experimental data and predicted column performance. Overall, CHB-CF-GLA is an efficient and functional adsorbent with strong potential for continuous Cu(II) removal in water treatment applications. Full article

The rapid growth of synthetic textile production has intensified the release of micro- and nanoplastics (MPs/NPs) into aquatic environments, primarily through industrial effluents and domestic laundering. Textile-derived microplastics, especially polyester fibers and polymeric coating fragments, constitute a significant fraction of plastic contamination in wastewater systems. Although wastewater treatment plants (WWTPs) can remove a large proportion of MPs, substantial quantities accumulate in sewage sludge, raising concerns about long-term environmental persistence and secondary release pathways. This review critically examines the sources, classification, and release mechanisms of textile-based micro- and nanoplastics, including fibrous debris and coating-derived fragments. Then it focuses on current identification and removal technologies, such as sedimentation, coagulation/flocculation, electrocoagulation, flotation, membrane filtration, adsorption, and biodegradation, and on the emerging strategy of converting recovered microplastics into value-added porous carbon materials via hydrothermal treatment and pyrolysis. Carbonized microplastics exhibit high surface area and adsorption capacity for dyes, heavy metals, and organic pollutants, offering a circular approach that simultaneously mitigates plastic pollution and enhances wastewater treatment efficiency. By integrating source control, optimized removal technologies, and carbonization-based valorization, this review proposes a dual-benefit framework that transforms textile-derived microplastic waste from an environmental liability into a functional resource for sustainable water purification. Full article

Soil erosion is a critical issue on the Loess Plateau due to weak soil and intense summer rainfall. Plant roots provide essential soil stabilization. A split-plot field experiment was conducted in Liulin County, Shanxi Province, to evaluate the effects of biodegradable mulch and organic amendments on maize root development and soil stabilization. The main plots included no mulch (N) and biodegradable mulch (M). The subplots comprised five treatments: control (CK, no amendment), peat (PT), biochar (BC), fermented pig manure (PM), and corn stover (CS). Correlation and principal component analyses were used to elucidate the underlying mechanisms. The results showed that organic amendments were the primary factor influencing the root and soil properties. Peat and biochar significantly raised the root surface area density (RSAD, p < 0.05) and root–soil composite cohesion (with increases of 122.56% and 109.06% for NPT and NBC compared to NCK, respectively). Biodegradable mulch, and its interaction with the organic amendments, had no statistically significant effect on either the root–soil composite cohesion or root system parameters. The strong positive correlations of cohesion with the root length density (RLD, r = 0.80) and root volume density (RVD, r = 0.81) highlight that root occupancy is the key mechanism for enhanced shear resistance. Therefore, biochar is recommended for its effectiveness in enhancing soil retention and its potential co-benefits for carbon sequestration. This study provides a technical reference for sustainable agriculture on the Loess Plateau, while also acknowledging the need for further research on long-term carbon dynamics. Full article

In recent years, sustainable biopolymers have attracted increasing attention in environmental engineering as alternatives to conventional synthetic materials due to their renewable origins, biodegradability, and functional versatility. However, their performance and technological viability are strongly influenced by structural design, modification strategies, and behavior under realistic environmental conditions. This review critically analyzes recent advances in biopolymers for environmental remediation, covering their main application formats such as hydrogels, membranes, beads, aerogels, and composites, their interaction mechanisms with contaminants, and their performance relative to conventional adsorbents. Particular emphasis is placed on emerging approaches, including advanced functionalization, integration with inorganic phases, and green synthesis technologies, which have significantly improved efficiency, selectivity, and operational stability. Despite these advances, key limitations persist, particularly regarding mechanical robustness, regenerability, reproducibility, and scalability, underscoring the need for standardized evaluation protocols in complex matrices. The role of biopolymers within circular economy frameworks is also examined, emphasizing their capacity to integrate material sustainability, resource recovery, and multifunctional environmental applications. Overall, sustainable biopolymers are positioned not only as substitutes for traditional materials but also as strategic platforms for the development of next-generation regenerative environmental technologies. Full article

Due to its affordability, widespread availability, non-toxicity, biodegradability, and renewability, cellulose is considered a crucial material for addressing the depletion of petroleum resources. In this study, a rotaxane-based supramolecular polymer derived from thermoplastic polyurethane (TPU) was synthesized and combined with cellulose to create a TPU–cellulose composite (TPU-C). This composite was employed as a separator for acrylate-based quasi-solid polymer electrolytes (QPEs). The polymer electrolyte demonstrated a high ionic conductivity of 0.16 mS cm⁻¹ at room temperature, a lithium-ion transference number of 0.63, and an electrochemical stability window extending up to 4.7 V. When paired with a LiFePO₄ (LFP) cathode, the coin cell retained 88.8% of its capacity after 100 cycles at 1 C. A cell assembled with Li and a high-voltage NCM622 cathode maintained a capacity of 65.8% after 100 cycles at 0.3 C. Additionally, the excellent electrochemical performance was analyzed through density functional theory (DFT) calculations to identify the underlying reasons for its outstanding behavior. This study offers new insights into expanding the application potential of cellulose-based composite materials. Full article