Search Results (740)

The complete removal of persistent aromatic organic pollutants from aqueous environments demands the development of sustainable and highly efficient filtration materials. In this study, novel bio-sourced mixed-matrix membranes (MMMs) were successfully fabricated by incorporating the highly porous metal–organic framework MIL-68(Al) into a biodegradable polylactic acid (PLA) matrix via a solvent-induced phase inversion method. The integration of MIL-68(Al) nanoparticles significantly tailored the membrane’s morphological structure, endowing the hybrid membranes with enhanced surface hydrophilicity (water contact angle reduced from 90.3° to 72.7°) and superior permeability. The pure water flux reached an optimal value of 42.2 L m⁻² h⁻¹ at a 15 wt.% MOF loading. Crucially, the hybrid membranes exhibited exceptionally high adsorptive removal performance for p-nitrophenol (PNP) and methylene blue (MB). Driven by the abundant accessible active sites of the MOF filler, the MIL-20/PLA membrane achieved a maximum equilibrium adsorption capacity of 121.03 μg/cm² (36.90 mg/g) for PNP, representing a remarkable 25.7-fold enhancement over the pristine PLA membrane. Kinetic analyses confirmed that the adsorption process is strictly governed by pseudo-second-order kinetics, indicating a chemisorption mechanism dominated by hydrogen bonding and π–π stacking interactions. Furthermore, the optimized membranes demonstrated outstanding dynamic filtration efficiencies (>80%) and robust regenerability over multiple continuous operating cycles. This work not only highlights the synergistic interfacial effects between MOFs and biodegradable polymers but also provides a highly effective, eco-friendly, and sustainable membrane platform for the advanced remediation of organic-contaminated wastewater. Full article

Polylactic acid (PLA), a biodegradable polymer derived from renewable resources, represents a promising candidate for sustainable textiles. Nevertheless, its practical application remains limited by the requirement for high-temperature dyeing, which can induce polymer hydrolysis and lead to the loss of fiber strength. To address this limitation, PLA fabric was treated with an eco-friendly natural deep eutectic solvent (NaDES) composed of glycerol and citric acid. The treatment was found to enhance fiber surface roughness and internal looseness, which facilitated dye diffusion and allowed for a significant reduction in dyeing temperature. When dyed with microbial prodigiosin, the treated PLA fabric achieved a color depth at 70 °C that was equivalent to untreated fabric at 90 °C, while also exhibiting a 93.56% bacteriostatic rate against Staphylococcus aureus due to the inherent antibacterial property of microbial prodigiosin. This work provides a novel and sustainable strategy for the eco-friendly dyeing of PLA textiles. Full article

Polysaccharides are structurally diverse biopolymers composed of multiple monosaccharide units linked through glycosidic bonds. Their complexity, biodegradability, and functional versatility make them integral to biological systems as well as modern industrial application. Sourced from plants, fungi, marine organisms, animals, and microbes, these natural polymers exhibit a broad spectrum of bioactivities, including antioxidant, antimicrobial, immunomodulatory, and physicochemical protective functions. In the context of food preservation, polysaccharides have gained significant attention as sustainable alternatives to synthetic preservatives and conventional packaging materials. This review summarizes the classification and structural attributes of polysaccharides that influence their functional performance, particularly their ability to scavenge free radicals, inhibit foodborne pathogens, and form protective barrier systems. Special emphasis is placed on their use in edible films, coatings, and encapsulation systems that enhance the shelf life of fruits, vegetables, meats, dairy, beverages, and bakery products. Challenges related to stability, sensory impact, and regulatory compliance are also discussed. Overall, polysaccharides demonstrate substantial potential as eco-friendly, bioactive packaging agents and controlled-release carriers, contributing to safer, greener, and more sustainable food preservation technologies. Full article

Polyelectrolyte complexes (PECs) are recognized as promising materials for the development of sustainable food packaging. In this study, eco-friendly PECs based on pectin (P) and chitosan (C) were prepared by solvent casting at different pH values and volume ratios (C, P, 1C:1P, 1C:2.5P, and 1C:5P) (v/v). The resulting films were characterized for numerous features, including thickness, opacity, moisture content, swelling degree, and water solubility, while mechanical performance (elongation at break and tensile strength), water vapor transmission rate (WVTR), surface energy, and anti-adhesive activity were evaluated for the most promising formulation. The results revealed that blending chitosan with pectin significantly improved the films’ physicochemical properties, notably by increasing thickness (up to 100 µm) and opacity (slightly above 2) while reducing the swelling degree (from over 1800% for pure chitosan to below 600% for 1C:2.5P film at pH 3.2) and the water solubility (from 100% for pectin films to around 45–50% for the blended films). The film 1C:2.5P at pH 3.2 showed improved barrier performance, with a lower WVTR (approximately 20 g/h·m²) compared to the single polymer films (more than 30 g/h·m²), and exhibited significant anti-adhesive activity by reducing bacterial adhesion to below 5% compared to 65% for the conventional packaging film. However, these improvements were accompanied by reduced tensile strength (From ~4.2 MPa to ~1.3 MPa) and in elongation at break (from ~50% to ~20%). Overall, PEC films demonstrate strong potential as sustainable packaging materials by combining improved barrier properties and anti-adhesive activity, despite some limitations in mechanical resistance. Full article

Plastic manufacturing depends heavily on petroleum-derived monomers like terephthalic acid, the main component of polyethylene terephthalate (PET). However, the depletion of fossil resources and increasing environmental concerns have heightened the need for sustainable alternatives. Lignocellulosic biomass has emerged as a promising resource due to its renewable, abundant, and eco-friendly nature. Understanding its chemical composition enables conversion of this biomass into platform chemicals, such as 2,5-furandicarboxylic acid (FDCA) and lactic acid, derived from cellulose and hemicellulose. These can be polymerized into bio-based plastics such as polyethylene furanoate (PEF), polylactic acid (PLA), and polyhydroxyalkanoates (PHAs), offering greener alternatives to fossil-based plastics. PEF features rigid furan rings that enhance thermal stability, mechanical strength, and barrier properties, and reduce gas permeability compared to PET. PLA is a renewable, biodegradable plastic widely used in packaging and medical applications. This review covers the chemical composition of lignocellulosic biomass cellulose, hemicellulose, and lignin, and various pretreatment strategies, chemical, physicochemical, and physical, to overcome biomass recalcitrance and improve conversion efficiency. It also highlights recent catalytic advances in transforming cellulosic carbohydrates into bio-based plastic precursors such as FDCA and lactic acid. Lastly, this review discusses polymerization pathways for producing PEF and PLA, emphasizing their role in reducing the environmental impact of polymer manufacturing and promoting green chemistry principles. Full article

Hydrocolloids are an extremely diverse and valuable group of materials, with various sources, properties and applications in many industries. Increasingly, naturally sourced colloids have gained the interest of the scientific world for their bio-availability, eco-friendliness and bio-degradability. This, coupled with emerging “green” extraction methods and modifying techniques, opens a wide range of uses. Pectin is a well-known, natural and abundant biomaterial, a heterogeneous anionic polysaccharide with vast applications in the food and pharmaceutical industries. Traditionally used in the food sector as a gelling agent and thickener, it is considered safe for human consumption. Pectin has found new applications in the pharmaceutical and medical worlds due to its complex structure, and it provides variety in its properties. This paper brings together information about this polysaccharide’s genuine usefulness in the context of growing interest for naturally sourced polymers, the reduction in wasteful industrial practices and environmental protection. Full article

This work describes the fabrication of an eco-friendly sponge for the removal of dyes from aqueous solutions. For this purpose, a reused cellulose sponge (CS) that is commercially sold for makeup was covered with polyaniline (PANI), a conductive polymer that allows the addition of functional groups that are compatible with dyes present in aqueous solutions. An SEM analysis showed the successful deposition of PANI over CS fibers and confirmed that the porosity of the sponge remained after the polymerization step. The adsorption performance of the PANI-CS was evaluated in batch mode using methyl orange (MO). The adsorption capacity was 308 mg/g at pH 4.0 and after 110 min. PANI-CS achieved an adsorption percentage of 84% (C_o = 25 mg/L MO) after only 20 min. The experimental data were adjusted to different isotherm adsorption models; the best fit was obtained using the Halsey model. Furthermore, the adsorption performance of PANI-CS was studied in continuous mode using a bespoke adsorption column with recirculation. The results indicated that after 5 min of interaction time, 59% of the initial MO concentration (25 mg/L) was adsorbed. These results show the potential of PANI-CS as an inexpensive adsorbent for large-scale adsorption of dyes from aqueous media. Full article

Ground granulated blast furnace slag (GGBFS)-based cementitious materials, known for their high strength and good fluidity, present an eco-friendly, low-carbon alternative to ordinary Portland cement (OPC). However, the high cost of activators poses a significant challenge, accounting for over 50% of alkali-activated material production costs. This study uses carbide slag (CS), a byproduct of polyvinylchloride (PVC) production, as an activator, along with other solid wastes such as GGBFS and fly ash (FA) as precursors to develop a novel, low-carbon alkali-activated material binder made entirely from solid waste. Various mixtures with different proportions of CS and GGBFS were prepared, and their workability and strength were tested at different ages. Additionally, the hydration characteristics and microstructure of the samples were analyzed using XRD, TG-DTG, FTIR, heat of hydration tests, and SEM-EDS. Results show that calcium hydroxide in CS activates the pozzolanic activity of GGBFS and FA, improving the strength as the proportion of CS increases. At the 5% CS content, the 7 days compressive strength of the GGBFS-based alkali-activated material increased by 79.7% compared to a 2% CS content. However, adding CS reduces the workability of the polymer slurry, with a spread decrease of 168.5 mm and 161.5 mm as the CS content increases from 2% to 8%. The inclusion of CS also increases the rate and total heat released during hydration, with the optimal performance observed at 5% CS. While FA incorporation reduces strength, it enhances slurry workability and reduces heat release during hydration. The strength development is attributed to the formation of AFt, C-S-H gel, C-(A)-S-H gel, and hydrocalumite-like hydrates. Full article

The development of sustainable plant protection strategies requires stable and environmentally compatible delivery systems for beneficial microorganisms. In this study, Bacillus subtilis was encapsulated within chitosan-based cast films to evaluate bacterial viability, sustained biological activity, and antifungal efficacy. Films prepared from chitooligosaccharide (COS) and chitosans of low, medium, and high molecular weight (CS-LMW, CS-MMW, CS-HMW) were characterized in terms of morphology, mechanical performance, and pH-dependent swelling behavior. The viscosity of the chitosan solutions increased markedly with molecular weight from 73 cP (COS) to 614 cP (CS-HMW), while film thickness ranged from 34 ± 1.5 to 57 ± 2.3 µm. Mechanical performance improved significantly with increasing molecular weight, with maximum tensile stress exceeding 200 MPa for CS-HMW films, while swelling studies confirmed pronounced pH-dependent behavior consistent with the polyelectrolyte nature of chitosan. Encapsulation effectively preserved bacterial viability and metabolic activity over time. The intrinsic antifungal activity of chitosan synergized with the biocontrol activity of B. subtilis against Fusarium avenaceum and Alternaria solani. The highest antifungal performance was observed for CS-HMW films, which produced inhibition zones up to 84.6 ± 5.0 mm against A. solani. These findings demonstrate that chitosan-based cast films serve as effective carriers for beneficial microorganisms, providing environmental protection and regulated biological activity. The combination of a bioactive polymer matrix with a potent biocontrol agent represents a promising eco-friendly approach to sustainable plant protection. Full article

In this work, a hybrid polymer electrolyte integrating single- and dual-ion conducting systems was developed for lithium-ion batteries using bio-based materials, namely oleic-acid derivatives and epoxidized soybean oil, through an in situ polymerization process. The fixed FSI anions in LiEFSOA enhance the selectivity of Li⁺ transport, while the cross-linked network formed by ESO provides mechanical stability, and the LiFSI incorporated into the polymer matrix helps maintain sufficient overall ionic conductivity. In addition, the long C18 oleic chains increase the internal free volume of the matrix, thereby improving segmental mobility within the amorphous phase. The in situ polymerization inside the cell causes intimate interfacial contact between the electrode and electrolyte, achieving an ionic conductivity of 1.05 × 10⁻⁴ S cm⁻¹ at 30 °C. Electrochemical evaluation using LiFePO₄/FSOA-2/Li cells shows an initial discharge capacity of 149.09 mAh g⁻¹ and a capacity retention of 81.09% after 100 cycles, and the average coulombic efficiency was 99.62%, demonstrating that the designed FSOA electrolyte exhibits stable cycling performance and competitive capacity. Overall, the combination of eco-friendly materials and a hybrid ion transport strategy provides a promising platform for developing sustainable and high-performance polymer electrolytes for lithium-ion batteries. Full article

This study explored the dual chemical modification of starch isolated from red lentils (Lens culinaris) to develop a biodegradable polymer with enhanced functionality for multifaceted applications. Native starch was isolated via combined salt–alkali treatment and sequentially modified through epichlorohydrin-mediated crosslinking, followed by cationization using glycidyl trimethylammonium chloride (GTAC). Utilizing a Quality by Design (QbD) strategy through Response Surface Methodology (RSM), the cationization endured fine-tuning to reach an optimal degree of substitution (DS = 0.572) under foremost conditions (GTAC: 2.1 mol, NaOH: 0.09 mol, reaction time: 18 h). Structural and functional characterization using FTIR, XRD, TGA, SEM, and zeta potential analysis confirmed the successful modification, indicating enhanced thermal stability, a transition to a more amorphous structure, and a moderately positive surface charge (+7.24 mV). The dual modified cationic lentil starch (CLS) demonstrated effective flocculation of kaolin suspensions, achieving a transmittance of up to 94%. Additionally, CLS showed significantly improved emulsion stability, maintaining over 70% stability after 24 h, compared to native starch, which dropped below 30%. These results emphasize the promising potential of CLS as an eco-friendly and high-performance alternative to synthetic polymers for water treatment and stabilization of emulsion-based formulations. Full article

Lignin nanoparticles (LNPs) offer sustainable alternatives to petroleum-derived nanofillers, yet their industrial application remains limited by poor dispersion control and trade-offs between loading, optical clarity, and mechanical performance. Here, we present a molecular architecture-driven design framework that systematically decouples polymer network physics from nanoparticle dispersion in poly(vinyl alcohol)/LNP nanocomposites. Through eco-friendly self-precipitation, we synthesize uniform LNPs with size tunability, overcoming persistent reproducibility challenges. Systematic investigation across PVA molecular weights and LNP loadings reveals entanglement-controlled dispersion behavior. Combined rheological and small-angle X-ray scattering analyses demonstrate that macroscopic suspension rheology is governed exclusively by polymer chain overlap, remaining invariant across LNP loadings. Conversely, the nanoscale LNP microstructural organization—ranging from depletion-driven clustering in weakly entangled networks to network-confinement stabilization in densely entangled systems—fundamentally dictates the film’s optical clarity and mechanical toughness. This rheology-microstructure decoupling establishes critical processing windows for industrial formulations, where polymer entanglement ensures suspension processability while the LNP dispersion state enables optical–mechanical tunability. The entangled network’s structure-filtering effect provides robust protocols for fabricating sustainable, transparent bio-composites suitable for packaging, optics, and functional films. Our quantitative composition–structure–performance framework advances fundamental understanding of entanglement-mediated interfacial phenomena while delivering practical design rules for next-generation sustainable bio-composites. Full article

Coastal ecosystems of the tropical Atlantic and the Mexican Caribbean have experienced recurrent massive influxes of pelagic brown macroalgae, Sargassum natans and Sargassum fluitans, generating severe environmental, social, and economic impacts. While the accumulation of this biomass poses a significant waste management challenge, it also represents an underexploited renewable resource aligned with circular economy and sustainability principles. This study investigated the valorisation of Sargassum spp. through comprehensive physicochemical characterisation and multiple value-added applications. The biomass collected in Tulum, Quintana Roo, Mexico, was analysed to determine its chemical composition, including lignin, holocellulose, α-cellulose, ash, and moisture content, using standardised methods of the Technical Association of the Pulp and Paper Industry (TAPPI). For mechanical testing, methods from the American Society for Testing and Materials (ASTM) were used. The biomass was subjected to controlled pretreatment and thermochemical conversion processes. Evaluated valorisation pathways included: (1) taxonomic identification and physicochemical characterisation, (2) polymer composites, (3) reinforcement in construction materials such as unfired clay bricks, and (4) biochar and activated carbon production for contaminant adsorption. The results demonstrated that Sargassum spp. biomass can be transformed from an environmental nuisance into a multifunctional, high-value biomaterial, providing scalable solutions that mitigate waste disposal challenges and contribute to climate and resource sustainability. Full article

This review examines biodegradable polymer-based core–shell nanoformulations encapsulating essential oils for acne treatment through the lens of physicochemical design and controlled delivery mechanisms. Acne is a common inflammatory skin disorder closely associated with sebum overproduction and microbial imbalance, while conventional therapies, although effective, may present long-term side effects. Increasing attention has therefore turned to sustainable dermatological materials derived from eco-friendly polymers combined with naturally active compounds. Recent advances show that core–shell nanostructures fabricated from biodegradable polymers function as physicochemically engineered carriers for volatile essential oils. They enhance their stability and protect them from premature degradation. They also enable controlled release governed by diffusion, polymer relaxation, interfacial interactions, and degradation kinetics. This review highlights how polymer chemistry, interfacial properties, particle morphology, and processing routes determine encapsulation efficiency, release profiles, and skin permeation behaviour. Particular emphasis is placed on structure–property–function relationships, including mass transport phenomena, thermodynamic compatibility between polymers and essential oils, surface charge, wettability, and nanostructure architecture, which collectively influence bioavailability and therapeutic performance. By integrating concepts from polymer physical chemistry, colloid and interface science, and drug delivery kinetics, these sustainable nanoformulations emerge as promising platforms for acne and sebum control. Overall, essential oil-loaded biodegradable polymeric core–shell systems represent a sustainable and scientifically grounded approach to acne management, although further physicochemical characterization, in vivo validation, and consideration of cost, technical challenges, and current limitations are required to support clinical translation. Full article

Microfibrillated cellulose (MFC) derived from wood sources is a biodegradable and eco-friendly reinforcing material for polymer composites. However, the high polarity of MFC is a challenge in homogeneous distribution into the hydrophobic PLA matrix, which limits its reinforcing efficiency. In this study, lignin-containing MFC (LMFC) with different residual lignin contents was prepared to investigate its dispersion behavior and reinforcing effect in polylactic acid (PLA). The aspect ratio and neutral sugar composition of LMFC remained similar regardless of lignin content, whereas the dispersion degree in PLA, quantified using a log-normal distribution model, increased from 24.2% to 35.1% with increasing lignin content. Mechanical testing showed that LMFC incorporation enhanced tensile strength and elastic modulus while reducing elongation at break. Higher residual lignin content in LMFC positively affected the tensile strength of the LMFC–PLA composites. Dynamic mechanical analysis revealed an increase in storage modulus and a decrease in loss factor with higher lignin content and LMFC loading (1–10 wt%), indicating enhanced interfacial interactions. Differential scanning calorimetry showed reductions in glass transition temperature (5–8 °C) and cold crystallization temperature (8–16 °C) compared to neat PLA. These findings indicate that residual lignin in LMFC enhances dispersion and interfacial interactions in PLA, leading to improved mechanical and thermal performance and highlighting its potential as an effective reinforcing component in sustainable biocomposites. Full article