Search Results (224)

The study investigated the tensile strength and elongation properties of abaca fiber-reinforced polymer (AFRP) composites after varying durations of seawater soaking, with a focus on their potential for reinforcing fiber-optic cables. It aims to bridge industrial technology education, experiential learning, and green technology by evaluating abaca fiber as a sustainable alternative to synthetic aramid yarn. Conducted at Caraga State University, Cabadbaran Campus (CSUCC), the research utilized a quasi-experimental product development design involving industrial technology students and instructors. Tensile strength testing and comparative analysis were performed on abaca fiber samples (A, B, and C) subjected to different seawater soaking durations. Results show that soaking time significantly affects the fiber strength, with Sample A achieving the highest tensile strength (5631.5 MPa) and Sample C the lowest (1679.8 MPa). Findings indicate that prolonged exposure to seawater weakens abaca fiber, emphasizing the need for controlled treatment to optimize its industrial applications. This study emphasizes the importance of hands-on learning in industrial technology education, promoting critical thinking and technical skills while underscoring sustainability. The research advocates for eco-friendly materials in industrial applications and highlights the potential of abaca fiber composites. Future studies should investigate pre-treatment methods to enhance fiber durability, assess the long-term environmental performance, and conduct large-scale pilot testing to evaluate commercial viability. By integrating sustainable innovations into industrial technology education, this study contributes to advancing natural fiber composites for manufacturing and telecommunications infrastructure. Full article

Ornamental fountains in the Alhambra and Generalife (Granada, Spain) constitute complex socio-ecological systems where water, stone, and biological communities interact, making them highly vulnerable to biodeterioration caused by phototrophic microorganisms such as cyanobacteria, green algae, and diatoms. Conventional chemical biocides, although widely applied, present significant drawbacks including toxicity, material degradation, ecological imbalance, and limited long-term effectiveness. In this context, this study evaluated the potential of algicidal bacteria as a sustainable alternative for controlling phototrophic growth in heritage environments. Water samples from eight ornamental fountains were analyzed using 16S ribosomal RNA (16S rRNA) gene sequencing to characterize bacterial communities and identify taxa previously reported with algicidal activity. Statistical analyses were conducted to assess relationships between microbial community structure and biofilm development. In parallel, functional screening assays using filtered fountain waters against Chlorella vulgaris were performed to evaluate intrinsic inhibitory capacity. The most active sample was selected for bacterial isolation and further validation through co-culture assays, cell density measurements, and pulse-amplitude-modulated (PAM) fluorometry. A total of 18 genera with reported algicidal capacity were detected, representing a substantial fraction of the microbiome across all samples. However, no significant association was found between these taxonomic metrics and biofilm development, highlighting a decoupling between taxonomic composition and functional activity. The most active isolate, identified as Stenotrophomonas maltophilia strain LIG25, caused a rapid decline in photosynthetic efficiency and achieved more than 98% inhibition of algal growth. These findings demonstrate that ornamental fountain microbiomes represent a reservoir of native biocontrol agents and support the development of eco-friendly strategies for cultural heritage conservation. Full article

Background: Increasing antifungal resistance, poor mucosal retention, and systemic side effects limit the effectiveness of currently available drugs. This study explores a novel topical nanotherapeutic approach for the targeted treatment of vulvovaginal candidiasis (VVC), employing green-synthesized silver nanoparticles (AgNPs) derived from Ascophyllum nodosum (AN) and incorporating ibrexafungerp citrate (IBC) into a liposomal formulation. Methods: AgNPs were biosynthesized using AN extract and characterized. Liposomes were prepared by thin-film hydration, and optimised using Central Composite design and characterized and optimized. Optimised liposomes, co-loaded with IBC and AN-AgNPs, were incorporated into a Carbopol-CMC-based topical gel. Results: FTIR shifts in the –OH (3332.31 cm⁻¹) and carbonyl (1636.87 cm⁻¹) bands with reduced intensity confirmed their involvement in Ag⁺ reduction and nanoparticle surface coordination, while the persistence of the 1015 cm⁻¹ band indicated the role of polysaccharides in capping and stabilizing the AN-AgNP. Characterization of the optimized liposomes (IBCL-11) revealed a particle size of 127.2 nm, a zeta potential of −43.8 mV, and a polydispersity index (PDI) of 0.35. Transmission Electron Microscopy (TEM) confirmed the presence of intact, spherical vesicles, while Differential Scanning Calorimetry (DSC) and X-ray diffraction (XRD) validated the molecular dispersion and amorphous characteristics of the films. In vitro evaluations of the IBC liposomal gel demonstrated a sustained drug release of 72.6% over 24 h, alongside enhanced drug penetration across all skin layers. Antifungal assays highlighted the formulation’s potent efficacy, yielding Minimum Inhibitory Concentration (MIC) and Minimum Fungicidal Concentration (MFC) values below 1 µg/mL. Furthermore, the treatments exhibited strong anti-biofilm properties; at MIC and MBC levels, AN-AgNPs achieved biofilm reductions of 45.27 ± 3.16% and 27.62 ± 2.13%, respectively, whereas IBCL-11 produced reductions of 34.25 ± 2.43% and 16.28 ± 1.72%. Conclusion: Ultimately, this study successfully developed an eco-friendly liposomal formulation co-loaded with AN-AgNPs and IBC, offering a promising and targeted therapeutic approach for the treatment of vulvovaginal candidiasis. Full article

Background: The invasive macroalga Rugulopteryx okamurae poses severe environmental challenges but presents an opportunity as a sustainable source of valuable carbohydrates. This study develops an eco-friendly method to extract monosaccharides from this biomass. Methods: Ultrasound-assisted extraction (with sonotrode) using water as the solvent was optimized with Design of Experiments, and the time, power and mass:solvent ratios were evaluated. The monosaccharide composition was evaluated by gas chromatography coupled to high-resolution mass spectrometry (GC-QTOF). Results: The analytical method was validated for accurate monosaccharide quantification using oximes and silylation, achieving a fast time of analysis (<20 min). The optimized UAE (1:15 mass:solvent ratio, 70% power, 30 min) yielded a total monosaccharide concentration of 210 mg mL⁻¹, significantly outperforming traditional acidic hydrolysis. Compared to the extraction of monosaccharides from the well-known seaweed Ulva ohnoi (31 mg mL⁻¹), it is far superior. Mannitol comprised 95% of the total extract. Conclusions: This scalable and green UAE methodology valorizes this seaweed by achieving high yields of simple sugars, offering a sustainable resource for industrial applications while mitigating the environmental impact of this invasive species. Full article

Silver nanoparticles (AgNPs) have attracted substantial scientific interest in biomedical research owing to their unique physicochemical characteristics, broad-spectrum antimicrobial activity, plasmonic properties, and therapeutic versatility. Although conventional physicochemical synthesis methods enable controlled NPs fabrication, their dependence on hazardous reagents, elevated energy input, and environmentally detrimental processing conditions has stimulated the development of sustainable biogenic alternatives. Biological synthesis utilizing plants, microorganisms, fungi, algae, and purified biomolecules has emerged as an eco-friendly and bio-compatible strategy for AgNP fabrication, enabling simultaneous reduction, stabilization, and intrinsic biofunctionalization of NPs. However, traditional biogenic synthesis remains constrained by limited mechanistic understanding, poor batch reproducibility, inadequate control over physicochemical properties, and challenges in large-scale manufacturing. Recent advances in bioengineering have transformed this field through the integration of metabolic engineering, synthetic biology, microfluidic-assisted synthesis, artificial intelligence-guided process optimization, and continuous-flow biomanufacturing, collectively enabling precision fabrication of biogenic AgNPs with enhanced uniformity, scalability, and functional tunability. Furthermore, strategic surface engineering and functionalization have expanded the applicability of biogenic AgNPs across targeted anticancer therapy, antimicrobial intervention, wound healing, regenerative medicine, drug delivery, and theranostic imaging. Despite these advancements, critical challenges remain regarding nano–bio interactions, toxicological safety, regulatory compliance, and translational scalability. Unlike conventional reviews focused primarily on green synthesis approaches, this review critically highlights emerging bioengineering paradigms that enable programmable, scalable, and precision-controlled biogenic AgNP fabrication. This review comprehensively examines next-generation paradigms and strategies for AgNPs biosynthesis, elucidates the molecular mechanisms governing their formation, highlights emerging functionalization and biomedical application paradigms, and discusses current translational barriers. Forming biogenic composites of AgNPs and heteroatom doped carbon nanodots needs intense research in near future. Full article

Covalent organic framework materials (COFs) are promising for pollutant adsorption owing to their high specific surface area, tunable pores and functional designability, but their microcrystalline powder form leads to poor mechanical strength and processability, limiting practical applications. This study presents a mild, eco-friendly strategy using polysulfonamide fiber (PSA) with excellent mechanical and thermal stability as the core matrix, and room-temperature-synthesized sulfonic acid-functionalized TFP-DABA-COFs as the shell layer. Via coaxial wet spinning, core–shell structured PSA-COF composite fibers were fabricated without harsh solvothermal conditions, improving COF dispersion and interfacial bonding. Characterizations revealed the fibers possessed favorable comprehensive properties: fracture strength of 14.97 MPa, elongation at break of 32.84%, specific surface area of 8 m²/g, and hierarchical porous structures dominated by micropores, with enhanced hydrophilicity beneficial to aqueous adsorption. Adsorption experiments on woven fabrics showed 93.6% methylene blue removal in 40 min and 98.9% in 120 min, following the quasi-second-order kinetics, indicating chemisorption (electrostatic attraction) as the main mechanism. This work provides a mild, green approach to prepare PSA-COFs core–shell fibers, effectively solving the formability and processing issues of COFs. Full article

The extensive use of 2,4-dichlorophenoxyacetic acid (2,4-D) in agriculture has led to water contamination and associated health risks, highlighting the need for eco-friendly detection strategies. Herein, Fe₃O₄ nanoparticles were green-synthesized for the first time using an aqueous extract of Rumex nervosus (R. nervosus) as a natural reducing and stabilizing agent and successfully employed for the electrochemical sensing of 2,4-D, representing the first reported application of R. nervosus-mediated Fe₃O₄ nanoparticles for this purpose. The phytochemical composition of the extract and synthesized R-Fe₃O₄ nanoparticles were systematically characterized. The R-Fe₃O₄-modified glassy carbon electrode (GCE) was evaluated for charge transfer properties using electrochemical impedance spectroscopy (EIS). Cyclic voltammetry (CV) showed no redox peak for 2,4-D at the bare GCE, whereas R-Fe₃O₄/GCE exhibited a distinct reduction peak at ~−1.5 V in 0.1 M phosphate buffer (pH 7), attributed to reductive dechlorination. Square-wave voltammetry (SWV) exhibited a linear response over the concentration range of 50–325 µM with a detection limit of 3.35 µM for 2,4-D. Although this performance is slightly above the guideline limits recommended by the World Health Organization (~0.14 µM) and the United States Environmental Protection Agency (~0.32 µM), it is suitable for the routine monitoring of elevated 2,4-D levels in environmental samples. The sensor demonstrated high selectivity with negligible interference and satisfactory recoveries of 96.6–98.3% in real water samples. Full article

With the rapid intensification of industrial and agricultural activities, water contamination by heavy metal ions has emerged as a critical global challenge, gravely imperiling ecosystem stability and public health. Among the various remediation technologies, adsorption has been widely adopted due to its high efficiency, low-cost water treatment, and simplicity of operation. However, conventional inorganic or synthetic adsorbents often exhibit poor degradability and pose a risk of secondary contamination, substantially limiting their sustainable application. Consequently, the development of environmentally benign and renewable adsorbent materials has become a central research focus in this field. Recently, cellulose-based composite hydrogels, derived from renewable resources and characterized by excellent eco-friendliness and highly tunable three-dimensional porous structures, have attracted considerable attention as promising green adsorption materials. These hydrogels demonstrate outstanding performance in the efficient sequestration of heavy metal contaminants from aqueous environments. This review systematically summarizes recent advances in cellulose-based composite hydrogels for heavy metal removal, to elucidate the structure–performance relationships linking material fabrication strategies, structural modulation, and adsorption efficiency. First, we outline the principal construction approaches, including physical crosslinking, chemical modification, and supramolecular self-assembly, and comprehensively analyze how different synthesis routes regulate pore architecture, mechanical properties, and the distribution of surface functional groups. Second, the underlying adsorption mechanisms, primarily coordination complexation, electrostatic interactions, and ion exchange, are discussed in detail. Finally, recent studies on the adsorption of cationic heavy metals (e.g., Pb(II), Cu(II), and Cd(II)) and anionic oxyanions (e.g., As(III) and Cr(VI)) are critically reviewed, with particular emphasis on the relationships between selective adsorption performance, material design principles, and specific recognition mechanisms. Overall, this review provides a theoretical foundation and practical guidance for the design and development of next-generation water treatment materials with high adsorption capacity, excellent selectivity, non-toxicity, and strong environmental compatibility, followed by future research recommendations. Full article

Conventional powdered biochar encounters severe bottlenecks in practical water treatment, such as difficult separation, easy loss, and potential secondary pollution. This work aimed to develop recyclable and high-performance adsorbents by preparing iron-doped biochar/sodium alginate composite microspheres (BC/MBC500-ALF) through Fe³⁺ cross-linking. Using corn stalk biochar and KMnO₄-modified biochar as adsorbent components and sodium alginate (SA) as a green shaping matrix, SA formed a stable egg-box hydrogel network to convert powdered biochar into uniform microspheres. Batch adsorption experiments revealed that the optimal pH for oxytetracycline (OTC) adsorption was 9, with adsorption capacities of 136.28 mg/g for BC500-ALF and 182.91 mg/g for MBC500-ALF. Kinetic analysis showed that BC500-ALF followed pseudo-first-order kinetics (R² = 0.983) dominated by physisorption, while MBC500-ALF fitted pseudo-second-order kinetics (R² = 0.994) dominated by chemisorption. The maximum Langmuir adsorption capacities at 308 K were 220.75 mg/g and 495.05 mg/g, respectively. Thermodynamic parameters confirmed a spontaneous and endothermic process. The adsorption mechanisms involved hydrogen bonding, π–π stacking, electrostatic attraction, metal-bridging complexation, and Fe–Mn oxide-mediated redox reactions. SA exerted dual functions in structure stabilization and adsorption enhancement. This composite provides an efficient and eco-friendly approach for tetracycline antibiotic pollution control in aqueous environments. Full article

The present work aimed to obtain antibacterial wound dressings using bacterial cellulose (BC) as a support, to improve wound treatment and reduce the incidence of infections. To enhance the antibacterial activity of the synthesized dressings, the introduction of ZnO nanoparticles into the BC network by precipitation was pursued. The method chosen to develop ZnO NPs was green synthesis, an ecological and sustainable method for obtaining nanomaterials using plant extracts as reducing agents or stabilizers. Thus, the chosen plants were Ginger rhizomes, Bay leaves, and Rose hips, in both fresh and dry form, due to the natural benefits they possess, and the Soxhlet method was used to obtain the plant extracts desired to be used in the synthesis. The composite dressings were developed in two distinct sample series, differentiated by the immersion time of BC in the precursor Zn²⁺ solution. The samples in the first series were obtained by precipitation in a mixture of Zn²⁺ solution and natural extract, whereas the samples in the second series were obtained by successive immersion in Zn²⁺ solution and then in natural extract, which demonstrated a considerable difference. The best antimicrobial activity tested against Gram-negative bacterium Escherichia coli was recorded for the composite material obtained in the presence of fresh rose hip extract, an aspect most likely related to the morphological and crystalline features of the ZnO phase, but also to the phytochemical profile of the extract used. Such eco-friendly materials represent valuable candidates for wound dressing applications due to their ability to support wound healing, relief burns, and skin irritation, provide antimicrobial protection, promote skin regeneration and reduce scarring, protect sensitive skin, and act as a barrier against external contaminants. Full article

Hybrid rocket technologies are gaining recognition as eco-friendly alternatives to traditional propulsion systems. Utah State University’s Propulsion Research Laboratory has developed a High-Performance Green Hybrid Propulsion (HPGHP) technology, leveraging 3D-printed ABS fuel for reliable, low-energy ignition. Among tested materials, only ABS shows suitable electrical-breakdown properties for arc ignition. Unfortunately, due to the proprietary formulations in commercial ABS blends, and its limited use as a rocket-propellant, related composition and combustion data are limited. This study uses spectroscopic evaluation and bomb calorimetry to estimate material compositions, enthalpies of formation, and combustion energies for multiple commercially available 3-D print feed stock ABS types, finding minimal differences amongst the samples tested. Based on these test results, “representative” ABS properties including chemical formula, mean molecular weight, enthalpy of formation, and Higher Heating Value, is recommended. Follow-on tests with 5 alternative, commonly used, 3D-printable thermoplastic feed stocks demonstrate that ABS has significantly higher energy content. This result supports ABS’s advantages and utility as a conveniently fabricated hybrid rocket fuel. 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

Currently, the resource wastage and safety hazards caused by fruit and vegetable spoilage are becoming increasingly prominent. Developing green, efficient, and non-toxic novel preservation materials has emerged as a hot spot in fruit and vegetable research. Based on this, this study utilized pomegranate peel as a raw material to prepare spherical multifunctional carbon dots (P-CDs) with an average particle size of 1.98 ± 0.58 nm through a one-step hydrothermal reaction. Subsequently, P-CDs were co-incorporated with L-cysteine (L-Cys) into a polyvinyl alcohol (PVA) and chitosan (CS) matrix to construct a novel composite coating material with combined antibacterial, antioxidant, and preservation functions. Experimental results demonstrate that P-CDs exhibit outstanding antioxidant activity and antibacterial performance. Compared to PVA/CS film, the P-CDs/L-Cys/PVA/CS film exhibited a 6.55 MPa increase in tensile strength and significantly enhanced thermal stability. Furthermore, the incorporation of P-CDs and L-Cys markedly boosted the PVA/CS film’s antioxidant activity (97% for ABTS; 85.69% for DPPH), antibacterial performance, and ultraviolet (UV) shielding capability. Coating cherry tomatoes with the P-CDs/L-cysteine/PVA/CS composite extended their shelf life by 6 days. This composite coating material exhibits preliminary biocompatibility and eco-friendly properties, aligning with green sustainable development needs and offering a novel potential solution for food preservation technology, while its practical applicability to food safety requires further comprehensive verification. Full article

An eco-friendly green synthesis approach was employed to produce copper nanoparticles (CuNPs) using a polyherbal extract derived from two medicinally important plant species, Hygrophila auriculata (Schumach.) Heine and Leucas aspera (Willd.) Link. The plant extracts were initially subjected to phytochemical screening to identify bioactive constituents potentially involved in nanoparticle synthesis. The synthesized CuNPs were characterized using UV-visible spectroscopy, Fourier-transform infrared spectroscopy (FTIR), gas chromatography–mass spectrometry (GC-MS), field-emission scanning electron microscopy coupled with energy-dispersive X-ray analysis (FESEM-EDAX), X-ray diffraction (XRD), and thin-layer chromatography (TLC). UV-visible spectroscopy revealed a characteristic absorption peak at 233.6 nm. FTIR analysis indicated the presence of functional groups associated with nanoparticle reduction and stabilization, whereas FESEM imaging showed predominantly spherical particles with sizes ranging 63–68 nm. Elemental composition was confirmed using EDAX analysis. XRD analysis demonstrated polycrystalline nature of the CuNPs, with an average crystallite size of 11.5 nm. GC-MS analysis and phytochemical screening further confirmed the presence of bioactive compounds, whereas TLC analysis revealed differences in mobility between the plant extract and synthesized CuNPs. Antibacterial activity of the synthesized CuNPs was evaluated using the agar well diffusion method against clinically relevant bacterial strains, including those of Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, and Streptococcus pyogenes. The polyherbal-derived CuNPs produced larger inhibition zones than the individual plant extracts, particularly against multidrug-resistant pathogens such as P. aeruginosa and S. aureus. Additionally, the nanoparticles exhibited concentration-dependent antioxidant activity in the 2,2-diphenyl-1-picrylhydrazyl assay at concentrations ranging 10–50 mg/mL, with radical scavenging activity increasing from 29.9% to 76.5% and a corresponding decrease in absorbance from 0.698 to 0.234 (p < 0.05). Cytotoxic evaluation in HepG2 cells after 48 h of exposure demonstrated dose-dependent morphological changes and reduced cell viability. These findings suggest that polyherbal-derived CuNPs possess antibacterial, antioxidant, and cytotoxic properties with potential relevance for biomedical applications. Full article

Fungal pigments have gained attention as eco-friendly and versatile materials for green nanotechnology because of their varied chemical structures, inherent redox properties, and strong metal ion-binding capabilities. These pigments, such as polyketides, azaphilones, melanins, and carotenoids, can function simultaneously as reducing, capping, and surface-functionalizing agents, facilitating the environmentally friendly production of metallic nanoparticles without the use of harmful chemicals. This review provides a critical overview of recent progress in the production, extraction, and application of fungal pigments for nanoparticle synthesis, focusing on the mechanistic roles of pigment functional groups in metal ion reduction, nanoparticle nucleation, growth, and stabilization. The impact of pigment chemistry and reaction conditions on the nanoparticle size, shape, crystallinity, and colloidal stability was thoroughly examined. Additionally, this review highlights the emerging biomedical, environmental, and industrial applications of pigment-mediated nanoparticles, emphasizing their biocompatibility and functional adaptability. Key challenges, such as variability in pigment yield and composition, limited mechanistic validation, lack of standardized synthesis protocols, and insufficient toxicity assessment, are critically analyzed in this review. Finally, future directions are outlined, emphasizing the importance of process optimization, omics-guided pigment discovery, and comprehensive safety evaluations as crucial steps toward the scalable and reliable use of fungal pigment-mediated nanoparticle synthesis in sustainable nanotechnology. Full article