Search Results (113)

With the rapid expansion of wind energy infrastructure, there is an increasing accumulation of wind turbine blade waste (WTBW), which is mainly composed of glass fiber-reinforced thermosetting composites. Due to the irreversible nature of polymer crosslinking, conventional recycling methods remain limited. In this study, plasma vitrification was employed to convert WTBW into a reactive calcium-aluminum-silicate slag suitable for use in geopolymer materials. Plasma treatment at a temperature of approximately 2750 K resulted in the formation of predominantly amorphous vitrified slag (VS). Structural characterization using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS) revealed the spatial heterogeneity of the VS. This heterogeneity was influenced by thermal gradients and varied between samples collected from different slag discharge zones, both vertically and horizontally from the reactor. All VS samples contained between 30 and 89% amorphous phase and 10–55% anorthite, with the proportions varying by sampling location. Chemical stability tests showed the dissolution of calcium and aluminum in acidic media, resulting in a silica-enriched residual structure in which the Ca and Al content decreased to less than 0.5 at.% after 100 days. In contrast, exposure to alkaline media caused only minimal surface reorganization—the addition of 5 wt.% VS to acid-based geopolymers made with two metakaolin precursors resulted in a 35% decrease in the mechanical strength of pure metakaolin-based systems. In contrast, when metakaolin containing illite impurities was used, strength values were similar to those of the reference geopolymer. The results quantitatively demonstrate that plasma-derived slag exhibits composition-dependent reactivity, directly linked to its amorphous content and dissolution behavior. 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

Colloidal amorphous structures comprise short-range ordered arrays of monodisperse submicrometer-sized particles. They exhibit angle-independent structural color and hence are expected to be promising candidates for advanced color materials. In particular, non-close-packed colloidal amorphous structures embedded in soft polymers can alter the angle-independent color through stimuli-induced volume changes in the polymer. Consequently, such materials should have significant potential for application in sensor devices. This paper reports the preparation of an elastomer-immobilized non-close-packed colloidal amorphous film with an angle-independent color using a hydrogel-immobilized non-close-packed colloidal amorphous film as the starting material. The swelling solvent (i.e., water) in the hydrogel film was replaced with a hydrophilic elastomer precursor solution, which was photopolymerized to immobilize the colloidal amorphous structure with the separated particles within the elastomer film. The color of the elastomer-immobilized non-close-packed colloidal amorphous film was angle-independent and was easily altered under stretching. Furthermore, hydrophilic carbon black dispersed well in the hydrophilic elastomer precursor solution, improving the saturation of the resultant elastomer-immobilized non-close-packed colloidal amorphous film. The flexible nature of the prepared film should allow it to be attached to curved surfaces, thereby promoting its application as a simple strain sensor to express invisible strains through color changes. Full article

Agricultural biomass has potential as a renewable and versatile carbon feedstock for developing eco-friendly and biodegradable polymers capable of replacing conventional petrochemical plastics. To address the growing environmental concerns associated with plastic waste and carbon emissions, lignocellulosic residues, edible crop by-products, and algal biomass were utilized as sustainable raw materials. These biomasses provided carbohydrate-, lipid-, and lignin-rich fractions that were deconstructed through optimised physical, chemical, and enzymatic pretreatments to yield fermentable intermediates, such as reducing sugars, organic acids, and fatty acids. The intermediates were subsequently converted through tailored microbial fermentation processes into biopolymer precursors, primarily polyhydroxyalkanoates (PHAs) and lactate-based monomers. The resulting monomers underwent polymerization via polycondensation and ring-opening reactions to produce high-performance biodegradable plastics with tunable structural and mechanical properties. Additionally, the direct extraction and modification of naturally occurring polymers, such as starch, cellulose, and lignin, were explored to develop blended and functionalized bioplastic formulations. Comparative evaluation revealed that these biomass-derived polymers possess favourable physical strength, thermal stability, and biodegradability under composting conditions. Life-cycle evaluation further indicated a significant reduction in greenhouse gas emissions and improved carbon recycling compared to fossil-derived counterparts. The study demonstrates that integrating agricultural residues into bioplastic production not only enhances waste valorization and rural bioeconomy but also supports sustainable material innovation for packaging, farming, and consumer goods industries. These findings position agriculture-based biodegradable polymers as a critical component of circular bioeconomy strategies, contributing to reduced plastic pollution and improved environmental sustainability. Full article

Low-melting bioabsorbable polymers, such as poly(caprolactone-co-lactide) (PCLA), hold significant promise for biomedical applications. However, achieving high-precision micro- and nanotopographical functionalization remains a formidable challenge due to the material’s susceptibility to thermal deformation during conventional thermal molding processes. In this study, functional microstructured PCLA coatings were engineered via low-temperature nanoimprint lithography utilizing a TiO₂–SiO₂ gas-permeable mold. These molds were synthesized via a sol–gel method utilizing titanium dioxide and silicon precursors. The gas-permeable nature of the mold facilitated the efficient evacuation of trapped air and volatiles during the imprinting process, enabling the high-fidelity replication of microstructures (1.3 μm height, 3 μm pitch) and nanostructured PCLA coatings featuring linewidths as narrow as 600 nm. The resultant microstructured PCLA coatings demonstrated modulated surface wettability, evidenced by an increase in water contact angles from 70.1° to 91.4°, and exhibited enhanced FD4 elution kinetics. These results confirm morphology-driven functionalities, specifically hydrophobicity and controlled release capabilities. Collectively, these findings underscore the efficacy of this microfabrication approach for polycaprolactone-based materials and highlight its potential to catalyze the development of high-value-added biomaterials for advanced medical and life science applications. This study establishes a foundational framework for the practical deployment of next-generation bioabsorbable materials and is anticipated to drive innovation in precision medical manufacturing. Full article

Membrane electrolytes play a critical role in energy conversion devices. The development of stable, efficient membrane electrolytes is urgent and demands paramount attention for the successful commercialization of fuel cells. Chitosan, a naturally occurring material, and silica particles were used as precursors for organic–inorganic membrane polymers. The silica nanoparticles were prepared by the sol–gel and Stober methods and characterized using various techniques, including XRD, FTIR, etc. The silica-incorporated membranes show improved properties, with the sulfur-functionalized membranes having optimal proton conductivity, ion-exchange capacity, and tensile strength of 0.0238 S/cm, 2.86 meq/g, and 7.3 MPa, respectively. It also showed the lowest methanol permeability. This was clear proof that membrane functionalization has a positive impact on tuning the properties of electrolyte membranes and should be further explored in membrane development. Full article

Carbon membranes have emerged as a promising class of inorganic membranes for desalination due to their tunable pore structures, superior chemical and thermal stability, and molecular-sieving properties. In pursuit of sustainability, recent research has shifted focus towards replacing petrochemical-based precursors with renewable natural polymers. This review provides a comprehensive examination of the fundamentals, developments, and prospects of carbon membranes derived from natural polymer precursors—such as cellulose, chitosan, lignin, starch, and sugars—specifically for pervaporation desalination. It begins by summarizing the fundamentals of membrane separation and the mechanisms of carbon membrane formation, emphasizing the critical relationships between precursor structure, carbonization conditions, and the resulting membrane performance. The core of the review is dedicated to a detailed analysis of various natural polymer precursors, discussing their unique chemistries, carbonization behaviors, and the characteristics of the derived carbon membranes. Particular attention is given to their application in pervaporation desalination, where they demonstrate competitive water flux and high salt rejection (>99%) under moderate operating conditions, highlighting their potential for treating hypersaline brines. Finally, the challenges of large-scale fabrication, structural durability, and data-driven optimization are discussed, along with future directions toward scalable and sustainable membrane technologies. Full article

Wood is one of the most widely used sustainable lignocellulosic materials, with numerous applications in consumer goods and the construction sector. Despite its positive properties, such as a high strength-to-weight ratio, thermal insulation, and low density, wood’s natural thermal degradation can limit its potential applications. In composite applications like wood–plastic composites, the particle morphology and surface topography must be preserved to support intimate polymer–wood contact and mechanical interlocking. This study investigated the efficacy of a thin silica coating for thermal protection, which was applied via an in situ sol–gel method using the precursor tetraethoxysilane (TEOS). The wood particles and treatments were characterized using particle size analysis, physisorption, FTIR, SEM, XRD, and TGA analyses. After treatment, the specific and microporous surface area of wood particles increased by 118% and 97%, respectively, an effect of the porosity of silica itself. FTIR spectra of the silica-treated wood displayed peaks corresponding to Si stretching, and SEM micrographs confirmed a successful silica coating formation. TGA showed that the silica coating increased the temperatures needed to degrade the underlying hemicellulose and cellulose by 16 °C for all treatment levels. This particle-scale coating provided a promising method for producing thermally protected, functionalizable wood fillers for composites that maintain the filler geometry and potential mechanical interlocking, offering an attractive upcycling pathway for wood residues. Full article

Hydrogen energy offers high energy density and carbon-free combustion, making it a promising fuel for next-generation propulsion and power generation systems. Hydrogen offers approximately three times more energy per unit mass than natural gas, and its combustion yields only water as a byproduct, making it an exceptionally clean and efficient energy source. Materials used in hydrogen-fueled combustion engines must exhibit high thermal stability as well as resistance to corrosion caused by high-temperature water vapor. This study introduces a novel ceramic matrix composite (CMC) designed for such harsh environments. The composite is made of yttria-stabilized zirconia (YSZ) fiber-reinforced silicoboron carbonitride [Si(B)CN]. CMCs were fabricated via the polymer infiltration and pyrolysis (PIP) method. Multiple PIP cycles, which help to reduce the porosity of the composite and enhance its properties, were utilized for CMC fabrication. The Si(B)CN precursor formed an amorphous ceramic matrix, where the presence of boron effectively suppressed crystallization and enhanced oxidation resistance, offering superior performance than their counter part. Thermogravimetric analysis (TGA) confirmed negligible mass loss (≤3%) after 30 min at 1350 °C. The real-time ablation performance of the CMC sample was assessed using a hydrogen torch test. The material withstood a constant heat flux of 185 W/cm² for 10 min, resulting in a front-surface temperature of ~1400 °C and a rear-surface temperature near 700 °C. No delamination, burn-through, or erosion was observed. A temperature gradient of more than 700 °C between the front and back surfaces confirmed the material’s effective thermal insulation performance during the hydrogen torch test. Post-hydrogen torch test X-ray diffraction indicated enhanced crystallinity, suggesting a synergistic effect of the oxidation-resistant amorphous Si(B)CN matrix and the thermally stable crystalline YSZ fibers. These results highlight the potential of YSZ/Si(B)CN composites as high-performance materials for hydrogen combustion environments and aerospace thermal protection systems. Full article

Chitosan is a natural biopolymer with intrinsic antimicrobial properties and strong metal ion chelating properties, making it an ideal matrix for the development of bioactive composites. In this study, silver and copper nanoparticles were synthesized using laser ablation in liquid (LAL) by the ablation of metallic targets into commercial chitosan (Cs) and chitosan produced from Hermetia illucens pupal exuviae (CsE) solutions, avoiding the use of chemical precursors or stabilizing agents. The nanocomposites obtained were characterized by UV–vis spectroscopy, TEM microscopy and FTIR spectroscopy in order to evaluate the size of the nanoparticles and the interactions between the polymer and metal nanoparticles. Antibacterial tests demonstrated the efficacy of Ag-based composites with a minimum inhibitory concentration (MIC) of 0.006 g/L, and Cu-based composites with a MIC of 0.003 g/L against both Escherichia coli and Micrococcus flavus. While the silver composites show antibacterial activity in both colloidal and film forms, the copper composites present antibacterial activity only in colloidal form. Swelling tests indicated that all films maintained a high water absorption capacity, with a swelling index over 200%, unaffected by nanoparticle integration. The results highlight the potential of LAL-synthesized metal–chitosan composites, particularly those based on insect chitosan, as sustainable and effective antimicrobial materials for biomedical and environmental applications. Full article

The shikimate pathway is the fundamental metabolic route for aromatic amino acid biosynthesis in bacteria, plants, and fungi, but is absent in mammals. This review explores how multi-enzyme synergy and allosteric regulation coordinate metabolic flux through this pathway by focusing on three key enzymes: 3-deoxy-d-arabino-heptulosonate-7-phosphate synthase, chorismate mutase, and tryptophan synthase. We examine the structural diversity and distribution of these enzymes across evolutionary domains, highlighting conserved catalytic mechanisms alongside species-specific regulatory adaptations. The review covers directed evolution strategies that have transformed naturally regulated enzymes into standalone biocatalysts with enhanced activity and expanded substrate scope, enabling synthesis of non-canonical amino acids and complex organic molecules. Industrial applications demonstrate the pathway’s potential for sustainable production of pharmaceuticals, polymer precursors, and specialty chemicals through engineered microbial platforms. Additionally, we discuss the therapeutic potential of inhibitors targeting pathogenic organisms, particularly their mechanisms of action and antimicrobial efficacy. This comprehensive review establishes the shikimate pathway as a paradigmatic system where understanding allosteric networks enables the rational design of biocatalytic platforms, providing blueprints for biotechnological innovation and demonstrating how evolutionary constraints can be overcome through protein engineering to create superior industrial biocatalysts. Full article

Hierarchical porous carbon materials hold great potential for energy storage applications due to their high porosity, large specific surface area, and excellent electrical conductivity. Cellulose and sodium alginate are naturally abundant high-molecular-weight biopolymer materials. Utilizing them as precursors for the fabrication of high-performance electrochemical carbon materials is highly significant for achieving carbon neutrality goals. In this study, porous carbon aerogels were successfully synthesized using a combination of freeze-drying and a simple carbonization process, with nanocellulose and sodium alginate as precursors. Among the prepared samples, SC-0.03 (sodium alginate: nanocellulose = 0.1:0.03) exhibited the best performance, achieving a specific surface area of 713.7 m² g⁻¹. This material features an optimized hierarchical pore structure and a substantial intrinsic oxygen doping content, resulting in excellent capacitance performance. Benefiting from these structural advantages and their synergistic effects, the SC-0.03 electrode demonstrated a high specific capacitance of 251.5 F g⁻¹ at a current density of 0.5 A g⁻¹. This study shows that the construction of three-dimensional porous structures by taking advantage of the self-supporting properties of natural polymer materials does not require the introduction of external binders. Due to the nanoscale dimensions and high aspect ratio, nanocellulose enables the formation of a more refined and interconnected hierarchical pore network, enhancing ion accessibility and conductivity. The hierarchical porous carbon aerogel developed in this study, based on a biomass self-reinforcement strategy, not only shows great promise as an advanced energy storage material but also possesses environmentally friendly properties, offering new insights for the development of sustainable energy materials. Full article

Ionic porous polymers have been widely utilized efficiently to anchor various metal atoms for the preparation of metal-embedded heteroatom-doped porous carbon composites as the active materials for electrocatalytic applications. However, the rational design of the heteroatom and metal elements in HPC-based composites remains a significant challenge, due to the tendency of the aggregation of metal nanoparticles during pyrolysis. In this study, a nitrogen (N)- and sulfur (S)-enriched ionic covalent organic framework (iCOF) incorporating viologen and thieno[3,4-b] thiophene (TbT) was constructed via Zincke-type polycondensation. The synthesized iCOF possesses a crystalline porous structure with a pore size of 3.05 nm, a low optical band gap of 1.88 eV, and superior ionic conductivity of 10^−2.672 S cm⁻¹ at 333 K, confirming the ionic and conjugated nature of our novel iCOF. By applying the iCOF as the precursor, a ruthenium and ruthenium(IV) oxide (Ru/RuO₂) nanoparticle-embedded N/S-co-doped porous carbon composite (NSPC-Ru) was prepared by using a two-step sequence of anion-exchange and pyrolysis processes. In the electrochemical nitrogen reduction reaction (eNRR) application, the NSPC-Ru achieves an impressive NH₃ yield rate of 32.0 μg h⁻¹ mg⁻¹ and a Faradaic efficiency of 13.2% at −0.34 V vs. RHE. Thus, this innovative approach proposes a new route for the design of iCOF-derived metal-embedded porous carbon composites for enhanced NRR performance. Full article

In this study, we report the findings of a morphological analysis of a resorcinol–formaldehyde (RF)-based carbon aerogel (CA) and its graphene oxide (GO)-doped version (CA-GO), prepared for possible applications as an electrode material. Beyond some electron microscopic and N₂ sorption investigations, we mostly used NMR cryoporometry and relaxometry to characterize the gels in a wet state, as they are usually applied. The precursor RF polymer aerogel was prepared both with and without GO and was subsequently carbonized into carbon aerogel. Modifying the polymer aerogel using GO resulted in a larger variety of C-O bonds in both polymer aerogels. However, the most important changes occurred in the morphology of the carbon aerogels. NMR relaxometry revealed the highly hydrophilic nature of the pore wall of the RF polymer aerogels, as demonstrated by their uniform wetting behavior. The carbonization resulted in a mostly hydrophobic pore wall decorated by some oxygen-containing spots and a macroporous system. Doping with GO after pyrolysis resulted in spherical pores in the CA and cylindrical pores in the CA-GO, which is potentially a more promising material for electrochemical use than CA. Full article

Polysaccharides offer a perfect option as raw materials for the development of a new generation of sustainable batteries and supercapacitors. This is due to their abundance and inherent structural characteristics. Polysaccharides can be chemically functionalized and engineered, offering a wide range of possibilities as electrode materials (as precursors of porous nanocarbons), binders and separators. Their hierarchical morphology also enables their exploitation as aerogel and hydrogel structures for quasi-solid and solid polymer electrolytes with high conductivity and wide voltage stability windows. In this review, we discuss how different polysaccharides, such as lignocellulosic biomass, starch, chitosan, natural gums, sugars and marine polysaccharides, can be applied in different components of energy storage systems (ESSs). An overview of the recent research work adhering to each functionality of different polysaccharides in various storage systems is provided. Full article