Search Results (775)

Raw lacquer, a natural polymer derived from the bast of lacquer trees (Toxicodendron vernicifluum), is renowned as the “King of Coatings” due to its exceptional film-forming properties, abrasion resistance, corrosion resistance, and biocompatibility. However, its inherent limitations—including stringent drying conditions, slow curing rates, deep coloration, and difficult application—have severely restricted its modernization and widespread adoption. This review systematically summarizes recent research advances in the modification and application of raw lacquer, focusing on four major modification strategies: (1) Nanocomposite modification—incorporating functional nanofillers such as Al₂O₃, cellulose nanofibrils (CNF), polydopamine (PDA) melanin-like nanoparticles, and SiO₂ to significantly enhance film hardness, compactness, UV-aging resistance, and drying kinetics. (2) Chemical structure modification—employing molecular design strategies including aminoanthraquinone grafting, tung oil blending, water-based emulsification, and terpene/allyl group functionalization to improve hydrophobicity, flexibility, fast-drying properties, and achieve dual photo/oxygen curing. (3) Biomass synergistic composites—utilizing natural polymers such as chitosan and lignin, along with bio-inspired adhesion mechanisms (e.g., PDA), to confer advanced functionalities including antibacterial and antifouling properties. (4) Curing behavior regulation—precisely controlling drying kinetics through inorganic salt ion microenvironment engineering, nonionic surfactants, and salicylaldehyde Schiff base-based driers. Building upon these foundations, this review further expands on the emerging high-value applications of modified lacquer in preventive conservation of cultural heritage, advanced functional coatings (anti-corrosion, super-hydrophobicity, flame retardancy), biomedical materials (hemostasis, antibacterial activity, drug-controlled release, water treatment adsorption), and intelligent responsive flexible electronics. Finally, addressing challenges including weak fundamental research, bottlenecks in green industrialization, and lack of standardization, future development directions are proposed encompassing interdisciplinary innovation, sustainable modification strategies, integration of multifunctional intelligent systems, and big data-driven research paradigms, aiming to provide theoretical guidance and technical references for the high-value utilization and modernization of lacquer resources. Full article

It is known that antimicrobial surface treatments are one of the measures that can reduce the spread of viral, bacterial or fungal infections that threaten humans’ life. The excessive use of antibiotics has led to the emergence of resistant microorganisms. This study presents the potential of nanocomposites to impart durable antimicrobial properties, which can be enhanced by the use of gamma radiation, even after two months of activation. Leather surfaces finished with composite titanium dioxide nanoparticles decorated with silver, copper oxide and/or graphene oxide were investigated before, immediately after, and after 60 days of gamma irradiation treatment. The antibacterial activity against Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 6538 was found to be maintained, and even slightly increased over time compared to unirradiated leathers. Analyses of the morphology and composition of the surface of treated leathers using SEM/EDS, ATR/FTIR, as well as photo activity tests allowed the identification of structural characteristics and the modifications induced by gamma radiation activation. Evaluating the resistance properties of leathers finished with the new nanoparticle composites compared to those finished classically confirmed the quality of the applied technologies. These results provide a solution for antimicrobial treatment of medical equipment, including footwear, with potential applications in other areas such as furniture, aircraft or car upholstery, clothing and bags. Full article

A synergistic approach to the photodegradation of polydimethylsiloxane-based composites upon photoaging was implemented by using La(III) complexes of Schiff base ligands with a silicon-containing spacer as fillers. The analysis methods were spectral, nanomechanical, and morphological. The results show that the accelerated oxidative degradation of the polydimethylsiloxane matrix is due to the combined actions of radicals, fragments, and photoproducts derived from the photolysis of the La(III) complexes and the water vapors in the photoaging chamber. Compared to the undoped polydimethylsiloxane, the photo-excited radical intermediates and photoproducts of the La(III) complexes, with aromatic or quinone structures, in ground or in excited state, have acted as photocatalysts and as new sources for reactive intermediates and for the generation of reactive oxygen species. Infrared, electron spin resonance, and nanomechanical investigations revealed that the chemistry of the photoaged surfaces comprises oxygen–containing species, photoreaction products, and an extended siloxane network with embedded ligand fragments. The key role of La(III) complexes in promoting the generation of reactive species is described. The study highlights the unexplored potential of La(III) complexes of Schiff base ligands bearing a silane/siloxane spacer as potential catalysts in the photodegradation of polymers and plastics. Full article

Wood, a renewable and sustainable resource with a hierarchical porous structure, exhibits significant potential for functional composites through integration with polymers. Wood/polymer composites are typically fabricated either via polymer impregnation into wood or through blending of wood powder with thermoplastic polymers to produce wood–plastic composites (WPCs). However, conventional thermosetting polymers cannot be reshaped or reprocessed, while thermoplastic polyolefins often exhibit poor compatibility with wood powder. Dynamic covalent polymer networks (DCPNs), which incorporate reversible covalent bonds into thermoset matrices, enable network reconfiguration in response to external stimuli such as heat. Replacing conventional polymers with DCPNs in delignified wood yields transparent wood with programmable shape-memory, photo-luminescent, and thermochromic properties, enabling the fabrication of advanced materials. DCPN-impregnated delignified wood is also reprocessable and degradable. Similarly, incorporating DCPNs into carbonized wood produces electrode materials with enhanced plasticity, shape-memory behavior, reshaping ability, and self-healing properties. DCPNs can replace thermoplastic polyolefins as matrices in WPCs. Consequently, repairable and reprocessable wood powder/DCPN composites can be fabricated with potential for carbon storage applications. This mini-review summarizes recent advances in wood/DCPN composites, focusing on two main fabrication approaches: DCPN impregnation into delignified wood and blending of DCPNs with wood powder. Wood/DCPN composites combine the characteristics of wood and dynamic DCPNs and have the potential to become an efficient, eco-friendly, and sustainable form of processing and utilization of wood. Full article

This study investigates the development and performance of polyolefin-based packaging materials reinforced with industrial mineral residues, specifically slate powder (SP) and bivalve shell powder (BSP). High-density polyethylene (HDPE) and polypropylene (PP) matrices were compounded with these fillers and processed by extrusion blow moulding to produce final prototypes. Thermal analyses (TGA and DSC) showed that incorporating SP and BSP does not compromise the thermal stability of the polymer matrices and increases stiffness in the filled formulations. Accelerated ageing (QUV, 200 h) revealed distinct photo-oxidative behaviours. PP and PP + BSP (30%) exhibited increased fragility and moderate colour changes, whereas PP + SP (10%) retained flexibility, indicating a partial protective effect of SP. HDPE-based formulations showed higher intrinsic UV resistance, with HDPE + BSP (30%) displaying excellent colour stability. Tensile tests before and after QUV exposure confirmed that fillers increase stiffness with limited influence on tensile strength. Air permeability results indicated that neat PP and HDPE were below the detection limit. At the same time, filled formulations exhibited measurable permeability, suggesting that filler incorporation may influence gas transport through interfacial effects. Overall, the results show that SP and BSP act as reinforcing additives and can modify functional properties such as stiffness and ageing resistance. However, their influence on barrier performance depends on the formulation and permeation mechanism. Full article

With the growing severity of water pollution, conventional treatment technologies are increasingly unable to satisfy the demand for deep purification. Catalytic wastewater treatment has emerged as an effective strategy for degrading refractory pollutants because of its high efficiency, mild operating conditions, and environmentally friendly nature. This review systematically summarizes recent progress in catalytic materials for wastewater treatment, covering four major categories: metal-based materials, carbon-based materials, multicomponent composites, and photo/electrocatalytic systems. Particular attention is given to their design strategies, structural characteristics, and performance advantages. On this basis, the full mechanistic chain is discussed, from interfacial adsorption and activation to reactive-species generation, including both radical and non-radical pathways, intermediate transformation, and macroscopic reaction kinetics. The review also highlights representative applications in practical wastewater streams, including textile dyeing and pharmaceutical, chemical, landfill leachate, and municipal tailwater treatment, thereby demonstrating the engineering potential of catalytic technologies. At the same time, several critical challenges remain, including insufficient long-term material stability, incomplete mechanistic understanding in complex water matrices, limited adaptability to real wastewater, and the high cost of large-scale preparation. Future research should therefore focus on the development of highly stable, low-cost, and interference-resistant catalytic materials, deeper mechanistic elucidation through in situ characterization and theoretical calculations, stronger integration with membrane separation, biological treatment, photovoltaic or electrochemical processes, and the establishment of standardized evaluation protocols and life-cycle assessment frameworks. These efforts will accelerate the transition of catalytic wastewater treatment toward greener, smarter, and more practical engineering applications. Full article

Graphene oxide (GO) was employed as an additive to improve the electrochemical activity of zinc oxide (ZnO) used as both a photoelectrocatalyst for water splitting and an electrochemical sensor for detection of diclofenac. To comprehend the influence of a small amount of GO on the electrochemical activity of ZnO, a series of ZnO/xGO (x = 0, 0.1, and 0.5) particles was synthesized by microwave processing of Zn(OH)₂ precipitate in the presence of 0.1 and 0.5 wt.% of previously prepared GO. The phase composition and crystal structure ordering of ZnO/xGO particles were investigated by XRD and Raman spectroscopy. The optical properties were studied by UV–Vis DRS and PL spectroscopy. The particle morphology was inspected by FE–SEM while the textural properties were analyzed by the low-temperature nitrogen adsorption–desorption method. The (photo)electrocatalytic and electrochemical sensing activities were examined on the ZnO/rxGO modified glassy carbon electrodes (GCEs) prepared by in situ reduction of the ZnO/xGO modified GCEs for 120 s. The electro- and photoelectrocatalytic activity of ZnO/rxGO modified GCEs for water splitting was tested in dark conditions and after 60 min under illumination, respectively, employing linear sweep voltammetry in 0.1 M NaOH and 0.1 M H₂SO₄ as electrolytes. The electrochemical sensing activity of ZnO/rxGO modified GCEs was tested for detection of diclofenac in aqueous solution. The improvement in the electrochemical activity of ZnO was correlated with the added amount of GO, structural defects, and particle morphology. Full article

Wood coatings play a critical role in protecting wood substrates from environmental degradation, particularly ultraviolet (UV)-induced photodegradation. This review comprehensively examines the mechanisms of wood coating photodegradation, the factors influencing their durability, and current anti-aging strategies. Photodegradation arises from polymer chain scission, chemical structure reorganization, and photo-oxidation of lignin and cellulose, leading to coating chalking, cracking, gloss loss, and color changes, ultimately compromising wood mechanical properties and service life. Key anti-aging strategies include UV absorbers, which convert harmful UV radiation into heat; hindered amine light stabilizers (HALSs) that capture free radicals and quench excited-state molecules; barrier and shielding materials that form dense physical or nanostructured networks to block UV penetration and enhance mechanical and water resistance; and antioxidants that neutralize free radicals or decompose peroxides at the molecular level. Each approach can be employed individually or synergistically to enhance coating durability. Challenges remain in achieving long-term outdoor stability, balancing transparency and UV shielding, optimizing nanoparticle dispersion, and maintaining the activity of natural antioxidants. Future research should focus on multifunctional composite coatings integrating bio-based materials and nanotechnology, smart responsive systems, adaptive protection mechanisms, and standardized long-term evaluation protocols. These advancements will facilitate the development of high-performance, sustainable wood coatings and promote the value-added utilization of wood resources. Full article

This work reports on the synthesis and electrochemical investigation of sustainable carbon–TiO₂ nanocomposites derived from marine biowaste, designed to elucidate light-assisted charge storage mechanisms in non-aqueous electrolytes. Porous carbons obtained from prawn chitin and blue shark gelatin were decorated in situ with TiO₂ nanoparticles using a deep eutectic solvent (DES) as a green synthesis medium. Structural and morphological characterisation revealed that TiO₂ incorporation induces significant nanoscale reorganisation of the carbon framework, resulting in hierarchical porosity, increased surface area, and intimate semiconductor–carbon interfaces. Electrochemical evaluation in a three-electrode configuration using an ethaline-based DES electrolyte demonstrated that TiO₂ decoration substantially enhances capacitive performance and cycling stability, with the prawn chitin-derived composite achieving a specific capacitance of 54 ± 3 F g⁻¹ and 91% retention after 10,000 cycles. Under illumination, all TiO₂-containing composites exhibited a pronounced increase in anodic current response and discharge time, indicating photo-assisted surface charge accumulation. Although the absolute capacitance values are modest compared to those of aqueous supercapacitor systems, the results provide mechanistic insight into the interplay among nanostructure, semiconductor photoactivity, and ion transport in viscous, hydrogen-bonded DES electrolytes. By combining waste-derived carbons, green synthesis routes, and photo-responsive nanostructures, this study highlights a sustainable strategy for developing multifunctional carbon-based nanomaterials with light-modulated electrochemical behaviour. Full article

Textile wastewater remains one of the most challenging industrial effluents to remediate due to its intense and persistent coloration, high organic load, elevated salinity, and fluctuating pH and the presence of recalcitrant dye structures and auxiliary chemicals. Conventional physicochemical and biological treatments frequently achieve incomplete removal, generate secondary wastes, or fail under high-salt and toxic dye matrices. Advanced oxidation processes (AOPs) provide molecular-level degradation via reactive oxygen species (ROS), yet their deployment is often constrained by narrow operating windows, catalyst instability, chemical/energy demand, and scale-up limitations. In this context, metal–organic frameworks (MOFs) have emerged as tunable porous catalytic platforms that integrate adsorption and oxidation within a single architecture through controllable metal nodes, functional linkers, and engineered pore environments. This critical review reimagines textile effluent treatment through the lens of MOF-based hybrid catalysts, synthesizing progress across Fenton/photo-Fenton catalysis, photocatalytic MOFs, persulfate activation, and MOF-derived/composite systems. Mechanistic pathways are discussed by linking pollutant enrichment, cyclic redox reactions, charge-transfer processes, and ROS-driven degradation toward mineralization, with emphasis on the distinction between rapid decolorization and true organic removal. A critical comparison highlights how hybridization improves charge transport, stability, and catalyst recovery, while persistent gaps remain in hydrolytic robustness, metal leaching control, intermediate toxicity assessment, real-wastewater validation, continuous-flow reactor integration, and techno-economic feasibility. Finally, the review outlines actionable research directions, including water-stable and defect-engineered MOFs, immobilized and structured catalysts, solar-driven operation, standardized performance metrics, and life-cycle-informed design, to accelerate translation toward scalable and sustainable textile wastewater remediation. By bridging material chemistry with reactor-level feasibility and sustainability assessment, this review provides an implementation-oriented perspective for next-generation textile wastewater treatment. Full article

We report the fabrication and electrochemical characterization of TiO₂-based impedimetric sensors for the analysis of artificial sweat compositions. Two-electrode topologies were patterned on indium tin oxide (ITO) substrates: an interdigitated electrode (IDE) configuration and a Hilbert fractal electrode (HFE) geometry. TiO₂ thin films with thickness up to 350 nm were deposited by dip-coating and evaluated as photoactive sensing layers. The impedimetric response of the sensors was investigated by electrochemical impedance spectroscopy in artificial sweat with composition varied in terms of ionic content (0–100 mM Na⁺) and organic content (2.5–30 mM lactic acid and 5–50 mM urea). Regardless of TiO₂ thickness, the high-frequency response is predominantly governed by electrode topology, with the HFE design exhibiting up to 2.5-fold higher modulation compared to the IDE configuration. Under UV illumination, a low-frequency, photo-assisted response emerges, influenced by the TiO₂ layer thickness and primarily sensitive to the organic components of the solution, particularly lactic acid. These results suggest that frequency-resolved impedance measurements in TiO₂|ITO structures may enable partial differentiation between ionic conductivity and organic contributions in sweat, providing a promising basis for multi-parameter sweat analysis. Full article

The photoelectrochemical water-splitting process for hydrogen production is limited by the large bandgap of semiconductor titanium dioxide (TiO₂) and by interfacial recombination at particle interfaces. The technique used in this paper is that of electrochemical anodization to produce robust, ordered TiO₂ nanotube arrays (TiO₂ nanorod arrays denoted as TNTAs). Using the immersion-annealing method, Nd₂O₃ nanoparticles can be immobilized in situ, and Nd₂O₃/TNTAs composite photoanodes are fabricated. The heterointerface caused between the Nd₂O₃ nanoparticles and TiO₂ results in the alignment of the Fermi levels and the formation of band bending and an internal electric field at the interface. It allows rapid photo-generated electron-hole (e⁻/h⁺) separation at the interface and, simultaneously, introduces novel localized electron states of Nd³⁺ within the TiO₂ bandgap. This triggers hybridisation between the 3d orbitals of Ti and the 2p orbitals of O, thereby altering the band structure of TiO₂. The best-performing Nd₂O₃/TNTAs photoelectrode outperforms pure TNTAs, with a photocurrent density of 1.59 mA·cm⁻² at 1.23 V vs. RHE. It produces 162.6 μmol·cm⁻² of hydrogen in a 3 h photocatalytic hydrogen production experiment, which is about 12.2 times that of pure TNTAs. This approach highlights the unique benefits and creative opportunities of applying rare-earth elements to address the critical issues of photocatalysts, such as significant band gaps and rapid recombination. Full article

Efficient charge transfer and effective separation of photo-generated charge carriers are pivotal to the photocatalytic process. In this study, a novel CoAl₂O₄@nitrogen-doped graphitic carbon (CoAl₂O₄@NGC) composite photocatalyst was fabricated via a stepwise hydrothermal method coupled with high-temperature calcination, and its photocatalytic performance for CO₂ reduction was systematically investigated. X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and photoelectrochemical measurements were employed to characterize the phase structure, microstructure, surface chemical state and photoelectrochemical properties of the catalyst. Spinel-structured CoAl₂O₄ nanoparticles were uniformly anchored on the NGC substrate, forming a well-integrated composite interface. XPS analysis confirmed the coexistence of Co²⁺/Co³⁺ mixed valence states in CoAl₂O₄ which provides abundant redox sites for CO₂ activation. Photocatalytic tests showed that CoAl₂O₄@NGC exhibits excellent catalytic activity and cycling stability, with CO and CH₄ yields of 27.88 μmol·g⁻¹·h⁻¹ and 23.90 μmol·g⁻¹·h⁻¹, respectively. The narrow bandgap (1.54 eV) enhances visible light absorption, while efficient electron-hole separation and reduced charge transfer resistance improve photocatalytic efficiency. Theoretical calculations further reveal that CoAl₂O₄@NGC lowers the adsorption free energy of CO₂ and the energy barrier for COOH formation, thus facilitating the photocatalytic CO₂ reduction. This work provides insights for the design of efficient and stable photocatalysts for CO₂ reduction and deepens the understanding of the synergistic catalytic mechanism in the spinel/nitrogen-doped carbon composite system. Full article

The hematite phase decorated with iron-doped cerium oxide nanoparticles (F@FC) was precipitated from cerium and iron oxalate intermediate products. The photocatalytic composite of graphitic carbon nitride (gCN) and F@FC was prepared by a simple method involving mixing the two components, followed by thermal treatment at 400 °C. According to electron microscopy, F@FC is composed of a submicron iron oxide (hematite) phase decorated with iron-doped cerium oxide nanoparticles deposited on gCN substrate. A hierarchically structured composite was observed instead of a simple mechanical mixture of α-Fe₂O₃, Fe-CeO₂, and gCN. To observe two types of degradation activity, photocatalytic and Photo-Fenton degradation activity, Rhodamine B (RhB) was applied as the model water pollutant. The influence of the amount of photocatalyst, the RhB concentration, the presence of cations and anions, the pH, and the effect of e⁻, h⁺, •OH, and •O₂⁻ scavenging reactants were studied. The Photo-Fenton degradation exhibited high efficiency across the entire tested pH range, whereas photocatalytic degradation showed comparable activity only at acidic pH. The F@FC-gCN composite catalyst exhibited a high degree of recyclability. The degradation pathways of photocatalytic and Photo-Fenton reactions were suggested by HPLC-MS analysis of the reaction products. A notable finding of this study was the observation that the green-yellow, fluorescent intermediate Rhodamine 110 was formed during the photocatalytic degradation of RhB. However, the high reactivity of the generated •OH radicals during Photo-Fenton degradation has been demonstrated to inhibit the formation of intermediate Rhodamine 110. Full article

Photochromic molecules, capable of reversible isomerization under specific light irradiation, are pivotal for developing advanced photo-responsive materials. Azobenzene derivatives, in particular, are renowned for their significant conformational change, excellent reversibility, and high photostability. This study presents a novel cyclic diazo compound (CDTA) comprising two azobenzene units connected via flexible glycol chains. The photo-responsive behavior of CDTA doped into the liquid crystal 4-cyano-4′-octylbiphenyl (8CB) was systematically investigated. The composite exhibits a pronounced photo-induced phase transition from a liquid crystalline to an isotropic state under 365 nm UV irradiation, accompanied by a reversible change in light transmittance. The response kinetics were found to be highly dependent on temperature and dopant concentration. At 35 °C, the UV response time was accelerated to 6.8 s, attributed to the transition of the host 8CB from a smectic to a nematic phase. Furthermore, the composite demonstrated dual responsiveness: optical switching under UV light and electrical switching under an applied field in its nematic state. This work elucidates the interaction between molecular structure and photo-response in a liquid crystalline matrix, offering insights for designing next-generation smart windows and adaptive optical devices. Full article