Search Results (84)

Photodegradation limits the accuracy of fast pressure-sensitive paints (PSPs), but its dependences on irradiance and operating conditions remain insufficiently researched. Here, the photodegradation kinetics of a polymer–ceramic PSP (PC-PSP) and a mesoporous-particle PSP (MP-PSP) were investigated under independently varied irradiance (50–122 mW/cm²), pressure (0.5–100 kPa), and temperature (20–100 °C). Normalized intensity histories acquired during 900 s of continuous irradiation were fitted with a bi-exponential model, whose composite degradation rate was correlated to the studied parameters using physical relations. PC-PSP exhibited greater absolute degradation and an approximately linear irradiance dependence (m = 1.28), whereas MP-PSP showed a nonlinear dependence (m = 2.13), consistent with a greater relative contribution from photooxidative processes. The degradation rate of PC-PSP decreased predominantly with increasing pressure because oxygen quenching reduced the excited-state luminophore population. MP-PSP exhibited a non-monotonic pressure dependence: decreasing pressure initially accelerated degradation by weakening oxygen quenching, whereas further pressure reduction below the half-saturation region suppressed oxygen-limited photooxidation. Increasing temperature generally accelerated degradation in both formulations; the fitted apparent activation energies were 12.99 kJ mol⁻¹ for PC-PSP and 33.12 kJ mol⁻¹ for MP-PSP, reflecticng the stronger overall temperature dependence of MP-PSP. These findings provide a basis for quantitatively evaluating PSP photostability and assessing photodegradation-induced measurement errors. Full article

Hybrid nanocomposites composed of dendritic fibrous nanosilica (DFNS) identified as KCC-1 and resorcinol–formaldehyde (RF) resin were synthesized via the polymer-assisted deposition (PAD) method for the incorporation of Ni and Fe in mono- and bimetallic configurations. The RF resin enabled uniform dispersion Fe-based and Ni-based nanoparticles through coordination with functional groups, while KCC-1 provided a high-surface-area, mesoporous support. A comprehensive structural and chemical characterization confirmed the formation of hematite in the Fe-based system; NiO and metallic Ni in the Ni-based material; and FeO, NiO and metallic Ni in the bimetallic composite, in the form of well-dispersed metal nanoparticles between 3–6 nm. Although a reduction in BET surface area was observed due to resin and metal loading, all nanocomposites retained mesoporous structures with Type IV isotherms and H3-type hysteresis, suitable for catalytic applications. The nanocomposites exhibited structural stability up to 800 °C under N₂, with a total mass loss of 12–14% dominated by moisture desorption below 100 °C (~8–11%) and minor surface group degradation at higher temperatures. These findings demonstrate the potential of the PAD method for fabricating functional hybrid materials with improved metal dispersion. Full article

The excessive emission of greenhouse gases (CO₂, CH₄, SF₆, and CF₄.) is a primary driver of global climate change, making the development of efficient adsorption and separation technologies critically important for achieving carbon reduction goals. Metal–organic frameworks (MOFs) have attracted considerable attention in this field due to their crystalline porous structures, ultrahigh surface areas, and tunable pore architectures. However, pristine MOFs face significant bottlenecks including poor water stability, high bed pressure drops caused by their powdered form, and limited mass transfer, which severely hinder their industrial application. The integration of MOFs with functional materials such as carbon materials, polymers, metal oxides, and porous SiO₂ offers a synergistic strategy to overcome these limitations. Carbon materials provide hydrophobic barriers and mesoporous transport channels, polymers enhance processability and mechanical strength, metal oxides introduce basic sites for enhanced chemisorption, and MOF-on-MOF heterostructures enable atomic-level interfacial integration and pore synergy. This review systematically summarizes recent advances in MOF composites for the separation of CO₂, CH₄, and fluorinated greenhouse gases (SF₆, CF₄.), with an emphasis on design strategies, structure–performance relationships, and synergistic mechanisms across different composite types. Finally, the current challenges including scalable synthesis, long-term stability, and separation performance under realistic conditions are discussed, and future directions toward rational design and functional synergy for industrial carbon capture and fluorinated gas emission reduction are envisioned. Full article

Biochar, a carbon-rich material derived from biomass pyrolysis, offers a promising pathway for valorising agricultural and industrial residues within a circular economy. This review analyses the evolution of biochar properties, including fixed carbon content, elemental composition, surface functional groups, porosity, pH, hydrophobicity, and thermal stability, as a function of pyrolysis temperature. The novelty of this work lies in the systematic correlation between the thermal history of biochar and its performance as a functional filler in polymer composites. In fact, increasing temperature enhances carbonisation and aromatic ordering, and in turn induces a transition from hydrophilic to hydrophobic behaviour, thereby promoting micro–mesoporous development. These shifts are critical for compatibility with polymer matrices and thus the production of light-weight, cost-effective, and environmentally friendly composite materials through processes such as melt extrusion and injection moulding. This study highlights how biochar can be tuned for compatibility: low-temperature biochar enhances adhesion in polar systems, while high-temperature biochar favours non-polar matrices, improving stiffness, thermal stability, and electrical conductivity. In biodegradable polymer composites, additional effects on crystallisation behaviour and degradation mechanisms emerge, further highlighting the complexity of designing biochar-reinforced systems. Full article

Conventional epoxy polymers and their composites are increasingly challenged by environmental concerns, high manufacturing costs, and limited recyclability, necessitating the exploration of sustainable alternatives. Many research groups have sought to develop alternate polymers from various renewable resources, such as lignin, polyphenols, natural resins, saccharides, and plant oils. This new type of polymer has led to the emergence of bio-based polymers, which are often used with different reinforcements as bio-based composites. In this review, the synthesis of different bio-epoxy resins is discussed in detail along with their chemical structures. Subsequently, the enhancements in the properties of these bio-composites with the addition of different nanomaterials such as carbonaceous nanofillers (carbon nanotubes, graphene nanoplatelets, graphene oxide, etc.), cellulose-based nanomaterials, inorganic nano-silica (spherical and mesoporous), and nano-clay is explained. Lastly, the properties of these bio-composites and their applications in civil engineering are highlighted. This review has provided a detailed overview of the developments in bio-composites that can be used as a guide for the development of a new class of bio-composites using other alternate resources. Full article

Magnesium alloys exhibit promising application prospects in medical orthopedic implants. However, their practical applications are limited by rapid corrosion, suboptimal osseointegration, and implant-related infections. Although conventional drug-eluting polymer coatings can provide various biological functions, the uncontrolled drug release often compromises long-term therapeutic efficacy. In this study, a self-healing Mg-poly(ε-caprolactone) (PCL)@OHF coating is designed and prepared on WE43 Mg by spin coating to achieve ultrasound-triggered release of osthole. OHF consists of osthole-loaded hollow mesoporous silica nanoparticles (HMSs) modified with Pluronic F127. Drug release studies show that the nanocapsules respond to ultrasound stimulation, with the cumulative release increasing from 39.94% to 75.93% after 7 days. Furthermore, the coating demonstrates intrinsic self-healing capacity upon thermal treatment at 50 °C. Electrochemical and immersion tests reveal that the composite coating provides good barrier protection for the WE43 Mg alloy, evidenced by a decrease in corrosion current density from 2.04 × 10⁻⁶ to 5.94 × 10⁻⁷ A/cm². In vitro biological assays confirm the antibacterial efficacy against Staphylococcus aureus and Escherichia coli, as well as the ability to promote osteogenic differentiation. The results reveal a surface modification strategy that combines self-healing, anticorrosion, and on-demand drug release, offering a promising approach for advanced orthopedic implants. Full article

Under dual challenges of global infrastructure expansion and industrial solid waste management, alkali-activated polymers (AAP), as industrial solid-waste-based low-carbon cementitious materials, exhibit immense potential in grouting engineering applications. This review synthesizes current research progress through three critical dimensions: reaction mechanisms, performance characteristics, and grouting applications (grouting for reinforcement and water-blocking). The reaction mechanism universally comprises three stages: dissolution, depolymerization, and polycondensation. Key performance determinants include precursor composition (e.g., slag, fly ash, metakaolin) and alkaline activator properties (type, modulus, concentration). The multifunctional advantages of AAP are fundamentally governed by their microstructural evolution. Specifically, the rapid formation of highly cross-linked C-(A)-S-H and N-A-S-H gels directly contributes to rapid setting and high early strength development, with high-calcium precursors such as slag exhibiting faster strength gain than low-calcium systems, such as fly ash and metakaolin. Furthermore, the absence of vulnerable calcium hydroxide phases, combined with a densified, low-porosity aluminosilicate network, provides superior thermal stability, corrosion resistance, frost durability, and low permeability. Nevertheless, pronounced autogenous shrinkage and drying shrinkage, driven by mesopore moisture loss and the highly viscoelastic solid skeleton, remain primary constraints for field implementation. In grouting reinforcement, AAP can effectively enhance the strength and structural integrity of weak soils, such as soft clay, loess, and sulfate-rich saline soils. For grouting water-blocking, particularly in sodium-silicate-based binary systems, AAP achieves rapid gelation, superior washout resistance, and high anti-seepage pressure, proving optimal for groundwater inflow control. Future research must prioritize (i) standardized mix design protocols for performance consistency, (ii) advanced shrinkage mitigation strategies, (iii) systematic durability assessment under coupled environmental stressors (e.g., wet–dry cycling, chemical attack, thermal fatigue), and (iv) cross-disciplinary collaboration for industrial-scale validation. Full article

Gel polymer electrolytes (GPEs), which combine the safety of solid electrolytes with the high ionic conductivity of liquid electrolytes, have long been regarded as ideal electrolyte materials. This study proposes a polymer/ceramics composite gel electrolyte aimed at improving the performance of lithium-ion batteries. A nanofiber membrane was fabricated by electrospinning a mixture of polyacrylonitrile and lithium-salt-grafted helical mesoporous silica nanoparticles, followed by plasticizer absorption to obtain the composite gel electrolyte film (PAN/SiO₂-Li). Experimental results indicate that this gel electrolyte membrane possesses high thermal stability, a wide electrochemical window (>5.3 V vs. Li/Li⁺), high room-temperature ionic conductivity (~4.4 × 10⁻³ S cm⁻¹), and a good lithium-ion transference number (0.72). In symmetric Li||Li cells, this electrolyte suppresses lithium dendrite growth and maintains stable lithium deposition/stripping. This work presents a practical electrolyte design strategy for developing GPEs with enhanced safety and performance. Full article

Organic dyes are critical components in industries ranging from textiles, plastics, and paper to food, cosmetics, and pharmaceuticals. However, their widespread use leads to significant environmental pollution. Consequently, developing efficient methods to treat dye wastewater is urgently needed. In this work, a high-performance composite membrane was developed with a poly(dibenzo-18-crown-6) covalent organic polymer (COP) interlayer. The chemical structure of the COP was verified by FT-IR, and BET analysis indicated that the as-synthesized material possesses a predominantly mesoporous structure with a minor microporous contribution. Subsequently, the membrane was fabricated by depositing a COP colloid on a nylon-66 support via vacuum filtration, followed by the formation of a dense polyamide (PA) active layer through interfacial polymerization (IP) between amine and acyl chloride monomers. Systematic evaluation of dye separation performance using a cross-flow filtration setup identified optimal operating conditions. Under these conditions, the membrane demonstrated effective molecular sieving behavior, achieving both high dye rejection and favorable solvent permeability. In long-term stability tests, the membrane maintained a rejection rate of over 99% for Congo red over 48 h, while sustaining a water flux of 103.2 L m⁻² h⁻¹ bar⁻¹ (LMH/bar). Furthermore, the membrane exhibited promising potential for dye desalination applications, achieving a high Congo red/potassium chloride separation selectivity of 186.8 with a flux of 138.2 LMH/bar. This study confirms that the poly(dibenzo-18-crown-6)-based composite membrane is a reliable and efficient material for molecular separation in wastewater treatment. Full article

Perfluorooctanesulfonate (PFOS) is a typical persistent organic pollutant, which presents a significant risk to the ecosystem and human health. Therefore, the development of a highly sensitive and effective detection technique for PFOS has aroused wide concern. In this study, for the mesoporous metal–organic frameworks (MOFs), Cr-MIL-101 were used as the precursor. And the poly(3,4-ethylenedioxythiophene) (PEDOT) using as molecularly imprinted polymers (MIPs) was loaded on Cr-MIL-101 to form a core–shell structure. The obtained Cr-MIL-101@PEDOT/MIP composites integrate the high specific surface area of Cr-MIL-101 and the specific recognition capability of PEDOT/MIP. The glassy carbon electrode (GCE) interface modified by them can specifically adsorb PFOS through electrostatic interactions, coordination by Cr metal nodes, hydrophobic interaction, and hydrogen bonding, etc. The adsorbed PFOS molecules could block the active sites at the electrode interface, causing the current decay of the redox probe. Following the quantitative analysis of peak current decay values using the Langmuir model and the Freundlich–Langmuir model, a wide detection range (0.1–200 nM) and a low detection limit (0.025 nM) were obtained. Characterization techniques including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), X-ray photoelectron spectroscopy (XPS), and electrochemical methods were employed to validate the fabrication of the composites. Moreover, Cr-MIL-101@PEDOT/MIP/GCE showed satisfactory stability, repeatability, and selectivity, providing an effective method for the detection of PFOS in practical samples, showing a wide prospective application. Full article

Architectural exterior wall coatings require a balance of elasticity, stain resistance, and durability. Although nano-SiO₂ enhances fracture resistance in elastic coatings, its limited hydrophobicity allows pollutant adhesion. Nano-TiO₂ can photocatalytically degrade organics but is often encapsulated by the polymer matrix, reducing its effectiveness. This study introduces a SiO₂-TiO₂ composite topcoat applied via aqueous dispersion to overcome these limitations. Experimental results demonstrate that the composite coating significantly outperforms single-component modifications, improving stain resistance by 21.3% after 12 months of outdoor exposure. The surface remains brighter with markedly reduced pollutant accumulation. Mechanistically, SiO₂ serves as an inert mesoporous carrier that improves the dispersion and photostability of TiO₂, minimizing agglomeration and photocorrosion. Its inherent hardness and hydrophobicity reduce physical adsorption sites. Together, SiO₂ and TiO₂ create a nanoscale rough surface that enhances hydrophobicity through a lotus-like effect. Under UV irradiation, TiO₂ generates radicals that decompose organic pollutants and inhibit microbial growth, enabling efficient self-cleaning with rainwater. This synergistic mechanism addresses the limitations of individual nanoparticles, successfully integrating elasticity with long-term anti-fouling and durability. This composite demonstrates a significant advancement in stain resistance and overall durability, offering potential applications in energy-efficient and environmentally sustainable building technologies. Full article

Delayed or non-healing of bone defects in an aging, multi-morbid population is still a medical challenge. Current replacement materials, like autografts, are limited. Thus, artificial substitutes from biodegradable polymers and bioactive glasses (BGs) are promising alternatives. Here, novel cerium-doped mesoporous BG microparticles (Ce-MBGs) with different cerium content were included in photocrosslinkable, methacrylated gelatin (GelMA) for promoting cellular functions of human mesenchymal stem cells (hBMSCs). The composites were studied for intrinsic morphology and Ce-MBGs distribution by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). They were gravimetrically analyzed for swelling and stability, compressive modulus via Microsquisher^® and bioactivity by Fluitest^® calcium assay and inductively coupled plasma-optical emission spectrometry (ICP-OES), also determining silicon and cerium ion release. Finally, seeding, proliferation, and differentiation of hBMSCs was investigated. Ce-MBGs were evenly distributed within composites. The latter displayed a concentration-dependent but cerium-independent decrease in swelling, while mechanical properties were comparable. A MBG type-dependent bioactivity was shown, while an enhanced osteogenic differentiation of hBMSCs was achieved for Ce-MBG-composites and related to different ion release profiles. These findings show their strong potential in promoting bone regeneration. Still, future work is required, e.g., analyzing the expression of osteogenic genes, providing further evidence for the composites’ osteogenic effect. Full article

Carbon nanostructures (CNs) are various low-dimensional allotropes of carbon that have attracted much scientific attention due to their interesting physicochemical properties. It was quickly discovered that the properties of CNs can be significantly improved by modifying their surface or synthesizing composites containing CNs. Composites combine two or more materials to create a final material with enhanced properties compared with their initial components. In this review, we focused on one group of carbon materials—composites containing CNs (carbon/CN composites), characterized by high mesoporosity. Particular attention was paid to the type of synthesis used, divided into hard- and soft-templating methods, the type of polymer matrix precursors and their preparation method, heteroatom doping, pore formation methods, and correlations between the applied experimental conditions of synthesis and the structural properties of the composite materials obtained. In the last part, we present an updated summary of the applications of mesoporous composites in energy storage systems, supercapacitors, electrocatalysis, etc. The correlations among porous structures of materials, heteroatom doping, and electrochemical or catalytic efficiency, including activity, selectivity, and stability, were also emphasized. To our knowledge, a single review has never summarized pyrolyzed mesoporous composites of polymer-CNs, their properties and applications in electrochemistry. Full article

Biogenic silica (SiO₂) sourced from living organisms, especially plants such as rice and other cereals, has recently been successfully applied in different polymeric compositions. Another rich source of biogenic silica is common horsetail (Equisetum arvense L.), containing up to 25% SiO₂ in the dry matter. In this study, biogenic silica was obtained from horsetail powder by acid leaching in sulfuric acid and calcination at 400 °C. The analysis, including measurements of specific surface area using the Brunauer–Emmett–Teller method, assessment of crystallinity by X-ray diffraction, as well as chemical content analysis by Fourier-transform infrared spectroscopy showed that high-purity, high-surface mesoporous silica was obtained. The biogenic silica and horsetail powders were also introduced to polylactide (PLA) to determine their influence on the polymer’s crystallization, which was studied in both non-isothermal and isothermal conditions by differential scanning calorimetry. The crystallization parameters were calculated according to the Avrami method based on isothermal crystallization curves at 100, 110 and 120 °C. The crystalline structures were observed by optical microscopy in polarized light. It was found that both fillers improve the crystallization of PLA, especially in low-supercooling conditions, so they can be successfully utilized in industrial applications, when high crystallinity of polylactide is needed. Full article

The aim of this work was the characterization of polymer microspheres obtained by the suspension polymerization of divinylbenzene (DVB) and glycidyl methacrylate (GMA), depending on the pore-forming diluents and molar ratio of monomers. The assessed properties included the chemical and porous structure, thermal stability, and sorption capacity of the obtained polymers towards methylene blue. The abovementioned characteristic was carried out for two series of copolymers with molar ratios of monomers of 1:2, 1:1 and 2:1, synthetized with toluene and a mixture of decanol and benzyl alcohol. The structure of the polymers was confirmed by FTIR and elemental analysis. The results of TGA demonstrated the main influence on thermal stability was the composition of polymers, whereas the impact of porogens was negligible. The S_BET varied in the range of 12–534 m²g⁻¹ for polymers obtained with toluene and 0–396 m²g⁻¹ with the mixture of alcohols. Toluene enhanced the formation of micro- and mesopores, while the mixture of alcohols enhanced the creation of meso- and macropores. For the polymers prepared with toluene, their effectiveness in water purification decreases in the following order: DVB-GMA 2:1 > DVB-GMA 1:1 > DVB-GMA 1:2, according to the decreasing values of porous structure parameters. In the case of a series obtained with a mixture of alcohols, such correlation was not observed. Full article