Search Results (479)

Primary aromatic amines (PAAs), such as 4,4′-methylenedianiline (MDA) and 4-chloroaniline (4-CA), are toxic, carcinogenic, and persistent pollutants widely detected in aquatic environments. To address this issue, UiO-66 was modified through nitro functionalization, copper doping, and defect regulation, and further integrated with chitosan (CS) to construct a composite aerogel (CS@CuUiO-66-NO₂) for the removal of MDA and 4-CA from wastewater. The adsorbent demonstrated relatively fast adsorption kinetics (MDA: 6 h; 4-CA: 4 h) and high adsorption capacities (MDA: 643.74 mg·g⁻¹; 4-CA: 491.54 mg·g⁻¹), showing improved performance compared to pristine UiO-66 and many previously reported adsorbents under similar conditions. The enhanced adsorption performance is likely attributed to the synergistic effects of multiple interactions, including hydrogen bonding, π-π interactions, and possible coordination interactions between functional groups of the adsorbent and PAAs. Moreover, the adsorbent maintained good adsorption performance after five adsorption–desorption cycles, with only a slight decrease in efficiency (~8%), and exhibited limited interference from coexisting anions. Overall, this study presents a feasible strategy for designing porous composite adsorbents with favorable reusability for potential applications in aqueous pollutant remediation. Full article

A warm-up is a critical procedure in sports science for enhancing muscular performance and optimizing subsequent athletic activities. However, the physiological and athletic performance effects of a warm-up are often transient, diminishing rapidly during the period of inactivity after the warm-up, which is known as the warm-up transition phase. In this study, a multi-functional thermoregulation wearable composite film of graphene–MXene–bacterial cellulose/polyethylene glycol (G-M-BC/PEG) was developed by integrating MXene (a two-dimensional material with good photothermal conversion performance) and graphene into a bacterial cellulose aerogel framework, subsequently impregnated with polyethylene glycol (PEG-2000). The film showed stable structure, efficient solar photothermal conversion and storage (SPCS), and improved mechanical properties. Under 1 sun irradiation, the optimized G-M-BC/PEG wearable film showed excellent SPCS performance, sustaining a temperature plateau of 38–40 °C for 10 min after the xenon lamp was switched off under 1 sun irradiation, with a leakage rate of only 5.32% after five cycles. By constructing a biomimetic sports human body model, the composite aerogel was shown to significantly elevate muscle surface temperature and effectively mitigate heat loss during the transition phase. In the warm-up effectiveness and sports performance tests, the wearable film improved 200 m sprint performance by 0.8% ± 0.4% (p = 0.039). It also maintained subjective thermal sensation during the warm-up transition phase, with no significant decline at 5 or 10 min after the warm-up and a significant decrease only at 15 min (p = 0.02), while thermal comfort remained stable, suggesting improved neuromuscular readiness. This research provided a novel strategy for the fabrication of advanced aerogel-based wearable devices aimed at precision thermal management and athletic performance optimization. Full article

Pesticides are a major cause of water contamination, making this issue a major environmental and public health concern. In this context, the development of advanced and effective remediation materials is needed. In this study, a titanium-functionalized magnetic silica aerogel (AG-Ti@Fe₃O₄-SA) was successfully prepared via microfluidics and evaluated for water decontamination. The structural and compositional features of the aerogel were determined using XRD, FT-IR, RAMAN, SEM, TEM, BET, and DLS, confirming the formation of the aerogel with dispersed Fe₃O₄-SA nanoparticles and the successful incorporation of titanium within the aerogel matrix. Regarding decontamination potential, the aerogel was tested against a pesticide mixture, yielding pesticide-dependent removal efficiencies (16–100%). Notably, the aerogel exhibited a high affinity for organophosphorus pesticides and a moderate affinity for polar compounds, whereas bulky hydrophobic pesticides showed lower adsorption. In vitro, the aerogel induced a moderate decrease in HaCaT cell viability after 48 h of exposure, accompanied by a slight increase in lactate dehydrogenase release, while HEK293 cells remained largely unaffected, indicating a cell-type-dependent biological response. Overall, the findings from this screening-level study recommend AG-Ti@Fe₃O₄-SA aerogel as a promising selective adsorbent for pesticide removal. Full article

Current strategies for treating organic dye wastewater are shifting from single-function removal processes and catalytic degradation methods toward more integrated treatment approaches. This study proposes a multifunctional composite integrating adsorption–photodegradation–intelligent recovery for photodegradation and recovery of methylene blue-contaminated wastewater. By optimizing the preparation process to precisely control the pore size and arrangement of the aerogel, a hierarchical porous framework with a high specific surface area is formed, featuring efficient mass transfer and ultra-multiple loading sites. The graphene framework enhances visible-light absorption by optimizing TiO₂ loading, agglomeration behavior and addressing detachable defects through a metal–polyphenol network. After 60 min of illumination, the degradation efficiency exceeds 99.5%, demonstrating superior cycling stability. After 100 cycles, the photocatalytic efficiency remains above 97%, showcasing excellent durability. Furthermore, the in situ polymerized thermoresponsive poly (N-isopropylacrylamide) (PNIPAm) composite exhibits smart responsiveness, enabling reversible temperature-responsive adsorption–desorption behavior within PNIPAm’s LCST range. with an adsorption capacity of 28,000 mg/g at LCST. Heating above LCST desorbs 90.2% of the wastewater, and adsorption stability remains above 98% after 100 thermal cycles, resolving operational challenges in mechanical wastewater recovery. The synergistic integration of an anisotropic porous structure, stable TiO₂ loading, and thermal responsiveness provides an efficient platform for integrated adsorption and recovery. Full article

Benefiting from their outstanding porosity, considerable specific surface area, and natural flexibility, cellulose nanofibers (CNFs)/MOF materials have emerged as competitive candidates for advanced flexible energy storage devices. However, conventional CNFs/MOFs aerogels or films often suffer from poor recoverability under compression, bending, and folding, accompanied by severe plastic deformation that compromises the cycling and structural stability of devices. To address this issue, we report a rationally designed flexible PU/CNFs/ZIF-8/PANI composite foam with an interconnected micro-mesoporous structure. Using polyurethane foam as a soft substrate and CNFs/ZIF-8 as building blocks, the composite was fabricated through a combined strategy of impregnation, in situ ZIF-8 growth, hot-pressing, and in situ aniline polymerization with simultaneous etching of the ZIF-8. The incorporation of carboxylated CNFs enhances the hydrophilicity of the PU skeleton. This, in combination with the hot-pressed framework, establishes an interconnected 3D network, thereby effectively preventing the agglomeration of active materials. Meanwhile, the hierarchical pores derived from the sacrificial ZIF-8 template provide abundant electroactive sites, accelerate ion transport, and facilitate high PANI loading. By virtue of this synergistic architectural effect, the resultant electrode achieves a high specific capacitance of 449 F/g at 0.2 A/g, with 97% capacitance retention after 2000 cycles at 5 A/g. Furthermore, the composite foam demonstrates excellent mechanical flexibility, with a tensile strength of 0.87 MPa and an elongation at break of 230%. This work offers a feasible approach for developing high-performance flexible supercapacitors and provides novel perspectives for the rational design of portable energy storage devices. Full article

Cellulose is a well-known biopolymer with excellent properties for a broad range of applications, including piezoelectricity for the development of nanogenerators. However, similar to other piezoelectric materials, the voltage outputs currently reported from cellulose-based piezoelectric nanogenerators (PENGs) could be overestimated due to the appearance of triboelectric processes. To understand the appearance of both phenomena, cellulose films and aerogels that had undergone several modifications to improve their piezoelectric behavior (i.e., thermal treatment and presence of piezoelectric/conductive particles) were developed and characterized. Our results show that these modifications significantly changed the dielectric properties (ε) and the piezoelectric coefficients (d₃₃), with increments as high as a factor of 4, although without a clear tendency regarding the sample characteristics. Under finger-tapping mechanical stimulation, nanogenerators (NGs) using pure cellulose films generated 6 V, whereas the modified cellulose films and aerogels either increased or decreased this value, with outputs between 2 and 10 V. Notably, ternary composites, having both conductive and piezoelectric ZnO particles, increased the generation up to 24 V. There was no correlation between the voltage generated and d₃₃ or d₃₃/ε values, although some relationship with ε was observed, meaning that a pure piezoelectric phenomenon was not observed. This lack of correlation and the drastic decrease in the voltage generated (around 0.2 V) after changing the NG configuration show that a triboelectric phenomenon from the multilayered structure significantly contributes to the voltage generation from cellulose samples. Full article

Fiber-reinforced aerogel composites are attractive for thermal protection applications because porous polymer networks can suppress heat transfer while maintaining structural stability. In this study, carbon fiber felt was integrated with a polyimide aerogel via a freeze-drying-assisted multicycle impregnation process to achieve controlled formation of interconnected aerogel networks within the fibrous scaffold. With increasing impregnation cycles, the composites exhibited progressive microstructural densification and improved structural stability. Although bulk density increased, thermal protection performance under prolonged butane-torch exposure was significantly enhanced, showing delayed backside temperature rise and improved resistance to structural degradation compared with bare carbon felt. Post-ablation analyses revealed the formation of a micro-/nanoporous polymer-derived char layer and a multilayer thermal-resistance structure, which contributed to suppressed heat transfer during flame exposure. These results indicate that effective thermal protection in CF/PA composites is governed by dynamic microstructural evolution and char-layer formation rather than intrinsic room-temperature thermal conductivity alone. The proposed multicycle impregnation strategy provides a scalable approach for designing lightweight polymer-based thermal protection materials operating in high-temperature environments. Full article

The global population explosion and accelerated industrialization have led to an increasing shortage of fossil fuels and environmental contamination, underscoring the urgent need to develop innovative energy storage technologies to improve energy utilization efficiency. As pivotal components in thermal energy storage (TES) systems, phase change materials (PCMs) enable spatiotemporal matching between thermal energy supply and demand through latent heat absorption and release during phase transitions. Organic PCMs are considered ideal candidates for thermal energy storage due to their high energy storage density, stable phase transition temperature, low supercooling, and negligible phase separation. However, inherent drawbacks such as low thermal conductivity, liquid leakage, limited light absorption, and lack of functionality have hindered their widespread application in advanced thermal management systems. Herein, we systematically summarize cutting-edge functionalization strategies for PCMs, progressing from conventional methods like thermal conductive particle blending and microencapsulation to the emerging design of 3D porous thermally conductive skeletons, including metal foams, boron nitride aerogels, carbon-based aerogels, and MXene aerogels. These frameworks not only enhance thermal transport via continuous conductive pathways and impart shape stability through capillary encapsulation but also, when integrated with photo-thermal, electro-thermal, and magneto-thermal conversion properties, enable broad applications in solar photo-thermal/photo-thermo-electric conversion, thermal management of electronics and batteries, building efficiency, and wearable thermal regulation. The review further addresses current challenges and future directions, highlighting scalable 3D framework fabrication, the shift to active thermal management, and innovative applications beyond conventional domains. By establishing a microstructure–property–application correlation, this work provides valuable insights for developing next-generation high-performance multifunctional phase change composites. Full article

A lightweight composite that simultaneously exhibits high strength and excellent thermal insulation is of great interest for thermal protection applications. In this study, dimensionally stable needled quartz fiber felt-reinforced phenolic aerogel composites were prepared using vacuum impregnation, sol–gel, and ambient pressure drying. The composites exhibit a multiscale porous structure formed by interconnected nanometer polymer skeletons and micronscale fibers. By regulating the thermoplastic phenolic resin concentration in the precursor solution, the pore structure of the material was refined; the average particle diameter reduced from 99.76 nm to 38.91 nm, and the average pore diameter decreased from 216.79 nm to 49.53 nm. At a phenolic resin concentration of 25%, the composite exhibits outstanding thermal insulation and mechanical properties: a low thermal conductivity of 0.0646 W·m⁻¹·K⁻¹ at room temperature, with a mere 19.5 °C temperature rise on the sample backside after 1800 s heating at 200 °C, and compressive strengths of 7.70 MPa in the XY-direction and 3.87 MPa in the Z-direction (at 10% strain). X-ray micro-CT characterized the internal structural evolution during loading, revealing a failure mechanism dominated by fiber buckling. Theoretical models and experimental data were used to analyze and quantify the contribution rates of gas and solid heat conduction in NQF/PR aerogel composites, with solid conduction accounting for over 80%. Combined with microstructural evolution, the mechanism for the high thermal insulation efficiency of NQF/PR aerogel composites was elucidated. This study prepared NQF/PR aerogel composites with promising application potential. By systematically evaluating their compressive behavior and quantifying the respective contributions of gas and solid conduction, this work provides a methodological framework to guide the rational design of similar aerogel composites. Full article

Silica aerogel microspheres demonstrate tremendous potential as fillers for diverse materials across various fields. Enhancing the strength of silica aerogel microspheres is therefore crucial for their practical applications. This study aims to develop novel hydrophobic polymer-reinforced silica aerogel microspheres using water glass as the precursor, hexamethyldisilazane (HMDS) as the modifier, and styrene as the crosslinking agent, with further strength enhancement achieved through short-term thermal post-treatment. The effects of varying polystyrene coating levels, crosslinker dosage, and short-term heat treatment on the structure and properties of silica aerogel were investigated. The optimized silica aerogel microspheres (Sample A-6) exhibited a specific surface area of 604.8 m²/g and a thermal conductivity of 0.030 W·m⁻¹·K⁻¹ and demonstrated excellent hydrophobicity and mechanical stability. Full article

To address the critical limitation of insufficient high-temperature structural stability in traditional formaldehyde-resorcinol aerogels for thermal protection applications, this study designed and fabricated a high-silica fiber felt-reinforced phenolic aerogel composite capable of in situ ceramization. The thermal insulation performance, structural stability, mechanical properties, and oxidation resistance mechanism after heat treatment at 1000 °C for 600 s were systematically investigated. Results demonstrated tunable density (0.398–0.629 g·cm⁻³), low room-temperature thermal conductivity (0.0414 W·m⁻¹·K⁻¹), and a stabilized back temperature of 408.6 °C during butane torch flame testing. After high-temperature treatment, the composite series exhibited a minimum volume shrinkage of 13.9% and a maximum mass retention of 77.6%. Specifically, the compressive strength and specific strength of the HS/C-75 sample reached 4.39 and 1.96 times those of the HS/C-0 sample, respectively. Further analysis revealed that the synergistic effect between the skeletal support of high-silica fibers and the in situ-formed ceramic phase effectively suppressed thermal shrinkage and improved oxidation resistance, achieving an optimized balance between thermal insulation and mechanical integrity. This work provides a theoretical foundation and viable technical pathway for developing advanced thermal protection materials with enhanced stability and reliability. Full article

Flexible supercapacitors have attracted significant attention as promising power sources for portable and wearable electronic devices. However, achieving simultaneous high power density, energy density and long-term cyclic stability in a simple device configuration remains a critical challenge. Herein, we report an all-solid-state flexible planar supercapacitor based on hierarchically structured cellulose nanofiber-carbon nanotube@manganese dioxide (CNF-CNT@MnO₂) composite aerogels. The electrode architecture is rationally designed by first dispersing CNTs within a hydrophilic CNF scaffold to form a conductive three-dimensional network, followed by in situ oxidative polymerization of MnO₂ onto the CNF-CNT fibrous skeleton. The hydrophilic CNFs network ensures thorough electrolyte penetration, the interconnected CNTs facilitate rapid electron transport, and the uniformly coated MnO₂ layer provides substantial pseudocapacitance. The aerogel electrode with a low density of 14.6 mg cm⁻³ and a high specific surface area of 214.4 m² g⁻¹ delivers a specific capacitance of 273.0 F g⁻¹ at 0.4 A g⁻¹. The assembled planar supercapacitor, incorporating gel electrolyte and a flexible hydrogel substrate, achieves an impressive areal capacitance of 885.0 mF cm⁻² at 2 mA cm⁻², energy density of 122.9 μWh cm⁻² and corresponding power density of 1000.0 μW cm⁻². The device exhibits excellent electrochemical stability, retaining 83.3% capacitance after 2500 charge–discharge cycles, and outstanding mechanical flexibility, with 96.3% capacitance retention after 200 repeated bending cycles. Furthermore, multiple devices can be connected in series or parallel to proportionally increase output voltage or current, meeting the practical power requirements of electronic applications. This work offers a viable pathway toward high-performance, durable energy storage solutions for next-generation wearable electronics. Full article

Aerogel-incorporated foam concrete has attracted significant attention in the construction sector owing to its light weight and superior thermal insulation properties. Nevertheless, its practical application in external wall insulation systems is hindered by the high cost of aerogel (AG) and the inherent trade-off between thermal efficiency and mechanical strength. To overcome these limitations, this study introduces a composite design that partially replaces AG with low-cost hollow glass microspheres (HGMs) and incorporates nano-silica (NS) as a strengthening agent. Foam concrete specimens with a constant dry density of 700 kg/m³ were fabricated with these additives. Through an orthogonal experimental approach, the synergistic effects of AG, HGMs, and NS on mechanical properties, porosity, water absorption, and durability were systematically evaluated. The results demonstrated that 4% AG content significantly reduced effective porosity by 33% and water absorption by 59%, while 4% HGM increased compressive and flexural strength by 13.5% and 19.7%, respectively. The addition of 2% NS further enhanced mechanical performance, yielding 25.9% and 21.6% improvements in compressive and flexural strength. The optimal formulation (A4H4N2) effectively balanced thermal insulation and mechanical properties, offering a viable strategy for producing cost-effective, high-performance foam concrete suitable for building envelope applications. Full article

In recent years, sustainable biopolymers have attracted increasing attention in environmental engineering as alternatives to conventional synthetic materials due to their renewable origins, biodegradability, and functional versatility. However, their performance and technological viability are strongly influenced by structural design, modification strategies, and behavior under realistic environmental conditions. This review critically analyzes recent advances in biopolymers for environmental remediation, covering their main application formats such as hydrogels, membranes, beads, aerogels, and composites, their interaction mechanisms with contaminants, and their performance relative to conventional adsorbents. Particular emphasis is placed on emerging approaches, including advanced functionalization, integration with inorganic phases, and green synthesis technologies, which have significantly improved efficiency, selectivity, and operational stability. Despite these advances, key limitations persist, particularly regarding mechanical robustness, regenerability, reproducibility, and scalability, underscoring the need for standardized evaluation protocols in complex matrices. The role of biopolymers within circular economy frameworks is also examined, emphasizing their capacity to integrate material sustainability, resource recovery, and multifunctional environmental applications. Overall, sustainable biopolymers are positioned not only as substitutes for traditional materials but also as strategic platforms for the development of next-generation regenerative environmental technologies. Full article

To address the integrated demands of structural reinforcement and energy-efficient retrofitting for existing buildings, a cementitious material modified with vitrified microspheres and SiO₂ aerogel was developed to realize the synergistic enhancement of thermal insulation and mechanical strength. By substituting fine sand with equal mass fractions of SiO₂ aerogel and vitrified microspheres in the cement matrix, this study systematically investigated the synergistic regulatory effects of this binary modification on two core performance metrics—thermal conductivity and compressive strength. All performance tests were conducted in triplicate, and the results are presented as the mean values. The results indicated that the thermal conductivity of the composite exhibited a trend of decreasing first and then increasing with the rise in aerogel content. At an aerogel dosage of 6%, the thermal conductivity dropped to 0.2237 W/(m·K), achieving optimal thermal insulation performance while retaining a compressive strength of 17.96 MPa. The subsequent incorporation of 15% vitrified microspheres further reduced the thermal conductivity to 0.1642 W/(m·K) while maintaining a compressive strength of 15.34 MPa, thereby achieving an optimal balance between thermal insulation and mechanical performance. Microstructural characterization revealed that the incorporation of aerogel significantly increased the internal porosity of the composite, effectively reducing thermal conductivity by obstructing heat transfer pathways. Vitrified microspheres enhance thermal resistance via their closed-cell structure and promote the formation and densification of C-S-H gel. Synergistically with SiO₂ aerogel, they construct a multi-scale porous composite system. By optimizing the interfacial bonding state and pore structure, this system achieves the synergistic optimization of mechanical strength and thermal insulation of cement-based composites, providing new materials and a theoretical basis for the functional integrated retrofitting of existing building structures. Full article