Search Results (156)

High-performance thermal protection materials are urgently required in harsh thermal environments, such as hypersonic vehicles, the thermal runaway of energy batteries and high-temperature equipment. Conventional aerogels only exhibit passive thermal insulation and fail to resist instantaneous high-temperature attack. Herein, a cooling material of ammonium oxalate (AO) was introduced to achieve efficient, active endothermic protection. A cellular isolation effect induced by graphene nanosheets combined with anti-solvent crystallization was adopted to significantly decrease the size of AO crystals by over 93%. Based on superfine morphology and the constructed conduction network, the decomposition rate and heat absorption capacity of obtained graphene-doped AO powders (GdAPs) are improved by 41.2% and 30.4%, respectively. The mechanisms of morphology regulation and enhanced heat absorption are explored specifically in this study. Furthermore, GdAPs are embedded in phenolic resin to prepare thermal protection composite materials. Benefiting from their nearly complete thermal decomposition, GdAPs serve as a sacrificial template to generate discrete micropores in pyrolyzed resin. So, the as-prepared carbon aerogels (CAs) with a regulable microstructure exhibit an extremely low thermal conductivity of 0.056 W/(m·K), which is lower than those of reported CAs with the same density. Based on the above advantages, a synergistic endothermic-insulating thermal protection material is reported for the first time, and its heating rate is only 28.6% of that of commercial silica aerogel under identical high-temperature shock. Therefore, a new accessible strategy is demonstrated to provide high-efficiency thermal protection for resisting both abrupt and prolonged high temperature. Full article

In recent years, oil spill accidents and oily wastewater discharge have posed severe threats to aquatic ecosystems and human health. Developing green, low-cost, efficient, and recyclable oil–water separation materials is therefore important for environmental remediation. In this work, kaolin/cellulose composite aerogels were fabricated through a low-temperature NaOH/urea dissolution system using N,N′-Methylenebisacrylamide (MBA) as the cross-linking agent, followed by freeze-drying and hydrophobic modification with Methyltrimethoxysilane (MTMS). The structure, morphology, thermal stability, wettability, mechanical behavior, oil adsorption capacity, and reusability of the aerogels were systematically investigated. The composite aerogels exhibited a honeycomb-like interconnected porous structure with low density and high porosity. Kaolin acted as an inorganic reinforcing and roughness-regulating component, which promoted the formation and anchoring of an MTMS-derived siloxane/SiO₂-like hydrophobic layer on the aerogel surface. The modified aerogels showed superhydrophobicity with a water contact angle above 152° and excellent oleophilicity. The optimized SC3K0.5 aerogel delivered adsorption capacities of 13.5 g/g for pump oil and 12.5 g/g for diesel. After 10 adsorption–desorption cycles, the adsorption capacity remained above 90% of the initial value, indicating good recyclability and mechanical stability. This recyclable kaolin/cellulose aerogel provides a feasible strategy for practical oil–water separation and oily wastewater treatment. Full article

Aerogels derived from microbial exopolysaccharides are useful in the food, pharmaceutical, and environmental sectors, but their application in anticancer therapy is constrained by inadequate characterization, especially regarding effects on normal cells. This study used ethanol precipitation and trichloroacetic acid deproteinization to extract crude exopolysaccharide from the fermentation broth of Bacillus amyloliquefaciens SQ-2. The pure fraction, EPS-3791, was obtained using Sephadex G-100 gel filtration chromatography and DEAE cellulose ion exchange. The weight–average molecular weight of EPS-3791 was 64.4 kDa. Monosaccharide analysis indicated fructan as the dominant component, which was consistent with the results of methylation analysis and NMR spectroscopy, confirming that EPS-3791 is a fructan mainly linked by →1)–Fruf–(2→bonds. UV scanning indicated high purity. FTIR analysis revealed functional groups including hydroxyl, carbonyl, and C–O–C groups. EPS-3791 exhibited a porous three-dimensional network morphology by SEM, with a decomposition temperature of 191.61 °C by TGA. Additionally, aerogels were prepared by freeze drying. EPS-3791 aerogels demonstrated minimal cytotoxicity to normal L929 cells while inhibiting the growth of human lung cancer A549, breast cancer MCF–7, and cervical cancer HeLa cells in a dose-dependent manner. Scratch wound healing experiments revealed that EPS-3791 aerogels hindered HeLa cell migration while promoting L929 wound closure. These findings identify EPS-3791 as a fructan-type exopolysaccharide aerogel with specific anticancer properties. Full article

Accurate thermal characterization of building insulation materials is essential for reliable energy performance assessment, regulatory compliance, and the development of high-performance envelopes. On one hand, the growing adoption of innovative insulating products, such as nanoporous materials, aerogel-based composites, bio-based panels, and thin insulating coatings, helps to enhance buildings’ energy efficiency by means of sustainable raw materials. On the other hand, conventional measurement techniques encounter significant challenges, due to their heterogeneity, reduced thickness, and unconventional geometries. In this study, an intra-laboratory comparison of three widely used methods for thermal conductivity determination is presented: the Transient Plane Source (TPS, Hot Disk) method, the Guarded Hot Plate (GHP) method, and the Heat Flow Meter (HFM) method. A total of twelve insulating materials, spanning super-insulating cores, insulating renders, bio-based panels, and nanocomposite coatings, were experimentally characterized under controlled laboratory conditions. A view on the analyzed insulating materials’ cradle-to-grave environmental impact is also given, to enhance the users’ awareness for the highly informed choice. The results highlight systematic differences between transient and steady-state approaches, with TPS measurements generally exhibiting larger deviations for materials characterized by surface roughness, limited thickness, or strong internal heterogeneity. In contrast, GHP and HFM methods show closer agreement when specimen geometry and stabilization requirements are satisfied. The influence of contact resistance, probing depth, specimen preparation, and uncertainty propagation is critically analyzed for each technique. The study provides practical insights into the applicability limits of commonly used thermal characterization methods and emphasizes the importance of selecting measurement techniques in relation to material morphology and testing constraints. These findings support more reliable thermal property assessment of emerging insulation materials and contribute to improved consistency between laboratory measurements and energy performance evaluations for buildings. Full article

Sol–gel processing provides an unusually controllable route to nanoporous solids, making silica aerogels the leading reference systems for extremely low thermal conductivity due to their high porosity, nanoscale pore sizes, and tunable solid frameworks. Under near-ambient conditions, thermal transport is multi-scale and multiphase, arising primarily from coupled solid conduction through the skeletal network and gas conduction within the pore space. Accordingly, aerogel design has emphasized suppressing solid-phase transport by reducing network connectivity, increasing tortuosity, and enhancing boundary scattering, while also limiting gaseous conduction through the control of pore size and gas pressure. This critical review provides an integrated overview of these mechanisms and the theory-to-experiment toolbox used to quantify the separate and combined contributions of the solid and gas phases to the effective thermal conductivity. We link key structural and environmental parameters (porosity, pore size distribution, density, backbone morphology, and pressure) to dominant transport regimes and the assumptions embedded in common models. Classical approaches, including effective-medium and percolation-based models, are assessed alongside phonon-scaling descriptions that incorporate characteristic length scales. Particular attention is given to the Knudsen effect and pressure-sensitive gas-conduction models, which are central to interpreting performance at atmospheric conditions and under vacuum or low-pressure operation. This review highlights inconsistencies across datasets and modeling practices, identifies persistent knowledge gaps, and outlines practical directions toward processable structure–property guidelines for manufacturing aerogels with targeted thermal performance, with regard to conduction-dominated heat transport mechanisms. Full article

This study evaluates the impact of a comprehensive design integrating precursor type, reduction and freeze-casting on the development of aerogels with high sorption capacity for engine oil. In this respect, the graphene oxide was varied from commercial to expanded; the reduction approach relied either on purely hydrothermal or combined hydrothermal–chemical reduction approaches. Following the synthesis, freeze-casting was applied at −5 °C and −196 °C. To further improve the reduction degree, annealing in an inert atmosphere was employed upon drying. The effects of precursors, reduction approach, freeze-casting and annealing were systematically investigated. Characterization techniques, including FT-IR, Raman spectroscopy, SEM, and EDS, were used to correlate the degree of reduction and morphological features of the porous structure with the absorption properties. The use of expanded GO as a precursor yielded aerogels with more homogeneous three-dimensional networks, a reduced bulk density of 3 mg cm⁻³, and lower oxygen-containing functional group content, thereby achieving consistently superior oil absorption of 270 g g⁻¹, with an oil occupancy of 94%. The process was found to fit well with the pseudo-first-order kinetic model. The results demonstrate that a comprehensive approach—considering combined reduction, freeze-casting, and thermal annealing—enables the tailored optimization of both the structure and absorption performance of GO aerogels for the remediation of oil spills. Full article

The selective removal of trace heteroatomic contaminants from fuel remains a critical challenge for clean combustion and refinery upgrading, particularly due to the chemical stability and structural similarity of sulfur- and nitrogen-containing aromatics. Herein, a surface-engineered graphene oxide aerogel functionalized with cyclodextrin (β-CD-CONH-GO) is developed via covalent grafting to introduce well-defined host–guest recognition sites within a porous framework. Spectroscopic and microscopic characterizations confirm successful functionalization, preserved aerogel morphology, and accessible hybrid interfaces. The removal process for monocyclic, bicyclic, and tricyclic impurities is governed by synergistic molecular inclusion within the cyclodextrin cavity, interfacial hydrogen bonding, and secondary confinement provided by the aerogel porosity. Thus, the β-CD-CONH-GO exhibits efficient adsorption toward representative bicyclic impurities, and the removal performance follows the order of indole > quinoline > benzothiophene. Kinetic analysis demonstrates pseudo-second-order adsorption behavior, indicating chemisorption dominated by cooperative host–guest recognition and hydrogen bonding. It possesses removal selectivity even in mixed systems containing structurally similar aliphatic and aromatic competitors and maintains > 95% efficiency after five regeneration cycles via ethanol extraction, confirming superb durability. This study demonstrates a feasible pathway to design adsorbents for deep fuel refining and highlights cyclodextrin-based graphene hybrid aerogels as promising candidates for separations. Full article

The development of cheap and efficient photocatalysts for the degradation of organic pollutants in textile printing and dyeing wastewater is of great importance for addressing environmental issues, although it remains challenging. In this study, nano-CuS particles were doped on cotton linter aerogels using a straightforward method for the degradation of methylene blue (MB) and organic pollutants in textile wastewater. Material morphology and structure were analyzed using XRD, SEM/EDS mapping, XPS, BET surface area measurements, and UV-Vis spectroscopy, while their performance was evaluated through various tests. The results demonstrated that a 10 mg catalyst material achieved complete degradation of a 20 mL methylene blue solution (15 mg/L) within 120 min. Moreover, the degradation rates of two types of textile wastewater, reactive red wastewater and reactive yellow wastewater, were both above 90% within 120 min and reached complete degradation within 150 min using the 10 mg catalyst material. The experimental results demonstrate that copper sulfide nanoparticles anchored in cotton linter carbon aerogel can increase the contact area of the photocatalytic reaction system, improve the photoelectron transfer, and thus enhance the photocatalytic reaction efficiency, providing a useful foundation for developing economical photocatalysts and effective dye degradation technologies. Full article

Recently, the state of the art of aerogels (AGs) has been reviewed, reporting first on their classification, based on the chemical origin of their precursors and the different methods existing to prepare them. Additionally, AGs of inorganic origin (IAGs) were contemplated, deeply discussing the properties, specific synthesis, and possible uses of silica and metal oxide-based AGs, since they are the most experimented and patented AGs already commercialized in several sectors. In this second part review, IAGs are examined again, but chalcogenide and metals AGs (CAGs and MAGs) are debated, since they are still too little studied, patented, and marketed, despite their nonpareil properties and vast range of possible applications. First, to give readers unaware of the previous work on AGs, a background about IAGs, all their main subclasses have been reported and their synthesis, including sol–gel, epoxide addition (EA), and dispersed inorganic (DIS) methods, as well as procedures involving the use of pre-synthesized nanoparticles as building blocks, have been discussed. Morphology and microstructure images of materials prepared by such synthetic method have been supplied. Conversely, the methods needed to prepare CAGs and MAGs, topics of this study, have been debated separately in the related sections, with illustrative SEM images. Their possible uses, properties, and some comparisons of their performance with that of other AGs and not AG materials traditionally tested for the same scopes, have also been disserted, reporting several case studies in reader-friendly tables. Full article

Hybrid polysaccharide-based aerogels offer significant potential as advanced drug delivery platforms due to their tunable structure, high porosity, and biocompatibility. In this study, aerogel microparticles were synthesized using alginate, pectin, carrageenan, and their hybrid formulations via an emulsion–gelation technique followed by supercritical fluid CO₂ extraction. The resulting aerogels exhibit mesoporous structures with specific surface areas ranging from 324 to 521 m²/g and pore volumes between 1.99 and 3.75 cm³/g. Comprehensive characterization (SEM, gas sorption, XRD, TGA, DSC, and FTIR) confirmed that hybridization improved morphological uniformity and thermal stability compared to single polymer aerogels. Ibuprofen was used as a model drug to evaluate loading efficiency and release kinetics. Among all formulations, the alginate/carrageenan (2:1) hybrid showed the highest drug loading efficiency (93.5%) and a rapid release profile (>90% within 15 min), closely matching the performance of commercial ibuprofen tablets. Drug release followed Fickian diffusion, as confirmed by the Korsmeyer–Peppas model (R² > 0.99). These results highlight the potential of hybrid polysaccharide aerogels as vehicles for drug delivery and other fast-acting therapeutic applications. Full article

Polymer gel-based triboelectric nanogenerators (TENGs) have emerged as versatile platforms for self-powered sensing due to their inherent softness, stretchability, and tunable conductivity. This review comprehensively explores the roles of polymer gels in TENG architecture, including their function as triboelectric layers, electrodes, and conductive matrices. We analyze four operational modes—vertical contact-separation, lateral-sliding, single-electrode, and freestanding configurations—alongside key performance metrics. Recent studies have reported output voltages of up to 545 V, short-circuit currents of 48.7 μA, and power densities exceeding 120 mW/m², demonstrating the high efficiency of gel-based TENGs. Gel materials are classified by network structure (single-, double-, and multi-network), matrix composition (hydrogels, aerogels, and ionic gels), and dielectric medium. Strategies to enhance conductivity using ionic salts, conductive polymers, and nanomaterials are discussed in relation to triboelectric output and sensing sensitivity. Morphological features such as surface roughness, porosity, and micro/nano-patterning are examined for their impact on charge generation. Application-focused sections detail the integration of gel-based TENGs in health monitoring (e.g., sweat, glucose, respiratory, and tremor sensing), environmental sensing (e.g., humidity, fire, marine, and gas detection), and tactile interfaces (e.g., e-skin and wearable electronics). Finally, we address current challenges, including mechanical durability, dehydration, and system integration, and outline future directions involving self-healing gels, hybrid architectures, and AI-assisted sensing. This review expands the subject area by synthesizing recent advances and offering a strategic roadmap for developing intelligent, sustainable, and multifunctional TENG-based sensing technologies. Full article

Aerogels (AGs) are highly porous, low-density, disordered, ultralight macroscopic materials with immense surface areas. Traditionally synthesized using aqueous sol–gel chemistry, starting by molecular precursors, the nanoparticles (NPs) dispersions gelation method is nowadays the most used procedure to obtain AGs with improved crystallinity and broader structural, morphological and compositional complexity. The Sol–gel process consists of preparing a solution by hydrolysis of different precursors, followed by gelation, ageing and a drying phase, via supercritical, freeze-drying or ambient evaporation. AGs can be classified based on various factors, such as appearance, synthetic methods, chemical origin, drying methods, microstructure, etc. Due to their nonpareil characteristics, AGs are completely different from common NPs, thus covering different and more extensive applications. AGs can be applied in supercapacitors, acoustic devices, drug delivery, thermal insulation, catalysis, electrocatalysis, gas absorption, gas separation, organic and inorganic xenobiotics removal from water and air and radionucleotides management. This review provides first an analysis on AGs according to data found in CAS Content Collection. Then, an AGs’ classification based on the chemical origin of their precursors, as well as the different methods existing to prepare AGs and the current optimization strategies are discussed. Following, focusing on AGs of inorganic origin, silica and metal oxide-based AGs are reviewed, deeply discussing their properties, specific synthesis and possible uses. These classes were chosen based on the evidence that they are the most experimented, patented and marketed AGs. Several related case studies are reported, some of which have been presented in reader-friendly tables and discussed. Full article

The development of advanced wound dressing materials with enhanced antibacterial properties is critical for improving patient outcomes and reducing infection risks. This study introduces a novel bio-based aerogel composed of copper-crosslinked alginate and hyaluronic acid, synthesized using supercritical gel drying techniques. Alginate and hyaluronic acid polymers are widely used in the pharmaceutical and medical industries because of their nontoxicity, biodegradability, and biocompatibility. This study aimed to create an aerogel that could be used as a potential wound dressing material by crosslinking hyaluronic acid and alginate with copper. The bio-based aerogel was prepared by ionic gelation and supercritical gel drying. The prepared materials were characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), BET surface area analysis, and energy-dispersive X-ray fluorescence (XRF). Moreover, the aerogel wound dressing properties were evaluated in terms of fluid uptake and antibacterial activity against S. aureus and E. coli. The physicochemical characterization of the prepared aerogels revealed their unique structural and morphological features, which are influenced by copper ion concentration and crosslinking time. Regarding their wound dressing evaluation, both aerogel and hydrogel were found to have antibacterial properties when tested on S. aureus with inhibition zones of (36 mm, 23 mm) and E. coli (31.6 mm, 21 mm) for hydrogel and aerogel, respectively. Also, excellent fluid uptake was found to reach up to 743%. These findings underscore the potential of copper-crosslinked alginate–hyaluronic acid aerogels as innovative wound dressing materials that combine superior antibacterial efficacy with excellent fluid management, paving the way for improved wound healing solutions. Full article

Although publications have documented the osteo-inductive effects of various bioactive materials on tissue sections, the associated morphologic patterns of tissue remodeling pathways at the cellular level have not been detailed. Therefore, we present a comparative histopathological follow-up evaluation of bone defect repair mediated by silica aerogels and methacrylate hydrogels over a 6-month period, which is the widely accepted time course for complete resolution. Time-dependent microscopic analysis was conducted using the “critical size model”. In untreated rat calvaria bone defects (control), re-ossification exclusively started at the lateral regions from the edges of the remaining bone. At the 6th month, only a few new bones were formed, which were independent of the lateral ossification. The overall ossification resulted in a 57% osseous encroachment of the defect. In contrast, aerogels (AE), hydrogels (H), and their β-tricalcium-phosphate (βTCP)-containing counterparts, which were used to fill the bone defects, characteristically induced rapid early ossification starting from the 1st month. This was accompanied by fibrous granulomatous inflammation with multinucleated giant macrophages, which persisted in decreasing intensity throughout the observational time. In addition to lateral ossification, multiple and intense intralesional osseous foci developed as early as the 1st month, and grew progressively thereafter, reflecting the osteo-inductive effects of all compounds. However, both βTCP-containing bone substituents generated larger amounts and more mature new bones inside the defects. Nevertheless, only 72.8–76.9% of the bone defects treated with AE and H and 80.5–82.9% of those treated with βTCP-containing counterparts were re-ossified by the 6th month. Remarkably, by this time, some intra-osseous hydrogels were found, and traces of silica from AE were still detectable, indicating these as the causative agents for the persistent osseous–fibrous granulomatous inflammation. When silica or methacrylate-based bone substituents are used, chronic ossifying fibrous granulomatous inflammation develops. Although 100% re-ossification takes more than 6 months, by this time, the degree of osteo-fibrous solidification provides functionally well-suited bone repair. Full article

Lithium–sulfur batteries (LSBs), possessing excellent theoretical capacities, advanced theoretical energy densities, low cost, and nontoxicity, are one of the most promising energy storage battery systems. However, some issues, including poor conductivity of elemental S, the “shuttle effect” of high-order lithium polysulfides (LiPSs), and sluggish reaction kinetics, hinder the commercialization of LSBs. To solve these problems, various carbon-based aerogels with developed surface morphology, tunable pores, and electrical conductivity have been examined for immobilizing sulfur, mitigating its volume variation and enhancing its electrochemical kinetics. In this paper, an extensive generalization about the effective preparation methods of carbon-based aerogels comprising the combined method of carbonization with the gelation of precursors and drying processes (ambient pressure drying, freeze-drying, and supercritical drying) is proposed. And we summarize various carbon carbon-based aerogels, mainly including graphene aerogels (Gas) and carbon nanofiber (CNF) and carbon nanotube (CNT) aerogels as cathodes, separators, and interlayers in LSBs. In addition, the mechanism of action of carbon-based aerogels in LSBs is described. Finally, we conclude with an outlook section to provide some insights into the application of carbon-based aerogels in electrochemical energy storage devices. Based on the discussion and proposed recommendations, we provide more approaches on nanomaterials in high-performance liquid or state LSBs with high electrochemical performance in the future. Full article