Search Results (215)

Silica aerogels are ideal candidates for gas adsorption due to their exceptional porosity and high specific surface area; however, the inherent mechanical fragility of their skeletal framework significantly compromises their operational stability in engineering applications. While the incorporation of carbon nanomaterials effectively enhances the mechanical robustness of aerogels, the specific microscopic mechanisms by which filler microstructure and surface chemistry dictate gas adsorption behavior remain insufficiently understood. In this study, we employed all-atom molecular dynamics (MD) simulations to develop a model of silicon-based porous composites synergistically doped with carbon nanotubes (CNTs) and graphene. The adsorption and diffusion characteristics of nitrogen (N₂) were systematically investigated across a CNT doping concentration range of 5% to 20%, and the influence of surface hydrophilicity/hydrophobicity on adsorption performance was quantitatively analyzed by modulating potential energy parameters. Our results demonstrate that the introduction of CNTs reconfigures the porous architecture, leading to an approximately 18.25% increase in the normalized specific surface area, which subsequently drives a 15% enhancement in the overall adsorption capacity of the composite. Nevertheless, analysis reveals that the weight-specific adsorption efficiency of the CNT component itself exhibits a declining trend as the doping concentration increases. This phenomenon is primarily attributed to the convex curvature of the CNTs, which restricts the effective contact area and weakens the adsorption potential, alongside the steric hindrance effects arising from local filler agglomeration at higher concentrations. Furthermore, surface chemical properties exert a significant regulatory influence on adsorption; a strongly hydrophilic modified surface (λ = 1.5) achieved an adsorption capacity approximately 98% higher than the baseline condition—an improvement that exceeds the gains provided by purely physical volume expansion. This research elucidates the synergistic mechanism between physical architecture and surface chemical modification in the adsorption process, suggesting that while the physical architecture determines the abundance of potential adsorption sites, the surface chemistry governs the actual efficiency of site utilization. These findings provide critical theoretical insights for the future design of composite aerogel materials that balance structural stability with superior adsorption performance. Full article

Graphene-based aerogels (GAs) exhibit outstanding performance in the adsorption of organic contaminants. Consequently, numerous studies have investigated the use of GAs for this purpose. In this work, the synthesis methods commonly used to produce GAs are first briefly described, and their key characteristics are summarized. Subsequently, GAs are classified according to the modifications applied to improve their adsorption properties toward organic pollutants. Furthermore, the quantitative relationships between surface area, density, surface chemistry, and adsorption performance for organic contaminants are systematically reviewed. The analysis revealed that the adsorption of two representative organic contaminants, toluene and methylene blue, is not dependent on the surface area of GAs. In contrast, GAs with lower density exhibit an improved adsorption capacity for toluene. Additionally, the relationship between the surface chemistry of GAs and their adsorption capacity toward methylene blue was analyzed considering the concentration of carboxylic sites. The available data suggests a potential correlation between the concentration of carboxylic groups on the surface of GAs and their adsorption capacity for methylene blue. This observation is supported by the analysis of methylene blue species in aqueous solution and the pH at the point of zero charge of GAs, which indicate that the interaction occurs mainly through electrostatic attractions resulting from the deprotonation of acidic surface sites. Finally, several opportunity areas and future research directions regarding the use of GAs for pollutant adsorption are discussed. 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

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

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

Phenolic aerogels offer low thermal conductivity, excellent thermal stability, and high char yield, but they suffer from intrinsic brittleness, low compressive modulus, and limited compressive strain. To overcome these limitations, phenolic aerogels modified with graphene oxide were synthesized and their structural, mechanical, and thermal insulation properties were evaluated. The GO fillers were uniformly dispersed in the phenolic matrix without disrupting its porous structure. Mechanical testing revealed that the modified aerogel achieved a compressive modulus of 265.52 MPa, representing a 67% increase over the pure phenolic aerogel’s value of 158.49 MPa, and a compressive strength of 40.19 MPa, compared to 6.18 MPa, for the pure sample. At the same time, the composite maintained good thermal insulation performance, with a thermal conductivity of 0.063 W·m⁻¹·K⁻¹. This work demonstrates a feasible approach to tailoring the structure–property relationship of phenolic aerogels via GO modification, supporting their potential use in high-temperature insulation and lightweight structural applications. 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

All-medium metamaterial absorbers (MMAs) have attracted considerable attention for ultra-broadband electromagnetic wave (EMW) absorption. Herein, a lightweight graphene aerogel (GA) was synthesized through a low-temperature, atmospheric-pressure reduction route. Benefiting from its 3D porous network, enriched oxygen-containing functional groups, and improved graphitization, the GA offers diverse intrinsic attenuation pathways and a limited effective absorption bandwidth (EAB) of only 6.46 GHz (11.54–18.00 GHz at 1.95 mm). To clarify its attenuation mechanism, nonlinear least-squares fitting was used to quantitatively separate electrical loss contributions. Compared with graphene, the GA shows markedly superior attenuation capability, making it a more suitable medium for MMA design. Guided by equivalent circuit modeling, a stacked frustum-configured GA-based MMA (GA-MMA) was developed, where structure-induced resonances compensate for the intrinsic absence of magnetic components in the GA, thereby substantially broadening its absorption range. The GA-MMA achieves an EAB of 40.7 GHz (9.1–49.8 GHz, reflection loss < −10 dB) and maintains stable absorption under incident angles up to ± 70°. Radar cross-section simulations further indicate its potential in electromagnetic interference mitigation, human health protection, and defense information security. This work provides a feasible route for constructing ultralight and broadband MMAs by coupling electrical loss with structural effects. Full article

Direct Air Capture (DAC) technology plays a crucial role in reducing atmospheric CO₂, but large-scale deployment faces challenges such as high energy consumption, operational costs, and slow material development. This study provides a comprehensive review of DAC principles, including chemical and solid adsorption methods, with a focus on emerging technologies like Metal–Organic Frameworks (MOFs) and graphene aerogels. MOFs have achieved adsorption capacities up to 1.5 mmol/g, while modified graphene aerogels reach 1.3 mmol/g. Other advancing approaches include DAC with Methanation (DACM), variable-humidity adsorption, photo-induced swing adsorption, and biosorption. The study also examines global industrialization trends, noting a significant rise in DAC projects since 2020, particularly in the U.S., China, and Europe. The integration of DAC with renewable energy sources, such as photovoltaic/electrochemical regeneration, offers significant cost-reduction potential and can cut reliance on conventional heat by 30%. This study focuses on the integration of Artificial Intelligence (AI) for accelerating material design and system optimization. AI and Machine Learning (ML) are accelerating DAC R&D: high-throughput screening shortens material design cycles by 60%, while AI-driven control systems optimize temperature, humidity, and adsorption dynamics in real time, improving CO₂ capture efficiency by 15–20%. The study emphasizes DAC’s future role in achieving carbon neutrality through enhanced material efficiency, integration with renewable energy, and expanded CO₂ utilization pathways, providing a roadmap for scaling DAC technology in the coming years. Full article

Honeycomb graphene aerogels offer a combination of graphene wall qualities, such as mechanical strength and binding, and the unique, engineered architecture of honeycombs. The honeycomb structure opens new opportunities for property modification, such as reinforcement with metal nanoparticles, which can increase strength and electrochemical performance. This study uses molecular dynamics simulations to examine the reinforcement of graphene honeycomb aerogels containing 2.7% and 5.8% randomly distributed Ni or Al nanoparticles. Metal nanoparticles considerably increase the resistance to compression: stress increase occurred for aerogels with Al nanoparticles at a density of 1.3 g/cm³, while for aerogels and filled with Ni, stress increase occurred at 2.0 g/cm³. The strengthening mechanism is volume repulsion when Al NPs repel the graphene cell walls, while Ni nanoparticles easily spread along the cell walls and provide less compression resistance, analogous to pure graphene aerogels. The tensile properties remained unaffected by the presence of either nanoparticle type since the same deformation mechanism (cell collapse) occurred for all aerogels. The maximal ultimate tensile strength achieved was 160 GPa. Temperatures ranging from 300 to 3000 K slightly affected the strength of all aerogels. Full article

By combining the superior capacity of graphene oxide with alginate matrix in a nanohybrid aerogel structure, great potential can be developed for technical features and use in areas such as biomedicine. The aim of this study is the production of graphene oxide incorporated nanohybrid aerogels using ambient pressure drying technique for drug loading and release. The produced nanostructures were identified with electron microscopy, X-ray diffraction, dynamic light scattering, and spectroscopic techniques. The surface area of the nanomaterials was examined by methylene blue method. Drug adsorption capacity of the nanohybrid aerogels was investigated by conducting batch adsorption studies using the model drug diclofenac sodium (DS). The equilibrium time of drug adsorption was determined and adsorption kinetics were modeled. The adsorption equilibrium time of the drug on the adsorbent was found to be 3 h. Equilibrium data were modeled by using the Langmuir and the Freundlich isotherms and according to the Langmuir isotherm, the maximum adsorption capacity was found to be 20.83 mg/g. Results showed the potential of the produced nanohybrid aerogels to be used as drug adsorbents for drug delivery applications. The results obtained from this study will be useful in drug production and treatment. Full article

In this work, samples of reduced graphene oxide (rGO) were prepared by treating graphite oxide (GrO) with thiourea (TU) and ascorbic acid (AA). Aerogels rGO-TU and rGO-AA were prepared using the freeze-drying method and were analyzed using X-ray diffraction, FTIR and Raman spectroscopy, ¹H and ¹³C NMR, TEM, and SEM-EDS. Based on the NMR, FTIR, SEM-EDS, and TEM data, GO with TU is reduced with simultaneous functionalization of its oxygen-containing groups. According to ¹H and ¹³C NMR data, the reduction of GO occurred simultaneously with an interaction of the amino groups of thiourea with carbonyl groups on the graphene sheets, forming an imine bond. This is evidenced by the appearance of additional signals in the ¹³C spectrum of GO-TU samples in the region of 140–230 ppm. The Boehm titration method showed that the number of oxygen-containing groups in rGO-TU aerogels decreased by about five times compared to GO. However, thiourea interacts with the GO surface, most likely due to electrostatic interaction and hydrogen bonds. The adsorption capacity of rGO-TU aerogel with respect to methylene blue (MB) after 1440 min was 60.2 mg/g, while for rGO-AA it was 71.4 mg/g. This fact indicates the importance of optimizing GO reduction to increase the number of active sites. Full article

Thermal energy storage (TES) plays a vital role in advancing energy efficiency and sustainability, with phase change materials (PCMs) receiving significant attention due to their high latent heat storage capacity. Nevertheless, conventional PCMs face critical challenges such as leakage, phase separation, and low thermal conductivity, which hinder large-scale applications. Encapsulation strategies have been developed to address these issues, and bio-based composite materials are increasingly recognised as sustainable alternatives. Materials such as lignin, nanocellulose, and biochar, as well as hybrid formulations with graphene and aerogels, show promise in improving thermal conductivity, mechanical integrity, and environmental performance. This review evaluates bio-based encapsulation approaches for PCMs, examining their effectiveness in enhancing heat transfer, durability under thermal cycling, and scalability. Applications in solar energy systems, building insulation, and electronic thermal regulation are highlighted, as are emerging AI-driven modelling tools for optimising encapsulation performance. Although bio-based PCM composites outperform conventional systems in terms of thermal stability and multifunctionality, they still face persistent challenges in terms of cost-effectiveness, scalability, and long-term reliability. Future research on smart, multifunctional PCMs and advanced bio-nanocomposites is essential for realising next-generation TES solutions that combine sustainability, efficiency, and durability. Full article

The development of effective materials for uranium extraction from seawater is vital for advancing sustainable energy solutions. However, the efficient recovery of uranium from seawater presents significant challenges due to its extremely low concentration, the presence of competing ions, and the complex marine environment. To address these issues, various materials such as inorganic and organic sorbents, chelating resins, nanostructured sorbents, and composite materials have been explored. More recently, the functionalization of carbon-based materials for enhanced adsorption properties has attracted much interest because of their high specific surface area, excellent chemical and thermal stability, and tunable porosity. These materials include activated carbon, graphene oxide, biochar, carbon cloths, carbon nanotubes, and carbon aerogels. The enhancement of carbonaceous materials is typically achieved through surface functionalization with chelating groups and the synthesis of composite materials that integrate other high-performance sorbents. This review aims to summarize the work of these functionalized carbon materials, focusing on their adsorption capacity, selectivity, and durability for uranium adsorption. This is followed by a discussion on the binding mechanisms of uranium with major chelating functional groups grafted on carbonaceous sorbents. Finally, an outlook for future research is suggested. We hope that this review will be helpful to researchers engaged in related studies. Full article