Search Results (278)

The increasing use of pharmaceutically active compounds (PhACs), endocrine-disrupting compounds (EDCs), and personal care products (PCPs) has led to the widespread presence of organic micropollutants (OMPs) in aquatic environments, posing a significant global challenge for environmental conservation. In recent years, advanced materials-based nanofiltration (NF) technologies have emerged as a promising solution for water and wastewater treatment. This review begins by examining the sources of OMPs, as well as the risk of OMPs. Subsequently, the key criteria of NF membranes for OMPs are discussed, with a focus on the roles of pore size, charge property, molecular interaction, and hydrophilicity in the separation performance. Against that background, this review summarizes and analyzes recent advancements in materials such as metal organic frameworks (MOFs), covalent organic frameworks (COFs), graphene oxide (GO), MXenes, hybrid materials, and environmentally friendly materials. It highlights the porous nature and structural diversity of organic framework materials, the advantage of inorganic layered materials in forming controllable nanochannels through stacking, the synergistic effects of hybrid materials, and the importance of green materials. Finally, the challenges related to the performance optimization, scalable fabrication, environmental sustainability, and complex separation of advanced materials-based membranes for OMP removal are discussed, along with future research directions and potential breakthroughs. Full article

In this study, we successfully synthesized olivine-type FePO₄ via an in situ oxidation method and further developed two composite cathode materials (o-FePO₄-1/GR-1 and o-FePO₄-1/GR-2) by incorporating graphene. The composites were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray Photoelectron Spectroscopy (XPS), revealing a three-dimensional porous layered structure with an enhanced surface area and strong interaction between FePO₄ nanoparticles and graphene layers. Electrochemical tests demonstrated that the composite electrodes exhibited significantly improved performance compared to pristine FePO₄, with discharge capacities of 147 mAh g⁻¹ at 1C and 163 mAh g⁻¹ at 0.1C for o-FePO₄-1/GR-2, approaching the level of LiFePO₄. The incorporation of graphene effectively enhanced the electrochemical reaction kinetics, highlighting the innovation of our method in developing high-performance cathode materials for lithium-ion batteries. Full article

Graphene oxide (GO) aerogels were discovered as lightweight, highly porous materials with exceptional mechanical, electrical, and thermal properties. These properties make them suitable for a wide range of advanced applications. This paper discusses GO aerogel synthesis processes, characterization, mechanical properties, applications, and future directions. The synthesis methods discussed include hydrothermal reduction, chemical reduction, crosslinking methods, and 3D printing, with major emphasis on their effects on the aerogel’s structural and functional attributes. A detailed analysis of mechanical characterization techniques is elaborated upon, along with highlighting the effects of parameters such as porosity, crosslinking, and graphene concentration on mechanical strength, elasticity, and stability. Research has been carried out to find GO aerogel applications in various sectors, such as energy storage, environmental remediation, sensors, and thermal management, showcasing their versatility and potential. Additionally, the combination of nanoparticles and doping strategies to improve specific properties is addressed. The review concludes by identifying current challenges in scalability, brittleness, and property optimization and proposes future directions for synthesis innovations. This work will be helpful for researchers and engineers exploring new possibilities for GO aerogels in both academic and industrial areas. Full article

This study reported covalent organic frameworks (COFs) and their hybrid composites with two-dimensional materials, graphene oxide (GO), graphitic carbon nitride (g-C₃N₄), and boron nitride (BN), to examine their structural, textural, and gas adsorption properties. Material characterization confirmed the crystallinity of COF-1 and the preservation of framework integrity after integrating the 2D nanomaterials. FT-IR spectra exhibited pronounced vibrational fingerprints of imine linkages and validated the functional groups from the COF and the integrated nanomaterials. TEM images revealed the integration of the two components, porous, layered structures with indications of interfacial interactions between COF and 2D nanosheets. Nitrogen adsorption–desorption isotherms revealed the microporous characteristics of the COFs, with hysteresis loops evident, indicating the development of supplementary mesopores at the interface between COF-1 and the 2D materials. The BET surface area of pristine COF-1 was maximal at 437 m²/g, accompanied by significant micropore and Langmuir surface areas of 348 and 1290 m²/g, respectively, offering enhanced average pore widths and hierarchical porous strcuture. CO₂ adsorption tests were investigated showing maximum adsorption capacitiy of 1.47 mmol/g, for COF-1, closely followed by COF@BN at 1.40 mmol/g, underscoring the preserved sorption capabilities of these materials. These findings demonstrate the promise of designed COF-based hybrids for gas capture, separation, and environmental remediation applications. Full article

Water pollution is a global problem that severely impacts human and environmental health, water recycling, and the economy. In Mexico, due to water scarcity, potable water contains significant amounts of heavy metals (i.e., arsenic (As)); thus, there is a need for efficient and sustainable water treatment strategies. Bismuth oxyhalides, BiOX (X = Cl, Br, I), exhibit three-dimensional (3D) porous structures suitable for efficient adsorption activity. In addition, bismuth is an abundant and biocompatible element appropriate for fabricating sustainable environmental remediation technologies, such as adsorptive BiOX nanomaterials (NMs). In this study, we examine the adsorption capacity of BiOX (X = Cl, I), BiOX-GO (GO: graphene oxide) and GO NMs to remove methylene blue (MB), methyl orange (MO) and arsenite (AsO₃³⁻) from aqueous solution. BiOCl-GO 10%, BiOI, BiOI-GO 1%, BiOI-GO 10% and GO have an enhanced adsorption capacity, removing MB (20 ppm) within one hour using a low dose of NMs (1 mg/mL). In addition, BiOX-GO NMs can be easily separated from the solution and regenerated upon visible light activation due to the photocatalytic activity of the materials. The efficiency of the NMs under study for MO removal decreases, with the GO material having the highest efficiency (96%), followed by BiOX-GO 10% (78%). BiOCl-GO 1% removes arsenic from aqueous solution at low doses and short treatment times; 5 mg As/g adsorbent takes five hours; however, at longer adsorption times (24 h), BiOI-GO 1% excels in its arsenic removal capacity. Perlite-supported BiOCl NMs exhibit a weak capacity for water treatment due to the poor mechanical strength of perlite and the amount of surface-exposed BiOCl material. For the photocatalytic removal of arsenic (oxidation–adsorption), BiOI-GO 1% excels in arsenic removal with efficiencies > 70%. Full article

Despite their outstanding thermal insulation and ultralight structure, silica aerogels suffer from inherent mechanical fragility, making the investigation of their mechanical behavior crucial for expanding their practical utility in advanced applications. To enhance their mechanical performance, this study introduces a dual-phase reinforcement strategy by anisotropically incorporating carbon nanotubes (CNTs) and graphene oxide (GO) sheets into the aerogel matrix. Using molecular dynamic simulations, we systematically investigate the tensile behavior and pore structure evolution of these hetero-structured composites. The results reveal a non-monotonic dependence of tensile strength on loading ratio, distinguishing three strain-dependent reinforcement regimes. High loading content (11.1%) significantly improves strength under low strain (0–26%), whereas low loading levels (1.8%) are more effective at preserving structural integrity under large strain (44–50%). Moderate loading (5.1%) yields balanced performance in intermediate regimes. While increasing carbon content reduces initial pore size by partially filling the framework, tensile deformation leads to interfacial debonding and the formation of larger pores due to CNT–GO hybrid structure interactions. This work elucidates a dual reinforcement mechanism—physical pore confinement and interfacial coupling—highlighting the critical role of nanostructure geometry in tuning strain-specific mechanical responses. The findings provide mechanistic insights into anisotropic nanocomposite behavior and offer guidance for designing robust porous materials for structural and functional applications. Full article

CO₂ capture by adsorption on proper solid materials appears to be a promising approach, due to its low energy requirements and ease of implementation. This study aimed to prepare efficient materials for CO₂ capture based on composites of nanocarbon and reduced graphene oxide, using graphite, L-ascorbic acid, and glycine as precursors. The materials were characterized by XRD, low-temperature N₂ adsorption, FTIR, Raman, and XPS spectroscopies, along with SEM and TEM. The CO₂ adsorption capacities, heats of adsorption, and selectivity were determined. A hierarchical porous structure was found for NC-LAA, NC/RGO-LAA, and NC/RGO-Gly. At 273 K and 100 kPa, the adsorption capacities for NC-LAA and NC-Gly reached 2.6 mmol/g and 2.5 mmol/g, respectively, while for the composites, the capacities were 1.7 mmol/g for NC/RGO-Gly and 3.5 mmol/g for NC/RGO-LAA. The adsorption ability of the glycine-derived materials is related to the presence of nitrogen-containing functional groups. The heats of adsorption for NC-LAA, NC-Gly, and NC/RGO-Gly reveal chemisorption with CO₂. Except for chemisorption, the NC/RGO-LAA material shows a sustained physical adsorption up to higher CO₂ coverage. The best adsorption of CO₂, observed for NC/RGO-LAA, is connected with the synergy between carbon dots and RGO. This composition ensures both sufficient oxygen surface functionalization and a proper hierarchical porous structure. Full article

In this study, the influence of (i) the degree of crosslinking and (ii) incorporating small amounts of graphene oxide—up to 0.2% by mass—into the matrix of ultra-porous hyaluronic acid scaffolds was analyzed in relation to their physicochemical and mechanical properties. Also studied was the effect of incorporating graphene oxide on the release profile of curcumin, a hydrophobic molecule of interest in tissue engineering, plus the potential antibacterial activity of graphene oxide against Escherichia coli, E.coli. This paper describes the development of a hybrid ultra-porous material composed of crosslinked hyaluronic acid and graphene oxide, representing a significant advance in the field of nanomedicine. The resulting material enables dual control over the release kinetics of curcumin, a compound with high pharmacological potential and neuroprotective properties. Full article

Background: In tissue engineering, developing injectable hydrogels with tailored mechanical and bioactive properties remains a challenge. This study introduces an injectable hydrogel composite for soft tissue regeneration, composed of oxidized alginate (OA) and N-succinyl chitosan (NSC) cross-linked via Schiff base reaction, reinforced with graphene oxide (GOx) and cyclic arginylglycylaspartic acid (c-RGD). The objective was to create a multifunctional platform combining injectability, bioactivity, and structural stability. Methods: The OA/NSC/GOx-cRGD hydrogel was synthesized through Schiff base cross-linking (aldehyde-amine reaction). Characterization included FTIR (C=N bond at 1650 cm⁻¹), Raman spectroscopy (D/G bands at 1338/1567 cm⁻¹), SEM (porous microstructure), and rheological analysis (shear-thinning behavior). In vitro assays assessed fibroblast viability (MTT) and macrophage TNF-α secretion (ELISA), while ex-vivo injectability and retention were evaluated using chicken cardiac tissue. Results: The hydrogel exhibited shear-thinning behavior (viscosity: 10 to <1 Pa·s) and elastic-dominated mechanics (G′ > G″), ensuring injectability. SEM revealed an interconnected porous structure mimicking native extracellular matrix. Fibroblast viability remained ≥95%, and TNF-α secretion in macrophages decreased by 80% (30 vs. 150 pg/μL in controls), demonstrating biocompatibility and anti-inflammatory effects. The hydrogel adhered stably to cardiac tissue without leakage. Conclusions: The OA/NSC/GOx-cRGD composite integrates injectability, bioactivity, and structural stability, offering a promising scaffold for tissue regeneration. Its modular design allows further functionalization with peptides or growth factors. Future work will focus on translational applications, including scalability and optimization for dynamic biological environments. Full article

All carbon-based sensors play a critical role in ensuring the sustainability of smart packaging while enabling real-time monitoring of parameters such as humidity, temperature, pressure, and strain during transit. This systematic review covers the literature between 2013 and 16 November 2024 in the Scopus, Web of Science, IEEE Xplore, and Wiley databases, focusing on carbon-based sensor materials, structural design, and fabrication technologies that contribute to maximizing the sensor performance and scalability with particular emphasis on food and pharmaceutical product packaging applications. After being subjected to the inclusion and exclusion criteria, 164 studies were included in this review. The results show that most humidity sensors are made using graphene oxide (GO), though there is some progress toward cellulose and cellulose-based materials. Graphene and carbon nanotubes (CNTs) are predominant in temperature and mechanical sensors. The application of composites with structural design (e.g., porous and 3D structures) significantly improves sensitivity, long-term stability, and multifunctionality, whereas manufacturing methods such as spray coating and 3D printing further drive production scalability. The transition from metal to carbon-based electrodes could also reduce the cost. However, the scalability, long-term stability, and real-world validation remain challenges to be addressed. Future research should further enhance the performance and scalability of carbon-based sensors through low-energy fabrication techniques and the development of sustainable advanced materials to provide solutions for practical applications in dynamic transportation environments. Full article

In this work, we developed 3D ionic liquid (IL) functionalized graphene assemblies (GAs) decorated by ultrafine RuCu alloy nanoparticles (RuCu-ANPs) via a one-step synthesis process, and integrated it into a microfluidic sensor chip for in situ electrochemical detection of NO released from living cells. Our findings have demonstrated that RuCu-ANPs on 3D IL-GA exhibit high density, uniform distribution, lattice-shaped arrangement of atoms, and extremely ultrafine size, and possess high electrocatalytic activity to NO oxidation on the electrode. Meanwhile, the 3D IL-GA with hierarchical porous structures can facilitate the efficient electron/mass transfer at the electrode/electrolyte interface and the cell culture. Moreover, the graft of IL molecules on GA endows it with high hydrophilicity for facile and well-controllable printing on the electrode. Consequently, the resultant electrochemical microfluidic sensor demonstrated excellent sensing performances including fast response time, high sensitivity, good anti-interference ability, high reproducibility, long-term stability, as well as good biocompatibility, which can be used as an on-chip sensing system for cell culture and real-time in situ electrochemical detection of NO released from living cells with accurate and stable characteristics in physiological conditions. Full article

Nickel hydroxide has ultra-high energy storage capacity in supercapacitors, but poor electrical conductivity limits their further application. The use of graphene to improve its conductivity is an effective measure, but how to suppress the stacking of graphene and improve the overall performance of composite materials has become a new challenge. In this work, a well-designed substrate of N-doped carbon nanowires with reduced graphene oxide (NCNWs/rGO) was fabricated by growing polypyrrole (PPy) nanowires between GO nanosheets layers and then calcining them at high temperatures. This NCNWs/rGO substrate can effectively avoid the stacking of rGO nanosheets, and provides sufficient sites for the subsequent in situ growth of Ni(OH)₂, forming a uniform and stable Ni(OH)₂/NCNWs/rGO composite material. Benefiting from the abundant pores, high specific surface area (107.2 m² g⁻¹), and conductive network throughout the NCNWs/rGO substrate, the deposited Ni(OH)₂ can not only realize an ultra-high loading ratio, but also exposes more active surfaces (221.3 m² g⁻¹). After a comprehensive electrochemical test, it was found that the Ni(OH)₂/NCNWs/rGO positive materials have a high specific capacitance of 2016.6 F g⁻¹ at a scan rate of 1 mV s⁻¹, and exhibit significantly better stability. The assembled Ni(OH)₂/NCNWs/rGO//AC asymmetric supercapacitor could achieve a high energy density of 85.2 Wh kg⁻¹ at power densities of 381 W kg⁻¹. In addition, the asymmetric supercapacitor has excellent stability and could retain 70.1% of initial capacitance after 10,000 cycles. These results demonstrate the feasibility of using NCNWs/rGO substrate to construct high-performance supercapacitor electrode materials, and it is also expected to be promoted in other active composite materials. Full article

A novel β-cyclodextrin–graphene oxide (β-CD/GO) composite adsorbent was synthesized via a hydrothermal method. Removal efficiency and mechanisms of typical pharmaceutical and personal care products (PPCPs) by the β-CD/GO composite were investigated in aqueous solutions. The results demonstrated that the β-CD/GO composite was successfully formed through cross-linking between β-CD and GO nanosheets, exhibiting enriched hydroxyl groups, a porous layered structure, and good thermal stability. The adsorption of cimetidine (CTD), sulfamethazine (SMZ), and diclofenac (DCF) onto the β-CD/GO composite was well described by pseudo-first-order and pseudo-second-order kinetic models, and Langmuir isotherm. The maximum adsorption capacities of CTD, SMZ, and DCF onto the β-CD/GO composite were 58.86, 35.62, and 29.11 mg g⁻¹ at 298 K, respectively. The adsorption process was rapid and reached equilibrium after 6 h. The adsorption followed a monolayer mechanism and was an exothermic process. The adsorption capacity decreased with increasing pH values and ion concentrations. The β-CD/GO composite exhibited maximum adsorption capacities of 17.69, 16.96, and 16.23 mg g⁻¹ for CTD, SMZ, and DCF, respectively, under a pH of 4 with a dosage of 1.0 g/L at 298 K for 6 h. Due to the combined impacts of electrostatic interaction, hydrogen bonding, and host–guest interaction, the adsorption of PPCPs onto β-CD/GO composite was fast and efficient. β-CD/GO composite exhibited superior adsorption efficacy and structural stability, which highlighted its promising application in the elimination of micropollutants from aqueous solutions. Full article

This review article provides a comprehensive overview of the pivotal role that nanomaterials, particularly graphene and its derivatives, play in advancing hydrogen energy technologies, with a focus on storage, production, and transport. As the quest for sustainable energy solutions intensifies, the use of nanoscale materials to store hydrogen in solid form emerges as a promising strategy toward mitigate challenges related to traditional storage methods. We begin by summarizing standard methods for producing modified graphene derivatives at the nanoscale and their impact on structural characteristics and properties. The article highlights recent advancements in hydrogen storage capacities achieved through innovative nanocomposite architectures, for example, multi-level porous graphene structures containing embedded nickel particles at nanoscale dimensions. The discussion covers the distinctive characteristics of these nanomaterials, particularly their expansive surface area and the hydrogen spillover effect, which enhance their effectiveness in energy storage applications, including supercapacitors and batteries. In addition to storage capabilities, this review explores the role of nanomaterials as efficient catalysts in the hydrogen evolution reaction (HER), emphasizing the potential of metal oxides and other composites to boost hydrogen production. The integration of nanomaterials in hydrogen transport systems is also examined, showcasing innovations that enhance safety and efficiency. As we move toward a hydrogen economy, the review underscores the urgent need for continued research aimed at optimizing existing materials and developing novel nanostructured systems. Addressing the primary challenges and potential future directions, this article aims to serve as a roadmap to enable scientists and industry experts to maximize the capabilities of nanomaterials for transforming hydrogen-based energy systems, thus contributing significantly to global sustainability efforts. Full article

Textile industry waste contains high concentrations of heavy metals such as Pb(II) and Cr(VI) that must be reduced before they are released to the environment. The adsorption method is one way to reduce the heavy metal content. In this work, we develop a porous cellulose nanofiber (CNF) aerogel modified with graphene oxide (GO) as an alternative aerogel adsorbent for Pb(II) and Cr(VI). Cellulose was extracted from banana peduncle, a biomass waste that remains largely underutilized. The addition of GO aims to increase the adsorption properties. The aerogel adsorbents were synthesized by varying the ultrasonication time to 45 min for CNF 45 and 60 min for CNF 60, and the amount of GO added to 1 mL and 2 mL. The aerogel adsorbents were successfully prepared using the freeze-drying method with CNF45, CNF60, CNF45/GO1, CNF45/GO2, CNF60/GO1, and CNF60/GO2 variations. CNF was successfully isolated from a banana peduncle with an average diameter of 44.16 nm for 45 min (CNF 45) and an average diameter of 14.6 nm for 60 min (CNF 60) of ultrasonication. Chemical treatment and ultrasonication reduced the crystallinity index value of cellulose by 73% and 61% for CNF 45 and CNF 60, respectively. CNF aerogel has a very low shrinkage rate (<7%), resulting in a larger surface area. CNF60/GO2 obtained the optimum adsorption ability for Pb(II) metal at a concentration of 100 ppm and 27.27 mg/g at 30 min. On the other hand, the adsorption ability of Cr(VI) metal was obtained by CNF60/GO2 at a concentration of 100 ppm and 13.48 mg/g at 30 min. SEM images show that all aerogel adsorbents are porous, with a porosity value range of 96–98%. In conclusion, CNF60/GO2 proved to be the most effective aerogel adsorbent, offering the potential for heavy metal removal from industrial wastewater. Full article