Search Results (744)

This study employed a sol–gel route to fabricate mesoporous silica (MS) carriers capable of simultaneously encapsulating two widely utilized UV absorbers—benzophenone-3 (BP-3) and octyl methoxycinnamate (OMC)—resulting in the composite sunscreen agent S4M1B1. Comprehensive characterization using FTIR, TGA, UV–vis spectroscopy, DSC, SEM, and standard photoprotective indices (SPF and UVA-PF) confirmed the successful immobilization of both active ingredients within the MS porous structure, achieving a notably high loading of up to 72 wt%. Sunscreen formulations incorporating the encapsulated composite demonstrated superior photoprotective performance, exhibiting SPF and UVA-PF values approximately 40% higher than equivalent physical mixtures of the same actives. Additionally, the MS encapsulation significantly enhanced the photostability of BP-3 and OMC, effectively maintaining their UV-protective efficacy after prolonged simulated solar exposure. Franz glass diffusion cell assays further revealed that encapsulation markedly reduced the in vitro skin permeation of both BP-3 and OMC by over 55%, substantially diminishing transdermal absorption risks. The dual benefits of enhanced UV-protection efficiency and reduced dermal penetration underscore the composite’s potential as a safer and more effective active ingredient in cosmetic sunscreen products, with promising applications in advanced skincare and cosmeceutical formulations. Full article

The rising level of atmospheric carbon dioxide (CO₂) is a major driver of climate change, highlighting the need to develop carbon capture and storage (CCS) technologies quickly. This paper offers a comparative review of three main groups of porous adsorbent materials—zeolites, metal–organic frameworks (MOFs), and activated carbons—for their roles in CO₂ capture and long-term storage. By examining their structural features, adsorption capacities, moisture stability, and economic viability, the strengths and weaknesses of each material are assessed. Additionally, five different methods for delivering these materials into depleted oil and gas reservoirs are discussed: direct suspension injection, polymer-assisted transport, foam-assisted delivery, encapsulation with controlled release, and preformed particle gels. The potential of hybrid systems, such as MOF–carbon composites and polymer-functionalized materials, is also examined for improved selectivity and durability in underground environments. This research aims to connect materials science with subsurface engineering, helping guide the selection and use of adsorbent materials in real-world CCS applications. The findings support the optimization of CCS deployment and contribute to broader climate change efforts and the goal of achieving net-zero emissions. Key findings include CO₂ adsorption capacities of 3.5–8.0 mmol/g and surface areas up to 7000 m²/g, with MOFs demonstrating the highest uptake and activated carbons offering cost-effective performance. Full article

Graphitic carbon nitride (g-C₃N₄)-based materials hold significant promise for environmental remediation, particularly water purification, owing to their unique electronic structure, metal-free composition, and robust chemical stability. However, powdered g-C₃N₄ faces challenges such as particle aggregation, poor recyclability, and limited exposure of active sites. Structuring g-C₃N₄ into hydrogels or aerogels—three-dimensional porous networks offering high surface area, rapid mass transport, and tunable porosity—represents a transformative solution. This review comprehensively examines recent advances in g-C₃N₄-based gels, covering synthesis strategies such as crosslinking (physical/chemical), in situ polymerization, and the sol–gel and template method. Modification approaches including chemical composition and structural engineering are systematically categorized to elucidate their roles in optimizing catalytic activity, stability, and multifunctionality. Special emphasis is placed on environmental applications, including the removal of emerging contaminants and heavy metal ions, as well as solar-driven interfacial evaporation for desalination. Throughout, the critical interplay between gel structure/composition and performance is evaluated to establish design principles for next-generation materials. Finally, this review identifies current challenges regarding scalable synthesis, long-term stability, in-depth mechanistic understanding, and performance in complex real wastewater matrices. This work aims to provide valuable insights and guidance for advancing g-C₃N₄-based hydrogel and aerogel technologies in environmental applications. Full article

To address the issues of poor thermal stability, inadequate salt tolerance, and environmental risks in conventional gel systems for the development of high-temperature, high-salinity heterogeneous reservoirs, a triple-synergy gel system comprising anionic polyacrylamide (APAM), polyethyleneimine (PEI), and phenolic resin (SMP) was developed in this study. The optimal synthesis parameters—APAM of 180 mg/L, PEI:SMP = 3:1, salinity of 150,000 ppm, and temperature of 110 °C—were determined via response surface methodology, and a time–viscosity model was established. Compared with existing binary systems, the proposed gel exhibited a mass retention rate of 93.48% at 110 °C, a uniform porous structure (pore size of 2–8 μm), and structural stability under high salinity (150,000 ppm). Nuclear magnetic resonance displacement tests showed that the utilization efficiency of crude oil in 0.1–1 μm micropores increased to 21.32%. Parallel dual-core flooding experiments further confirmed the selective plugging capability in heterogeneous systems with a permeability contrast of 10:1: The high-permeability layer (500 mD) achieved a plugging rate of 98.7%, while the recovery factor of the low-permeability layer increased by 13.6%. This gel system provides a green and efficient profile control solution for deep, high-temperature, high-salinity reservoirs. Full article

This study modified corn, oat, barley, and buckwheat starches using a Henan-specific sourdough starter, revealing that the initial starch architecture governs differentiated functional transformations. Pore-dominant starches (corn/buckwheat) underwent “inside-out” enzymatic pathways—corn starch exhibited a 38.21% reduced particle size through pore expansion, with long amylopectin chain degradation forming thermally stable gels, establishing it as an ideal base for anti-staling sauces and frozen dough. Buckwheat starch demonstrated a 44% increased amylose content facilitated by porous structures, where post digestion double helix formation elevated the resistant starch (RS) content by 7%, achieving a significant 28.19% GI (Glycemic Index) reduction. Conversely, fissure-dominant starches (oat/barley) experienced “surface-inward” limited erosion—oat starch, constrained by surface cracks, showed amorphous region degradation and short-chain proliferation, accelerating glucose release and adapting it for rapid digestion products like energy bars. Barley starch primarily underwent amorphous zone modification, enhancing the pasting efficiency to provide raw materials for instant meal replacement powders. Full article

Atmospheric water harvesting, as an emerging water collection technology, is expected to mitigate water resource crises. Adsorption-based atmospheric water harvesting technology offers distinct advantages, including geographical independence and reduced reliance on ambient humidity levels. Herein, a thermoresponsive gel (PNIPAM/TO-CNF) integrated with lithium chloride was constructed to achieve accelerated moisture sorption and rapid desorption capabilities. In the designated PNIPAM/TO-CNF/LiCl gel, PNIPAM provided a temperature-responsive hydrophilic–hydrophobic transition network; the hydrophilicity and structural strength were enhanced by TO-CNF, the moisture absorption capacity was dramatically elevated by hygroscopic salt LiCl, and pore-forming agent polyethylene glycol created a favorable porous structure. This synergistic design endows the gel with an optimized hydrophilic network, temperature-responsive behavior, and a porous architecture conducive to water vapor transportation, thereby achieving rapid moisture absorption and desorption. Under 60% relative humidity, the gel exhibited a water vapor adsorption capacity of 144% within 1 h, reaching its maximum absorption capacity of 178% after 140 min. The gel exhibited an even more superior desorption performance: when heated to 70 °C, its moisture content rapidly decreased to 16% of its initial weight within 1 h, corresponding to the desorption of 91% of the total absorbed water. A simplified pore-forming methodology that enables the integration of temperature-responsive properties with efficient moisture transfer channels was reported in this paper, providing a viable design pathway for achieving accelerated adsorption–desorption cycles in atmospheric water harvesting. Full article

Vanadium-based electrode materials are limited in practical applications, due to their low energy density, cycling instability, and poor electrochemical stability. To address these limitations, a wood-derived vanadium oxide (VO_x) electrode was developed through sol–gel assembly followed by thermal annealing, in which VO_x aerogel formed within the vertically aligned wood channels, resulting in a continuous porous network to mitigate particle aggregation and enhance ion diffusion. After thermal annealing at 800 °C, V⁵⁺ partially converts to V⁴⁺, forming a mixed-valence heterostructure that significantly increases the density of redox-active sites and facilitates efficient charge transfer. The optimized VO_x@Wood-800 °C (VOW-800) electrode exhibits a high specific capacitance of 317.8 F g⁻¹ at 2 mA cm⁻² and a specific surface area of 111.22 m⁻² g⁻¹, attributed to the synergistic effects of the mixed-valence structure and the enhanced ion accessibility provided by the wood-derived porous framework. This approach offers a promising pathway for developing vanadium-based electrodes with improved charge storage capacity and interface stability. Full article

Tests during methane hydrate (MH) production in Japan have shown that excessive water production is a primary challenge in MH development. It can lead to sand production, inhibit effective reservoir depressurization, and hinder gas production. This study investigated the ability of a reactive grout, produced by the in situ reaction of CO₂ with sodium silicate (SS), to inhibit water generation from unconsolidated sand layers by forming a water-blocking gel barrier. The performance of this grout was evaluated through laboratory experiments using silica sand as a porous medium. Under controlled conditions, diluted SS and CO₂ were sequentially injected. The injection and gelation processes were monitored in real time using CT scanning, and SEM was employed to analyze the microstructure of the reaction products. The results indicated that SS exhibited piston-like flow, with elevated concentrations increasing viscosity and promoting more uniform injection. CO₂ injection resulted in successful in situ gel formation. A homogeneous gel distribution decreased permeability by ~98% when the SS concentration was 25 wt%. However, at 50 wt%, rapid localized gelation caused preferential flow paths and reduced sealing efficiency. These findings highlight the potential of CO₂ reactive grouting for water management in MH exploitation and the importance of optimizing injection parameters. Full article

Solid–liquid phase change materials (PCMs) have attracted significant attention due to their high enthalpy, which enables superior energy storage density. However, it is difficult to maintain their original shapes in a molten state. Therefore, confining PCMs within porous materials is an important method, either through mixing molten polymers and PCMs or confining PCMs in pre-prepared porous materials (e.g., aerogels). The former method is straightforward and easy to execute but its stability is severely limited, and the latter is exactly the opposite. Herein, aerogel-confined functional liquid made via in situ solid–liquid host–guest composite strategy is reported. As a proof of concept, Nylon 66 and 1,6-hexanediol are selected as the solid and liquid phases, respectively. 1,6-hexanediol not only serves as a solvent to dissolve Nylon 66 but also induces sol–gel transition during the cooling process and acts as a PCM to store energy. Unlike aerogel-supported systems requiring multi-step processing, this approach integrates porous host formation and PCM encapsulation in one step. The resulting shape-stabilized PCMs (ss-PCMs) exhibit obscure leakage, high latent heat (160 J/g), mechanical robustness (compressive modulus of 3.6 MPa), and low thermal conductivity (0.081 W/(m·K)) above 75 wt% loading of 1,6-hexanediol. These ss-PCMs enable infrared stealth by delaying thermal detection and passive thermal buffering that suppress temperature fluctuations. The in situ solid–liquid host–guest composite strategy is straightforward, being achievable through a one-pot method involving heating and cooling cycles, with high raw material utilization and minimal waste generation, thus maximizing the conversion rate of raw materials into the final product. By combining the excellent liquid retention capability of aerogels with process simplicity, this methodology opens new avenues for the development of ss-PCMs. Full article

Water pollution remains one of the most pressing global environmental challenges, posing significant threats to ecosystems and human health. Among the various pollutants, heavy metal contamination is particularly concerning, even at trace concentrations, due to its bioaccumulative and toxic effects. The Efficient detection of heavy metals is therefore essential for effective environmental monitoring and public health protection. In this study, we present the development of an advanced electrochemical sensor based on polyaniline (PANI) incorporated into a sodium alginate (SA) matrix. The PANI/SA composite was synthesized via in-situ polymerization, improving both the material’s electrical conductivity and mechanical stability. The Scanning Electron microscopy (SEM) analysis confirmed a porous, interconnected structure favorable for electrochemical activity. Excellent sensitivity, stability, selectivity and rapid response times for Pb²⁺ and Cd²⁺ detection were demonstrated by the sensor that was created by fusing the high conductivity of PANI with the biocompatibility and gel-like qualities of SA. Notably, the sensor modified with 10 µL of PANI/SA suspension achieved a sensitivity of 3.183 µA µM⁻¹ cm⁻² for Cd²⁺ detection, representing an eightfold increase compared to the sensor using 5 µL (0.394 µA µM⁻¹ cm⁻²). These results highlight the potential of the PANI/SA-based sensor for real-time and low-level heavy metal ion monitoring in environmental applications. Full article

A facile and cost-effective sol–gel method for the synthesis of uniformly porous alumina (Al₂O₃) was developed using stable CTAB/hexanol/water microemulsions as soft templates. The phase behavior of the ternary system was investigated to identify compositions that form kinetically stable microemulsions, with an optimal ratio of 7.5 wt.% CTAB, 5 wt.% hexanol, and 87.5 wt.% water exhibiting minimal droplet size variation over one week. Gelation was induced by partial neutralization to pH 4.2 with ammonium carbonate, promoting the formation of polynuclear Al species and enabling the uniform entrapment of hexanol droplets. Lyophilization preserved the porous network, and calcination at 500 °C yielded η-Al₂O₃ with a large specific surface area (~225 m²·g⁻¹) and a narrow mesopore size distribution centered around 100 nm, consistent with the original droplet size. Mercury porosimetry and SEM analyses confirmed a highly porous, low-density material (0.75 g·cm⁻³) with an interconnected pore morphology. This scalable synthesis method, supported by the high kinetic stability of the microemulsion, provides sufficient processing time and eliminates the need for post-synthesis purification. It shows strong potential for producing advanced alumina materials for use in energy storage, catalysis, and sensor applications. Full article

Porous carbon-loaded MnO was prepared via a combination of the sol–gel method and the chemical blow molding method using polyvinylpyrrolidone (PVP) and manganese nitrate as starting materials. SEM, EDX, TEM, FTIR, XRD, XPS, nitrogen adsorption–desorption, and elemental analysis were used to assess its physical and chemical characteristics. Furthermore, the adsorption property of porous carbon-loaded MnO for hexavalent chromium (Cr(VI)) in polluted water was investigated in detail. The results demonstrated that large numbers of MnO nanoparticles were evenly mounted on the surfaces of carbon walls, with a uniform distribution of C, N, and O elements. The BET surface area was 46.728 m²/g, and the pore sizes of porous carbon ranged from 2 nm to 10 nm. Additionally, abundant surface functional groups were found in porous carbon-loaded MnO, a result consistent with XPS data and applicable to the adsorption of heavy metals from aqueous solutions containing Cr(VI). The Freundlich model fitted the adsorption isotherm well, and the pseudo−second−order model precisely matched the adsorption kinetics. According to the study results, the adsorption was multilayer, and the adsorption process involved an endothermic reaction. These results indicate that this is a feasible way to synthesize a high−efficiency adsorbent for the removal of harmful heavy−metal ions from wastewater. Full article

This study aimed to develop a functional powder using whey and milk matrices, leveraging the protective capacity of chia–alginate hydrogels and the advantages of electrohydrodynamic spraying (EHDA), a non-thermal technique suitable for encapsulating probiotic cells under stress conditions commonly encountered in food processing. A hydrogel matrix composed of chia seed mucilage and sodium alginate was used to form a biopolymeric network that protected probiotic cells during processing. The encapsulation efficiency reached 99.0 ± 0.01%, and bacterial viability remained above 9.9 log₁₀ CFU/mL after lyophilization, demonstrating the excellent protective capacity of the hydrogel matrix. Microstructural analysis using confocal laser scanning microscopy (CLSM) revealed well-retained cell morphology and homogeneous distribution within the hydrogel matrix while, in contrast, scanning electron microscopy (SEM) showed spherical, porous microcapsules with distinct surface characteristics influenced by the encapsulation method. Encapsulates were incorporated into beverages flavored with red fruits and pear and subsequently freeze-dried. The resulting powders were analyzed for moisture, protein, lipids, carbohydrates, fiber, and color determinations. The results were statistically analyzed using ANOVA and response surface methodology, highlighting the impact of ingredient ratios on nutritional composition. Raman spectroscopy identified molecular features associated with casein, lactose, pectins, anthocyanins, and other functional compounds, confirming the contribution of both matrix and encapsulants maintaining the structural characteristics of the product. The presence of antioxidant bands supported the functional potential of the powder formulations. Chia–alginate hydrogels effectively encapsulated L. reuteri, maintaining cell viability and enabling their incorporation into freeze-dried beverage powders. This approach offers a promising strategy for the development of next-generation functional food gels with enhanced probiotic stability, nutritional properties, and potential application in health-promoting dairy systems. Full article

Infection control and bleeding management in deep wounds remain urgent and unmet clinical challenges that demand innovative, multifunctional, and sustainable solutions. Unlike previously reported sodium alginate and silk fibroin-based gel formulations, the present work introduces a dual-functional system combining antimicrobial and haemostatic activity in the form of conformable aerogel beads. This dual-functional formulation is designed to absorb exudate, promote clotting, and provide localized antimicrobial action, all essential for accelerating wound repair in high-risk scenarios within a single biocompatible system. Aerogel beads were obtained by supercritical drying of a silk fibroin–sodium alginate blend, resulting in highly porous, spherical structures measuring 3–4 mm in diameter. The formulations demonstrated efficient ciprofloxacin encapsulation (42.75–49.05%) and sustained drug release for up to 12 h. Fluid absorption reached up to four times their weight in simulated wound fluid and was accompanied by significantly enhanced blood clotting, outperforming a commercial haemostatic dressing. These findings highlight the potential of silk-based aerogel beads as a multifunctional wound healing platform that combines localized antimicrobial delivery, efficient fluid and exudate management, biodegradability, and superior haemostatic performance in a single formulation. This work also shows for the first time how the prilling encapsulation technique with supercritical drying is able to successfully produce silk fibroin and sodium alginate composite aerogel beads. Full article

Freshwater surimi typically exhibits poor gel-forming capability and is prone to gel deterioration, limiting its applications in food products. This study successfully prepared silver carp surimi gels with improved gel strength and water-holding capacity (WHC) using carboxymethyl konjac glucomannan (CKGM) as a functional modifier. Furthermore, the regulatory mechanism of CKGM with different degrees of substitution (DS) on the gel properties of silver carp surimi was systematically investigated. Results demonstrated that DS significantly influenced gel strength, WHC, and microstructure. CKGM (DS = 0.21%) substantially enhanced the gel strength and WHC through strengthened hydrophobic interactions and hydrogen-bond networks. However, CKGM with a higher DS (0.41%) induced a steric hindrance effect, decreasing elastic modulus and WHC and resulting in a more porous gel network. Raman spectroscopy analysis revealed that CKGM facilitated the conformational transition of myofibrillar proteins from α-helix to β-sheet, thereby improving the density of the gel network. The study provides theoretical foundations and technical guidance for the quality improvement of surimi products. Full article