Gels最新文献

Mucilage extracted from cladodes of Opuntia ficus-indica (L.) Mill. has attracted growing interest as a natural food additive due to its gelling and nutritional properties. In this study, the chemical characteristics of Opuntia ficus-indica mucilage were comparatively evaluated against commercial pectin, with particular emphasis on volatile compounds, mineral composition, and monosaccharide profiles by ¹³C-NMR spectroscopic analysis. The volatile components were analysed using gas chromatography-mass spectrometry (GC-MS), revealing distinct aromatic profiles between the two matrices, with the mucilage showing a significant presence of methoxypyrazines, but not detected in the powdered pectin studied. These compounds could negatively affect the sensory perception of mucilage. Mineral analysis demonstrated significantly higher levels of calcium, magnesium, and potassium, supporting its potential contribution to nutritional enrichment. The spectroscopic analysis, used to identify monosaccharide composition of polysaccharide chains, highlighted the presence of arabinose, galactose, glucose, and rhamnose in the mucilage sample compared to the predominantly glucose/galacturonic acid-based structure of pectin. Overall, the results indicate that Opuntia ficus-indica mucilage represents a promising alternative to pectin, offering unique chemical properties that may expand its application as a multifunctional, natural food additive.

Enhanced oil recovery (EOR) in fractured reservoirs presents significant challenges due to fluid channeling and poor sweep efficiency. In this study, a synergistic EOR system was developed with polymer-based weak gel as the primary component and foam as the auxiliary enhancer. The system utilizes a low-concentration polymer (1000 mg·L^-1) that forms a weakly cross-linked three-dimensional viscoelastic gel network in the aqueous phase, inheriting the core functions of viscosity enhancement and profile control from polymer flooding. Foam acts as an auxiliary component, leveraging the high sweep efficiency and strong displacement capability of gas in fractures. These two components synergistically create a multiscale enhancement mechanism of "bulk-phase stability control and interfacial-driven displacement." Systematic screening of seven foaming agents identified an optimal formulation of 0.5% SDS and 1000 mg·L^-1 polymer. Two-dimensional visual flow experiments demonstrated that the polymer-induced gel network significantly improves mobility control and sweep efficiency under various injection volumes (0.1-0.7 PV) and gravity segregation conditions. Numerical simulation in a 3D fractured network model confirmed the superiority of this enhanced system, achieving a final oil recovery rate of 75%, significantly outperforming gas flooding (65%) and water flooding (59%). These findings confirm that weakly cross-linked polymer gels serve as the principal EOR material, with foam providing complementary reinforcement, offering robust conformance control and enhanced recovery potential in fracture-dominated reservoirs.

The regeneration of bone and the repair of large segmental bone defects represent critical challenges in regenerative medicine. Natural bone tissue is an anisotropic material characterized by an intricate gradient distribution in structure, mechanical properties, and biochemical composition; this multi-dimensional heterogeneity is crucial for maintaining its physiological functions and guiding regeneration. Although tissue engineering scaffolds have demonstrated significant potential in the treatment of bone defects, homogeneous or single-gradient scaffolds often struggle to precisely recapitulate the high degree of heterogeneity and anisotropy of natural bone from the macroscopic to the microscopic level, thereby limiting their capability in repairing complex bone defects. In recent years, biomimetic gradient scaffolds-particularly those employing multi-gradient synergistic designs that integrate physical structure, biochemical composition, and mechanical properties-have emerged as a research frontier in this field due to their ability to accurately mimic the natural bone microenvironment and regulate cellular behavior. This research aims to systematically review the latest research progress in gradient scaffolds for bone tissue engineering. First, gradient characteristics of biomimetic gradient bone scaffolds are summarized; second, the design strategies for gradient scaffolds are discussed in depth, with a focus on the applications and advantages of advanced fabrication techniques, such as additive manufacturing, in constructing multi-dimensional gradient structures; finally, based on current research findings, the emerging development trends and future research directions of biomimetic gradient bone scaffolds are outlined to provide a reference for innovative breakthroughs in the field of bone tissue engineering.

Stimuli-responsive hydrogels are an emerging class of smart materials with immense potential across biomedical engineering, soft robotics, environmental systems, and advanced manufacturing. In this review, we present an in-depth exploration of their material design, classification, fabrication strategies, and real-world applications. We examine how a wide range of external stimuli-such as temperature, pH, moisture, ions, electricity, magnetism, redox conditions, and light-interact with polymer composition and crosslinking chemistry to shape the responsive behavior of hydrogels. Special attention is given to the growing field of 4D printing, where time-dependent shape and property changes enable dynamic, programmable systems. Unlike existing reviews that often treat materials, stimuli, or applications in isolation, this work introduces a multidimensional comparative framework that connects stimulus-response behavior with fabrication techniques and end-use domains. We also highlight key challenges that limit practical deployment-including mechanical fragility, slow actuation, and scale-up difficulties-and outline engineering solutions such as hybrid material design, anisotropic structuring, and multi-stimuli integration. Our aim is to offer a forward-looking perspective that bridges material innovation with functional design, serving as a resource for researchers and engineers working to develop next-generation adaptive systems.

Eco-friendly chitosan nanogels (CSNG) with an average diameter of 48.5 nm were synthesized via alkali/urea dissolution and employed as templates for in situ silver nanoparticle fabrication. Silver nanoparticle size was controlled by adjusting CSNG to AgNO₃ mass ratios, with the optimal ratio of 18:1 producing ultrasmall particles of 3.72 nm, uniformly dispersed in the matrix. The nanocomposites demonstrated superior antibacterial activity, with inhibition zones of 14.3 mm against E. coli and 12.1 mm against S. aureus, significantly exceeding pure CSNGs at 7.4 mm and 6.9 mm, respectively. Rheological analysis revealed shear-thinning behavior, with viscosity decreasing from 450 Pa·s to 0.1 Pa·s, confirming excellent injectability. Cytotoxicity evaluation showed cell viability exceeding 82.3% at 100 μg/mL, which was substantially superior to conventional silver formulations. Thermogravimetric analysis and FTIR spectroscopy verified enhanced thermal stability and coordination interactions between chitosan and silver species. This green synthesis approach yields injectable, size-tunable nanocomposites with combined antibacterial efficacy and biocompatibility for biomedical applications.

Unconventional low-permeability reservoirs present significant production challenges due to the poor imbibition and displacement efficiency of conventional polymer fracturing fluids. The injection of nanoparticle (NP) compounds into polymer fracturing fluid base systems, such as linear gels or slickwater, has garnered significant research interest due to their superior performance. However, previous studies have primarily focused on evaluating the fluid's properties, while its imbibition and oil displacement mechanisms within reservoirs remain unclear. Herein, the imbibition mechanism of nanoparticle composite polymer fracturing fluid was systematically investigated from macro and micro perspectives using low-field nuclear magnetic resonance (LF-NMR), atomic force microscopy (AFM), interfacial rheology, and other technical means. The results showed that the imbibition recovery using polymer fracturing fluid was 10.91% higher than that achieved with conventional slickwater. Small and medium pores were identified as the primary contributors to oil drainage. Nanoparticles can be adsorbed on the rock wall in the deep reservoir to realize wettability reversal from oil-wet to water-wet, reducing crude oil adhesion. Furthermore, a strong interaction between the adsorbed NPs and cleanup agents at the oil-water interface was observed, which reduces interfacial tension to 0.95 mN·m^-1, mitigates the Jamin effect, and enhances interfacial film deformability. NPs increase the interfacial dilatational modulus from 6.0 to 14.4 mN·m^-1, accelerating fluid exchange and oil stripping. This work provides a consolidated mechanistic framework linking NP-induced interfacial modifications to enhanced pore-scale drainage, offering a scientific basis for designing next-generation fracturing fluids. We conclude that NP-compound systems hold strong potential for low-permeability reservoir development, and future efforts must focus on optimizing NP parameters for specific reservoir conditions and overcoming scalability challenges for field deployment.

Wound-related inflammatory pain is a major contributor to wound healing success and requires wound-specific therapeutic platforms with minimal systemic adverse effects. This study builds a dual-crosslinked polyvinyl alcohol (PVOH)/carboxymethyl cellulose (CMC)/gellan gum hydrogel system with optimized mechanical strength and sustained anti-inflammatory drug delivery by developing predictive mathematical models using response surface methodology with central composite design. The effects of citric acid (5-15% w/w) and dialdehyde carboxymethyl cellulose (DCMC, 0.0125-0.0375% w/w) on mechanical properties were systematically evaluated. The optimal formulation (2.23 g low-acyl gellan gum, 1.00 g high-acyl gellan gum, 0.02% DCMC, 10.21% citric acid) achieved firmness of 1.27 ± 0.06 N, rupture strength of 24.24 ± 0.52 N, and compressive strength of 41.91 ± 0.62 kPa. Curcumin oil incorporation yielded 82% cumulative release over 360 min following Korsmeyer-Peppas kinetics (R² = 0.9887, n = 0.8773). Cell viability exceeded 70% throughout the release period, confirming biocompatibility. The hydrogel strongly inhibited reactive oxygen species (ROS) and nitric oxide (NO) production in lipopolysaccharide-stimulated macrophages (p < 0.001) and enhanced macrophage migration, increasing wound closure from 40-80% (p < 0.001). This dual-crosslinked hydrogel shows great potential for localized inflammatory pain relief.

Metallogels constitute a rapidly expanding class of hybrid soft materials in which metal ions, metal complexes, or metal-containing nanoparticles play a decisive structural and functional role within a three-dimensional gel network. Their unique combination of supramolecular assembly, metal-ligand coordination, and dynamic network behaviour provides tunable mechanical, optical, electrical, redox, and catalytic properties that are not accessible in conventional hydrogels or organogels. This review systematically summarises current knowledge on metallogels, beginning with a classification based on matrix type, dominant metal interaction and functional output, spanning metallohydrogels, metal-organic gels, metal-phenolic gels, nanoparticle-based gels, polymer-based metallogels and low-molecular-weight metallogels. Key synthesis pathways are discussed, including coordination-chemistry-driven formation, metal-ligand self-assembly, in situ reduction, diffusion-mediated strategies, sol-gel-like polymerisation, enzyme-assisted routes, and bio-derived fabrication. Particular emphasis is placed on structure-function relationships that enable the development of catalytic, conductive, luminescent, antimicrobial, and biomedical metallogels. The examples compiled here highlight the versatility and transformative potential of metallogels in next-generation soft technologies, including sensing, energy conversion, wound healing, drug delivery, and emerging applications such as soft electronics and on-skin catalytic or bioactive patches. By mapping current progress and emerging design principles, this review aims to support the rational engineering of metallogels for advanced technological and biomedical applications.

Silica aerogels are critical for thermal protection in extreme environments; however, their mechanical response mechanisms under high temperatures remain elusive. This study employs large-scale molecular dynamics simulations to systematically investigate the mechanical behavior of silica aerogels (0.43-0.71 g/cm³) across a temperature range of 298-1800 K. The results reveal a fundamental competition between thermal softening and sintering-induced strengthening. Under tensile loading, the thermal softening effect dominates, leading to a significant fracture strength reduction of up to 49.6% at 1800 K, while simultaneously enhancing ductility, extending fracture strain to 80%. Conversely, under compressive loading, the sintering effect induced by temperatures above 900 K outweighs softening, resulting in a ~20% increase in the elastic modulus for high-density samples at 1300 K. Microstructural analysis attributes this enhancement to the preferential collapse of large pores and densification into an atomic-scale micropore range (0.5-1.0 nm). This work elucidates how the interplay between softening and sintering dictates material failure or strengthening, providing a microscopic theoretical basis for designing thermal shock-resistant materials for new energy batteries.

A targeted modification approach involving the synthesis of Ce/C co-doped TiO₂ aerogels (CeCTi) via a sol-gel method combined with supercritical CO₂ drying and subsequent heat treatment is employed to enhance the photocatalytic CO₂ reduction performance of cost-effective and stable TiO₂ aerogels. The results demonstrate that the CeCTi exhibits a pearl-like porous network structure, an optical band gap of 2.90 eV, and a maximum specific surface area of 188.81 m²/g. The black aerogel sample shows an enhanced light absorption capability resulting from the Ce/C co-doping, which is attributed to the formation of oxygen vacancies. Under simulated sunlight irradiation, the production rates of CH₄ and CO reach 27.06 and 97.11 μmol g^-1 h^-1 without any co-catalysts or sacrificial agents, respectively, which are 82.0 and 5.7 times higher than those of the pristine TiO₂ aerogel. DFT reveals that C-doping facilitates the formation of oxygen vacancies, which introduces defect states within the calculational band gap of TiO₂. The proposed photocatalytic mechanism involves the light-induced excitation of electrons from the valence band to the conduction band, their trapping by oxygen vacancies to prolong the charge carrier lifetime, and their subsequent transfer to adsorbed CO₂ molecules, thereby enabling efficient CO₂ reduction, which is experimentally supported by photoluminescence measurements.