Search Results (504)

Inulin, a type of fructan primarily extracted from chicory, Jerusalem artichoke, and dahlia, is a prebiotic dietary fiber increasingly valued for its multifunctional roles in food systems. Beyond its well-established nutritional benefits linked to gut microbiota modulation and metabolic health, inulin also provides unique techno-functional properties that make it a versatile structuring ingredient. This review emphasizes inulin’s ability to form gel-like networks and emulsion gels, examining the mechanisms of gelation and the influence of chain length, degree of polymerization, and processing conditions on gel stability and performance. Inulin-based gels act as effective fat replacers, texture modifiers, and carriers of bioactive compounds, supporting the reformulation of foods with reduced fat and sugar while maintaining desirable texture and sensory quality. Applications span a wide range of food systems, including dairy, meat, bakery, confectionery, plant-based, and gluten-free products, where inulin contributes to enhanced structure, stability, and palatability. Furthermore, the potential to obtain inulin from agro-industrial by-products strengthens its role in sustainable food design within a circular economy framework. By integrating nutritional, structural, and technological functionalities, inulin and inulin-based gels emerge as promising tools for the development of innovative and health-oriented food products. Full article

As styrene–butadiene rubber (SBR) is widely used and tends to age, the performance improvement in aging resistance is greatly important to rubber industrial fields. To this end, this study considered using layered double hydroxides (LDHs) as inorganic fillers and subsequently modified them by silane coupling agent KH−580 to obtain organically functionalized LDHs (m−LDHs) for solving the compatibility and aging concerns. The modified fillers were incorporated into styrene–butadiene rubber (SBR) to prepare m−LDHs/SBR composites. To evaluate their aging resistance, both SBR and m−LDHs/SBR samples were subjected to ultraviolet (UV) accelerated aging tests. Comprehensive characterizations were carried out using Fourier−transform infrared spectroscopy (FT−IR), thermogravimetric analysis (TGA), and standard mechanical property testing. FT−IR confirmed the successful grafting of KH−580 onto LDHs surfaces, while TGA demonstrated a ~50 °C increase in decomposition temperature of the modified SBR compared to the pristine sample, indicating enhanced thermal stability. Mechanical performance, including tensile strength, elongation at break, and hardness, was better retained in m−LDHs/SBR after aging, revealing the role of m−LDHs as both UV shielding and interfacial reinforcing agents. These findings highlight the potential of surface−functionalized LDHs as multifunctional fillers to enhance the durability and service lifetime of rubber materials. Full article

This work presents the development of carbon nanotubes functionalised with carboxylic acid groups (CNT-COOH) as an oxygen-sensitive electrochemical platform for parallel multi-analyte enzymatic biosensing. The platform was constructed by depositing carboxylic-acid-functionalised single-walled carbon nanotubes covalently onto nanostructured gold electrodes modified with a self-assembled monolayer of 4-aminothiophenol. Atomic force microscopy characterization revealed that the nanotubes attached via their ends to the surface and had a predominantly horizontal orientation. Glucose oxidase, lactate oxidase, glutamate oxidase, and tyrosinase were immobilised onto the electrodes to create selective biosensor for lactate, glucose, glutamate, and dopamine, respectively. A key finding is that incorporating catalase significantly extends the linear detection range for analytes by mitigating the accumulation of hydrogen peroxide. The resulting multifunctional biosensor demonstrated its capability for the simultaneous and independent measurement of glucose, lactate as the key bioanalytes under uniform conditions in blood plasma samples, highlighting its potential for applications in health and food technologies. Full article

In this work, hydrogel nanocomposites, as films, were prepared by embedding cerium oxide nanoparticles (CeO₂NPs) within xanthan gum (Xn)/poly(vinylalcohol) (PVA) matrices. Their physicochemical properties were tuned by adjusting the ratio between components and thermal treatment conditions. The cross-linking of the polymer network was confirmed by attenuated total reflectance–Fourier transform infrared (ATR-FTIR), thermal analysis, and swelling behavior. Morphological features were evaluated by atomic force microscopy (AFM), scanning electron microscopy (SEM), while optical properties were investigated by UV–Vis spectroscopy. Undoped films displayed high transparency (~80% transmittance at 400 nm), with thermal cross-linking determined only slight yellowing and negligible changes in absorption edge (300 ± 2 nm). In contrast, CeO₂NPs incorporation increased reflectance and introduced a new absorption threshold around 400 ± 2 nm, indicating nanoparticle–matrix interactions that modify optical behavior. Sorption studies with Methylene Blue (MB) and Crystal Violet (CV) dyes highlighted the influence of nanoparticle content and cross-linking on functional performance, with thermally treated samples showing the highest efficiency (~97–98% MB and 71–83% CV removal). Overall, the results demonstrate how structural tailoring and cross-linking control the characteristics of Xn/PVA/CeO₂ nanocomposites, providing insight into their design as multifunctional hydrogel materials for environmental applications. Full article

Waste cooking oil (WCO), a significant urban waste stream, presents untapped potential for synthesizing high-value materials. This study introduces an innovative “epoxidation-hydrolysis-blending” strategy to conveniently transform WCO into a highly flexible, photocurable elastomer suitable for 3D printing. Initially, WCO is converted into WCO-based hydroxy fatty acids (WHFA) via epoxidation and hydrolysis, yielding linear chains functionalized with multiple hydrogen-bonding sites. Subsequently, blending WHFA with hydroxyethyl acrylate (HEA) yields a novel photocurable WHFA/HEA elastomer. This elastomer exhibits excellent dimensional accuracy during vat photopolymerization 3D printing. Within the WHFA/HEA system, WHFA acts as a dual-functional modifier: its flexible alkyl chains enhance conformational freedom through plasticization while serving as dynamic hydrogen-bonding cross-linking sites that synergize with HEA chains to achieve unprecedented flexibility via reversible bond reconfiguration. Mechanical testing reveals that the optimized WHFA/HEA elastomer (mass ratio 1:3) exhibits ultra-high flexibility, with an elongation at break of 1184.66% (surpassing pure HEA by 360%). Furthermore, the elastomer demonstrates significant weldability (44.23% elongation retention after 12 h at 25 °C), physical reprocessability (7.60% elongation retention after two cycles), pressure-sensitive adhesion (glass interface adhesion toughness: 32.60 J/m²), and notable biodegradability (14.35% mass loss after 30-day soil burial). These properties indicate broad application potential in flexible electronics, biomedical scaffolds, and related fields. This research not only pioneers a low-cost route to multifunctional photocurable 3D printing materials but also provides a novel, sustainable solution for the high-value valorization of waste cooking oil. Full article

Pulmonary fibrosis (PF) is a progressive and fatal lung disease characterized by irreversible alveolar destruction and pathological extracellular matrix (ECM) deposition. Currently approved agents (pirfenidone and nintedanib) slow functional decline but do not reverse established fibrosis or restore functional alveoli. Multifunctional bioscaffolds present a promising therapeutic strategy through targeted modulation of critical cellular processes, including proliferation, migration, and differentiation. This review synthesizes recent advances in scaffold-based interventions for PF, with a focus on their dual mechano-epigenetic regulatory functions. We delineate how scaffold properties (elastic modulus, stiffness gradients, dynamic mechanical cues) direct cell fate decisions via mechanotransduction pathways, exemplified by focal adhesion–cytoskeleton coupling. Critically, we highlight how pathological mechanical inputs establish and perpetuate self-reinforcing epigenetic barriers to regeneration through aberrant chromatin states. Furthermore, we examine scaffolds as platforms for precision epigenetic drug delivery, particularly controlled release of inhibitors targeting DNA methyltransferases (DNMTi) and histone deacetylases (HDACi) to disrupt this mechano-reinforced barrier. Evidence from PF murine models and ex vivo lung slice cultures demonstrate scaffold-mediated remodeling of the fibrotic niche, with key studies reporting substantial reductions in collagen deposition and significant increases in alveolar epithelial cell markers following intervention. These quantitative outcomes highlight enhanced alveolar epithelial plasticity and upregulating antifibrotic gene networks. Emerging integration of stimuli-responsive biomaterials, CRISPR/dCas9-based epigenetic editors, and AI-driven design to enhance scaffold functionality is discussed. Collectively, multifunctional bioscaffolds hold significant potential for clinical translation by uniquely co-targeting mechanotransduction and epigenetic reprogramming. Future work will need to resolve persistent challenges, including the erasure of pathological mechanical memory and precise spatiotemporal control of epigenetic modifiers in vivo, to unlock their full therapeutic potential. Full article

The rapid advancement of modern infrastructure and construction industries demands cementitious materials with superior mechanical performance, durability, and sustainability, surpassing the limitations of conventional concrete. To address these challenges, carbon-based nanomaterials—including carbon nanofibers (CNFs), carbon nanotubes (CNTs), and graphene—have gained significant attention as next-generation reinforcement agents due to their exceptional strength, high aspect ratio, and unique interfacial properties. This review presents a critical analysis of the latest technological developments in carbon-enhanced cement and concrete composites, focusing on their role in achieving high-performance construction materials, as there is a shortage of reviews of cement concretes based on carbon nanoadditives. We systematically explore the underlying mechanisms, processing techniques, and structure–property relationships governing carbon-modified cementitious systems. First, we discuss advanced synthesis methods and dispersion strategies for carbon nanomaterials to ensure uniform reinforcement within the cement matrix. Subsequently, we analyze the mechanical enhancement mechanisms, including crack bridging, nucleation seeding, and interfacial bonding, supported by experimental and computational studies. Despite notable progress, challenges such as long-term durability, cost-effectiveness, and large-scale processing remain key barriers to practical implementation. Finally, we outline emerging trends, including multifunctional smart composites and sustainable hybrid systems, to guide future research toward scalable and eco-friendly solutions. By integrating fundamental insights with technological advancements, this review not only advances the understanding of carbon-reinforced cement composites but also provides strategic recommendations for their optimization and industrial adoption in next-generation construction. Full article

The success of mRNA-based SARS-CoV-2 vaccines has been confirmed in both preclinical and clinical settings. However, the development of safe and efficient mRNA vaccine delivery platforms remains challenging. In this report, PBAE-G-B-SS-modified CaO₂ nanofibers and Au@OVA@Cu@Dendrobium huoshanense polysaccharides were employed to establish novel self-assembling polymeric micelles (CaO₂@Au@OVA@Cu@DHPs) capable of serving as both an adjuvant and a delivery system for mRNA vaccines. In vitro, CaO₂@Au@OVA@Cu@DHPs nanoparticles (NPs) were conducive to effective macrophage antigen uptake and efficient antigen processing. In vivo, P-CaO₂@Au@OVA@Cu@DHPs NP administration was associated with a reduction in the ovalbumin (OVA) release rate that was conducive to the sustained induction of long-term immunity and to the production of higher levels of different IgG subtypes, suggesting that these effects were attributable to enhanced antigen uptake by antigen-presenting cells. Overall, these present data highlight the promise of these P-CaO₂@Au@OVA@Cu@DHPs NPs as an effective and safe platform amenable to vaccine delivery through their ability to provide robust adjuvant activity and sustained antigen release capable of eliciting long-term immunological memory while potentiating humoral and cellular immune responses. Full article

This paper presents the development and characteristics of geopolymer foams modified with paraffin-based phase change materials (PCMs) encapsulated in diatomite. The aim was to increase both the thermal insulation and heat storage capacity of the foams while maintaining sufficient mechanical strength for construction applications. Eleven variants of composites with different PCM fractions (5–10% by mass) and grain sizes (<1.6 mm to >2.5 mm) were synthesized and tested. The inclusion of PCM encapsulated in diatomite modified the porous structure: the total porosity increased from 6.6% in the reference sample to 19.6% for the 1.6–1.8 mm_10% wt. variant, with pore diameters ranging from ~4 to 280 µm. Thermal conductivity (λ) ranged between 0.090–0.129 W/m·K, with the lowest values observed for composites 2.0–2.5 mm_5–10% wt. (≈0.090–0.091 W/m·K), which also showed high thermal resistance (R ≈ 0.287–0.289 m²·K/W). The specific heat (Cp) increased from 1.28 kJ/kg·K (reference value) to a maximum value of 1.87 kJ/kg·K for the 2.0–2.5 mm_10% mass variant, confirming the effective energy storage capacity of PCM-modified foams. Mechanical tests showed compressive strength values in the range of 0.7–3.1 MPa. The best structural performance was obtained for the 1.6–1.8 mm_10% wt. variant (3.1 MPa), albeit with a higher λ (≈0.129 W/m·K), illustrating the classic trade-off between porosity-based insulation and mechanical strength. SEM microstructural analysis and mercury porosimetry confirmed the presence of mesopores, which determine both thermal and mechanical properties. The results show that medium-sized PCM fractions (1.6–2.0 mm) with moderate content (≈10% by weight) offer the most favorable compromise between insulation and strength, while thicker fractions (2.0–2.5 mm) maximize thermal energy storage capacity. These findings confirm the possibility of incorporating natural PCMs into geopolymer foams to create multifunctional materials for sustainable and energy-efficient building applications. A unique contribution to this work is the use of diatomite as a natural PCM carrier, ensuring stability, compatibility, and environmental friendliness compared to conventional encapsulation methods. Full article

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and one of the most pressing global health challenges. Increasing evidence highlights oxidative stress as a key factor in its pathogenesis, contributing to amyloid-β accumulation, tau hyperphosphorylation, neuroinflammation, and mitochondrial dysfunction. Oxidative stress markers, detected in the bodily fluids of AD patients, are considered promising diagnostic and prognostic tools. Despite extensive research, currently available therapies remain largely symptomatic, which emphasizes the need to develop novel, disease-modifying strategies. The aim of this review is to summarize current knowledge on the role of oxidative stress in the pathogenesis of AD and to evaluate therapeutic approaches aimed at its reduction. We discuss molecular mechanisms linking reactive oxygen species to neurodegeneration and present pharmacological strategies such as monoamine oxidase inhibitors and multifunctional agents, as well as natural antioxidants, dietary interventions, and novel therapeutic technologies. We pay particular attention to their efficacy, limitations, and translational challenges. A more profound understanding of oxidative stress-related mechanisms may facilitate the development of combined antioxidant, anti-inflammatory, and neuroprotective approaches, offering new perspectives for delaying disease progression and improving patient outcomes. Full article

This study investigates the influence of pectin and copper incorporation on the catalytic properties of Pd/ZnO catalysts in the liquid-phase hydrogenation of 2-hexyn-1-ol and photocatalytic hydrogen evolution. A series of monometallic Pd/ZnO catalysts with varying pectin contents (0–8.1 wt%) and bimetallic PdCu-Pec/ZnO catalysts with different Pd to Cu mass ratios (3:1, 1:1, 1:3) were synthesized via sequential adsorption of the polymer and metal ions onto ZnO. The catalysts were characterized using TGA, EDX, IR spectroscopy, XRD, TEM, UV–Vis DRS, and XPS. Characterization confirmed successful modification and changes in surface properties. Pectin modification improved the distribution of Pd nanoparticles on the surface of ZnO, resulting in the enhanced catalytic performance of Pd-Pec/ZnO in both hydrogenation and hydrogen evolution reactions compared to unmodified Pd/ZnO. In contrast, copper addition led to a deterioration of catalytic properties in both processes, likely due to the inhibited reduction of Pd caused by Pd–Cu interactions. Among the catalysts studied, Pd-Pec/ZnO with low pectin content (1.8 wt%) exhibited the highest activity in both reactions. The hydrogenation of 2-hexyn-1-ol to cis-2-hexen-1-ol proceeded with high selectivity (96%) at a rate (W_C≡C) of 3.3 × 10⁻⁶ mol/s, and the catalyst retained its activity over 30 consecutive runs. In the photocatalytic hydrogen evolution reaction, the rate reached 1.11 mmol/(h·g_cat) and the catalyst maintained ~94% of its initial activity after three consecutive runs. These findings demonstrate the potential of biopolymer-modified ZnO composites for the design of multifunctional catalysts combining hydrogenation and photocatalytic activity. Full article

Zeolites are widely used as solid acid catalysts and also as supports in complex multifunctional heterogeneous systems. In recent years, there has been an increase in the development of zeolite-based catalysts with hierarchical porosity combined with metal dopants (modifiers or catalysts). These modifications can significantly improve the catalytic characteristics of such materials. In this review, we discuss the application of hierarchically porous zeolites, including metal-doped ones, in catalytic reactions employed in the production and upgrading of liquid fuels, i.e., pyrolysis of biomass and polymeric wastes; conversion of alcohols to fuel hydrocarbons, aromatics and olefins; cracking and hydrocracking of polymeric wastes and hydrocarbons; and hydroisomerization. It is revealed that, in many cases, higher activity, selectivity and stability can be achieved for metal-doped hierarchical zeolites in comparison with parent ones due to control over the diffusion, surface acidity and coke deposition processes. Full article

The rehabilitation of underground infrastructure requires cement grouts that combine high injectability into micro-cracks with superior mechanical strength and durability. Conventional grouts, however, are limited by excessive yield stress and the formation of weak crystalline phases. This study investigated sodium polyacrylate (PAAS) as a multi-functional modifier to address these limitations. Through a multi-scale approach combining rheological measurements, spectroscopic analysis (FTIR, LF-NMR), diffraction (XRD), and electron microscopy (SEM), we elucidated the synergistic modification mechanisms of PAAS. The results demonstrated that PAAS operated via two pathways: (i) chemically, its carboxyl groups chelated Ca²⁺ ions, suppressing Ca(OH)₂ crystallization and refining C-S-H gel; (ii) physically, it provided electrostatic and steric dispersion, dismantling flocculated networks to reduce yield stress by 80.3% and enhance fluidity by 30.7%. This drastically improved injectability was complemented by micro-structural optimization, where PAAS eliminated percolation pores (>1 μm) and promoted a homogeneous, dense matrix. Consequently, the mechanical properties were significantly enhanced, with a 0.04% PAAS dosage maximizing compressive strength (15.56 MPa, +26.2%) and a 0.06% dosage elevating flexural strength (5.74 MPa, +29.3%). This work establishes that low-dosage PAAS modification enables a unique combination of high fluidity, strength, and durability by leveraging synergistic chemical and physical mechanisms, providing a tailored, cost-effective solution for advanced grouting applications. Full article

This paper presents the results of a rheological and spectral study characterising the change in the microstructure of lubricants depending on the type of vegetable oil base. The three lubricating compositions were prepared based on vegetable oils (rapeseed, sunflower and abyssinian), where amorphous silica of a specific particle size was used as a thickener. These three lubricating compositions were then modified by introducing the AW/EP additive (BCH 351) into their structure. Rheological tests were performed for the prepared lubricating compositions on a DWS diffusion spectrometer. Based on the tests, the dependence of ICF function values on time, MSD function values on time and G’ and G” modulus values on frequency were determined. From the collected data, rheological parameters such as the elasticity coefficient, MSD curve slope factor, diffusion coefficients and the value at which the G’ and G” curves intersect were determined, which characterise the microstructure of the tested lubricants. Raman and FTIR spectra were also performed to characterise the chemical structure of the compositions studied, and the intensity of integration of characteristic bands of vegetable greases was calculated. For vegetable greases made from different vegetable oils, a change in the value of the MSD function was observed, and the calculated value of the elasticity index indicates better viscoelastic properties for the grease made from rapeseed oil. Modification of vegetable greases with a multifunctional additive leads to a change in rheological parameters, indicating a change in the structure of the greases studied. The results of tests of diffusion coefficients for vegetable greases show a change in microstructure for greases made with different vegetable oils. Such results testify to moderately strong viscoelastic properties, leading to the conclusion that the produced greases are substances stable to changes in chemical structure depending on the base oil and modifying additive used. Raman and FTIR spectroscopy is a technique that enables changes in the chemical composition of vegetable oils to be assessed by analysing the degree of unsaturation of fatty acids in vegetable oils, making it a very good diagnostic method for quality control of lubricants based on vegetable oils. The results obtained make it possible to differentiate lubricants prepared with different vegetable oils and allow the chemical structure of the vegetable lubricants studied to be assessed on the basis of the intensity of integration of characteristic bands. Full article

Superhydrophobic surfaces, characterized by water contact angles greater than 150°, have attracted widespread interest due to their exceptional water repellency and multifunctional applications. However, traditional fabrication methods often rely on fluorinated compounds and petroleum-based polymers, raising environmental and health concerns. In response to growing environmental and health problems, recent research has increasingly focused on developing green superhydrophobic surfaces, employing eco-friendly materials, energy-efficient processes, and non-toxic modifiers. This review systematically summarizes recent progress in the development of green superhydrophobic materials, focusing on the use of natural substrates such as cellulose, chitosan, starch, lignin, and silk fibroin. Sustainable fabrication techniques, including spray coating, dip coating, sol–gel processing, electrospinning, laser texturing, and self-assembly, are critically discussed with regards to their environmental compatibility, scalability, and integration with biodegradable components. Furthermore, the functional performance of these coatings is explored in diverse application fields, including self-cleaning, oil–water separation, anti-corrosion, anti-icing, food packaging, and biomedical devices. Key challenges such as mechanical durability, substrate adhesion, and large-scale processing are addressed, alongside emerging strategies that combine green chemistry with surface engineering. This review provides a comprehensive perspective on the design and deployment of eco-friendly superhydrophobic surfaces, aiming to accelerate their practical implementation across sustainable technologies. Full article